Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6096 |
| ensemblid | ENSG00000198963.11 |
| hgncid | 10259 |
| symbol | RORB |
| name | RAR related orphan receptor B |
| refseq_nuc | NM_006914.4 |
| refseq_prot | NP_008845.2 |
| ensembl_nuc | ENST00000376896.8 |
| ensembl_prot | ENSP00000366093.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 74497335 |
| end | 74693177 |
| strand | + |
| ver | v1.2 |
| region | chr9:74497335-74693177 |
| region5000 | chr9:74492335-74698177 |
| regionname0 | RORB_chr9_74497335_74693177 |
| regionname5000 | RORB_chr9_74492335_74698177 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 459 | 224 | 69 | 46 | 79 | 8 | 20 | 59 | RORB_chr9_74492335_74698177 | RORB | MRAQI others(454): Show |
chr9 | 74492335 | 74698177 |
| a0002 | 0/0 | 459 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | MRAQI others(454): Show |
chr9 | 74492335 | 74698177 |
| a0003 | 0/0 | 459 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | MRAQI others(454): Show |
chr9 | 74492335 | 74698177 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1377 | 194 | 67 | 37 | 64 | 6 | 18 | RORB_chr9_74492335_74698177 | RORB | ATGCG others(1372): Show |
chr9 | 74492335 | 74698177 | ||
| a0001c0002 | 0/0 | 1377 | 29 | 2 | 8 | 15 | 2 | 2 | RORB_chr9_74492335_74698177 | RORB | ATGCG others(1372): Show |
chr9 | 74492335 | 74698177 | ||
| a0001c0005 | 0/0 | 1377 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATGCG others(1372): Show |
chr9 | 74492335 | 74698177 | ||
| a0002c0004 | 0/0 | 1377 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATGCG others(1372): Show |
chr9 | 74492335 | 74698177 | ||
| a0003c0003 | 0/0 | 1377 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATGCG others(1372): Show |
chr9 | 74492335 | 74698177 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 9581 | 60 | 10 | 15 | 22 | 4 | 9 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0002 | 0/0 | 9582 | 14 | 1 | 2 | 9 | 0 | 2 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0003 | 0/0 | 9581 | 3 | 1 | 0 | 0 | 1 | 1 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0004 | 0/0 | 9581 | 10 | 4 | 3 | 2 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0005 | 0/0 | 9582 | 5 | 0 | 0 | 5 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0006 | 0/1 | 9582 | 7 | 1 | 4 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0007 | 0/0 | 9581 | 7 | 6 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0008 | 0/0 | 9582 | 5 | 0 | 0 | 5 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0009 | 0/0 | 9582 | 4 | 0 | 1 | 3 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0010 | 0/0 | 9581 | 4 | 4 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0011 | 0/0 | 9581 | 3 | 0 | 2 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0012 | 0/0 | 9581 | 4 | 3 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0013 | 0/0 | 9578 | 4 | 4 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9573): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0014 | 0/0 | 9578 | 4 | 4 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9573): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0015 | 0/0 | 9581 | 3 | 3 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0016 | 1/0 | 9581 | 3 | 2 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0017 | 0/0 | 9581 | 3 | 3 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0018 | 0/0 | 9581 | 3 | 2 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0019 | 0/0 | 9581 | 3 | 3 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0020 | 0/0 | 9581 | 2 | 2 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0021 | 0/0 | 9581 | 2 | 2 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0022 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0024 | 0/0 | 9581 | 2 | 0 | 0 | 1 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0025 | 0/0 | 9582 | 2 | 0 | 0 | 2 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0026 | 0/0 | 9582 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0027 | 0/0 | 9581 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0028 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0029 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0031 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0032 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0033 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0034 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0035 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0036 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0037 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0038 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0039 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0040 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0041 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0042 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0043 | 0/0 | 9581 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0044 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0045 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0046 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0047 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0048 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0049 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0050 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0051 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0052 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0053 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0054 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0055 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0056 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9573): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0057 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0059 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9573): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0062 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0063 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9556): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0064 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0001t0066 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0001 | 0/0 | 9581 | 3 | 0 | 1 | 0 | 2 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0002 | 0/0 | 9582 | 4 | 0 | 0 | 4 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0003 | 0/0 | 9581 | 9 | 0 | 1 | 7 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0004 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0005 | 0/0 | 9582 | 3 | 0 | 0 | 3 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0009 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0011 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0022 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0023 | 0/0 | 9581 | 2 | 0 | 1 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0058 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0060 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0061 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0002t0065 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0001c0005t0006 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0002c0004t0030 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9577): Show |
chr9 | 74492335 | 74698177 |
| a0003c0003t0001 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | ATCTC others(9576): Show |
chr9 | 74492335 | 74698177 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0103 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0009g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0009g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0010g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0010g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0010g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0010g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0011g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0011g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0011g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0012g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0012g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0012g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0013g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0013g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0014g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0014g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0015g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0015g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0016g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0016g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0017g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0017g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0017g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0018g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0018g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0018g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0019g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0019g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0019g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0020g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0020g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0021g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0021g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0022g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0024g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0024g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0025g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0025g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0026g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0027g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0028g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0029g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0031g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0032g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0033g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0034g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0035g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0036g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0037g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0038g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0039g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0040g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0041g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0042g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0043g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0044g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0045g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0046g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0047g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0048g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0049g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0050g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0051g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0052g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0053g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0054g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0055g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0056g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0057g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0059g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0062g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0063g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0064g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0066g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0005g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0009g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0011g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0022g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0023g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0023g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0058g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0060g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0061g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0065g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0005t0006g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0002c0004t0030g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0047 | EUR | GBR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00323 | hp1 | a0001 | c0001 | t0027 | g0082 | EUR | FIN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | FIN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00408 | hp2 | a0001 | c0001 | t0025 | g0217 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00597 | hp1 | a0001 | c0001 | t0008 | g0078 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00609 | hp1 | a0001 | c0001 | t0025 | g0054 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0165 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0214 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0127 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0181 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0063 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0126 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01081 | hp1 | a0001 | c0002 | t0061 | g0045 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0102 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0172 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01109 | hp1 | a0001 | c0001 | t0041 | g0074 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01168 | hp1 | a0001 | c0005 | t0006 | g0218 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01168 | hp2 | a0001 | c0001 | t0018 | g0018 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01175 | hp2 | a0001 | c0002 | t0023 | g0215 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01192 | hp1 | a0001 | c0001 | t0036 | g0150 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01243 | hp1 | a0001 | c0001 | t0066 | g0182 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0212 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0100 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01256 | hp1 | a0001 | c0001 | t0031 | g0121 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0084 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01433 | hp2 | a0001 | c0002 | t0011 | g0123 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01496 | hp1 | a0001 | c0001 | t0064 | g0101 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0152 | EUR | IBS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01884 | hp1 | a0001 | c0001 | t0056 | g0220 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01891 | hp1 | a0001 | c0001 | t0040 | g0022 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01891 | hp2 | a0001 | c0001 | t0042 | g0155 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01975 | hp1 | a0001 | c0001 | t0022 | g0069 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01975 | hp2 | a0001 | c0002 | t0009 | g0116 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01978 | hp1 | a0001 | c0001 | t0048 | g0144 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01981 | hp1 | a0001 | c0001 | t0011 | g0179 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02004 | hp1 | a0001 | c0001 | t0009 | g0070 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0023 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02080 | hp2 | a0001 | c0001 | t0024 | g0176 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02135 | hp1 | a0001 | c0001 | t0045 | g0061 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02135 | hp2 | a0001 | c0001 | t0044 | g0187 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02148 | hp1 | a0001 | c0002 | t0022 | g0028 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02155 | hp1 | a0001 | c0001 | t0050 | g0145 | EAS | CDX | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02155 | hp2 | a0001 | c0001 | t0032 | g0076 | EAS | CDX | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02257 | hp1 | a0001 | c0001 | t0018 | g0030 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02258 | hp2 | a0001 | c0001 | t0057 | g0037 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02280 | hp1 | a0001 | c0001 | t0038 | g0162 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02280 | hp2 | a0001 | c0002 | t0058 | g0109 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02293 | hp1 | a0001 | c0002 | t0004 | g0027 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0021 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0091 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02523 | hp2 | a0001 | c0001 | t0029 | g0057 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0160 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0210 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02622 | hp2 | a0001 | c0001 | t0014 | g0019 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0213 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02630 | hp2 | a0001 | c0001 | t0014 | g0010 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02647 | hp1 | a0001 | c0001 | t0054 | g0163 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02647 | hp2 | a0001 | c0001 | t0012 | g0211 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02698 | hp1 | a0001 | c0002 | t0023 | g0044 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0096 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02723 | hp1 | a0001 | c0001 | t0016 | g0099 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0224 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0137 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0158 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0004 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0015 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02895 | hp1 | a0001 | c0001 | t0020 | g0139 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02895 | hp2 | a0001 | c0001 | t0021 | g0003 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0110 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02897 | hp2 | a0001 | c0001 | t0020 | g0138 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02965 | hp1 | a0001 | c0002 | t0060 | g0016 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0051 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0107 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02970 | hp2 | a0002 | c0004 | t0030 | g0014 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02976 | hp1 | a0001 | c0001 | t0010 | g0143 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02976 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03017 | hp1 | a0001 | c0001 | t0043 | g0048 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0024 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03041 | hp1 | a0001 | c0001 | t0052 | g0147 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0036 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03098 | hp2 | a0001 | c0001 | t0051 | g0203 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0086 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0111 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0052 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03209 | hp2 | a0001 | c0001 | t0015 | g0142 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03225 | hp1 | a0001 | c0001 | t0019 | g0090 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0159 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03453 | hp1 | a0001 | c0001 | t0017 | g0141 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03453 | hp2 | a0001 | c0001 | t0021 | g0112 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03486 | hp1 | a0001 | c0001 | t0059 | g0205 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03516 | hp2 | a0001 | c0001 | t0046 | g0094 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03579 | hp1 | a0001 | c0001 | t0047 | g0087 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0221 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0038 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03927 | hp2 | a0001 | c0001 | t0024 | g0095 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04115 | hp2 | a0001 | c0001 | t0011 | g0207 | SAS | STU | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04199 | hp1 | a0001 | c0001 | t0026 | g0186 | SAS | STU | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0124 | SAS | STU | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0209 | SAS | STU | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0065 | SAS | STU | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18747 | hp1 | a0001 | c0002 | t0003 | g0042 | EAS | CHB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | CHB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0020 | AFR | YRI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | YRI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0092 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18947 | hp2 | a0001 | c0001 | t0034 | g0064 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18952 | hp1 | a0001 | c0001 | t0009 | g0075 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18960 | hp1 | a0001 | c0001 | t0028 | g0188 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18960 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18965 | hp1 | a0001 | c0002 | t0003 | g0026 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18965 | hp2 | a0003 | c0003 | t0001 | g0194 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18969 | hp1 | a0001 | c0001 | t0009 | g0025 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18983 | hp1 | a0001 | c0001 | t0037 | g0184 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18999 | hp1 | a0001 | c0001 | t0033 | g0079 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19001 | hp1 | a0001 | c0001 | t0063 | g0197 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19001 | hp2 | a0001 | c0001 | t0039 | g0033 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19002 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0169 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19010 | hp1 | a0001 | c0001 | t0049 | g0105 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19010 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19043 | hp1 | a0001 | c0001 | t0018 | g0089 | AFR | LWK | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | LWK | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0050 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0196 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19060 | hp2 | a0001 | c0001 | t0035 | g0146 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19062 | hp1 | a0001 | c0002 | t0065 | g0031 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19064 | hp2 | a0001 | c0001 | t0008 | g0131 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0130 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0041 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19076 | hp1 | a0001 | c0001 | t0062 | g0104 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19078 | hp1 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19082 | hp1 | a0001 | c0002 | t0003 | g0164 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19087 | hp1 | a0001 | c0002 | t0005 | g0077 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19087 | hp2 | a0001 | c0001 | t0053 | g0174 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0097 | AFR | YRI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19240 | hp2 | a0001 | c0001 | t0016 | g0029 | AFR | YRI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0170 | EUR | TSI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | TSI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | USA | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG06807 | hp2 | a0001 | c0001 | t0055 | g0017 | AFR | USA | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | USA | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | USA | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0103 | REF | REF | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0016 | g0204 | REF | REF | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:74642766 | C | A | 1 | a0003 | 1 | NA18965.hp2 | missense_variant | MODERATE | c.588C>A | p.Ser196Arg | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/10 | 1230/9581 | 588/1380 | 196/459 | chr9 | 74642766 | |||
| chr9:74665542 | A | G | 1 | a0002 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.947A>G | p.Asn316Ser | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/10 | 1589/9581 | 947/1380 | 316/459 | chr9 | 74665542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:74630349 | C | T | 1 | a0001c0005 | 1 | HG01168.hp1 | synonymous_variant | LOW | c.75C>T | p.Ile25Ile | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/10 | 717/9581 | 75/1380 | 25/459 | chr9 | 74630349 | |||
| chr9:74642430 | G | A | 1 | a0001c0002 | 29 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(26): Show |
synonymous_variant | LOW | c.252G>A | p.Arg84Arg | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/10 | 894/9581 | 252/1380 | 84/459 | chr9 | 74642430 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:74497507 | C | T | 1 | a0001c0001t0019 | 3 | HG02451.hp2 HG03130.hp1 HG03225.hp1 |
5_prime_UTR_variant | MODIFIER | c.-470C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/10 | 470 | chr9 | 74497507 | ||||||
| chr9:74497790 | A | G | 1 | a0001c0001t0066 | 1 | HG01243.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-187A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/10 | chr9 | 74497790 | |||||||
| chr9:74685648 | G | A | 1 | a0001c0001t0026 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 30 | chr9 | 74685648 | ||||||
| chr9:74685732 | C | T | 2 | a0001c0001t0025 a0001c0002t0065 |
3 | HG00408.hp2 HG00609.hp1 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*114C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 114 | chr9 | 74685732 | ||||||
| chr9:74686073 | G | T | 1 | a0001c0001t0024 | 2 | HG02080.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*455G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 455 | chr9 | 74686073 | ||||||
| chr9:74686229 | T | C | 1 | a0001c0001t0027 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 611 | chr9 | 74686229 | ||||||
| chr9:74686246 | A | G | 1 | a0001c0001t0018 | 3 | HG01168.hp2 HG02257.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*628A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 628 | chr9 | 74686246 | ||||||
| chr9:74686388 | C | T | 11 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0025 others(8): Show |
31 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*770C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 770 | chr9 | 74686388 | ||||||
| chr9:74686593 | T | C | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0028 others(7): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*975T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 975 | chr9 | 74686593 | ||||||
| chr9:74686858 | A | C | 8 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0057 others(5): Show |
19 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1240A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 1240 | chr9 | 74686858 | ||||||
| chr9:74686982 | T | C | 1 | a0001c0001t0035 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1364T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 1364 | chr9 | 74686982 | ||||||
| chr9:74687266 | C | G | 5 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0055 others(2): Show |
11 | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1648C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 1648 | chr9 | 74687266 | ||||||
| chr9:74687356 | G | A | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0028 others(7): Show |
20 | HG00597.hp1 HG01192.hp1 HG01256.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1738G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 1738 | chr9 | 74687356 | ||||||
| chr9:74687357 | T | C | 1 | a0001c0001t0024 | 2 | HG02080.hp2 HG03927.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1739T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 1739 | chr9 | 74687357 | ||||||
| chr9:74687455 | A | G | 1 | a0001c0001t0054 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1837A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 1837 | chr9 | 74687455 | ||||||
| chr9:74687920 | T | C | 1 | a0001c0002t0060 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2302T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 2302 | chr9 | 74687920 | ||||||
| chr9:74688102 | A | G | 1 | a0001c0001t0053 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2484A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 2484 | chr9 | 74688102 | ||||||
| chr9:74688368 | C | T | 4 | a0001c0001t0008 a0001c0001t0032 a0001c0001t0033 others(1): Show |
8 | HG00597.hp1 HG01192.hp1 HG02155.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2750C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 2750 | chr9 | 74688368 | ||||||
| chr9:74688447 | C | T | 4 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0051 others(1): Show |
8 | HG02451.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2829C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 2829 | chr9 | 74688447 | ||||||
| chr9:74688584 | T | TA | 30 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(27): Show |
71 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*2978dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 2979 | INFO_REALIGN_3_PRIME | chr9 | 74688584 | |||||
| chr9:74688941 | A | G | 1 | a0001c0001t0033 | 1 | NA18999.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3323A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 3323 | chr9 | 74688941 | ||||||
| chr9:74689027 | C | G | 1 | a0001c0001t0063 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3409C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 3409 | chr9 | 74689027 | ||||||
| chr9:74689028 | C | G | 1 | a0001c0001t0063 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3410C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 3410 | chr9 | 74689028 | ||||||
| chr9:74689049 | ATATGCCC others(24): Show |
A | 1 | a0001c0001t0063 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3433_*3463delATGC others(27): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 3433 | INFO_REALIGN_3_PRIME | chr9 | 74689049 | |||||
| chr9:74689107 | T | TTTTGTGG others(3): Show |
1 | a0001c0001t0063 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3492_*3493insGTGG others(6): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 3493 | INFO_REALIGN_3_PRIME | chr9 | 74689107 | |||||
| chr9:74689252 | C | T | 1 | a0001c0001t0021 | 2 | HG02895.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3634C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 3634 | chr9 | 74689252 | ||||||
| chr9:74689294 | G | A | 2 | a0001c0001t0015 a0001c0001t0054 |
4 | HG02647.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3676G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 3676 | chr9 | 74689294 | ||||||
| chr9:74689372 | A | G | 4 | a0001c0001t0003 a0001c0001t0031 a0001c0002t0003 others(1): Show |
15 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3754A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 3754 | chr9 | 74689372 | ||||||
| chr9:74689395 | C | T | 10 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0028 others(7): Show |
20 | HG00597.hp1 HG01192.hp1 HG01256.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3777C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 3777 | chr9 | 74689395 | ||||||
| chr9:74689724 | A | G | 7 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0050 others(4): Show |
18 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*4106A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4106 | chr9 | 74689724 | ||||||
| chr9:74689751 | A | G | 1 | a0001c0001t0049 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4133A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4133 | chr9 | 74689751 | ||||||
| chr9:74689760 | T | C | 9 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0038 others(6): Show |
20 | HG00609.hp2 HG00738.hp1 HG01081.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4142T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4142 | chr9 | 74689760 | ||||||
| chr9:74689766 | C | T | 1 | a0001c0002t0065 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4148C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4148 | chr9 | 74689766 | ||||||
| chr9:74689952 | CTCTT | C | 4 | a0001c0001t0013 a0001c0001t0014 a0001c0001t0056 others(1): Show |
10 | HG01884.hp1 HG02451.hp1 HG02622.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4336_*4339delCTTT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4336 | INFO_REALIGN_3_PRIME | chr9 | 74689952 | |||||
| chr9:74690037 | A | G | 1 | a0001c0001t0048 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4419A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4419 | chr9 | 74690037 | ||||||
| chr9:74690060 | C | T | 3 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0052 |
7 | HG02451.hp2 HG02970.hp1 HG03041.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4442C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4442 | chr9 | 74690060 | ||||||
| chr9:74690200 | A | G | 1 | a0001c0001t0047 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4582A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4582 | chr9 | 74690200 | ||||||
| chr9:74690333 | G | A | 4 | a0001c0001t0013 a0001c0001t0015 a0001c0001t0038 others(1): Show |
9 | HG02280.hp1 HG02886.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4715G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4715 | chr9 | 74690333 | ||||||
| chr9:74690383 | G | A | 1 | a0001c0001t0039 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4765G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4765 | chr9 | 74690383 | ||||||
| chr9:74690469 | T | C | 2 | a0001c0001t0010 a0001c0001t0040 |
5 | HG01891.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4851T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4851 | chr9 | 74690469 | ||||||
| chr9:74690553 | G | A | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(39): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*4935G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4935 | chr9 | 74690553 | ||||||
| chr9:74690564 | G | A | 42 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(39): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*4946G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 4946 | chr9 | 74690564 | ||||||
| chr9:74690675 | A | G | 2 | a0001c0001t0046 a0001c0002t0058 |
2 | HG02280.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5057A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5057 | chr9 | 74690675 | ||||||
| chr9:74690779 | A | C | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0025 others(8): Show |
37 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5161A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5161 | chr9 | 74690779 | ||||||
| chr9:74690860 | T | C | 34 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0009 others(31): Show |
111 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*5242T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5242 | chr9 | 74690860 | ||||||
| chr9:74690875 | G | A | 74 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(71): Show |
220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*5257G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5257 | chr9 | 74690875 | ||||||
| chr9:74691017 | T | C | 13 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0017 others(10): Show |
27 | HG00597.hp1 HG01192.hp1 HG01256.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*5399T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5399 | chr9 | 74691017 | ||||||
| chr9:74691117 | C | A | 1 | a0001c0002t0058 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5499C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5499 | chr9 | 74691117 | ||||||
| chr9:74691284 | G | A | 1 | a0001c0001t0031 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5666G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5666 | chr9 | 74691284 | ||||||
| chr9:74691300 | T | C | 4 | a0001c0001t0017 a0001c0001t0019 a0001c0001t0051 others(1): Show |
8 | HG02451.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*5682T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5682 | chr9 | 74691300 | ||||||
| chr9:74691465 | C | T | 2 | a0001c0001t0046 a0001c0002t0058 |
2 | HG02280.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5847C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5847 | chr9 | 74691465 | ||||||
| chr9:74691590 | A | G | 1 | a0001c0001t0043 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5972A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 5972 | chr9 | 74691590 | ||||||
| chr9:74691758 | C | T | 1 | a0001c0001t0052 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6140C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 6140 | chr9 | 74691758 | ||||||
| chr9:74691923 | A | G | 2 | a0001c0001t0011 a0001c0002t0011 |
4 | HG01106.hp2 HG01433.hp2 HG01981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6305A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 6305 | chr9 | 74691923 | ||||||
| chr9:74692085 | T | C | 2 | a0001c0001t0010 a0001c0001t0038 |
5 | HG02280.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6467T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 6467 | chr9 | 74692085 | ||||||
| chr9:74692329 | A | G | 6 | a0001c0001t0014 a0001c0001t0017 a0001c0001t0019 others(3): Show |
13 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*6711A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 6711 | chr9 | 74692329 | ||||||
| chr9:74692892 | A | G | 2 | a0001c0001t0037 a0001c0001t0062 |
2 | NA18983.hp1 NA19076.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7274A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 7274 | chr9 | 74692892 | ||||||
| chr9:74692911 | T | C | 1 | a0001c0001t0041 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7293T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 7293 | chr9 | 74692911 | ||||||
| chr9:74692924 | T | C | 1 | a0001c0001t0020 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7306T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 7306 | chr9 | 74692924 | ||||||
| chr9:74693133 | T | C | 74 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(71): Show |
220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*7515T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 7515 | chr9 | 74693133 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:74498003 | C | A | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+20C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498003 | |||||||
| chr9:74498003 | C | T | 5 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(2): Show |
5 | HG01884.hp1 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+20C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498003 | |||||||
| chr9:74498066 | A | T | 2 | a0001c0001t0001g0219 a0001c0005t0006g0218 |
2 | HG01168.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.7+83A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498066 | |||||||
| chr9:74498198 | A | G | 1 | a0001c0001t0025g0217 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.7+215A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498198 | |||||||
| chr9:74498328 | G | T | 1 | a0001c0002t0002g0216 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.7+345G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498328 | |||||||
| chr9:74498386 | G | A | 1 | a0001c0001t0001g0005 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.7+403G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498386 | |||||||
| chr9:74498412 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0007g0008 others(2): Show |
5 | HG02630.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+429G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498412 | |||||||
| chr9:74498668 | G | A | 1 | a0001c0001t0005g0011 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.7+685G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498668 | |||||||
| chr9:74498680 | T | A | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+697T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498680 | |||||||
| chr9:74498859 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7+876G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498859 | |||||||
| chr9:74498866 | A | G | 8 | a0001c0001t0007g0213 a0001c0001t0010g0004 a0001c0001t0012g0210 others(5): Show |
8 | HG00738.hp1 HG01175.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+883A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498866 | |||||||
| chr9:74498925 | G | A | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG01884.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+942G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498925 | |||||||
| chr9:74498962 | C | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+979C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498962 | |||||||
| chr9:74498976 | T | G | 4 | a0001c0001t0007g0013 a0001c0001t0015g0015 a0001c0002t0060g0016 others(1): Show |
4 | HG02886.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+993T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74498976 | |||||||
| chr9:74499026 | T | C | 5 | a0001c0001t0014g0019 a0001c0001t0014g0020 a0001c0001t0014g0021 others(2): Show |
5 | HG01168.hp2 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+1043T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74499026 | |||||||
| chr9:74499096 | C | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+1113C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74499096 | |||||||
| chr9:74499097 | T | C | 171 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
172 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.7+1114T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74499097 | |||||||
| chr9:74499127 | T | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+1144T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74499127 | |||||||
| chr9:74499242 | G | A | 1 | a0001c0001t0040g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.7+1259G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74499242 | |||||||
| chr9:74499331 | C | T | 2 | a0001c0002t0003g0164 a0001c0002t0003g0165 |
2 | HG00609.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.7+1348C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74499331 | |||||||
| chr9:74499358 | G | A | 98 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0043 others(95): Show |
99 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.7+1375G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74499358 | |||||||
| chr9:74499508 | A | G | 4 | a0001c0001t0013g0110 a0001c0001t0015g0111 a0001c0001t0021g0112 others(1): Show |
4 | HG01891.hp1 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+1525A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74499508 | |||||||
| chr9:74499773 | A | G | 8 | a0001c0001t0007g0213 a0001c0001t0010g0004 a0001c0001t0012g0210 others(5): Show |
8 | HG00738.hp1 HG01175.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+1790A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74499773 | |||||||
| chr9:74500010 | C | T | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7+2027C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74500010 | |||||||
| chr9:74500088 | A | G | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+2105A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74500088 | |||||||
| chr9:74500125 | G | A | 27 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0114 others(24): Show |
27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.7+2142G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74500125 | |||||||
| chr9:74500195 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+2212G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74500195 | |||||||
| chr9:74500213 | T | C | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+2230T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74500213 | |||||||
| chr9:74500302 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0010g0160 a0001c0001t0038g0162 |
3 | HG02280.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+2319A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74500302 | |||||||
| chr9:74500443 | G | T | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+2460G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74500443 | |||||||
| chr9:74500765 | G | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+2782G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74500765 | |||||||
| chr9:74501014 | A | G | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+3031A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74501014 | |||||||
| chr9:74501045 | G | T | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+3062G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74501045 | |||||||
| chr9:74501080 | G | A | 3 | a0001c0001t0001g0161 a0001c0001t0010g0160 a0001c0001t0038g0162 |
3 | HG02280.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+3097G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74501080 | |||||||
| chr9:74501158 | G | T | 3 | a0001c0001t0014g0019 a0001c0001t0014g0020 a0001c0001t0014g0021 |
3 | HG02451.hp1 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7+3175G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74501158 | |||||||
| chr9:74501166 | G | T | 1 | a0001c0001t0021g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.7+3183G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74501166 | |||||||
| chr9:74501755 | GA | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+3773delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74501755 | |||||||
| chr9:74501933 | A | G | 1 | a0001c0001t0001g0108 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.7+3950A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74501933 | |||||||
| chr9:74502015 | A | T | 1 | a0001c0001t0006g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.7+4032A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74502015 | |||||||
| chr9:74502116 | T | C | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG01884.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+4133T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74502116 | |||||||
| chr9:74502139 | G | A | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7+4156G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74502139 | |||||||
| chr9:74502299 | A | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.7+4316A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74502299 | |||||||
| chr9:74502756 | C | G | 8 | a0001c0001t0007g0213 a0001c0001t0010g0004 a0001c0001t0012g0210 others(5): Show |
8 | HG00738.hp1 HG01175.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+4773C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74502756 | |||||||
| chr9:74503014 | A | T | 1 | a0001c0001t0001g0136 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.7+5031A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74503014 | |||||||
| chr9:74503072 | G | A | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7+5089G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74503072 | |||||||
| chr9:74503091 | T | C | 1 | a0001c0001t0009g0023 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.7+5108T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74503091 | |||||||
| chr9:74503415 | A | C | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.7+5432A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74503415 | |||||||
| chr9:74503540 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.7+5557C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74503540 | |||||||
| chr9:74503610 | A | G | 1 | a0001c0001t0017g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7+5627A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74503610 | |||||||
| chr9:74503661 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+5678A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74503661 | |||||||
| chr9:74503975 | T | A | 1 | a0001c0001t0003g0024 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.7+5992T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74503975 | |||||||
| chr9:74504028 | T | C | 1 | a0001c0001t0009g0025 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.7+6045T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74504028 | |||||||
| chr9:74504045 | A | G | 6 | a0001c0001t0007g0213 a0001c0001t0010g0004 a0001c0001t0012g0210 others(3): Show |
6 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+6062A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74504045 | |||||||
| chr9:74504071 | C | T | 27 | a0001c0001t0001g0012 a0001c0001t0001g0113 a0001c0001t0001g0114 others(24): Show |
27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.7+6088C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74504071 | |||||||
| chr9:74504412 | T | C | 1 | a0001c0001t0014g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+6429T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74504412 | |||||||
| chr9:74504414 | T | C | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+6431T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74504414 | |||||||
| chr9:74504447 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0011g0207 |
2 | HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.7+6464C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74504447 | |||||||
| chr9:74504632 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.7+6649T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74504632 | |||||||
| chr9:74504729 | C | G | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+6746C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74504729 | |||||||
| chr9:74504858 | G | A | 3 | a0001c0002t0003g0026 a0001c0002t0004g0027 a0001c0002t0022g0028 |
3 | HG02148.hp1 HG02293.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.7+6875G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74504858 | |||||||
| chr9:74505054 | T | C | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | NA18944.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.7+7071T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74505054 | |||||||
| chr9:74505116 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.7+7133T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74505116 | |||||||
| chr9:74505131 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.7+7148G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74505131 | |||||||
| chr9:74505481 | G | C | 2 | a0001c0001t0016g0029 a0001c0001t0018g0030 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7+7498G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74505481 | |||||||
| chr9:74505916 | A | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+7933A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74505916 | |||||||
| chr9:74505991 | C | A | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7+8008C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74505991 | |||||||
| chr9:74506217 | C | T | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7+8234C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74506217 | |||||||
| chr9:74506342 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.7+8359C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74506342 | |||||||
| chr9:74506462 | A | G | 1 | a0001c0001t0008g0106 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.7+8479A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74506462 | |||||||
| chr9:74506768 | G | A | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.7+8785G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74506768 | |||||||
| chr9:74506781 | A | G | 1 | a0001c0001t0049g0105 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.7+8798A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74506781 | |||||||
| chr9:74507074 | C | T | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+9091C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74507074 | |||||||
| chr9:74507079 | T | G | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+9096T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74507079 | |||||||
| chr9:74507503 | C | A | 1 | a0001c0002t0065g0031 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.7+9520C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74507503 | |||||||
| chr9:74508156 | T | C | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+10173T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74508156 | |||||||
| chr9:74508275 | C | A | 1 | a0001c0001t0001g0032 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7+10292C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74508275 | |||||||
| chr9:74508412 | A | G | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+10429A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74508412 | |||||||
| chr9:74508473 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+10490T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74508473 | |||||||
| chr9:74508564 | G | T | 1 | a0001c0001t0002g0167 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.7+10581G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74508564 | |||||||
| chr9:74508585 | A | G | 1 | a0001c0001t0062g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.7+10602A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74508585 | |||||||
| chr9:74508593 | G | T | 1 | a0001c0001t0006g0102 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7+10610G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74508593 | |||||||
| chr9:74508638 | T | A | 45 | a0001c0001t0001g0002 a0001c0001t0001g0168 a0001c0001t0001g0171 others(42): Show |
46 | HG00140.hp2 HG01070.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.7+10655T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74508638 | |||||||
| chr9:74508900 | G | GCT | 2 | a0001c0001t0014g0010 a0001c0001t0039g0033 |
2 | HG02630.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.7+10938_7+10939dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74508900 | ||||||
| chr9:74508900 | GCT | G | 61 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(58): Show |
61 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.7+10938_7+10939del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74508900 | ||||||
| chr9:74509188 | G | A | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7+11205G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74509188 | |||||||
| chr9:74509716 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+11733T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74509716 | |||||||
| chr9:74509768 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(60): Show |
63 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.7+11785G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74509768 | |||||||
| chr9:74509959 | A | G | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+11976A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74509959 | |||||||
| chr9:74509977 | A | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+11994A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74509977 | |||||||
| chr9:74510167 | A | T | 1 | a0001c0001t0010g0224 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7+12184A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510167 | |||||||
| chr9:74510191 | T | C | 6 | a0001c0001t0007g0213 a0001c0001t0010g0004 a0001c0001t0012g0210 others(3): Show |
6 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+12208T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510191 | |||||||
| chr9:74510322 | G | T | 1 | a0001c0001t0010g0224 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7+12339G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510322 | |||||||
| chr9:74510410 | T | G | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG01884.hp1 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+12427T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510410 | |||||||
| chr9:74510425 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0010g0160 a0001c0001t0038g0162 |
3 | HG02280.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+12442C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510425 | |||||||
| chr9:74510447 | T | C | 1 | a0001c0001t0005g0169 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.7+12464T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510447 | |||||||
| chr9:74510492 | C | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
57 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.7+12509C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510492 | |||||||
| chr9:74510609 | C | A | 1 | a0001c0001t0005g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7+12626C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510609 | |||||||
| chr9:74510655 | G | A | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+12672G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510655 | |||||||
| chr9:74510684 | C | T | 171 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
172 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.7+12701C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74510684 | |||||||
| chr9:74511044 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+13061C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511044 | |||||||
| chr9:74511098 | C | A | 3 | a0001c0001t0001g0171 a0001c0001t0011g0172 a0001c0002t0001g0170 |
3 | HG01106.hp2 HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.7+13115C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511098 | |||||||
| chr9:74511141 | T | A | 4 | a0001c0001t0007g0013 a0001c0001t0015g0015 a0001c0002t0060g0016 others(1): Show |
4 | HG02886.hp2 HG02965.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+13158T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511141 | |||||||
| chr9:74511149 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.7+13166G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511149 | |||||||
| chr9:74511174 | G | A | 1 | a0001c0001t0014g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+13191G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511174 | |||||||
| chr9:74511209 | A | G | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7+13226A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511209 | |||||||
| chr9:74511211 | G | T | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+13228G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511211 | |||||||
| chr9:74511253 | G | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+13270G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511253 | |||||||
| chr9:74511388 | T | G | 10 | a0001c0001t0001g0161 a0001c0001t0001g0222 a0001c0001t0004g0221 others(7): Show |
10 | HG01884.hp1 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+13405T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511388 | |||||||
| chr9:74511529 | G | T | 6 | a0001c0001t0007g0213 a0001c0001t0010g0004 a0001c0001t0012g0210 others(3): Show |
6 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+13546G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511529 | |||||||
| chr9:74511687 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0003g0152 others(2): Show |
5 | HG01517.hp2 HG01891.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+13704C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511687 | |||||||
| chr9:74511719 | G | T | 1 | a0001c0001t0010g0224 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7+13736G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511719 | |||||||
| chr9:74511803 | G | A | 6 | a0001c0001t0007g0213 a0001c0001t0010g0004 a0001c0001t0012g0210 others(3): Show |
6 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+13820G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511803 | |||||||
| chr9:74511829 | A | T | 1 | a0001c0001t0011g0172 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.7+13846A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74511829 | |||||||
| chr9:74512015 | T | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+14032T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74512015 | |||||||
| chr9:74512060 | T | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+14077T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74512060 | |||||||
| chr9:74512577 | G | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.7+14594G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74512577 | |||||||
| chr9:74512729 | C | T | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+14746C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74512729 | |||||||
| chr9:74512768 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.7+14785T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74512768 | |||||||
| chr9:74513182 | G | A | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+15199G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74513182 | |||||||
| chr9:74513248 | C | A | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+15265C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74513248 | |||||||
| chr9:74513289 | A | G | 3 | a0001c0001t0007g0100 a0001c0001t0016g0099 a0001c0001t0064g0101 |
3 | HG01255.hp1 HG01496.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.7+15306A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74513289 | |||||||
| chr9:74514077 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7+16094A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74514077 | |||||||
| chr9:74514127 | T | C | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+16144T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74514127 | |||||||
| chr9:74514586 | G | T | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+16603G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74514586 | |||||||
| chr9:74514635 | C | A | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+16652C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74514635 | |||||||
| chr9:74514743 | G | A | 1 | a0001c0001t0006g0102 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7+16760G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74514743 | |||||||
| chr9:74514804 | A | ACTACAGT others(19): Show |
1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+16824_7+16825ins others(26): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74514804 | ||||||
| chr9:74514804 | A | G | 57 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(54): Show |
57 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.7+16821A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74514804 | |||||||
| chr9:74514845 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7+16862T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74514845 | |||||||
| chr9:74514928 | A | G | 98 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0043 others(95): Show |
99 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.7+16945A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74514928 | |||||||
| chr9:74515055 | G | A | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+17072G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515055 | |||||||
| chr9:74515110 | A | T | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+17127A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515110 | |||||||
| chr9:74515111 | T | C | 2 | a0001c0001t0013g0036 a0001c0001t0057g0037 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.7+17128T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515111 | |||||||
| chr9:74515205 | A | T | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+17222A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515205 | |||||||
| chr9:74515228 | T | G | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+17245T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515228 | |||||||
| chr9:74515404 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0017g0097 |
2 | HG02257.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7+17421C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515404 | |||||||
| chr9:74515411 | A | G | 1 | a0001c0001t0004g0096 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.7+17428A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515411 | |||||||
| chr9:74515463 | T | G | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+17480T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515463 | |||||||
| chr9:74515465 | G | T | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+17482G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515465 | |||||||
| chr9:74515466 | T | G | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+17483T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515466 | |||||||
| chr9:74515567 | C | T | 171 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(168): Show |
172 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.7+17584C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515567 | |||||||
| chr9:74515568 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.7+17585T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515568 | |||||||
| chr9:74515598 | T | G | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+17615T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515598 | |||||||
| chr9:74515750 | T | C | 1 | a0001c0001t0016g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.7+17767T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515750 | |||||||
| chr9:74515877 | T | A | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+17894T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74515877 | |||||||
| chr9:74516093 | G | T | 1 | a0001c0001t0018g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7+18110G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74516093 | |||||||
| chr9:74516099 | G | C | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7+18116G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74516099 | |||||||
| chr9:74516221 | T | C | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+18238T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74516221 | |||||||
| chr9:74516261 | T | G | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.7+18278T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74516261 | |||||||
| chr9:74516502 | T | C | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.7+18519T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74516502 | |||||||
| chr9:74517290 | C | T | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+19307C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74517290 | |||||||
| chr9:74517632 | G | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
64 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.7+19649G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74517632 | |||||||
| chr9:74517744 | C | A | 5 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+19761C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74517744 | |||||||
| chr9:74518370 | C | G | 5 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+20387C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74518370 | |||||||
| chr9:74518578 | A | G | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+20595A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74518578 | |||||||
| chr9:74518580 | G | C | 3 | a0001c0001t0001g0161 a0001c0001t0010g0160 a0001c0001t0038g0162 |
3 | HG02280.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+20597G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74518580 | |||||||
| chr9:74519183 | G | A | 1 | a0001c0001t0002g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.7+21200G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74519183 | |||||||
| chr9:74519274 | G | A | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+21291G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74519274 | |||||||
| chr9:74519363 | A | G | 1 | a0001c0001t0005g0011 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.7+21380A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74519363 | |||||||
| chr9:74519905 | G | A | 1 | a0001c0001t0007g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.7+21922G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74519905 | |||||||
| chr9:74520017 | A | G | 1 | a0001c0001t0024g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7+22034A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74520017 | |||||||
| chr9:74520132 | A | G | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+22149A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74520132 | |||||||
| chr9:74520450 | C | A | 1 | a0001c0001t0004g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.7+22467C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74520450 | |||||||
| chr9:74520462 | ATC | A | 2 | a0001c0001t0004g0093 a0001c0001t0046g0094 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.7+22481_7+22482del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74520462 | ||||||
| chr9:74520483 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0222 a0001c0001t0004g0221 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+22500A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74520483 | |||||||
| chr9:74520562 | T | C | 1 | a0001c0001t0024g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.7+22579T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74520562 | |||||||
| chr9:74520944 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.7+22961G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74520944 | |||||||
| chr9:74521261 | T | A | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+23278T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74521261 | |||||||
| chr9:74521432 | A | G | 157 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
157 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.7+23449A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74521432 | |||||||
| chr9:74521609 | C | T | 1 | a0001c0001t0008g0092 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.7+23626C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74521609 | |||||||
| chr9:74521873 | C | T | 221 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.7+23890C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74521873 | |||||||
| chr9:74521980 | C | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0168 others(53): Show |
58 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.7+23997C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74521980 | |||||||
| chr9:74522053 | G | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0168 others(53): Show |
58 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.7+24070G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522053 | |||||||
| chr9:74522063 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0168 others(54): Show |
59 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.7+24080G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522063 | |||||||
| chr9:74522228 | A | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0222 a0001c0001t0004g0221 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+24245A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522228 | |||||||
| chr9:74522232 | G | T | 2 | a0001c0001t0013g0051 a0001c0001t0013g0052 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.7+24249G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522232 | |||||||
| chr9:74522364 | A | G | 1 | a0001c0001t0008g0092 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.7+24381A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522364 | |||||||
| chr9:74522396 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0222 a0001c0001t0004g0221 others(6): Show |
9 | HG02258.hp2 HG02280.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.7+24413A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522396 | |||||||
| chr9:74522413 | C | T | 2 | a0001c0001t0010g0004 a0001c0001t0021g0003 |
2 | HG02886.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.7+24430C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522413 | |||||||
| chr9:74522682 | T | G | 1 | a0001c0001t0001g0012 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7+24699T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522682 | |||||||
| chr9:74522742 | C | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.7+24759C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522742 | |||||||
| chr9:74522743 | A | T | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.7+24760A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74522743 | |||||||
| chr9:74523025 | T | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0168 others(53): Show |
58 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.7+25042T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74523025 | |||||||
| chr9:74523103 | C | T | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
64 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.7+25120C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74523103 | |||||||
| chr9:74523298 | T | C | 4 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG01261.hp2 HG01975.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+25315T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74523298 | |||||||
| chr9:74523330 | C | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
64 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.7+25347C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74523330 | |||||||
| chr9:74523609 | C | A | 1 | a0001c0001t0055g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7+25626C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74523609 | |||||||
| chr9:74523631 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.7+25648C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74523631 | |||||||
| chr9:74523729 | C | T | 2 | a0001c0001t0019g0090 a0001c0001t0019g0091 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7+25746C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74523729 | |||||||
| chr9:74523842 | C | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.7+25859C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74523842 | |||||||
| chr9:74523997 | C | T | 1 | a0001c0001t0049g0105 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.7+26014C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74523997 | |||||||
| chr9:74524003 | C | CT | 135 | a0001c0001t0001g0002 a0001c0001t0001g0035 a0001c0001t0001g0043 others(132): Show |
137 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.7+26040dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74524003 | ||||||
| chr9:74524003 | C | CTT | 68 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(65): Show |
68 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.7+26039_7+26040dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74524003 | ||||||
| chr9:74524063 | G | A | 1 | a0001c0001t0039g0033 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.7+26080G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74524063 | |||||||
| chr9:74524360 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0173 a0001c0001t0001g0177 others(17): Show |
21 | HG02040.hp1 HG02523.hp1 HG04184.hp1 others(18): Show |
intron_variant | MODIFIER | c.7+26377C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74524360 | |||||||
| chr9:74524559 | T | C | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+26576T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74524559 | |||||||
| chr9:74524641 | A | C | 56 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0168 others(53): Show |
58 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.7+26658A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74524641 | |||||||
| chr9:74524807 | G | T | 1 | a0001c0002t0003g0050 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.7+26824G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74524807 | |||||||
| chr9:74524904 | T | G | 3 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0011g0179 |
3 | HG00140.hp2 HG01261.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.7+26921T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74524904 | |||||||
| chr9:74525095 | A | T | 3 | a0001c0001t0001g0088 a0001c0001t0018g0089 a0001c0001t0047g0087 |
3 | HG01884.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7+27112A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74525095 | |||||||
| chr9:74525462 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.7+27479T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74525462 | |||||||
| chr9:74525549 | T | C | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
64 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.7+27566T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74525549 | |||||||
| chr9:74525606 | A | AT | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+27627dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74525606 | ||||||
| chr9:74525904 | A | G | 3 | a0001c0001t0019g0086 a0001c0001t0019g0090 a0001c0001t0019g0091 |
3 | HG02451.hp2 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.7+27921A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74525904 | |||||||
| chr9:74526035 | C | T | 83 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(80): Show |
83 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.7+28052C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74526035 | |||||||
| chr9:74526203 | C | A | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.7+28220C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74526203 | |||||||
| chr9:74526236 | A | G | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+28253A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74526236 | |||||||
| chr9:74526333 | T | C | 5 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+28350T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74526333 | |||||||
| chr9:74526487 | A | G | 1 | a0001c0001t0013g0036 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.7+28504A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74526487 | |||||||
| chr9:74527014 | G | C | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7+29031G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74527014 | |||||||
| chr9:74527104 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.7+29121C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74527104 | |||||||
| chr9:74527167 | G | T | 1 | a0001c0001t0001g0032 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.7+29184G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74527167 | |||||||
| chr9:74527298 | A | T | 1 | a0001c0002t0002g0049 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.7+29315A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74527298 | |||||||
| chr9:74527430 | T | A | 64 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(61): Show |
64 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.7+29447T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74527430 | |||||||
| chr9:74527475 | G | GT | 2 | a0001c0001t0016g0029 a0001c0001t0018g0030 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7+29493dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74527475 | ||||||
| chr9:74527664 | T | C | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+29681T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74527664 | |||||||
| chr9:74527905 | A | G | 2 | a0001c0001t0005g0201 a0001c0001t0053g0174 |
2 | NA19002.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.7+29922A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74527905 | |||||||
| chr9:74529020 | G | A | 5 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+31037G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74529020 | |||||||
| chr9:74529127 | C | A | 83 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(80): Show |
83 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.7+31144C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74529127 | |||||||
| chr9:74529284 | A | G | 77 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(74): Show |
77 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.7+31301A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74529284 | |||||||
| chr9:74529494 | C | T | 2 | a0001c0001t0016g0029 a0001c0001t0018g0030 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7+31511C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74529494 | |||||||
| chr9:74529775 | G | A | 1 | a0001c0001t0006g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.7+31792G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74529775 | |||||||
| chr9:74529956 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.7+31973A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74529956 | |||||||
| chr9:74530070 | T | C | 5 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.7+32087T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74530070 | |||||||
| chr9:74530076 | T | C | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+32093T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74530076 | |||||||
| chr9:74530375 | T | C | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+32392T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74530375 | |||||||
| chr9:74530460 | T | A | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+32477T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74530460 | |||||||
| chr9:74530866 | T | C | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7+32883T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74530866 | |||||||
| chr9:74530873 | T | G | 5 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(2): Show |
5 | HG02258.hp2 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+32890T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74530873 | |||||||
| chr9:74531181 | T | A | 6 | a0001c0001t0007g0013 a0001c0001t0015g0015 a0001c0001t0016g0029 others(3): Show |
6 | HG02257.hp1 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+33198T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531181 | |||||||
| chr9:74531239 | G | T | 1 | a0001c0001t0039g0033 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.7+33256G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531239 | |||||||
| chr9:74531355 | T | G | 1 | a0001c0002t0003g0041 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.7+33372T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531355 | |||||||
| chr9:74531376 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0007g0137 a0001c0001t0020g0138 others(1): Show |
4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+33393T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531376 | |||||||
| chr9:74531386 | G | C | 8 | a0001c0001t0013g0051 a0001c0001t0013g0052 a0001c0001t0014g0019 others(5): Show |
8 | HG01168.hp1 HG01168.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+33403G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531386 | |||||||
| chr9:74531552 | G | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
134 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.7+33569G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531552 | |||||||
| chr9:74531653 | T | C | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+33670T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531653 | |||||||
| chr9:74531686 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.7+33703A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531686 | |||||||
| chr9:74531708 | A | G | 1 | a0001c0001t0043g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.7+33725A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531708 | |||||||
| chr9:74531813 | C | T | 1 | a0001c0001t0024g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.7+33830C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531813 | |||||||
| chr9:74531817 | AGACTTTT others(626): Show |
A | 1 | a0001c0002t0002g0049 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.7+33835_7+34467del | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531817 | |||||||
| chr9:74531818 | G | A | 1 | a0001c0001t0041g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.7+33835G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74531818 | |||||||
| chr9:74532402 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0002t0009g0116 |
3 | HG01261.hp2 HG01975.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.7+34419A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532402 | |||||||
| chr9:74532452 | C | G | 1 | a0001c0002t0002g0049 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.7+34469C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532452 | |||||||
| chr9:74532454 | C | T | 1 | a0001c0002t0002g0049 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.7+34471C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532454 | |||||||
| chr9:74532500 | T | C | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
134 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.7+34517T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532500 | |||||||
| chr9:74532677 | C | T | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
134 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.7+34694C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532677 | |||||||
| chr9:74532740 | C | T | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7+34757C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532740 | |||||||
| chr9:74532778 | G | A | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
134 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.7+34795G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532778 | |||||||
| chr9:74532784 | A | G | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+34801A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532784 | |||||||
| chr9:74532793 | T | C | 77 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(74): Show |
77 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.7+34810T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532793 | |||||||
| chr9:74532803 | C | CGTATATA others(17): Show |
10 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(7): Show |
10 | HG01884.hp1 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+34843_7+34866dup others(24): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74532803 | ||||||
| chr9:74532803 | C | CGTATATA others(41): Show |
3 | a0001c0001t0001g0161 a0001c0001t0010g0160 a0001c0001t0038g0162 |
3 | HG02280.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+34866_7+34867ins others(48): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74532803 | ||||||
| chr9:74532804 | G | A | 77 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(74): Show |
77 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.7+34821G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532804 | |||||||
| chr9:74532805 | TATATATA others(29): Show |
T | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+34847_7+34882del others(36): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74532805 | ||||||
| chr9:74532826 | GTGTATAT others(27): Show |
G | 132 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
132 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.7+34847_7+34880del others(34): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74532826 | ||||||
| chr9:74532870 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.7+34887G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532870 | |||||||
| chr9:74532872 | G | A | 132 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(129): Show |
132 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.7+34889G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532872 | |||||||
| chr9:74532874 | A | G | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7+34891A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532874 | |||||||
| chr9:74532955 | G | T | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+34972G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74532955 | |||||||
| chr9:74533034 | G | A | 1 | a0001c0001t0055g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7+35051G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74533034 | |||||||
| chr9:74533068 | T | A | 1 | a0001c0001t0024g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.7+35085T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74533068 | |||||||
| chr9:74533148 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.7+35165G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74533148 | |||||||
| chr9:74533183 | C | T | 1 | a0001c0001t0014g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+35200C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74533183 | |||||||
| chr9:74533674 | A | G | 6 | a0001c0001t0007g0013 a0001c0001t0015g0015 a0001c0001t0016g0029 others(3): Show |
6 | HG02257.hp1 HG02886.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.7+35691A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74533674 | |||||||
| chr9:74533726 | T | G | 1 | a0001c0001t0049g0105 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.7+35743T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74533726 | |||||||
| chr9:74533919 | C | T | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
134 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.7+35936C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74533919 | |||||||
| chr9:74534017 | G | A | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+36034G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74534017 | |||||||
| chr9:74534029 | A | G | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+36046A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74534029 | |||||||
| chr9:74534113 | C | G | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+36130C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74534113 | |||||||
| chr9:74534162 | C | T | 3 | a0001c0001t0001g0161 a0001c0001t0010g0160 a0001c0001t0038g0162 |
3 | HG02280.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+36179C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74534162 | |||||||
| chr9:74534213 | G | A | 1 | a0001c0002t0003g0042 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.7+36230G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74534213 | |||||||
| chr9:74534546 | G | A | 1 | a0001c0002t0001g0170 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.7+36563G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74534546 | |||||||
| chr9:74534631 | T | C | 128 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
128 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.7+36648T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74534631 | |||||||
| chr9:74534921 | A | G | 80 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(77): Show |
80 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.7+36938A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74534921 | |||||||
| chr9:74535012 | C | T | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+37029C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74535012 | |||||||
| chr9:74535016 | C | A | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+37033C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74535016 | |||||||
| chr9:74535148 | GGT | G | 133 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
133 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.7+37176_7+37177del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74535148 | ||||||
| chr9:74535185 | T | G | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.7+37202T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74535185 | |||||||
| chr9:74535228 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.7+37245T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74535228 | |||||||
| chr9:74535373 | T | C | 157 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
158 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.7+37390T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74535373 | |||||||
| chr9:74535926 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.7+37943T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74535926 | |||||||
| chr9:74535943 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.7+37960T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74535943 | |||||||
| chr9:74536099 | T | C | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+38116T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74536099 | |||||||
| chr9:74536564 | C | T | 1 | a0001c0001t0036g0150 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.7+38581C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74536564 | |||||||
| chr9:74536595 | A | G | 2 | a0001c0001t0016g0029 a0001c0001t0018g0030 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7+38612A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74536595 | |||||||
| chr9:74537123 | A | G | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+39140A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74537123 | |||||||
| chr9:74537186 | A | G | 1 | a0001c0001t0049g0105 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.7+39203A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74537186 | |||||||
| chr9:74537222 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.7+39239A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74537222 | |||||||
| chr9:74537406 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.7+39423A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74537406 | |||||||
| chr9:74537711 | T | C | 75 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(72): Show |
75 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.7+39728T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74537711 | |||||||
| chr9:74538294 | G | A | 2 | a0001c0001t0016g0029 a0001c0001t0018g0030 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7+40311G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74538294 | |||||||
| chr9:74538327 | C | A | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+40344C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74538327 | |||||||
| chr9:74538549 | T | C | 60 | a0001c0001t0001g0002 a0001c0001t0001g0168 a0001c0001t0001g0171 others(57): Show |
61 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.7+40566T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74538549 | |||||||
| chr9:74538728 | C | CA | 124 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0035 others(121): Show |
125 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.7+40758dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74538728 | ||||||
| chr9:74538728 | C | CAA | 18 | a0001c0001t0001g0177 a0001c0001t0001g0190 a0001c0001t0001g0192 others(15): Show |
18 | HG01168.hp2 HG02148.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.7+40757_7+40758dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74538728 | ||||||
| chr9:74538728 | C | G | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
52 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.7+40745C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74538728 | |||||||
| chr9:74538729 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.7+40746A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74538729 | |||||||
| chr9:74538801 | A | T | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7+40818A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74538801 | |||||||
| chr9:74538881 | A | G | 7 | a0001c0001t0001g0128 a0001c0001t0001g0132 a0001c0001t0001g0133 others(4): Show |
7 | HG00597.hp2 NA18968.hp2 NA19062.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+40898A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74538881 | |||||||
| chr9:74538971 | T | C | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+40988T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74538971 | |||||||
| chr9:74539045 | C | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0168 a0001c0001t0001g0171 others(56): Show |
60 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.7+41062C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74539045 | |||||||
| chr9:74539084 | G | A | 215 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.7+41101G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74539084 | |||||||
| chr9:74539201 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.7+41218G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74539201 | |||||||
| chr9:74539289 | G | A | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+41306G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74539289 | |||||||
| chr9:74539535 | G | A | 75 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(72): Show |
75 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.7+41552G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74539535 | |||||||
| chr9:74539565 | C | T | 1 | a0001c0001t0010g0224 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7+41582C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74539565 | |||||||
| chr9:74539750 | C | A | 17 | a0001c0001t0001g0043 a0001c0001t0001g0135 a0001c0001t0007g0213 others(14): Show |
18 | HG01081.hp1 HG01175.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.7+41767C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74539750 | |||||||
| chr9:74539868 | C | CA | 16 | a0001c0001t0001g0222 a0001c0001t0003g0024 a0001c0001t0004g0221 others(13): Show |
16 | HG01168.hp2 HG02135.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.7+41905dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74539868 | ||||||
| chr9:74539868 | CA | C | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
80 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.7+41905delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74539868 | ||||||
| chr9:74539868 | CAA | C | 5 | a0001c0001t0001g0114 a0001c0001t0001g0133 a0001c0001t0001g0148 others(2): Show |
5 | HG00597.hp2 HG01081.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+41904_7+41905del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74539868 | ||||||
| chr9:74540093 | A | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
120 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.7+42110A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540093 | |||||||
| chr9:74540227 | G | T | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+42244G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540227 | |||||||
| chr9:74540271 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.7+42288A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540271 | |||||||
| chr9:74540311 | G | C | 1 | a0001c0001t0006g0102 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7+42328G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540311 | |||||||
| chr9:74540358 | C | T | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+42375C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540358 | |||||||
| chr9:74540360 | C | T | 4 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(1): Show |
4 | HG02258.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+42377C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540360 | |||||||
| chr9:74540466 | A | T | 75 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(72): Show |
75 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.7+42483A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540466 | |||||||
| chr9:74540637 | A | T | 10 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(7): Show |
10 | HG01168.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.7+42654A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540637 | |||||||
| chr9:74540692 | T | C | 219 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.7+42709T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540692 | |||||||
| chr9:74540818 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0018g0089 a0001c0001t0047g0087 |
3 | HG01884.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.7+42835G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74540818 | |||||||
| chr9:74541085 | A | C | 2 | a0001c0001t0016g0029 a0001c0001t0018g0030 |
2 | HG02257.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.7+43102A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74541085 | |||||||
| chr9:74541139 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.7+43156G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74541139 | |||||||
| chr9:74541279 | C | CA | 12 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0002g0065 others(9): Show |
12 | HG00408.hp2 HG00738.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.7+43323dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAA | 22 | a0001c0001t0001g0002 a0001c0001t0001g0168 a0001c0001t0001g0173 others(19): Show |
23 | HG00140.hp1 HG02040.hp1 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.7+43320_7+43323dup others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAAA | 14 | a0001c0001t0001g0007 a0001c0001t0001g0114 a0001c0001t0001g0140 others(11): Show |
14 | HG00738.hp2 HG01081.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.7+43319_7+43323dup others(5): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAAAA | 28 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(25): Show |
28 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.7+43318_7+43323dup others(6): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAAAAA | 14 | a0001c0001t0001g0113 a0001c0001t0001g0133 a0001c0001t0001g0149 others(11): Show |
14 | HG00597.hp2 HG01074.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.7+43317_7+43323dup others(7): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0004g0221 a0001c0001t0057g0037 |
2 | HG02258.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.7+43314_7+43323dup others(10): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+43312_7+43323dup others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAAAAA others(7): Show |
2 | a0001c0001t0014g0021 a0001c0001t0018g0018 |
2 | HG01168.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.7+43310_7+43323dup others(14): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0014g0019 a0001c0001t0014g0020 |
2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.7+43309_7+43323dup others(15): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0013g0052 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7+43308_7+43323dup others(16): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0013g0051 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.7+43307_7+43323dup others(17): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | CAAAAAAA others(1): Show |
C | 32 | a0001c0001t0001g0043 a0001c0001t0001g0135 a0001c0001t0001g0171 others(29): Show |
33 | HG00140.hp2 HG01074.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.7+43316_7+43323del others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541279 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0052g0147 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.7+43314_7+43323del others(10): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74541279 | ||||||
| chr9:74541499 | G | A | 1 | a0001c0001t0019g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.7+43516G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74541499 | |||||||
| chr9:74541716 | A | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
9 | HG00323.hp1 HG02148.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+43733A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74541716 | |||||||
| chr9:74541990 | A | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0140 a0001c0001t0001g0148 others(7): Show |
10 | HG00738.hp2 HG01192.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+44007A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74541990 | |||||||
| chr9:74542011 | A | G | 1 | a0001c0001t0008g0078 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.7+44028A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74542011 | |||||||
| chr9:74542316 | A | G | 2 | a0001c0002t0003g0214 a0001c0002t0023g0215 |
2 | HG00738.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.7+44333A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74542316 | |||||||
| chr9:74542390 | T | C | 59 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(56): Show |
59 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.7+44407T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74542390 | |||||||
| chr9:74542624 | C | T | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+44641C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74542624 | |||||||
| chr9:74542684 | T | G | 1 | a0001c0001t0066g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.7+44701T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74542684 | |||||||
| chr9:74542728 | A | T | 1 | a0001c0002t0001g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7+44745A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74542728 | |||||||
| chr9:74542802 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0193 |
2 | NA18977.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.7+44819T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74542802 | |||||||
| chr9:74543015 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.7+45032C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543015 | |||||||
| chr9:74543060 | A | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.7+45077A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543060 | |||||||
| chr9:74543232 | C | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(212): Show |
217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.7+45249C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543232 | |||||||
| chr9:74543233 | G | A | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7+45250G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543233 | |||||||
| chr9:74543320 | C | T | 17 | a0001c0001t0001g0043 a0001c0001t0001g0135 a0001c0001t0007g0213 others(14): Show |
18 | HG01081.hp1 HG01175.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.7+45337C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543320 | |||||||
| chr9:74543369 | G | A | 10 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(7): Show |
10 | HG01168.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.7+45386G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543369 | |||||||
| chr9:74543490 | T | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(216): Show |
221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.7+45507T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543490 | |||||||
| chr9:74543573 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.7+45590G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543573 | |||||||
| chr9:74543606 | A | AT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0168 a0001c0001t0001g0171 others(46): Show |
50 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.7+45633dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74543606 | ||||||
| chr9:74543752 | C | T | 1 | a0001c0001t0014g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+45769C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543752 | |||||||
| chr9:74543792 | CT | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.7+45812delT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74543792 | ||||||
| chr9:74544085 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.7+46102G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74544085 | |||||||
| chr9:74544297 | C | G | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+46314C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74544297 | |||||||
| chr9:74544349 | C | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.7+46366C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74544349 | |||||||
| chr9:74544799 | C | T | 75 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0053 others(72): Show |
75 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.7+46816C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74544799 | |||||||
| chr9:74544900 | G | C | 3 | a0001c0001t0001g0161 a0001c0001t0010g0160 a0001c0001t0038g0162 |
3 | HG02280.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.7+46917G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74544900 | |||||||
| chr9:74545099 | G | GT | 9 | a0001c0001t0001g0068 a0001c0001t0001g0157 a0001c0001t0003g0153 others(6): Show |
9 | HG01891.hp1 HG01891.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.7+47129dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74545099 | ||||||
| chr9:74545099 | G | GTT | 42 | a0001c0001t0001g0002 a0001c0001t0001g0135 a0001c0001t0001g0140 others(39): Show |
43 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.7+47128_7+47129dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74545099 | ||||||
| chr9:74545099 | G | GTTT | 7 | a0001c0001t0001g0173 a0001c0001t0001g0192 a0001c0001t0001g0206 others(4): Show |
7 | HG03704.hp1 HG03831.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+47127_7+47129dup others(3): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74545099 | ||||||
| chr9:74545336 | C | T | 2 | a0001c0002t0060g0016 a0002c0004t0030g0014 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7+47353C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545336 | |||||||
| chr9:74545459 | A | G | 1 | a0001c0001t0049g0105 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.7+47476A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545459 | |||||||
| chr9:74545595 | A | T | 1 | a0001c0001t0002g0040 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.7+47612A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545595 | |||||||
| chr9:74545600 | T | G | 12 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(9): Show |
12 | HG01168.hp2 HG01884.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.7+47617T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545600 | |||||||
| chr9:74545634 | G | T | 204 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.7+47651G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545634 | |||||||
| chr9:74545738 | G | A | 2 | a0001c0002t0060g0016 a0002c0004t0030g0014 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7+47755G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545738 | |||||||
| chr9:74545801 | C | T | 2 | a0001c0002t0060g0016 a0002c0004t0030g0014 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7+47818C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545801 | |||||||
| chr9:74545807 | G | GT | 94 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0043 others(91): Show |
95 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.7+47834dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74545807 | ||||||
| chr9:74545868 | T | C | 2 | a0001c0002t0060g0016 a0002c0004t0030g0014 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7+47885T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545868 | |||||||
| chr9:74545872 | G | A | 2 | a0001c0002t0060g0016 a0002c0004t0030g0014 |
2 | HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.7+47889G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545872 | |||||||
| chr9:74545899 | A | G | 106 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0043 others(103): Show |
107 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.7+47916A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545899 | |||||||
| chr9:74545948 | G | A | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+47965G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545948 | |||||||
| chr9:74545954 | A | G | 1 | a0001c0002t0001g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.7+47971A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74545954 | |||||||
| chr9:74546013 | G | C | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7+48030G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74546013 | |||||||
| chr9:74546168 | A | T | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7+48185A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74546168 | |||||||
| chr9:74546214 | G | A | 1 | a0001c0001t0010g0224 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.7+48231G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74546214 | |||||||
| chr9:74546437 | A | T | 2 | a0001c0001t0001g0059 a0001c0001t0008g0092 |
2 | NA18944.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.7+48454A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74546437 | |||||||
| chr9:74546715 | C | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(122): Show |
126 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.7+48732C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74546715 | |||||||
| chr9:74546795 | T | G | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7+48812T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74546795 | |||||||
| chr9:74546875 | C | T | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7+48892C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74546875 | |||||||
| chr9:74546965 | G | A | 1 | a0001c0001t0002g0060 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.7+48982G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74546965 | |||||||
| chr9:74547121 | G | T | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7+49138G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74547121 | |||||||
| chr9:74547129 | T | C | 6 | a0001c0001t0004g0093 a0001c0001t0013g0110 a0001c0001t0015g0111 others(3): Show |
6 | HG01891.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+49146T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74547129 | |||||||
| chr9:74547243 | A | C | 48 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0113 others(45): Show |
48 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.7+49260A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74547243 | |||||||
| chr9:74547281 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7+49298T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74547281 | |||||||
| chr9:74547416 | C | G | 2 | a0001c0001t0012g0159 a0002c0004t0030g0014 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.7+49433C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74547416 | |||||||
| chr9:74547464 | T | A | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7+49481T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74547464 | |||||||
| chr9:74547988 | G | A | 1 | a0001c0001t0017g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.7+50005G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74547988 | |||||||
| chr9:74548168 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0067 others(78): Show |
82 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.7+50185G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74548168 | |||||||
| chr9:74548193 | C | T | 2 | a0001c0001t0012g0159 a0002c0004t0030g0014 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.7+50210C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74548193 | |||||||
| chr9:74548526 | T | C | 81 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0067 others(78): Show |
82 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.7+50543T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74548526 | |||||||
| chr9:74548680 | G | A | 1 | a0001c0001t0017g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.7+50697G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74548680 | |||||||
| chr9:74548900 | G | C | 1 | a0001c0001t0005g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.7+50917G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74548900 | |||||||
| chr9:74548966 | A | G | 47 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0113 others(44): Show |
47 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.7+50983A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74548966 | |||||||
| chr9:74549090 | C | A | 136 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
137 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.7+51107C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549090 | |||||||
| chr9:74549185 | C | T | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7+51202C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549185 | |||||||
| chr9:74549261 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+51278C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549261 | |||||||
| chr9:74549300 | T | C | 2 | a0001c0002t0065g0031 a0002c0004t0030g0014 |
2 | HG02970.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.7+51317T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549300 | |||||||
| chr9:74549406 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+51423C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549406 | |||||||
| chr9:74549439 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.7+51456G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549439 | |||||||
| chr9:74549441 | C | CAA | 132 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0067 others(129): Show |
133 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.7+51470_7+51471dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549441 | ||||||
| chr9:74549454 | AG | A | 2 | a0001c0001t0001g0007 a0001c0001t0054g0163 |
2 | HG02647.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.7+51472delG | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549454 | |||||||
| chr9:74549462 | G | A | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.7+51479G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549462 | |||||||
| chr9:74549464 | G | A | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.7+51481G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549464 | |||||||
| chr9:74549478 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+51495T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549478 | |||||||
| chr9:74549517 | AAGGGAGG others(5): Show |
A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0202 a0001c0001t0002g0056 others(1): Show |
4 | HG00609.hp1 HG03831.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+51556_7+51567del others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549517 | ||||||
| chr9:74549519 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+51536G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549519 | |||||||
| chr9:74549521 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+51538G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549521 | |||||||
| chr9:74549529 | G | GAGGGAGG others(26): Show |
1 | a0001c0001t0034g0064 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.7+51567_7+51568ins others(33): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549529 | ||||||
| chr9:74549531 | GGGAGGGA others(25): Show |
G | 1 | a0001c0001t0019g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.7+51552_7+51583del others(32): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549531 | ||||||
| chr9:74549535 | GGGAGGGA others(9): Show |
G | 1 | a0001c0002t0065g0031 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.7+51556_7+51571del others(16): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549535 | ||||||
| chr9:74549535 | GGGAGGGA others(13): Show |
G | 1 | a0001c0001t0025g0217 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.7+51556_7+51575del others(20): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549535 | ||||||
| chr9:74549535 | GGGAGGGA others(17): Show |
G | 3 | a0001c0001t0005g0169 a0001c0001t0008g0196 a0001c0001t0063g0197 |
3 | NA19001.hp1 NA19007.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.7+51556_7+51579del others(24): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549535 | ||||||
| chr9:74549535 | GGGAGGGA others(21): Show |
G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0173 a0001c0001t0002g0167 others(5): Show |
8 | HG02135.hp2 HG02523.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+51556_7+51583del others(28): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549535 | ||||||
| chr9:74549535 | GGGAGGGA others(25): Show |
G | 12 | a0001c0001t0001g0168 a0001c0001t0001g0177 a0001c0001t0001g0183 others(9): Show |
12 | HG02723.hp2 HG02976.hp1 HG03098.hp2 others(9): Show |
intron_variant | MODIFIER | c.7+51556_7+51587del others(32): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549535 | ||||||
| chr9:74549535 | GGGAGGGA others(28): Show |
G | 1 | a0001c0001t0037g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.7+51553_7+51587del others(35): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549535 | |||||||
| chr9:74549535 | GGGAGGGA others(29): Show |
G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0190 a0001c0001t0001g0192 others(10): Show |
13 | HG01168.hp1 HG01255.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.7+51556_7+51591del others(36): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549535 | ||||||
| chr9:74549535 | GGGAGGGA others(33): Show |
G | 2 | a0001c0001t0001g0206 a0001c0001t0066g0182 |
2 | HG01243.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.7+51556_7+51595del others(40): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549535 | ||||||
| chr9:74549535 | GGGAGGGA others(37): Show |
G | 1 | a0001c0001t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.7+51556_7+51599del others(44): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549535 | ||||||
| chr9:74549535 | GGGAGGGA others(41): Show |
G | 2 | a0001c0001t0001g0208 a0001c0001t0018g0030 |
2 | HG02257.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.7+51556_7+51603del others(48): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549535 | ||||||
| chr9:74549539 | GGGAGGGA others(5): Show |
G | 1 | a0001c0001t0002g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.7+51560_7+51571del others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549539 | GGGAGGGA others(13): Show |
G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0148 others(3): Show |
6 | HG01496.hp2 HG01981.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+51560_7+51579del others(20): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549539 | GGGAGGGA others(17): Show |
G | 14 | a0001c0001t0001g0149 a0001c0001t0001g0157 a0001c0001t0001g0222 others(11): Show |
14 | HG01243.hp2 HG02074.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.7+51560_7+51583del others(24): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549539 | GGGAGGGA others(21): Show |
G | 8 | a0001c0001t0001g0007 a0001c0001t0002g0055 a0001c0001t0007g0013 others(5): Show |
8 | HG01168.hp2 HG01891.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+51560_7+51587del others(28): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549539 | GGGAGGGA others(25): Show |
G | 13 | a0001c0001t0001g0132 a0001c0001t0003g0024 a0001c0001t0007g0100 others(10): Show |
13 | HG01192.hp1 HG01255.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.7+51560_7+51591del others(32): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549539 | GGGAGGGA others(29): Show |
G | 15 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(12): Show |
15 | HG01070.hp2 HG01081.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.7+51560_7+51595del others(36): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549539 | GGGAGGGA others(33): Show |
G | 22 | a0001c0001t0001g0035 a0001c0001t0001g0133 a0001c0001t0001g0135 others(19): Show |
22 | HG00140.hp2 HG00597.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.7+51560_7+51599del others(40): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549539 | GGGAGGGA others(37): Show |
G | 16 | a0001c0001t0001g0067 a0001c0001t0001g0120 a0001c0001t0001g0134 others(13): Show |
16 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.7+51560_7+51603del others(44): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549539 | GGGAGGGA others(41): Show |
G | 1 | a0001c0001t0006g0102 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.7+51560_7+51607del others(48): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549539 | GGGAGGGA others(45): Show |
G | 2 | a0001c0001t0001g0136 a0001c0001t0004g0125 |
2 | HG00408.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.7+51560_7+51611del others(52): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549539 | ||||||
| chr9:74549543 | GGGAGGGA others(5): Show |
G | 1 | a0001c0001t0014g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.7+51564_7+51575del others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549543 | ||||||
| chr9:74549543 | GGGAGGGA others(9): Show |
G | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7+51564_7+51579del others(16): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549543 | ||||||
| chr9:74549547 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0032g0076 |
2 | HG02074.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.7+51564G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549547 | |||||||
| chr9:74549547 | G | GGGAA | 7 | a0001c0001t0001g0108 a0001c0001t0001g0171 a0001c0001t0002g0066 others(4): Show |
7 | HG01074.hp1 HG01081.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.7+51622_7+51625dup others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549547 | ||||||
| chr9:74549547 | G | GGGAAGGA others(1): Show |
3 | a0001c0001t0008g0106 a0001c0001t0031g0121 a0001c0002t0002g0049 |
3 | HG01256.hp1 NA18977.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.7+51618_7+51625dup others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549547 | ||||||
| chr9:74549547 | G | GGGAAGGA others(30): Show |
1 | a0001c0001t0002g0060 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.7+51578_7+51579ins others(37): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549547 | ||||||
| chr9:74549547 | GGGAA | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0098 others(14): Show |
17 | HG00140.hp1 HG00597.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.7+51622_7+51625del others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549547 | ||||||
| chr9:74549547 | GGGAAGGA others(1): Show |
G | 9 | a0001c0001t0001g0068 a0001c0001t0008g0092 a0001c0001t0009g0075 others(6): Show |
10 | HG02523.hp2 HG02886.hp1 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.7+51618_7+51625del others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549547 | ||||||
| chr9:74549547 | GGGAAGGA others(5): Show |
G | 10 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0002g0038 others(7): Show |
10 | HG00323.hp1 HG01109.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.7+51614_7+51625del others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549547 | ||||||
| chr9:74549547 | GGGAAGGA others(9): Show |
G | 2 | a0001c0001t0053g0174 a0001c0002t0003g0041 |
2 | NA19074.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.7+51610_7+51625del others(16): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549547 | ||||||
| chr9:74549547 | GGGAAGGA others(13): Show |
G | 4 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0018g0089 others(1): Show |
4 | HG01884.hp2 HG03516.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+51606_7+51625del others(20): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549547 | ||||||
| chr9:74549551 | A | G | 2 | a0001c0001t0009g0070 a0001c0001t0034g0064 |
2 | HG02004.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.7+51568A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549551 | |||||||
| chr9:74549559 | A | G | 1 | a0001c0001t0029g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.7+51576A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549559 | |||||||
| chr9:74549601 | G | A | 1 | a0001c0001t0024g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7+51618G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549601 | |||||||
| chr9:74549605 | GAAGA | G | 2 | a0001c0001t0024g0095 a0001c0001t0043g0048 |
2 | HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.7+51626_7+51629del others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549605 | ||||||
| chr9:74549609 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(137): Show |
141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.7+51626A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549609 | |||||||
| chr9:74549613 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7+51630G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549613 | |||||||
| chr9:74549629 | A | G | 40 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0113 others(37): Show |
40 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.7+51646A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549629 | |||||||
| chr9:74549632 | G | A | 5 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(2): Show |
5 | HG02258.hp2 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+51649G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549632 | |||||||
| chr9:74549643 | AAG | A | 5 | a0001c0001t0013g0110 a0001c0001t0015g0111 a0001c0001t0015g0142 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+51662_7+51663del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74549643 | ||||||
| chr9:74549845 | T | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+51862T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549845 | |||||||
| chr9:74549854 | G | T | 1 | a0001c0001t0019g0086 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.7+51871G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549854 | |||||||
| chr9:74549889 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.7+51906C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549889 | |||||||
| chr9:74549909 | T | C | 7 | a0001c0001t0001g0071 a0001c0001t0002g0040 a0001c0001t0002g0060 others(4): Show |
7 | HG01433.hp1 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+51926T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549909 | |||||||
| chr9:74550090 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+52107C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74550090 | |||||||
| chr9:74550146 | T | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+52163T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74550146 | |||||||
| chr9:74550146 | T | C | 2 | a0001c0001t0001g0080 a0001c0001t0033g0079 |
2 | NA18999.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.7+52163T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74550146 | |||||||
| chr9:74550447 | A | C | 1 | a0001c0001t0032g0076 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.7+52464A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74550447 | |||||||
| chr9:74550470 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7+52487G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74550470 | |||||||
| chr9:74550476 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7+52493T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74550476 | |||||||
| chr9:74550618 | T | C | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+52635T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74550618 | |||||||
| chr9:74550908 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.7+52925A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74550908 | |||||||
| chr9:74551091 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+53108C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551091 | |||||||
| chr9:74551111 | C | T | 1 | a0001c0002t0061g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.7+53128C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551111 | |||||||
| chr9:74551225 | C | T | 6 | a0001c0001t0013g0110 a0001c0001t0015g0111 a0001c0001t0015g0142 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+53242C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551225 | |||||||
| chr9:74551231 | A | G | 2 | a0001c0002t0004g0027 a0001c0002t0022g0028 |
2 | HG02148.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.7+53248A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551231 | |||||||
| chr9:74551311 | T | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+53328T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551311 | |||||||
| chr9:74551319 | G | A | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+53336G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551319 | |||||||
| chr9:74551412 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+53429C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551412 | |||||||
| chr9:74551449 | C | T | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7+53466C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551449 | |||||||
| chr9:74551486 | C | T | 16 | a0001c0001t0001g0071 a0001c0001t0001g0108 a0001c0001t0002g0038 others(13): Show |
16 | HG00597.hp1 HG01433.hp1 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.7+53503C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551486 | |||||||
| chr9:74551658 | C | T | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7+53675C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551658 | |||||||
| chr9:74551662 | G | C | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+53679G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551662 | |||||||
| chr9:74551666 | T | C | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7+53683T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551666 | |||||||
| chr9:74551794 | A | G | 2 | a0001c0001t0012g0159 a0002c0004t0030g0014 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.7+53811A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551794 | |||||||
| chr9:74551810 | G | A | 1 | a0001c0002t0003g0050 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.7+53827G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551810 | |||||||
| chr9:74551919 | G | A | 1 | a0001c0001t0052g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.7+53936G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551919 | |||||||
| chr9:74551967 | A | G | 2 | a0001c0001t0012g0159 a0002c0004t0030g0014 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.7+53984A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74551967 | |||||||
| chr9:74552058 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.7+54075G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552058 | |||||||
| chr9:74552111 | T | C | 1 | a0001c0001t0011g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.7+54128T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552111 | |||||||
| chr9:74552120 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+54137G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552120 | |||||||
| chr9:74552361 | T | G | 4 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0137 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+54378T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552361 | |||||||
| chr9:74552423 | C | T | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+54440C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552423 | |||||||
| chr9:74552541 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+54558G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552541 | |||||||
| chr9:74552586 | C | T | 3 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0017g0107 |
3 | HG02723.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7+54603C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552586 | |||||||
| chr9:74552598 | T | C | 1 | a0001c0002t0003g0042 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.7+54615T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552598 | |||||||
| chr9:74552766 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.7+54783G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552766 | |||||||
| chr9:74552788 | C | T | 1 | a0001c0001t0024g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.7+54805C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74552788 | |||||||
| chr9:74553183 | C | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0067 others(68): Show |
72 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.7+55200C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553183 | |||||||
| chr9:74553184 | G | A | 1 | a0001c0002t0005g0001 | 2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.7+55201G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553184 | |||||||
| chr9:74553195 | C | T | 1 | a0001c0001t0004g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.7+55212C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553195 | |||||||
| chr9:74553289 | T | C | 23 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0001t0001g0114 others(20): Show |
23 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.7+55306T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553289 | |||||||
| chr9:74553524 | C | T | 1 | a0001c0001t0008g0106 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.7+55541C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553524 | |||||||
| chr9:74553533 | G | A | 1 | a0001c0001t0038g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.7+55550G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553533 | |||||||
| chr9:74553535 | A | T | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.7+55552A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553535 | |||||||
| chr9:74553576 | T | TA | 52 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0113 others(49): Show |
52 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.7+55596dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74553576 | ||||||
| chr9:74553832 | G | A | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+55849G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553832 | |||||||
| chr9:74553873 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.7+55890T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553873 | |||||||
| chr9:74553916 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.7+55933A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74553916 | |||||||
| chr9:74554062 | G | A | 1 | a0001c0001t0008g0106 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.7+56079G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74554062 | |||||||
| chr9:74554072 | C | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+56089C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74554072 | |||||||
| chr9:74554102 | G | A | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7+56119G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74554102 | |||||||
| chr9:74554331 | C | T | 3 | a0001c0001t0012g0159 a0001c0001t0051g0203 a0002c0004t0030g0014 |
3 | HG02970.hp2 HG03098.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.7+56348C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74554331 | |||||||
| chr9:74554485 | ACAGT | A | 8 | a0001c0001t0004g0158 a0001c0001t0010g0143 a0001c0001t0010g0224 others(5): Show |
8 | HG02257.hp1 HG02723.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.7+56506_7+56509del others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74554485 | ||||||
| chr9:74554576 | TA | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+56605delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74554576 | ||||||
| chr9:74554626 | C | T | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7+56643C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74554626 | |||||||
| chr9:74554805 | A | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+56822A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74554805 | |||||||
| chr9:74554963 | A | G | 6 | a0001c0001t0013g0110 a0001c0001t0015g0111 a0001c0001t0015g0142 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.7+56980A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74554963 | |||||||
| chr9:74555002 | G | A | 1 | a0001c0001t0002g0166 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.7+57019G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74555002 | |||||||
| chr9:74555107 | C | T | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.7+57124C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74555107 | |||||||
| chr9:74555417 | G | A | 1 | a0001c0001t0015g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.7+57434G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74555417 | |||||||
| chr9:74555471 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+57488A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74555471 | |||||||
| chr9:74555748 | G | A | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7+57765G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74555748 | |||||||
| chr9:74555750 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0173 a0001c0001t0001g0177 others(10): Show |
14 | HG02040.hp1 HG02523.hp1 HG04184.hp1 others(11): Show |
intron_variant | MODIFIER | c.7+57767A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74555750 | |||||||
| chr9:74555930 | G | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.7+57947G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74555930 | |||||||
| chr9:74556102 | G | T | 1 | a0001c0001t0014g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.7+58119G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74556102 | |||||||
| chr9:74556370 | C | T | 1 | a0001c0002t0023g0044 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.7+58387C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74556370 | |||||||
| chr9:74556371 | A | G | 1 | a0001c0002t0023g0044 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.7+58388A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74556371 | |||||||
| chr9:74556481 | C | A | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7+58498C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74556481 | |||||||
| chr9:74556526 | A | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
140 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.7+58543A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74556526 | |||||||
| chr9:74556670 | C | T | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7+58687C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74556670 | |||||||
| chr9:74556676 | CA | C | 2 | a0001c0001t0004g0096 a0001c0001t0041g0074 |
2 | HG01109.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.7+58695delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74556676 | ||||||
| chr9:74556870 | C | G | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.7+58887C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74556870 | |||||||
| chr9:74557138 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.7+59155G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74557138 | |||||||
| chr9:74557292 | A | G | 3 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0017g0107 |
3 | HG02723.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.7+59309A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74557292 | |||||||
| chr9:74557319 | C | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(78): Show |
82 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.7+59336C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74557319 | |||||||
| chr9:74557447 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.7+59464T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74557447 | |||||||
| chr9:74557570 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0113 others(30): Show |
33 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.7+59587C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74557570 | |||||||
| chr9:74557701 | G | A | 5 | a0001c0001t0013g0110 a0001c0001t0015g0111 a0001c0001t0015g0142 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.7+59718G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74557701 | |||||||
| chr9:74557728 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+59745G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74557728 | |||||||
| chr9:74557870 | G | T | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7+59887G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74557870 | |||||||
| chr9:74557957 | C | T | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.7+59974C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74557957 | |||||||
| chr9:74558263 | G | A | 1 | a0001c0002t0004g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.7+60280G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74558263 | |||||||
| chr9:74558590 | T | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(78): Show |
82 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.7+60607T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74558590 | |||||||
| chr9:74558638 | AAATATCA others(59): Show |
A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+60725_7+60790del others(66): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74558638 | ||||||
| chr9:74558881 | G | A | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+60898G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74558881 | |||||||
| chr9:74559314 | A | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+61331A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74559314 | |||||||
| chr9:74559380 | T | C | 1 | a0001c0001t0004g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.7+61397T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74559380 | |||||||
| chr9:74559517 | A | C | 1 | a0001c0001t0008g0196 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.7+61534A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74559517 | |||||||
| chr9:74559735 | G | T | 1 | a0001c0002t0002g0049 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.7+61752G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74559735 | |||||||
| chr9:74559894 | A | C | 83 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(80): Show |
84 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.7+61911A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74559894 | |||||||
| chr9:74560101 | G | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+62118G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74560101 | |||||||
| chr9:74560166 | C | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(80): Show |
84 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.7+62183C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74560166 | |||||||
| chr9:74560218 | A | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+62235A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74560218 | |||||||
| chr9:74560426 | C | T | 4 | a0001c0001t0031g0121 a0001c0002t0001g0122 a0001c0002t0003g0124 others(1): Show |
4 | HG01074.hp1 HG01256.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.7+62443C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74560426 | |||||||
| chr9:74560539 | CAGA | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(78): Show |
82 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.7+62559_7+62561del others(3): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74560539 | ||||||
| chr9:74560664 | T | G | 3 | a0001c0001t0016g0029 a0001c0001t0018g0030 a0001c0001t0046g0094 |
3 | HG02257.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7+62681T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74560664 | |||||||
| chr9:74560747 | G | T | 1 | a0001c0002t0002g0049 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.7+62764G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74560747 | |||||||
| chr9:74561253 | A | G | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+63270A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74561253 | |||||||
| chr9:74561318 | T | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+63335T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74561318 | |||||||
| chr9:74561327 | A | C | 4 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0137 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+63344A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74561327 | |||||||
| chr9:74561475 | A | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+63492A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74561475 | |||||||
| chr9:74561978 | A | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+63995A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74561978 | |||||||
| chr9:74561992 | C | T | 3 | a0001c0001t0016g0029 a0001c0001t0018g0030 a0001c0001t0046g0094 |
3 | HG02257.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.7+64009C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74561992 | |||||||
| chr9:74562052 | G | A | 1 | a0001c0001t0063g0197 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.7+64069G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562052 | |||||||
| chr9:74562226 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+64243G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562226 | |||||||
| chr9:74562263 | G | A | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+64280G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562263 | |||||||
| chr9:74562265 | A | G | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+64282A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562265 | |||||||
| chr9:74562619 | G | C | 1 | a0001c0001t0001g0012 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.7+64636G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562619 | |||||||
| chr9:74562691 | C | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+64708C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562691 | |||||||
| chr9:74562725 | T | C | 1 | a0001c0001t0006g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.7+64742T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562725 | |||||||
| chr9:74562732 | A | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.7+64749A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562732 | |||||||
| chr9:74562955 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.7+64972T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562955 | |||||||
| chr9:74562956 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.7+64973C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562956 | |||||||
| chr9:74563118 | G | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.7+65135G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74563118 | |||||||
| chr9:74563141 | G | T | 81 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(78): Show |
82 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.7+65158G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74563141 | |||||||
| chr9:74563184 | C | CT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0071 others(20): Show |
23 | HG00609.hp1 HG01106.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.7+65222dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74563184 | ||||||
| chr9:74563184 | CT | C | 8 | a0001c0001t0001g0148 a0001c0001t0001g0173 a0001c0001t0001g0177 others(5): Show |
8 | HG01496.hp1 HG01496.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.7+65222delT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74563184 | ||||||
| chr9:74563225 | G | A | 2 | a0001c0001t0001g0043 a0001c0002t0023g0044 |
2 | HG01175.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.7+65242G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74563225 | |||||||
| chr9:74563281 | A | G | 1 | a0001c0001t0055g0017 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.7+65298A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74563281 | |||||||
| chr9:74563310 | C | T | 3 | a0001c0001t0001g0183 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | NA18944.hp1 NA18979.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.7+65327C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74563310 | |||||||
| chr9:74563614 | C | T | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7+65631C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74563614 | |||||||
| chr9:74563803 | A | C | 2 | a0001c0002t0002g0049 a0001c0002t0005g0001 |
3 | NA18960.hp2 NA18977.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.7+65820A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74563803 | |||||||
| chr9:74563937 | G | A | 1 | a0001c0001t0045g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.7+65954G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74563937 | |||||||
| chr9:74564124 | A | G | 4 | a0001c0001t0006g0102 a0001c0001t0006g0181 a0001c0001t0026g0186 others(1): Show |
4 | HG01070.hp2 HG01106.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.7+66141A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74564124 | |||||||
| chr9:74564464 | T | C | 1 | a0001c0002t0003g0041 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.8-65818T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74564464 | |||||||
| chr9:74564616 | A | G | 5 | a0001c0001t0013g0110 a0001c0001t0015g0111 a0001c0001t0015g0142 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-65666A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74564616 | |||||||
| chr9:74564721 | A | G | 1 | a0001c0001t0029g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.8-65561A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74564721 | |||||||
| chr9:74564981 | T | C | 1 | a0001c0001t0049g0105 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.8-65301T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74564981 | |||||||
| chr9:74565186 | A | T | 2 | a0001c0001t0038g0162 a0001c0001t0051g0203 |
2 | HG02280.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-65096A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74565186 | |||||||
| chr9:74565392 | C | T | 1 | a0001c0001t0009g0023 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.8-64890C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74565392 | |||||||
| chr9:74565732 | G | T | 1 | a0001c0001t0062g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.8-64550G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74565732 | |||||||
| chr9:74566077 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.8-64205G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74566077 | |||||||
| chr9:74566237 | C | T | 1 | a0001c0001t0007g0213 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.8-64045C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74566237 | |||||||
| chr9:74566715 | T | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(78): Show |
82 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.8-63567T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74566715 | |||||||
| chr9:74566753 | T | C | 81 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(78): Show |
82 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.8-63529T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74566753 | |||||||
| chr9:74566771 | T | C | 5 | a0001c0001t0013g0110 a0001c0001t0015g0111 a0001c0001t0015g0142 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-63511T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74566771 | |||||||
| chr9:74566970 | T | C | 1 | a0001c0001t0019g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.8-63312T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74566970 | |||||||
| chr9:74567026 | C | T | 1 | a0001c0002t0003g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.8-63256C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74567026 | |||||||
| chr9:74567032 | CT | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0148 others(4): Show |
7 | HG01192.hp1 HG01496.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-63239delT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74567032 | ||||||
| chr9:74567066 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.8-63216C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74567066 | |||||||
| chr9:74567107 | A | C | 1 | a0001c0001t0017g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8-63175A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74567107 | |||||||
| chr9:74567192 | A | AT | 3 | a0001c0001t0016g0029 a0001c0001t0018g0030 a0001c0001t0046g0094 |
3 | HG02257.hp1 HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.8-63084dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74567192 | ||||||
| chr9:74567278 | T | C | 1 | a0001c0001t0014g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-63004T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74567278 | |||||||
| chr9:74567482 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.8-62800A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74567482 | |||||||
| chr9:74567730 | C | T | 1 | a0001c0002t0022g0028 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.8-62552C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74567730 | |||||||
| chr9:74568356 | A | C | 18 | a0001c0001t0001g0043 a0001c0001t0002g0119 a0001c0001t0039g0033 others(15): Show |
19 | HG00140.hp1 HG01081.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.8-61926A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568356 | |||||||
| chr9:74568365 | A | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0148 others(4): Show |
7 | HG01192.hp1 HG01496.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-61917A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568365 | |||||||
| chr9:74568417 | C | T | 5 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0003g0152 others(2): Show |
5 | HG01168.hp2 HG01517.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-61865C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568417 | |||||||
| chr9:74568435 | C | T | 1 | a0001c0001t0006g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.8-61847C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568435 | |||||||
| chr9:74568528 | C | A | 1 | a0001c0001t0038g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.8-61754C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568528 | |||||||
| chr9:74568542 | A | C | 1 | a0001c0001t0038g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.8-61740A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568542 | |||||||
| chr9:74568554 | G | A | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-61728G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568554 | |||||||
| chr9:74568593 | G | C | 3 | a0001c0001t0001g0043 a0001c0002t0003g0050 a0001c0002t0023g0044 |
3 | HG01175.hp1 HG02698.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.8-61689G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568593 | |||||||
| chr9:74568642 | G | A | 81 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(78): Show |
82 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.8-61640G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568642 | |||||||
| chr9:74568699 | C | CA | 73 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(70): Show |
74 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.8-61568dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74568699 | ||||||
| chr9:74568699 | C | CAA | 8 | a0001c0001t0001g0043 a0001c0002t0003g0026 a0001c0002t0003g0041 others(5): Show |
8 | HG01175.hp1 HG02148.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-61569_8-61568dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74568699 | ||||||
| chr9:74568710 | A | G | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8-61572A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74568710 | |||||||
| chr9:74569113 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-61169T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74569113 | |||||||
| chr9:74569133 | T | C | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-61149T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74569133 | |||||||
| chr9:74569300 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.8-60982C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74569300 | |||||||
| chr9:74569597 | A | G | 1 | a0001c0001t0056g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8-60685A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74569597 | |||||||
| chr9:74569750 | A | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.8-60532A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74569750 | |||||||
| chr9:74570073 | C | G | 1 | a0001c0001t0007g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-60209C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74570073 | |||||||
| chr9:74570484 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.8-59798G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74570484 | |||||||
| chr9:74570601 | T | C | 9 | a0001c0001t0012g0159 a0001c0001t0013g0110 a0001c0001t0015g0111 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-59681T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74570601 | |||||||
| chr9:74570730 | C | CGT | 83 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(80): Show |
84 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.8-59543_8-59542dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74570730 | ||||||
| chr9:74570890 | T | C | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8-59392T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74570890 | |||||||
| chr9:74571017 | A | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.8-59265A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74571017 | |||||||
| chr9:74571070 | A | T | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-59212A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74571070 | |||||||
| chr9:74571343 | A | G | 1 | a0001c0002t0002g0049 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.8-58939A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74571343 | |||||||
| chr9:74571384 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-58898T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74571384 | |||||||
| chr9:74571401 | T | TA | 9 | a0001c0001t0001g0071 a0001c0001t0001g0154 a0001c0001t0003g0152 others(6): Show |
9 | HG01517.hp2 HG01978.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-58865dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74571401 | ||||||
| chr9:74571401 | TA | T | 7 | a0001c0001t0001g0208 a0001c0001t0003g0024 a0001c0001t0004g0127 others(4): Show |
7 | HG01070.hp1 HG01168.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-58865delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74571401 | ||||||
| chr9:74571414 | A | T | 2 | a0001c0001t0001g0067 a0001c0001t0010g0160 |
2 | HG02572.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.8-58868A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74571414 | |||||||
| chr9:74571514 | A | G | 6 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0016g0029 others(3): Show |
6 | HG02257.hp1 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-58768A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74571514 | |||||||
| chr9:74571851 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.8-58431T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74571851 | |||||||
| chr9:74571879 | A | G | 2 | a0001c0001t0007g0100 a0001c0001t0016g0099 |
2 | HG01255.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.8-58403A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74571879 | |||||||
| chr9:74572864 | C | T | 4 | a0001c0001t0031g0121 a0001c0002t0001g0122 a0001c0002t0003g0124 others(1): Show |
4 | HG01074.hp1 HG01256.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-57418C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74572864 | |||||||
| chr9:74572865 | G | A | 2 | a0001c0001t0012g0159 a0002c0004t0030g0014 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.8-57417G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74572865 | |||||||
| chr9:74572950 | C | T | 1 | a0001c0002t0003g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.8-57332C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74572950 | |||||||
| chr9:74572951 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.8-57331G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74572951 | |||||||
| chr9:74573251 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.8-57031T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74573251 | |||||||
| chr9:74573464 | TA | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.8-56797delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74573464 | ||||||
| chr9:74573464 | TAA | T | 12 | a0001c0001t0001g0108 a0001c0001t0001g0132 a0001c0001t0006g0084 others(9): Show |
12 | HG01106.hp1 HG01168.hp2 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.8-56798_8-56797del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74573464 | ||||||
| chr9:74573480 | A | C | 2 | a0001c0001t0001g0043 a0001c0002t0003g0050 |
2 | HG01175.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.8-56802A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74573480 | |||||||
| chr9:74573651 | C | T | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-56631C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74573651 | |||||||
| chr9:74573742 | C | T | 71 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0067 others(68): Show |
72 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.8-56540C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74573742 | |||||||
| chr9:74573797 | G | C | 1 | a0001c0001t0056g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8-56485G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74573797 | |||||||
| chr9:74573802 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.8-56480G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74573802 | |||||||
| chr9:74573895 | T | C | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-56387T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74573895 | |||||||
| chr9:74573958 | T | G | 1 | a0001c0001t0036g0150 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.8-56324T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74573958 | |||||||
| chr9:74573969 | G | A | 5 | a0001c0001t0006g0102 a0001c0001t0006g0181 a0001c0001t0006g0209 others(2): Show |
5 | HG01070.hp2 HG01106.hp1 HG04199.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-56313G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74573969 | |||||||
| chr9:74574205 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(77): Show |
81 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.8-56077A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74574205 | |||||||
| chr9:74574236 | C | A | 1 | a0001c0001t0043g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.8-56046C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74574236 | |||||||
| chr9:74574266 | G | C | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8-56016G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74574266 | |||||||
| chr9:74574303 | T | C | 24 | a0001c0001t0001g0035 a0001c0001t0001g0108 a0001c0001t0001g0113 others(21): Show |
24 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.8-55979T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74574303 | |||||||
| chr9:74574318 | C | T | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.8-55964C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74574318 | |||||||
| chr9:74574701 | C | A | 1 | a0001c0005t0006g0218 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.8-55581C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74574701 | |||||||
| chr9:74574887 | C | T | 1 | a0001c0001t0039g0033 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.8-55395C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74574887 | |||||||
| chr9:74574919 | C | T | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-55363C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74574919 | |||||||
| chr9:74574935 | G | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-55347G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74574935 | |||||||
| chr9:74575083 | C | T | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.8-55199C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74575083 | |||||||
| chr9:74575318 | A | G | 6 | a0001c0001t0013g0036 a0001c0001t0013g0051 a0001c0001t0013g0052 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-54964A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74575318 | |||||||
| chr9:74575334 | C | T | 1 | a0001c0001t0004g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.8-54948C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74575334 | |||||||
| chr9:74575464 | T | C | 34 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0108 others(31): Show |
34 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.8-54818T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74575464 | |||||||
| chr9:74575489 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.8-54793A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74575489 | |||||||
| chr9:74575507 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.8-54775G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74575507 | |||||||
| chr9:74575564 | T | A | 4 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0137 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-54718T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74575564 | |||||||
| chr9:74576381 | C | T | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-53901C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74576381 | |||||||
| chr9:74576466 | A | AGATTT | 186 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(183): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.8-53814_8-53813ins others(5): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74576466 | ||||||
| chr9:74576546 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-53736T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74576546 | |||||||
| chr9:74576632 | A | G | 1 | a0001c0001t0008g0078 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.8-53650A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74576632 | |||||||
| chr9:74576634 | C | A | 1 | a0001c0001t0008g0078 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.8-53648C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74576634 | |||||||
| chr9:74576780 | T | C | 1 | a0001c0001t0005g0011 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.8-53502T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74576780 | |||||||
| chr9:74576834 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-53448A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74576834 | |||||||
| chr9:74577176 | G | T | 1 | a0001c0001t0042g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8-53106G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74577176 | |||||||
| chr9:74577245 | T | G | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-53037T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74577245 | |||||||
| chr9:74577453 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-52829A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74577453 | |||||||
| chr9:74577461 | A | G | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-52821A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74577461 | |||||||
| chr9:74577677 | C | T | 137 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(134): Show |
138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.8-52605C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74577677 | |||||||
| chr9:74577727 | T | G | 137 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(134): Show |
138 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.8-52555T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74577727 | |||||||
| chr9:74577782 | T | A | 83 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(80): Show |
84 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.8-52500T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74577782 | |||||||
| chr9:74577842 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.8-52440C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74577842 | |||||||
| chr9:74577925 | C | T | 52 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0108 others(49): Show |
52 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.8-52357C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74577925 | |||||||
| chr9:74578202 | A | C | 71 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0067 others(68): Show |
72 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.8-52080A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74578202 | |||||||
| chr9:74578301 | C | T | 2 | a0001c0001t0001g0206 a0001c0001t0011g0207 |
2 | HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.8-51981C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74578301 | |||||||
| chr9:74578340 | A | G | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-51942A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74578340 | |||||||
| chr9:74578642 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.8-51640A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74578642 | |||||||
| chr9:74578686 | CT | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-51591delT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74578686 | ||||||
| chr9:74579037 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(64): Show |
68 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.8-51245C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579037 | |||||||
| chr9:74579039 | C | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-51243C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579039 | |||||||
| chr9:74579171 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0020g0138 a0001c0001t0020g0139 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.8-51111T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579171 | |||||||
| chr9:74579265 | C | G | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.8-51017C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579265 | |||||||
| chr9:74579277 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-51005T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579277 | |||||||
| chr9:74579298 | T | C | 1 | a0001c0001t0056g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8-50984T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579298 | |||||||
| chr9:74579371 | T | G | 1 | a0001c0001t0029g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.8-50911T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579371 | |||||||
| chr9:74579612 | A | G | 140 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(137): Show |
141 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.8-50670A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579612 | |||||||
| chr9:74579643 | C | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-50639C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579643 | |||||||
| chr9:74579696 | C | T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0108 others(27): Show |
30 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.8-50586C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579696 | |||||||
| chr9:74579889 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.8-50393G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579889 | |||||||
| chr9:74579907 | T | G | 1 | a0001c0001t0034g0064 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.8-50375T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579907 | |||||||
| chr9:74580180 | G | A | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-50102G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74580180 | |||||||
| chr9:74580448 | T | C | 1 | a0001c0001t0006g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.8-49834T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74580448 | |||||||
| chr9:74580592 | A | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-49690A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74580592 | |||||||
| chr9:74580616 | T | C | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8-49666T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74580616 | |||||||
| chr9:74580771 | T | C | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-49511T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74580771 | |||||||
| chr9:74581833 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.8-48449T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74581833 | |||||||
| chr9:74581933 | G | A | 3 | a0001c0001t0025g0054 a0001c0001t0025g0217 a0001c0002t0065g0031 |
3 | HG00408.hp2 HG00609.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.8-48349G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74581933 | |||||||
| chr9:74582002 | A | C | 1 | a0001c0001t0006g0063 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.8-48280A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582002 | |||||||
| chr9:74582111 | T | C | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-48171T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582111 | |||||||
| chr9:74582245 | G | A | 42 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0108 others(39): Show |
42 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.8-48037G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582245 | |||||||
| chr9:74582457 | T | C | 1 | a0001c0001t0017g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8-47825T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582457 | |||||||
| chr9:74582555 | G | A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.8-47727G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582555 | |||||||
| chr9:74582685 | C | T | 1 | a0001c0001t0011g0172 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.8-47597C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582685 | |||||||
| chr9:74582699 | G | A | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-47583G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582699 | |||||||
| chr9:74582728 | C | T | 1 | a0001c0005t0006g0218 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.8-47554C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582728 | |||||||
| chr9:74582739 | G | A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(81): Show |
85 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.8-47543G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582739 | |||||||
| chr9:74582774 | T | C | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-47508T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582774 | |||||||
| chr9:74582786 | T | C | 3 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0017g0107 |
3 | HG02723.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8-47496T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582786 | |||||||
| chr9:74582805 | G | C | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-47477G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582805 | |||||||
| chr9:74582892 | T | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.8-47390T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582892 | |||||||
| chr9:74582968 | G | A | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8-47314G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582968 | |||||||
| chr9:74582972 | C | T | 3 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0010g0160 |
3 | HG02572.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-47310C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74582972 | |||||||
| chr9:74583104 | C | G | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8-47178C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74583104 | |||||||
| chr9:74583137 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.8-47145C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74583137 | |||||||
| chr9:74583167 | C | T | 1 | a0001c0001t0001g0012 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.8-47115C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74583167 | |||||||
| chr9:74583228 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.8-47054T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74583228 | |||||||
| chr9:74583320 | G | A | 2 | a0001c0001t0007g0013 a0001c0001t0056g0220 |
2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.8-46962G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74583320 | |||||||
| chr9:74583365 | A | G | 84 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(81): Show |
85 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.8-46917A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74583365 | |||||||
| chr9:74584007 | T | C | 2 | a0001c0001t0051g0203 a0001c0002t0060g0016 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-46275T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74584007 | |||||||
| chr9:74584031 | T | C | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-46251T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74584031 | |||||||
| chr9:74584095 | T | G | 2 | a0001c0001t0001g0133 a0001c0001t0001g0136 |
2 | HG00597.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.8-46187T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74584095 | |||||||
| chr9:74584136 | G | A | 2 | a0001c0001t0051g0203 a0001c0002t0060g0016 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-46146G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74584136 | |||||||
| chr9:74584165 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-46117G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74584165 | |||||||
| chr9:74584241 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-46041C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74584241 | |||||||
| chr9:74584299 | G | A | 1 | a0001c0001t0024g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.8-45983G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74584299 | |||||||
| chr9:74584760 | G | A | 1 | a0001c0001t0062g0104 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.8-45522G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74584760 | |||||||
| chr9:74585085 | C | A | 1 | a0001c0001t0004g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.8-45197C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585085 | |||||||
| chr9:74585120 | T | G | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(64): Show |
68 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.8-45162T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585120 | |||||||
| chr9:74585270 | C | G | 19 | a0001c0001t0001g0043 a0001c0001t0039g0033 a0001c0001t0043g0048 others(16): Show |
20 | HG00140.hp1 HG01081.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.8-45012C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585270 | |||||||
| chr9:74585375 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(64): Show |
68 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.8-44907C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585375 | |||||||
| chr9:74585752 | T | A | 3 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0017g0107 |
3 | HG02723.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8-44530T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585752 | |||||||
| chr9:74585784 | A | AATATTTA others(10): Show |
1 | a0001c0001t0018g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.8-44498_8-44497ins others(17): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585784 | |||||||
| chr9:74585784 | A | ATATT | 45 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0067 others(42): Show |
45 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.8-44473_8-44470dup others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74585784 | ||||||
| chr9:74585784 | A | ATATTTAT others(1): Show |
11 | a0001c0001t0001g0202 a0001c0001t0007g0213 a0001c0001t0012g0210 others(8): Show |
11 | HG00609.hp2 HG01891.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.8-44477_8-44470dup others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74585784 | ||||||
| chr9:74585784 | A | ATATTTAT others(5): Show |
35 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0059 others(32): Show |
36 | HG00140.hp1 HG01074.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.8-44481_8-44470dup others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74585784 | ||||||
| chr9:74585784 | A | ATATTTAT others(9): Show |
44 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0068 others(41): Show |
44 | HG00323.hp1 HG00597.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.8-44485_8-44470dup others(16): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74585784 | ||||||
| chr9:74585784 | A | ATATTTAT others(13): Show |
65 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0032 others(62): Show |
66 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.8-44489_8-44470dup others(20): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74585784 | ||||||
| chr9:74585784 | A | ATATTTAT others(17): Show |
8 | a0001c0001t0001g0088 a0001c0001t0001g0148 a0001c0001t0001g0208 others(5): Show |
8 | HG01106.hp1 HG01496.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-44493_8-44470dup others(24): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74585784 | ||||||
| chr9:74585834 | G | A | 85 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(82): Show |
86 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.8-44448G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585834 | |||||||
| chr9:74585840 | A | G | 3 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0010g0160 |
3 | HG02572.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-44442A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585840 | |||||||
| chr9:74585940 | G | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0161 |
2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-44342G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585940 | |||||||
| chr9:74585970 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-44312G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74585970 | |||||||
| chr9:74586054 | A | G | 3 | a0001c0001t0025g0054 a0001c0001t0025g0217 a0001c0002t0065g0031 |
3 | HG00408.hp2 HG00609.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.8-44228A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586054 | |||||||
| chr9:74586110 | A | G | 84 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(81): Show |
85 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.8-44172A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586110 | |||||||
| chr9:74586215 | G | C | 8 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0004g0158 others(5): Show |
8 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-44067G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586215 | |||||||
| chr9:74586249 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.8-44033G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586249 | |||||||
| chr9:74586267 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0185 |
2 | HG01109.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.8-44015G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586267 | |||||||
| chr9:74586301 | C | T | 5 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0137 others(2): Show |
5 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-43981C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586301 | |||||||
| chr9:74586354 | C | T | 139 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(136): Show |
140 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.8-43928C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586354 | |||||||
| chr9:74586571 | C | T | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
210 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.8-43711C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586571 | |||||||
| chr9:74586572 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-43710G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586572 | |||||||
| chr9:74586600 | C | CGT | 7 | a0001c0001t0001g0035 a0001c0001t0007g0013 a0001c0001t0007g0039 others(4): Show |
7 | HG01109.hp1 HG02080.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-43645_8-43644dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74586600 | ||||||
| chr9:74586600 | C | CGTGT | 29 | a0001c0001t0001g0108 a0001c0001t0001g0113 a0001c0001t0001g0114 others(26): Show |
29 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.8-43647_8-43644dup others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74586600 | ||||||
| chr9:74586600 | C | CGTGTGT | 52 | a0001c0001t0001g0043 a0001c0001t0001g0067 a0001c0001t0001g0135 others(49): Show |
53 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.8-43649_8-43644dup others(6): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74586600 | ||||||
| chr9:74586600 | C | CGTGTGTG others(1): Show |
52 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0080 others(49): Show |
53 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.8-43651_8-43644dup others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74586600 | ||||||
| chr9:74586600 | C | CGTGTGTG others(3): Show |
49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(46): Show |
49 | HG00323.hp1 HG00597.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.8-43653_8-43644dup others(10): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74586600 | ||||||
| chr9:74586600 | C | CGTGTGTG others(5): Show |
9 | a0001c0001t0001g0068 a0001c0001t0001g0200 a0001c0001t0005g0011 others(6): Show |
9 | HG01071.hp1 HG01256.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.8-43655_8-43644dup others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74586600 | ||||||
| chr9:74586600 | C | CGTGTGTG others(7): Show |
6 | a0001c0001t0001g0208 a0001c0001t0010g0160 a0001c0001t0018g0030 others(3): Show |
6 | HG01978.hp1 HG02257.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-43657_8-43644dup others(14): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74586600 | ||||||
| chr9:74586600 | CGT | C | 2 | a0001c0001t0004g0096 a0001c0002t0003g0164 |
2 | HG02698.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.8-43645_8-43644del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74586600 | ||||||
| chr9:74586600 | CGTGTGTG others(1): Show |
C | 3 | a0001c0001t0001g0007 a0001c0001t0020g0138 a0001c0001t0020g0139 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.8-43651_8-43644del others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74586600 | ||||||
| chr9:74586670 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-43612G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586670 | |||||||
| chr9:74586706 | T | C | 3 | a0001c0001t0004g0175 a0001c0001t0005g0169 a0001c0001t0063g0197 |
3 | NA19001.hp1 NA19007.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.8-43576T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586706 | |||||||
| chr9:74586826 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-43456T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586826 | |||||||
| chr9:74586909 | A | G | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8-43373A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74586909 | |||||||
| chr9:74587021 | G | C | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-43261G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74587021 | |||||||
| chr9:74587024 | T | C | 1 | a0001c0001t0004g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.8-43258T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74587024 | |||||||
| chr9:74587163 | C | T | 3 | a0001c0001t0005g0189 a0001c0001t0005g0201 a0001c0001t0028g0188 |
3 | NA18960.hp1 NA18969.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.8-43119C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74587163 | |||||||
| chr9:74587164 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.8-43118G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74587164 | |||||||
| chr9:74587460 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-42822T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74587460 | |||||||
| chr9:74587573 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.8-42709C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74587573 | |||||||
| chr9:74587965 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-42317G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74587965 | |||||||
| chr9:74588140 | C | T | 1 | a0001c0001t0027g0082 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.8-42142C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74588140 | |||||||
| chr9:74588208 | A | G | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-42074A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74588208 | |||||||
| chr9:74588542 | A | G | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-41740A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74588542 | |||||||
| chr9:74588559 | T | A | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-41723T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74588559 | |||||||
| chr9:74588611 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-41671A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74588611 | |||||||
| chr9:74588635 | C | T | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-41647C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74588635 | |||||||
| chr9:74588938 | TA | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-41332delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74588938 | ||||||
| chr9:74589149 | C | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(135): Show |
139 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.8-41133C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74589149 | |||||||
| chr9:74589254 | T | G | 5 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0137 others(2): Show |
5 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-41028T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74589254 | |||||||
| chr9:74589328 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0002g0083 |
2 | NA18951.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.8-40954A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74589328 | |||||||
| chr9:74589382 | A | G | 1 | a0001c0001t0017g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.8-40900A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74589382 | |||||||
| chr9:74589776 | C | T | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-40506C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74589776 | |||||||
| chr9:74590146 | A | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-40136A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590146 | |||||||
| chr9:74590194 | A | G | 2 | a0001c0001t0007g0013 a0001c0001t0056g0220 |
2 | HG01884.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.8-40088A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590194 | |||||||
| chr9:74590394 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0011g0179 |
3 | HG00140.hp2 HG01261.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.8-39888G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590394 | |||||||
| chr9:74590434 | C | T | 2 | a0001c0001t0004g0126 a0001c0001t0004g0127 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.8-39848C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590434 | |||||||
| chr9:74590537 | A | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.8-39745A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590537 | |||||||
| chr9:74590696 | G | T | 1 | a0001c0001t0009g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.8-39586G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590696 | |||||||
| chr9:74590710 | A | C | 3 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0052g0147 |
3 | HG02896.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.8-39572A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590710 | |||||||
| chr9:74590769 | T | TTTTTGTT others(3): Show |
1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-39493_8-39484dup others(10): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74590769 | ||||||
| chr9:74590769 | TTTTTGTT others(3): Show |
T | 2 | a0001c0001t0001g0080 a0001c0001t0033g0079 |
2 | NA18999.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.8-39493_8-39484del others(10): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74590769 | ||||||
| chr9:74590799 | A | G | 3 | a0001c0001t0014g0010 a0001c0001t0051g0203 a0001c0002t0060g0016 |
3 | HG02630.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-39483A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590799 | |||||||
| chr9:74590823 | G | T | 1 | a0001c0001t0014g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.8-39459G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590823 | |||||||
| chr9:74590967 | T | C | 1 | a0001c0001t0004g0096 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.8-39315T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590967 | |||||||
| chr9:74590975 | T | G | 1 | a0001c0002t0061g0045 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.8-39307T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74590975 | |||||||
| chr9:74591214 | A | G | 2 | a0001c0001t0010g0143 a0001c0001t0010g0224 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.8-39068A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74591214 | |||||||
| chr9:74591292 | T | C | 1 | a0001c0001t0042g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.8-38990T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74591292 | |||||||
| chr9:74591316 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-38966A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74591316 | |||||||
| chr9:74591327 | G | A | 5 | a0001c0001t0001g0071 a0001c0001t0002g0040 a0001c0001t0002g0072 others(2): Show |
5 | HG01433.hp1 HG01975.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-38955G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74591327 | |||||||
| chr9:74591607 | C | T | 1 | a0001c0002t0002g0049 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.8-38675C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74591607 | |||||||
| chr9:74591798 | T | A | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.8-38484T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74591798 | |||||||
| chr9:74591958 | CAG | C | 3 | a0001c0001t0001g0178 a0001c0001t0035g0146 a0001c0002t0003g0214 |
3 | HG00738.hp1 HG01261.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.8-38307_8-38306del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74591958 | ||||||
| chr9:74591976 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.8-38306G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74591976 | |||||||
| chr9:74592024 | C | T | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8-38258C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74592024 | |||||||
| chr9:74592425 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-37857G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74592425 | |||||||
| chr9:74592504 | T | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-37778T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74592504 | |||||||
| chr9:74592585 | C | T | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8-37697C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74592585 | |||||||
| chr9:74593071 | G | A | 8 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0004g0158 others(5): Show |
8 | HG02723.hp2 HG02818.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-37211G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593071 | |||||||
| chr9:74593097 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-37185T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593097 | |||||||
| chr9:74593194 | C | T | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-37088C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593194 | |||||||
| chr9:74593305 | A | G | 2 | a0001c0001t0051g0203 a0001c0002t0060g0016 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-36977A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593305 | |||||||
| chr9:74593322 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-36960C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593322 | |||||||
| chr9:74593395 | G | T | 2 | a0001c0001t0051g0203 a0001c0002t0060g0016 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-36887G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593395 | |||||||
| chr9:74593415 | G | A | 1 | a0001c0001t0010g0004 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.8-36867G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593415 | |||||||
| chr9:74593455 | C | G | 4 | a0001c0001t0002g0066 a0001c0001t0002g0073 a0001c0001t0002g0085 others(1): Show |
4 | HG02135.hp1 NA18982.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-36827C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593455 | |||||||
| chr9:74593466 | T | TA | 64 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(61): Show |
65 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(62): Show |
intron_variant | MODIFIER | c.8-36798dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74593466 | ||||||
| chr9:74593466 | TA | T | 133 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(130): Show |
134 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.8-36798delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74593466 | ||||||
| chr9:74593466 | TAA | T | 5 | a0001c0001t0002g0066 a0001c0001t0002g0073 a0001c0001t0002g0085 others(2): Show |
5 | HG02135.hp1 NA18982.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-36799_8-36798del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74593466 | ||||||
| chr9:74593483 | A | G | 1 | a0001c0002t0005g0077 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.8-36799A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593483 | |||||||
| chr9:74593485 | C | A | 1 | a0001c0001t0004g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.8-36797C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593485 | |||||||
| chr9:74593525 | G | A | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8-36757G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593525 | |||||||
| chr9:74593531 | T | C | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-36751T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593531 | |||||||
| chr9:74593546 | T | C | 2 | a0001c0001t0051g0203 a0001c0002t0060g0016 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-36736T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593546 | |||||||
| chr9:74593754 | A | G | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-36528A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593754 | |||||||
| chr9:74593760 | A | G | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8-36522A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593760 | |||||||
| chr9:74593966 | C | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(81): Show |
85 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.8-36316C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74593966 | |||||||
| chr9:74594121 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(64): Show |
68 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.8-36161C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74594121 | |||||||
| chr9:74594376 | C | A | 2 | a0001c0001t0007g0100 a0001c0001t0016g0099 |
2 | HG01255.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.8-35906C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74594376 | |||||||
| chr9:74594554 | T | C | 62 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(59): Show |
63 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.8-35728T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74594554 | |||||||
| chr9:74594955 | C | T | 1 | a0001c0001t0056g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8-35327C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74594955 | |||||||
| chr9:74595280 | T | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.8-35002T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74595280 | |||||||
| chr9:74595375 | C | T | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-34907C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74595375 | |||||||
| chr9:74595432 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0048g0144 |
2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.8-34850A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74595432 | |||||||
| chr9:74595838 | T | C | 5 | a0001c0001t0013g0110 a0001c0001t0015g0111 a0001c0001t0015g0142 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-34444T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74595838 | |||||||
| chr9:74595867 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-34415C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74595867 | |||||||
| chr9:74595873 | G | A | 2 | a0001c0001t0013g0051 a0001c0001t0013g0052 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.8-34409G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74595873 | |||||||
| chr9:74596055 | A | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-34227A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74596055 | |||||||
| chr9:74596101 | A | G | 2 | a0001c0001t0014g0020 a0001c0001t0014g0021 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.8-34181A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74596101 | |||||||
| chr9:74596213 | G | A | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-34069G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74596213 | |||||||
| chr9:74596412 | C | T | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(64): Show |
68 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.8-33870C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74596412 | |||||||
| chr9:74596577 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.8-33705C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74596577 | |||||||
| chr9:74596800 | G | A | 3 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0017g0107 |
3 | HG02723.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8-33482G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74596800 | |||||||
| chr9:74596979 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.8-33303C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74596979 | |||||||
| chr9:74597117 | G | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0108 others(39): Show |
42 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.8-33165G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597117 | |||||||
| chr9:74597167 | G | C | 32 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0108 others(29): Show |
32 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.8-33115G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597167 | |||||||
| chr9:74597194 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.8-33088G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597194 | |||||||
| chr9:74597398 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-32884C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597398 | |||||||
| chr9:74597635 | TA | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.8-32639delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74597635 | ||||||
| chr9:74597685 | A | T | 97 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(94): Show |
98 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.8-32597A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597685 | |||||||
| chr9:74597713 | C | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0148 others(4): Show |
7 | HG01192.hp1 HG01496.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-32569C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597713 | |||||||
| chr9:74597756 | C | T | 2 | a0001c0001t0016g0029 a0001c0001t0046g0094 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.8-32526C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597756 | |||||||
| chr9:74597787 | C | T | 1 | a0001c0001t0009g0023 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.8-32495C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597787 | |||||||
| chr9:74597882 | C | T | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-32400C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597882 | |||||||
| chr9:74597893 | G | C | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-32389G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597893 | |||||||
| chr9:74597913 | G | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0018g0030 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-32369G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74597913 | |||||||
| chr9:74598298 | T | C | 1 | a0001c0001t0050g0145 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.8-31984T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74598298 | |||||||
| chr9:74598350 | G | C | 97 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(94): Show |
98 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.8-31932G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74598350 | |||||||
| chr9:74598356 | A | G | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-31926A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74598356 | |||||||
| chr9:74598456 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-31826C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74598456 | |||||||
| chr9:74598728 | G | GGA | 45 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0108 others(42): Show |
45 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.8-31554_8-31553ins others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74598728 | |||||||
| chr9:74598742 | G | A | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-31540G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74598742 | |||||||
| chr9:74599420 | A | C | 1 | a0001c0001t0056g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8-30862A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74599420 | |||||||
| chr9:74599728 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-30554G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74599728 | |||||||
| chr9:74599792 | T | G | 1 | a0001c0001t0016g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.8-30490T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74599792 | |||||||
| chr9:74599853 | G | T | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.8-30429G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74599853 | |||||||
| chr9:74599986 | C | A | 96 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(93): Show |
97 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.8-30296C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74599986 | |||||||
| chr9:74600096 | C | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.8-30186C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74600096 | |||||||
| chr9:74600139 | C | T | 1 | a0001c0001t0041g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.8-30143C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74600139 | |||||||
| chr9:74600496 | A | G | 3 | a0001c0001t0001g0183 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | NA18944.hp1 NA18979.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.8-29786A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74600496 | |||||||
| chr9:74600536 | C | G | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-29746C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74600536 | |||||||
| chr9:74600730 | A | G | 1 | a0001c0001t0004g0096 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.8-29552A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74600730 | |||||||
| chr9:74601305 | T | C | 3 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0017g0107 |
3 | HG02723.hp2 HG02970.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.8-28977T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74601305 | |||||||
| chr9:74601371 | T | TTA | 96 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(93): Show |
97 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.8-28901_8-28900dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74601371 | ||||||
| chr9:74601417 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0007g0013 |
2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8-28865G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74601417 | |||||||
| chr9:74601458 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.8-28824C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74601458 | |||||||
| chr9:74601654 | A | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-28628A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74601654 | |||||||
| chr9:74601674 | G | A | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8-28608G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74601674 | |||||||
| chr9:74601981 | C | T | 5 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0016g0029 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-28301C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74601981 | |||||||
| chr9:74601982 | G | T | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8-28300G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74601982 | |||||||
| chr9:74602173 | C | A | 6 | a0001c0001t0013g0036 a0001c0001t0013g0051 a0001c0001t0013g0052 others(3): Show |
6 | HG02451.hp1 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-28109C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74602173 | |||||||
| chr9:74602177 | C | A | 12 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0004g0158 others(9): Show |
12 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.8-28105C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74602177 | |||||||
| chr9:74602289 | G | T | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-27993G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74602289 | |||||||
| chr9:74602342 | G | T | 2 | a0001c0001t0012g0159 a0002c0004t0030g0014 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.8-27940G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74602342 | |||||||
| chr9:74602508 | G | A | 95 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(92): Show |
96 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.8-27774G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74602508 | |||||||
| chr9:74602512 | C | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0132 a0001c0001t0008g0131 |
3 | NA18968.hp2 NA19064.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.8-27770C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74602512 | |||||||
| chr9:74602935 | C | T | 1 | a0001c0002t0003g0050 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.8-27347C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74602935 | |||||||
| chr9:74602963 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-27319A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74602963 | |||||||
| chr9:74602967 | A | G | 1 | a0001c0001t0066g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.8-27315A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74602967 | |||||||
| chr9:74603186 | G | A | 3 | a0001c0001t0014g0019 a0001c0001t0014g0020 a0001c0001t0014g0021 |
3 | HG02451.hp1 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.8-27096G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74603186 | |||||||
| chr9:74603300 | G | A | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.8-26982G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74603300 | |||||||
| chr9:74603341 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(64): Show |
68 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.8-26941G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74603341 | |||||||
| chr9:74603429 | C | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(89): Show |
93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.8-26853C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74603429 | |||||||
| chr9:74603674 | C | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(90): Show |
94 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.8-26608C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74603674 | |||||||
| chr9:74603685 | G | A | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.8-26597G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74603685 | |||||||
| chr9:74603758 | C | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(64): Show |
68 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.8-26524C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74603758 | |||||||
| chr9:74603929 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-26353C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74603929 | |||||||
| chr9:74603990 | C | T | 1 | a0001c0001t0056g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8-26292C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74603990 | |||||||
| chr9:74604012 | A | G | 94 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(91): Show |
95 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.8-26270A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604012 | |||||||
| chr9:74604042 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.8-26240C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604042 | |||||||
| chr9:74604050 | A | ATTATT | 160 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(157): Show |
162 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.8-26229_8-26225dup others(5): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74604050 | ||||||
| chr9:74604139 | C | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.8-26143C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604139 | |||||||
| chr9:74604361 | C | A | 5 | a0001c0001t0031g0121 a0001c0001t0041g0074 a0001c0002t0001g0122 others(2): Show |
5 | HG01074.hp1 HG01109.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-25921C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604361 | |||||||
| chr9:74604412 | T | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(89): Show |
93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.8-25870T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604412 | |||||||
| chr9:74604479 | T | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0098 others(43): Show |
46 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.8-25803T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604479 | |||||||
| chr9:74604523 | T | G | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-25759T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604523 | |||||||
| chr9:74604667 | T | C | 2 | a0001c0001t0007g0100 a0001c0001t0016g0099 |
2 | HG01255.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.8-25615T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604667 | |||||||
| chr9:74604708 | T | C | 1 | a0001c0001t0017g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8-25574T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604708 | |||||||
| chr9:74604759 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.8-25523C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74604759 | |||||||
| chr9:74605309 | G | C | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-24973G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74605309 | |||||||
| chr9:74605386 | G | C | 43 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0098 others(40): Show |
43 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.8-24896G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74605386 | |||||||
| chr9:74605562 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.8-24720G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74605562 | |||||||
| chr9:74605689 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.8-24593G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74605689 | |||||||
| chr9:74605747 | C | T | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-24535C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74605747 | |||||||
| chr9:74605787 | T | A | 1 | a0001c0001t0049g0105 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.8-24495T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74605787 | |||||||
| chr9:74605995 | C | T | 1 | a0001c0001t0029g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.8-24287C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74605995 | |||||||
| chr9:74606133 | G | A | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8-24149G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74606133 | |||||||
| chr9:74606414 | A | G | 2 | a0001c0001t0051g0203 a0001c0002t0060g0016 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-23868A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74606414 | |||||||
| chr9:74606452 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-23830C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74606452 | |||||||
| chr9:74606675 | G | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(87): Show |
91 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.8-23607G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74606675 | |||||||
| chr9:74606682 | G | A | 3 | a0001c0001t0004g0158 a0001c0001t0051g0203 a0001c0002t0060g0016 |
3 | HG02818.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-23600G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74606682 | |||||||
| chr9:74606771 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-23511T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74606771 | |||||||
| chr9:74607076 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.8-23206G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607076 | |||||||
| chr9:74607155 | T | C | 1 | a0001c0001t0038g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.8-23127T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607155 | |||||||
| chr9:74607165 | T | C | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8-23117T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607165 | |||||||
| chr9:74607217 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.8-23065A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607217 | |||||||
| chr9:74607264 | C | T | 1 | a0001c0001t0017g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.8-23018C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607264 | |||||||
| chr9:74607367 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0168 a0001c0001t0001g0173 others(26): Show |
30 | HG01243.hp1 HG02040.hp1 HG02135.hp2 others(27): Show |
intron_variant | MODIFIER | c.8-22915T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607367 | |||||||
| chr9:74607394 | T | C | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-22888T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607394 | |||||||
| chr9:74607557 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.8-22725T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607557 | |||||||
| chr9:74607589 | T | C | 2 | a0001c0001t0010g0143 a0001c0001t0010g0224 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.8-22693T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607589 | |||||||
| chr9:74607600 | T | TTA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-22673_8-22672dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74607600 | ||||||
| chr9:74607611 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-22671C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607611 | |||||||
| chr9:74607653 | T | C | 1 | a0001c0002t0009g0116 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.8-22629T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607653 | |||||||
| chr9:74607724 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-22558G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607724 | |||||||
| chr9:74607912 | G | A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.8-22370G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74607912 | |||||||
| chr9:74608326 | G | C | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-21956G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74608326 | |||||||
| chr9:74608541 | G | T | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8-21741G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74608541 | |||||||
| chr9:74608563 | C | CA | 86 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0043 others(83): Show |
87 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.8-21701dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74608563 | ||||||
| chr9:74608563 | C | CAA | 43 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0117 others(40): Show |
43 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.8-21702_8-21701dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74608563 | ||||||
| chr9:74608563 | C | CAAA | 27 | a0001c0001t0001g0002 a0001c0001t0001g0168 a0001c0001t0001g0173 others(24): Show |
28 | HG00140.hp2 HG01243.hp1 HG01981.hp1 others(25): Show |
intron_variant | MODIFIER | c.8-21703_8-21701dup others(3): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74608563 | ||||||
| chr9:74608563 | CA | C | 6 | a0001c0001t0003g0152 a0001c0001t0010g0143 a0001c0001t0010g0224 others(3): Show |
6 | HG00738.hp1 HG01517.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.8-21701delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74608563 | ||||||
| chr9:74608587 | A | G | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8-21695A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74608587 | |||||||
| chr9:74608634 | C | A | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-21648C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74608634 | |||||||
| chr9:74608635 | C | A | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-21647C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74608635 | |||||||
| chr9:74608691 | G | GT | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.8-21586dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74608691 | ||||||
| chr9:74608969 | C | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.8-21313C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74608969 | |||||||
| chr9:74609088 | T | C | 162 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.8-21194T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609088 | |||||||
| chr9:74609106 | G | A | 1 | a0001c0001t0004g0096 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.8-21176G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609106 | |||||||
| chr9:74609172 | T | C | 83 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(80): Show |
84 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.8-21110T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609172 | |||||||
| chr9:74609226 | T | G | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8-21056T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609226 | |||||||
| chr9:74609282 | T | C | 1 | a0001c0001t0002g0040 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.8-21000T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609282 | |||||||
| chr9:74609357 | C | T | 3 | a0001c0001t0004g0175 a0001c0001t0005g0169 a0001c0001t0063g0197 |
3 | NA19001.hp1 NA19007.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.8-20925C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609357 | |||||||
| chr9:74609508 | T | C | 72 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(69): Show |
73 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.8-20774T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609508 | |||||||
| chr9:74609575 | G | T | 22 | a0001c0001t0001g0035 a0001c0001t0001g0108 a0001c0001t0001g0113 others(19): Show |
22 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.8-20707G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609575 | |||||||
| chr9:74609715 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(64): Show |
68 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.8-20567G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609715 | |||||||
| chr9:74609769 | G | T | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.8-20513G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609769 | |||||||
| chr9:74609811 | A | G | 91 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(88): Show |
92 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.8-20471A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609811 | |||||||
| chr9:74609902 | A | G | 5 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0016g0029 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-20380A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609902 | |||||||
| chr9:74609976 | T | C | 2 | a0001c0001t0031g0121 a0001c0002t0001g0122 |
2 | HG01074.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.8-20306T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74609976 | |||||||
| chr9:74610065 | T | C | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.8-20217T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74610065 | |||||||
| chr9:74610178 | T | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0098 others(41): Show |
44 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.8-20104T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74610178 | |||||||
| chr9:74610204 | T | C | 1 | a0001c0001t0021g0003 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.8-20078T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74610204 | |||||||
| chr9:74610294 | A | G | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.8-19988A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74610294 | |||||||
| chr9:74610384 | T | G | 3 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0010g0160 |
3 | HG02572.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-19898T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74610384 | |||||||
| chr9:74610429 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-19853C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74610429 | |||||||
| chr9:74610628 | C | A | 3 | a0001c0001t0005g0189 a0001c0001t0005g0201 a0001c0001t0028g0188 |
3 | NA18960.hp1 NA18969.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.8-19654C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74610628 | |||||||
| chr9:74610687 | G | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-19595G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74610687 | |||||||
| chr9:74611119 | C | A | 1 | a0001c0002t0009g0116 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.8-19163C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74611119 | |||||||
| chr9:74611384 | C | A | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-18898C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74611384 | |||||||
| chr9:74611437 | G | A | 7 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0010g0143 others(4): Show |
7 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-18845G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74611437 | |||||||
| chr9:74611608 | T | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(88): Show |
92 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.8-18674T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74611608 | |||||||
| chr9:74611670 | A | T | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-18612A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74611670 | |||||||
| chr9:74611680 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.8-18602G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74611680 | |||||||
| chr9:74611830 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0011g0207 |
2 | HG03831.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.8-18452A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74611830 | |||||||
| chr9:74611833 | A | G | 7 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0010g0143 others(4): Show |
7 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-18449A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74611833 | |||||||
| chr9:74612166 | G | A | 1 | a0001c0002t0003g0050 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.8-18116G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74612166 | |||||||
| chr9:74612203 | G | T | 1 | a0001c0002t0004g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.8-18079G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74612203 | |||||||
| chr9:74612386 | G | A | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-17896G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74612386 | |||||||
| chr9:74612557 | T | G | 3 | a0001c0001t0004g0158 a0001c0001t0051g0203 a0001c0002t0060g0016 |
3 | HG02818.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-17725T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74612557 | |||||||
| chr9:74612671 | A | G | 7 | a0001c0001t0013g0036 a0001c0001t0013g0051 a0001c0001t0013g0052 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-17611A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74612671 | |||||||
| chr9:74612831 | C | A | 89 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(86): Show |
90 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.8-17451C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74612831 | |||||||
| chr9:74612852 | CA | C | 5 | a0001c0001t0001g0120 a0001c0001t0007g0213 a0001c0001t0012g0210 others(2): Show |
5 | HG01243.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-17421delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74612852 | ||||||
| chr9:74613092 | T | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.8-17190T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74613092 | |||||||
| chr9:74613473 | C | T | 1 | a0001c0001t0005g0034 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.8-16809C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74613473 | |||||||
| chr9:74613518 | C | T | 1 | a0001c0001t0066g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.8-16764C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74613518 | |||||||
| chr9:74613603 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-16679T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74613603 | |||||||
| chr9:74613665 | T | C | 3 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0010g0160 |
3 | HG02572.hp2 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-16617T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74613665 | |||||||
| chr9:74613883 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.8-16399T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74613883 | |||||||
| chr9:74613887 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-16395G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74613887 | |||||||
| chr9:74613899 | G | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(87): Show |
91 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.8-16383G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74613899 | |||||||
| chr9:74614245 | G | A | 46 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0098 others(43): Show |
46 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.8-16037G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74614245 | |||||||
| chr9:74614389 | T | A | 7 | a0001c0001t0004g0126 a0001c0001t0004g0127 a0001c0001t0004g0175 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-15893T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74614389 | |||||||
| chr9:74614472 | T | A | 13 | a0001c0001t0001g0002 a0001c0001t0001g0173 a0001c0001t0001g0177 others(10): Show |
14 | HG02040.hp1 HG02523.hp1 HG04184.hp1 others(11): Show |
intron_variant | MODIFIER | c.8-15810T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74614472 | |||||||
| chr9:74614726 | CTAAG | C | 3 | a0001c0001t0004g0158 a0001c0001t0051g0203 a0001c0002t0060g0016 |
3 | HG02818.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-15552_8-15549del others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74614726 | ||||||
| chr9:74614742 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.8-15540A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74614742 | |||||||
| chr9:74614821 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.8-15461C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74614821 | |||||||
| chr9:74614839 | T | C | 5 | a0001c0001t0001g0222 a0001c0001t0004g0221 a0001c0001t0004g0223 others(2): Show |
5 | HG02258.hp2 HG02886.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-15443T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74614839 | |||||||
| chr9:74614995 | C | T | 4 | a0001c0001t0004g0058 a0001c0001t0006g0062 a0001c0001t0006g0063 others(1): Show |
4 | HG01071.hp1 HG01074.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.8-15287C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74614995 | |||||||
| chr9:74615307 | G | A | 67 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(64): Show |
68 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.8-14975G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74615307 | |||||||
| chr9:74615505 | G | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG01081.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.8-14777G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74615505 | |||||||
| chr9:74615507 | A | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(80): Show |
84 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.8-14775A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74615507 | |||||||
| chr9:74615561 | A | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.8-14721A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74615561 | |||||||
| chr9:74615576 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0007g0013 |
2 | HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8-14706T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74615576 | |||||||
| chr9:74615871 | C | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-14411C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74615871 | |||||||
| chr9:74616156 | A | T | 1 | a0001c0001t0014g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.8-14126A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74616156 | |||||||
| chr9:74616304 | G | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0161 |
2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-13978G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74616304 | |||||||
| chr9:74616354 | T | C | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-13928T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74616354 | |||||||
| chr9:74616968 | T | G | 7 | a0001c0001t0001g0108 a0001c0001t0001g0128 a0001c0001t0001g0132 others(4): Show |
7 | HG00597.hp2 NA18968.hp2 NA19064.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-13314T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74616968 | |||||||
| chr9:74616990 | T | TA | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-13280dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74616990 | ||||||
| chr9:74617018 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.8-13264T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617018 | |||||||
| chr9:74617088 | CT | C | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
156 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.8-13193delT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617088 | |||||||
| chr9:74617089 | T | C | 55 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0098 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.8-13193T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617089 | |||||||
| chr9:74617268 | C | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-13014C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617268 | |||||||
| chr9:74617333 | T | C | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-12949T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617333 | |||||||
| chr9:74617602 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8-12680G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617602 | |||||||
| chr9:74617742 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0008g0092 |
2 | NA18944.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.8-12540C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617742 | |||||||
| chr9:74618312 | T | TTAAA | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.8-11969_8-11966dup others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74618312 | ||||||
| chr9:74618474 | A | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-11808A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74618474 | |||||||
| chr9:74618543 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0161 |
2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-11739G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74618543 | |||||||
| chr9:74618668 | G | A | 1 | a0001c0002t0022g0028 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.8-11614G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74618668 | |||||||
| chr9:74618714 | C | A | 2 | a0001c0001t0009g0023 a0001c0002t0002g0216 |
2 | HG02080.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.8-11568C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74618714 | |||||||
| chr9:74618775 | TG | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0202 a0001c0001t0002g0056 others(3): Show |
6 | HG00408.hp2 HG00609.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.8-11501delG | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74618775 | ||||||
| chr9:74618804 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0020g0138 a0001c0001t0020g0139 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.8-11478C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74618804 | |||||||
| chr9:74619041 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.8-11241G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619041 | |||||||
| chr9:74619144 | T | C | 90 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(87): Show |
91 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.8-11138T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619144 | |||||||
| chr9:74619255 | C | T | 1 | a0001c0001t0011g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.8-11027C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619255 | |||||||
| chr9:74619302 | T | C | 1 | a0001c0001t0039g0033 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.8-10980T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619302 | |||||||
| chr9:74619468 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.8-10814T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619468 | |||||||
| chr9:74619476 | G | C | 22 | a0001c0001t0001g0035 a0001c0001t0001g0108 a0001c0001t0001g0113 others(19): Show |
22 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.8-10806G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619476 | |||||||
| chr9:74619491 | G | C | 2 | a0001c0001t0051g0203 a0001c0002t0060g0016 |
2 | HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-10791G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619491 | |||||||
| chr9:74619555 | G | A | 3 | a0001c0001t0019g0086 a0001c0001t0019g0090 a0001c0001t0019g0091 |
3 | HG02451.hp2 HG03130.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.8-10727G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619555 | |||||||
| chr9:74619711 | A | T | 5 | a0001c0001t0013g0110 a0001c0001t0015g0111 a0001c0001t0015g0142 others(2): Show |
5 | HG01891.hp1 HG02896.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-10571A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619711 | |||||||
| chr9:74619766 | G | C | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-10516G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619766 | |||||||
| chr9:74619768 | C | T | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-10514C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619768 | |||||||
| chr9:74619773 | A | T | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-10509A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619773 | |||||||
| chr9:74619788 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0011g0179 |
2 | HG00140.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.8-10494A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619788 | |||||||
| chr9:74619794 | A | G | 9 | a0001c0001t0001g0135 a0001c0001t0001g0140 a0001c0001t0001g0178 others(6): Show |
9 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.8-10488A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619794 | |||||||
| chr9:74619942 | C | T | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-10340C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74619942 | |||||||
| chr9:74620309 | G | C | 2 | a0001c0001t0002g0119 a0001c0001t0008g0106 |
2 | HG02040.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.8-9973G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74620309 | |||||||
| chr9:74620312 | G | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0108 others(28): Show |
31 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.8-9970G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74620312 | |||||||
| chr9:74620327 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-9955C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74620327 | |||||||
| chr9:74620360 | T | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.8-9922T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74620360 | |||||||
| chr9:74620379 | G | A | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.8-9903G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74620379 | |||||||
| chr9:74620483 | C | CA | 69 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(66): Show |
70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.8-9792dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74620483 | ||||||
| chr9:74621125 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.8-9157C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621125 | |||||||
| chr9:74621154 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0193 |
2 | NA18977.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.8-9128T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621154 | |||||||
| chr9:74621228 | A | C | 1 | a0001c0001t0056g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.8-9054A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621228 | |||||||
| chr9:74621297 | TG | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0161 |
2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-8984delG | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621297 | |||||||
| chr9:74621347 | G | A | 74 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0043 others(71): Show |
75 | HG00140.hp1 HG00323.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.8-8935G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621347 | |||||||
| chr9:74621351 | G | C | 2 | a0001c0001t0007g0100 a0001c0001t0016g0099 |
2 | HG01255.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.8-8931G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621351 | |||||||
| chr9:74621382 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0007g0013 a0001c0001t0056g0220 |
3 | HG01884.hp1 HG02257.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.8-8900T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621382 | |||||||
| chr9:74621494 | A | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0098 others(44): Show |
47 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.8-8788A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621494 | |||||||
| chr9:74621504 | A | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-8778A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621504 | |||||||
| chr9:74621505 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-8777A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621505 | |||||||
| chr9:74621575 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.8-8707G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621575 | |||||||
| chr9:74621678 | T | C | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.8-8604T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621678 | |||||||
| chr9:74621787 | C | A | 8 | a0001c0001t0012g0159 a0001c0001t0013g0110 a0001c0001t0015g0111 others(5): Show |
8 | HG01496.hp1 HG01891.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-8495C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621787 | |||||||
| chr9:74622027 | A | G | 20 | a0001c0001t0001g0043 a0001c0001t0039g0033 a0001c0001t0043g0048 others(17): Show |
21 | HG00140.hp1 HG01081.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.8-8255A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622027 | |||||||
| chr9:74622109 | C | T | 3 | a0001c0001t0004g0158 a0001c0001t0051g0203 a0001c0002t0060g0016 |
3 | HG02818.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-8173C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622109 | |||||||
| chr9:74622162 | T | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-8120T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622162 | |||||||
| chr9:74622234 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(79): Show |
83 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.8-8048G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622234 | |||||||
| chr9:74622269 | G | A | 18 | a0001c0001t0001g0043 a0001c0001t0039g0033 a0001c0001t0043g0048 others(15): Show |
19 | HG01175.hp1 HG01175.hp2 HG01975.hp2 others(16): Show |
intron_variant | MODIFIER | c.8-8013G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622269 | |||||||
| chr9:74622273 | C | T | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-8009C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622273 | |||||||
| chr9:74622365 | G | C | 5 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0016g0029 others(2): Show |
5 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-7917G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622365 | |||||||
| chr9:74622519 | A | AT | 69 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(66): Show |
70 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.8-7738dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74622519 | ||||||
| chr9:74622519 | A | ATT | 25 | a0001c0001t0001g0012 a0001c0001t0001g0032 a0001c0001t0001g0067 others(22): Show |
25 | HG01109.hp2 HG01255.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.8-7739_8-7738dupTT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74622519 | ||||||
| chr9:74622519 | A | ATTT | 66 | a0001c0001t0001g0043 a0001c0001t0001g0053 a0001c0001t0001g0059 others(63): Show |
67 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.8-7740_8-7738dupTT others(1): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74622519 | ||||||
| chr9:74622519 | A | ATTTT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0088 others(17): Show |
20 | HG01243.hp2 HG01884.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.8-7741_8-7738dupTT others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74622519 | ||||||
| chr9:74622558 | G | A | 1 | a0001c0001t0018g0018 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.8-7724G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622558 | |||||||
| chr9:74622652 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-7630G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622652 | |||||||
| chr9:74622882 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.8-7400A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74622882 | |||||||
| chr9:74623061 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-7221T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623061 | |||||||
| chr9:74623160 | A | G | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-7122A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623160 | |||||||
| chr9:74623177 | T | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.8-7105T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623177 | |||||||
| chr9:74623187 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.8-7095A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623187 | |||||||
| chr9:74623198 | A | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-7084A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623198 | |||||||
| chr9:74623274 | C | T | 2 | a0001c0001t0007g0100 a0001c0001t0016g0099 |
2 | HG01255.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.8-7008C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623274 | |||||||
| chr9:74623343 | G | A | 1 | a0001c0001t0024g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.8-6939G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623343 | |||||||
| chr9:74623344 | T | G | 1 | a0001c0001t0024g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.8-6938T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623344 | |||||||
| chr9:74623380 | C | T | 3 | a0001c0001t0004g0158 a0001c0001t0051g0203 a0001c0002t0060g0016 |
3 | HG02818.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.8-6902C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623380 | |||||||
| chr9:74623441 | C | CT | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
183 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.8-6828dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74623441 | ||||||
| chr9:74623642 | A | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.8-6640A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623642 | |||||||
| chr9:74623944 | T | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.8-6338T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623944 | |||||||
| chr9:74623946 | A | G | 8 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0010g0143 others(5): Show |
8 | HG02572.hp2 HG02723.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.8-6336A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623946 | |||||||
| chr9:74624227 | G | A | 32 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0108 others(29): Show |
32 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.8-6055G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74624227 | |||||||
| chr9:74624320 | A | T | 1 | a0001c0001t0004g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.8-5962A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74624320 | |||||||
| chr9:74624383 | T | A | 1 | a0001c0001t0039g0033 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.8-5899T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74624383 | |||||||
| chr9:74624474 | C | T | 1 | a0001c0001t0021g0112 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.8-5808C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74624474 | |||||||
| chr9:74624519 | T | G | 1 | a0001c0002t0003g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.8-5763T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74624519 | |||||||
| chr9:74624624 | C | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.8-5658C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74624624 | |||||||
| chr9:74624948 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.8-5334T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74624948 | |||||||
| chr9:74625225 | G | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.8-5057G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625225 | |||||||
| chr9:74625225 | G | T | 2 | a0001c0001t0001g0067 a0001c0001t0001g0161 |
2 | HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.8-5057G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625225 | |||||||
| chr9:74625264 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.8-5018G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625264 | |||||||
| chr9:74625265 | C | T | 35 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0098 others(32): Show |
35 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.8-5017C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625265 | |||||||
| chr9:74625331 | A | G | 1 | a0001c0001t0007g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.8-4951A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625331 | |||||||
| chr9:74625333 | AC | A | 47 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0098 others(44): Show |
47 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.8-4946delC | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74625333 | ||||||
| chr9:74625389 | G | A | 1 | a0001c0001t0053g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.8-4893G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625389 | |||||||
| chr9:74625425 | A | G | 1 | a0001c0002t0003g0214 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-4857A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625425 | |||||||
| chr9:74625666 | C | T | 7 | a0001c0001t0001g0067 a0001c0001t0001g0161 a0001c0001t0010g0143 others(4): Show |
7 | HG02723.hp2 HG02970.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-4616C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625666 | |||||||
| chr9:74625826 | G | C | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-4456G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625826 | |||||||
| chr9:74625877 | A | G | 1 | a0001c0001t0007g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.8-4405A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625877 | |||||||
| chr9:74625896 | G | A | 1 | a0001c0002t0009g0116 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.8-4386G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625896 | |||||||
| chr9:74625921 | T | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-4361T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625921 | |||||||
| chr9:74625929 | T | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-4353T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625929 | |||||||
| chr9:74626035 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.8-4247G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74626035 | |||||||
| chr9:74626141 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-4141G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74626141 | |||||||
| chr9:74626326 | A | G | 68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(65): Show |
69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-3956A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74626326 | |||||||
| chr9:74626631 | C | T | 7 | a0001c0001t0013g0036 a0001c0001t0013g0051 a0001c0001t0013g0052 others(4): Show |
7 | HG02451.hp1 HG02622.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-3651C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74626631 | |||||||
| chr9:74626861 | C | T | 94 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(91): Show |
95 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.8-3421C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74626861 | |||||||
| chr9:74627031 | A | G | 1 | a0001c0002t0005g0001 | 2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.8-3251A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74627031 | |||||||
| chr9:74627032 | C | G | 1 | a0001c0002t0005g0001 | 2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.8-3250C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74627032 | |||||||
| chr9:74627033 | A | G | 1 | a0001c0002t0005g0001 | 2 | NA18960.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.8-3249A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74627033 | |||||||
| chr9:74627144 | G | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0018g0030 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.8-3138G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74627144 | |||||||
| chr9:74627160 | C | CA | 106 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0032 others(103): Show |
108 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.8-3107dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74627160 | ||||||
| chr9:74627160 | C | CAA | 48 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0053 others(45): Show |
48 | HG00323.hp1 HG00597.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.8-3108_8-3107dupAA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 74627160 | ||||||
| chr9:74627180 | A | G | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.8-3102A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74627180 | |||||||
| chr9:74627255 | G | A | 1 | a0001c0001t0006g0181 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.8-3027G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74627255 | |||||||
| chr9:74627763 | G | C | 24 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0071 others(21): Show |
24 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.8-2519G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74627763 | |||||||
| chr9:74627829 | T | G | 2 | a0001c0001t0012g0159 a0002c0004t0030g0014 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.8-2453T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74627829 | |||||||
| chr9:74627985 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.8-2297T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74627985 | |||||||
| chr9:74628104 | G | A | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.8-2178G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74628104 | |||||||
| chr9:74628176 | T | G | 2 | a0001c0001t0002g0038 a0001c0001t0049g0105 |
2 | HG03704.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.8-2106T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74628176 | |||||||
| chr9:74628275 | G | T | 1 | a0001c0001t0004g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.8-2007G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74628275 | |||||||
| chr9:74628345 | T | A | 3 | a0001c0001t0001g0007 a0001c0001t0020g0138 a0001c0001t0020g0139 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.8-1937T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74628345 | |||||||
| chr9:74628701 | A | G | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.8-1581A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74628701 | |||||||
| chr9:74628751 | A | C | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.8-1531A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74628751 | |||||||
| chr9:74629092 | G | C | 1 | a0001c0001t0044g0187 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.8-1190G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74629092 | |||||||
| chr9:74629095 | G | A | 1 | a0001c0001t0032g0076 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.8-1187G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74629095 | |||||||
| chr9:74629103 | T | G | 2 | a0001c0001t0025g0054 a0001c0001t0025g0217 |
2 | HG00408.hp2 HG00609.hp1 |
intron_variant | MODIFIER | c.8-1179T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74629103 | |||||||
| chr9:74629305 | T | C | 8 | a0001c0001t0001g0067 a0001c0001t0010g0143 a0001c0001t0010g0160 others(5): Show |
8 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.8-977T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74629305 | |||||||
| chr9:74629537 | G | A | 43 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0043 others(40): Show |
43 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.8-745G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74629537 | |||||||
| chr9:74629538 | T | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
210 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.8-744T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74629538 | |||||||
| chr9:74629866 | T | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(201): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.8-416T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74629866 | |||||||
| chr9:74629951 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.8-331G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74629951 | |||||||
| chr9:74630102 | G | A | 7 | a0001c0001t0001g0067 a0001c0001t0010g0143 a0001c0001t0010g0224 others(4): Show |
7 | HG02630.hp2 HG02723.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.8-180G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74630102 | |||||||
| chr9:74630246 | A | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.8-36A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74630246 | |||||||
| chr9:74630390 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.93+23G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74630390 | |||||||
| chr9:74630432 | CG | C | 8 | a0001c0001t0006g0062 a0001c0001t0006g0063 a0001c0001t0006g0084 others(5): Show |
8 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.93+67delG | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 74630432 | ||||||
| chr9:74630578 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.93+211T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74630578 | |||||||
| chr9:74630588 | G | T | 7 | a0001c0001t0001g0067 a0001c0001t0010g0143 a0001c0001t0010g0224 others(4): Show |
7 | HG02630.hp2 HG02723.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.93+221G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74630588 | |||||||
| chr9:74630826 | GA | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(56): Show |
60 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.93+468delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 74630826 | ||||||
| chr9:74630830 | AAAAAAG | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+468_93+473delAG others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 74630830 | ||||||
| chr9:74630835 | AG | A | 134 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0012 others(131): Show |
135 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.93+469delG | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74630835 | |||||||
| chr9:74630836 | G | A | 11 | a0001c0001t0001g0067 a0001c0001t0004g0158 a0001c0001t0010g0143 others(8): Show |
11 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.93+469G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74630836 | |||||||
| chr9:74630868 | T | C | 8 | a0001c0001t0001g0059 a0001c0001t0002g0066 a0001c0001t0002g0073 others(5): Show |
8 | HG02135.hp1 HG02155.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.93+501T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74630868 | |||||||
| chr9:74630957 | A | G | 59 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(56): Show |
60 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(57): Show |
intron_variant | MODIFIER | c.93+590A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74630957 | |||||||
| chr9:74631088 | G | A | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.93+721G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74631088 | |||||||
| chr9:74631224 | A | G | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.93+857A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74631224 | |||||||
| chr9:74631461 | CT | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.93+1096delT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 74631461 | ||||||
| chr9:74631480 | C | T | 1 | a0001c0002t0005g0077 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.93+1113C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74631480 | |||||||
| chr9:74631651 | G | A | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.93+1284G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74631651 | |||||||
| chr9:74631725 | A | C | 3 | a0001c0001t0013g0051 a0001c0001t0013g0052 a0001c0001t0055g0017 |
3 | HG02965.hp2 HG03209.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.93+1358A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74631725 | |||||||
| chr9:74631909 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.93+1542G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74631909 | |||||||
| chr9:74632185 | G | A | 2 | a0001c0001t0012g0159 a0002c0004t0030g0014 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.93+1818G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74632185 | |||||||
| chr9:74632407 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.93+2040C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74632407 | |||||||
| chr9:74632681 | A | G | 87 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0032 others(84): Show |
88 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(85): Show |
intron_variant | MODIFIER | c.94-1950A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74632681 | |||||||
| chr9:74632836 | T | C | 6 | a0001c0001t0010g0143 a0001c0001t0010g0224 a0001c0001t0014g0010 others(3): Show |
6 | HG02630.hp2 HG02723.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94-1795T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74632836 | |||||||
| chr9:74632869 | G | A | 1 | a0001c0002t0023g0215 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.94-1762G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74632869 | |||||||
| chr9:74632936 | A | C | 1 | a0001c0001t0008g0106 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.94-1695A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74632936 | |||||||
| chr9:74633047 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.94-1584C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74633047 | |||||||
| chr9:74633280 | C | T | 4 | a0001c0001t0002g0040 a0001c0001t0002g0072 a0001c0001t0009g0070 others(1): Show |
4 | HG01433.hp1 HG01975.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.94-1351C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74633280 | |||||||
| chr9:74633286 | AG | A | 5 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0003g0152 others(2): Show |
5 | HG01168.hp2 HG01517.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.94-1343delG | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 74633286 | ||||||
| chr9:74633356 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.94-1275G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74633356 | |||||||
| chr9:74633423 | C | T | 1 | a0001c0001t0017g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94-1208C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74633423 | |||||||
| chr9:74633815 | A | G | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(57): Show |
61 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.94-816A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74633815 | |||||||
| chr9:74634018 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.94-613C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74634018 | |||||||
| chr9:74634078 | T | TA | 50 | a0001c0001t0001g0012 a0001c0001t0001g0053 a0001c0001t0001g0059 others(47): Show |
50 | HG00597.hp1 HG01106.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.94-539dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 74634078 | ||||||
| chr9:74634078 | T | TAA | 57 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(54): Show |
58 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(55): Show |
intron_variant | MODIFIER | c.94-540_94-539dupAA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 74634078 | ||||||
| chr9:74634141 | GA | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0088 others(46): Show |
50 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.94-485delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 74634141 | ||||||
| chr9:74634326 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0020g0138 a0001c0001t0020g0139 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.94-305G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74634326 | |||||||
| chr9:74634463 | T | C | 7 | a0001c0001t0001g0161 a0001c0001t0013g0110 a0001c0001t0015g0111 others(4): Show |
7 | HG01496.hp1 HG01891.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-168T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74634463 | |||||||
| chr9:74634466 | C | T | 78 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0035 others(75): Show |
78 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.94-165C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | chr9 | 74634466 | |||||||
| chr9:74634880 | A | G | 2 | a0001c0001t0013g0051 a0001c0001t0013g0052 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.235+108A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74634880 | |||||||
| chr9:74634980 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.235+208A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74634980 | |||||||
| chr9:74635046 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.235+274A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74635046 | |||||||
| chr9:74635191 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+419G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74635191 | |||||||
| chr9:74635572 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(57): Show |
61 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.235+800G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74635572 | |||||||
| chr9:74635588 | G | A | 11 | a0001c0001t0001g0067 a0001c0001t0007g0213 a0001c0001t0010g0143 others(8): Show |
11 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.235+816G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74635588 | |||||||
| chr9:74635762 | T | A | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.235+990T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74635762 | |||||||
| chr9:74635795 | A | G | 11 | a0001c0001t0001g0067 a0001c0001t0007g0213 a0001c0001t0010g0143 others(8): Show |
11 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.235+1023A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74635795 | |||||||
| chr9:74635805 | A | G | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.235+1033A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74635805 | |||||||
| chr9:74635845 | A | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.235+1073A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74635845 | |||||||
| chr9:74635956 | C | CA | 10 | a0001c0001t0001g0081 a0001c0001t0001g0098 a0001c0001t0007g0013 others(7): Show |
10 | HG01243.hp2 HG02257.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.235+1200dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74635956 | ||||||
| chr9:74635956 | C | CAAA | 35 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0148 others(32): Show |
35 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.235+1198_235+1200d others(5): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74635956 | ||||||
| chr9:74635956 | C | CAAAA | 30 | a0001c0001t0001g0002 a0001c0001t0001g0151 a0001c0001t0001g0168 others(27): Show |
31 | HG01243.hp1 HG02040.hp1 HG02135.hp2 others(28): Show |
intron_variant | MODIFIER | c.235+1197_235+1200d others(6): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74635956 | ||||||
| chr9:74635956 | CA | C | 51 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0088 others(48): Show |
52 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.235+1200delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74635956 | ||||||
| chr9:74635977 | A | G | 1 | a0001c0001t0018g0018 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.235+1205A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74635977 | |||||||
| chr9:74636056 | A | AT | 56 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0088 others(53): Show |
57 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.235+1293dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74636056 | ||||||
| chr9:74636171 | G | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0117 others(58): Show |
62 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(59): Show |
intron_variant | MODIFIER | c.235+1399G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74636171 | |||||||
| chr9:74636234 | C | A | 1 | a0001c0001t0066g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.235+1462C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74636234 | |||||||
| chr9:74636323 | T | C | 4 | a0001c0002t0002g0049 a0001c0002t0002g0129 a0001c0002t0002g0130 others(1): Show |
4 | NA18977.hp2 NA19062.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.235+1551T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74636323 | |||||||
| chr9:74636420 | A | G | 1 | a0001c0001t0014g0019 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.235+1648A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74636420 | |||||||
| chr9:74636547 | C | T | 1 | a0001c0002t0003g0046 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.235+1775C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74636547 | |||||||
| chr9:74636682 | T | C | 1 | a0001c0001t0017g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.235+1910T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74636682 | |||||||
| chr9:74637087 | C | A | 13 | a0001c0001t0001g0032 a0001c0001t0001g0202 a0001c0001t0002g0056 others(10): Show |
13 | HG00408.hp2 HG00609.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+2315C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74637087 | |||||||
| chr9:74637355 | C | T | 3 | a0001c0002t0003g0050 a0001c0002t0023g0044 a0001c0002t0023g0215 |
3 | HG01175.hp2 HG02698.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.235+2583C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74637355 | |||||||
| chr9:74637440 | C | T | 58 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0171 others(55): Show |
59 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.235+2668C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74637440 | |||||||
| chr9:74637587 | A | AT | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.235+2822dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74637587 | ||||||
| chr9:74637958 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0066g0182 |
2 | HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.235+3186G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74637958 | |||||||
| chr9:74638076 | G | A | 6 | a0001c0001t0001g0161 a0001c0001t0013g0110 a0001c0001t0015g0111 others(3): Show |
6 | HG01891.hp1 HG02896.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+3304G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74638076 | |||||||
| chr9:74638259 | C | A | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.235+3487C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74638259 | |||||||
| chr9:74638354 | T | C | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+3582T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74638354 | |||||||
| chr9:74638365 | T | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.235+3593T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74638365 | |||||||
| chr9:74638451 | C | T | 2 | a0001c0001t0010g0004 a0001c0001t0051g0203 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.235+3679C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74638451 | |||||||
| chr9:74638552 | G | GT | 60 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0171 others(57): Show |
61 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.235+3783dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74638552 | ||||||
| chr9:74638710 | A | G | 31 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0171 others(28): Show |
31 | HG00597.hp1 HG01106.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.236-3704A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74638710 | |||||||
| chr9:74638804 | G | A | 1 | a0001c0001t0025g0217 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.236-3610G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74638804 | |||||||
| chr9:74638847 | T | A | 2 | a0001c0001t0010g0004 a0001c0001t0051g0203 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.236-3567T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74638847 | |||||||
| chr9:74638977 | T | A | 1 | a0001c0001t0009g0075 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.236-3437T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74638977 | |||||||
| chr9:74639051 | T | G | 2 | a0001c0001t0010g0004 a0001c0001t0051g0203 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.236-3363T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639051 | |||||||
| chr9:74639265 | G | A | 1 | a0001c0001t0042g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.236-3149G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639265 | |||||||
| chr9:74639395 | G | T | 5 | a0001c0001t0007g0008 a0001c0001t0007g0009 a0001c0001t0007g0137 others(2): Show |
5 | HG02809.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-3019G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639395 | |||||||
| chr9:74639412 | G | A | 13 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0098 others(10): Show |
13 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.236-3002G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639412 | |||||||
| chr9:74639418 | A | G | 60 | a0001c0001t0001g0053 a0001c0001t0001g0059 a0001c0001t0001g0171 others(57): Show |
61 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.236-2996A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639418 | |||||||
| chr9:74639513 | T | A | 1 | a0001c0001t0066g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.236-2901T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639513 | |||||||
| chr9:74639513 | TA | T | 9 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0007g0213 others(6): Show |
9 | HG01081.hp2 HG01192.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.236-2889delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74639513 | ||||||
| chr9:74639566 | CAA | C | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-2847_236-2846d others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639566 | |||||||
| chr9:74639582 | T | C | 2 | a0001c0001t0004g0126 a0001c0001t0004g0127 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.236-2832T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639582 | |||||||
| chr9:74639902 | T | C | 1 | a0001c0001t0012g0212 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.236-2512T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639902 | |||||||
| chr9:74639908 | G | C | 1 | a0001c0001t0038g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.236-2506G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74639908 | |||||||
| chr9:74640194 | T | C | 184 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(181): Show |
186 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.236-2220T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640194 | |||||||
| chr9:74640225 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0098 others(10): Show |
13 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.236-2189C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640225 | |||||||
| chr9:74640321 | G | A | 207 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
209 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.236-2093G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640321 | |||||||
| chr9:74640365 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.236-2049C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640365 | |||||||
| chr9:74640433 | C | CTG | 92 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0035 others(89): Show |
93 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.236-1957_236-1956d others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74640433 | ||||||
| chr9:74640433 | C | CTGTG | 24 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0080 others(21): Show |
24 | HG00140.hp2 HG00323.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.236-1959_236-1956d others(6): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74640433 | ||||||
| chr9:74640433 | C | CTGTGTG | 2 | a0001c0001t0010g0004 a0001c0001t0051g0203 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.236-1961_236-1956d others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74640433 | ||||||
| chr9:74640433 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.236-1965_236-1956d others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74640433 | ||||||
| chr9:74640483 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0018g0030 others(9): Show |
12 | HG01109.hp1 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.236-1931C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640483 | |||||||
| chr9:74640494 | A | C | 1 | a0001c0001t0004g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.236-1920A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640494 | |||||||
| chr9:74640500 | G | A | 216 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.236-1914G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640500 | |||||||
| chr9:74640702 | C | G | 1 | a0001c0001t0012g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.236-1712C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640702 | |||||||
| chr9:74640827 | TG | T | 6 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0219 others(3): Show |
6 | HG00140.hp2 HG00738.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.236-1585delG | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74640827 | ||||||
| chr9:74640840 | C | T | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.236-1574C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640840 | |||||||
| chr9:74640888 | G | A | 11 | a0001c0001t0001g0067 a0001c0001t0004g0058 a0001c0001t0007g0008 others(8): Show |
11 | HG01074.hp2 HG01891.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.236-1526G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640888 | |||||||
| chr9:74640913 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.236-1501G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640913 | |||||||
| chr9:74640991 | A | C | 1 | a0001c0001t0007g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.236-1423A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74640991 | |||||||
| chr9:74641020 | C | T | 3 | a0001c0002t0003g0042 a0001c0002t0003g0164 a0001c0002t0003g0165 |
3 | HG00609.hp2 NA18747.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.236-1394C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74641020 | |||||||
| chr9:74641223 | TA | T | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(48): Show |
52 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.236-1186delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74641223 | ||||||
| chr9:74641462 | TA | T | 7 | a0001c0001t0001g0161 a0001c0001t0013g0110 a0001c0001t0015g0015 others(4): Show |
7 | HG01891.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-951delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74641462 | |||||||
| chr9:74641744 | T | TA | 5 | a0001c0001t0029g0057 a0001c0002t0003g0042 a0001c0002t0003g0164 others(2): Show |
5 | HG00609.hp2 HG01168.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.236-656dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 74641744 | ||||||
| chr9:74641745 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.236-669A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74641745 | |||||||
| chr9:74642345 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0148 others(4): Show |
7 | HG01192.hp1 HG01496.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-69G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 3/9 | chr9 | 74642345 | |||||||
| chr9:74643349 | A | G | 63 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0035 others(60): Show |
63 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.637+534A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74643349 | |||||||
| chr9:74643496 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.637+681T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74643496 | |||||||
| chr9:74643503 | G | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0156 a0001c0001t0003g0152 others(1): Show |
4 | HG01517.hp2 HG02572.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+688G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74643503 | |||||||
| chr9:74643866 | T | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0035 others(43): Show |
46 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.637+1051T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74643866 | |||||||
| chr9:74643920 | A | G | 5 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0018g0030 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1105A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74643920 | |||||||
| chr9:74644048 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.637+1233C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74644048 | |||||||
| chr9:74644244 | G | C | 2 | a0001c0001t0002g0066 a0001c0001t0002g0073 |
2 | NA18982.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.637+1429G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74644244 | |||||||
| chr9:74644401 | C | A | 1 | a0001c0001t0004g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.637+1586C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74644401 | |||||||
| chr9:74644440 | A | C | 14 | a0001c0001t0001g0067 a0001c0001t0004g0058 a0001c0001t0004g0158 others(11): Show |
14 | HG01074.hp2 HG01891.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.637+1625A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74644440 | |||||||
| chr9:74644576 | G | A | 2 | a0001c0001t0010g0004 a0001c0001t0051g0203 |
2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.637+1761G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74644576 | |||||||
| chr9:74644764 | G | A | 2 | a0001c0001t0007g0008 a0001c0001t0007g0009 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.637+1949G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74644764 | |||||||
| chr9:74644798 | AG | A | 2 | a0001c0001t0016g0029 a0001c0001t0046g0094 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.637+1984delG | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74644798 | |||||||
| chr9:74644859 | T | C | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.637+2044T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74644859 | |||||||
| chr9:74644877 | C | A | 1 | a0001c0001t0041g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.637+2062C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74644877 | |||||||
| chr9:74645182 | T | C | 1 | a0001c0001t0004g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.637+2367T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74645182 | |||||||
| chr9:74645313 | T | A | 16 | a0001c0001t0001g0067 a0001c0001t0004g0058 a0001c0001t0004g0158 others(13): Show |
16 | HG01074.hp2 HG01255.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.637+2498T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74645313 | |||||||
| chr9:74645394 | A | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+2579A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74645394 | |||||||
| chr9:74645400 | C | G | 1 | a0001c0001t0031g0121 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.637+2585C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74645400 | |||||||
| chr9:74645581 | A | T | 2 | a0001c0002t0001g0170 a0001c0002t0003g0124 |
2 | HG04199.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.637+2766A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74645581 | |||||||
| chr9:74645615 | T | C | 1 | a0001c0001t0006g0063 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.637+2800T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74645615 | |||||||
| chr9:74645643 | G | A | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.637+2828G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74645643 | |||||||
| chr9:74645809 | C | T | 2 | a0001c0001t0016g0029 a0001c0001t0046g0094 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.637+2994C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74645809 | |||||||
| chr9:74646015 | A | C | 46 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0035 others(43): Show |
46 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.637+3200A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74646015 | |||||||
| chr9:74646129 | CA | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(173): Show |
178 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.637+3328delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74646129 | ||||||
| chr9:74646470 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.637+3655G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74646470 | |||||||
| chr9:74646506 | T | C | 1 | a0001c0001t0017g0097 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.637+3691T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74646506 | |||||||
| chr9:74646531 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+3716G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74646531 | |||||||
| chr9:74646561 | T | C | 1 | a0001c0002t0011g0123 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.637+3746T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74646561 | |||||||
| chr9:74646667 | G | GAGTT | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.637+3854_637+3857d others(6): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74646667 | ||||||
| chr9:74646934 | T | C | 7 | a0001c0001t0001g0161 a0001c0001t0013g0110 a0001c0001t0015g0015 others(4): Show |
7 | HG01891.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+4119T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74646934 | |||||||
| chr9:74646952 | T | G | 1 | a0001c0001t0013g0036 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.637+4137T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74646952 | |||||||
| chr9:74647458 | C | T | 1 | a0001c0001t0012g0212 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.637+4643C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74647458 | |||||||
| chr9:74647469 | A | C | 1 | a0001c0001t0014g0010 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.637+4654A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74647469 | |||||||
| chr9:74647561 | C | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(202): Show |
207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.637+4746C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74647561 | |||||||
| chr9:74647627 | G | A | 7 | a0001c0001t0001g0161 a0001c0001t0013g0110 a0001c0001t0015g0015 others(4): Show |
7 | HG01891.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+4812G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74647627 | |||||||
| chr9:74647858 | A | G | 8 | a0001c0002t0003g0026 a0001c0002t0003g0041 a0001c0002t0003g0046 others(5): Show |
8 | HG01175.hp2 HG02148.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.637+5043A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74647858 | |||||||
| chr9:74648185 | T | C | 3 | a0001c0001t0001g0068 a0001c0001t0002g0083 a0001c0001t0027g0082 |
3 | HG00323.hp1 NA18951.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.637+5370T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74648185 | |||||||
| chr9:74648590 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.637+5775C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74648590 | |||||||
| chr9:74648676 | G | A | 19 | a0001c0001t0001g0067 a0001c0001t0001g0178 a0001c0001t0001g0180 others(16): Show |
19 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.637+5861G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74648676 | |||||||
| chr9:74648760 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.637+5945T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74648760 | |||||||
| chr9:74648832 | A | G | 6 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0219 others(3): Show |
6 | HG00140.hp2 HG01168.hp1 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.637+6017A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74648832 | |||||||
| chr9:74648970 | CT | C | 7 | a0001c0001t0001g0161 a0001c0001t0013g0110 a0001c0001t0015g0015 others(4): Show |
7 | HG01891.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+6169delT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74648970 | ||||||
| chr9:74649020 | G | T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0098 others(43): Show |
47 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.637+6205G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649020 | |||||||
| chr9:74649133 | A | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+6318A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649133 | |||||||
| chr9:74649140 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.637+6325G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649140 | |||||||
| chr9:74649247 | G | A | 6 | a0001c0001t0001g0171 a0001c0001t0007g0213 a0001c0001t0011g0172 others(3): Show |
6 | HG01106.hp2 HG01243.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.637+6432G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649247 | |||||||
| chr9:74649312 | T | A | 44 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0035 others(41): Show |
44 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.637+6497T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649312 | |||||||
| chr9:74649371 | C | T | 1 | a0001c0001t0004g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.637+6556C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649371 | |||||||
| chr9:74649512 | C | T | 203 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.637+6697C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649512 | |||||||
| chr9:74649601 | C | G | 11 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0004g0093 others(8): Show |
11 | HG01884.hp2 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.637+6786C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649601 | |||||||
| chr9:74649606 | A | G | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.637+6791A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649606 | |||||||
| chr9:74649630 | T | C | 38 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0035 others(35): Show |
38 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.637+6815T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649630 | |||||||
| chr9:74649652 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+6837G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649652 | |||||||
| chr9:74649680 | A | C | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.637+6865A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649680 | |||||||
| chr9:74649705 | C | T | 1 | a0001c0001t0025g0054 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.637+6890C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649705 | |||||||
| chr9:74649751 | T | C | 2 | a0001c0001t0001g0202 a0001c0001t0003g0024 |
2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.637+6936T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649751 | |||||||
| chr9:74649873 | T | C | 24 | a0001c0002t0001g0047 a0001c0002t0001g0122 a0001c0002t0002g0049 others(21): Show |
25 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.637+7058T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74649873 | |||||||
| chr9:74650020 | A | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0098 others(36): Show |
40 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.637+7205A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74650020 | |||||||
| chr9:74650412 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.637+7597T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74650412 | |||||||
| chr9:74650458 | G | A | 17 | a0001c0001t0001g0053 a0001c0001t0001g0202 a0001c0001t0003g0024 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.637+7643G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74650458 | |||||||
| chr9:74650659 | T | C | 2 | a0001c0001t0005g0169 a0001c0001t0063g0197 |
2 | NA19001.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.637+7844T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74650659 | |||||||
| chr9:74650716 | G | A | 5 | a0001c0001t0001g0120 a0001c0001t0001g0134 a0001c0001t0001g0135 others(2): Show |
5 | HG00323.hp2 HG00738.hp2 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+7901G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74650716 | |||||||
| chr9:74650845 | C | T | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.637+8030C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74650845 | |||||||
| chr9:74650952 | A | G | 17 | a0001c0001t0001g0053 a0001c0001t0001g0202 a0001c0001t0003g0024 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.637+8137A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74650952 | |||||||
| chr9:74651008 | C | T | 1 | a0001c0001t0004g0158 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.637+8193C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74651008 | |||||||
| chr9:74651048 | C | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.637+8233C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74651048 | |||||||
| chr9:74651063 | T | C | 1 | a0001c0001t0037g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.637+8248T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74651063 | |||||||
| chr9:74651384 | A | T | 4 | a0001c0001t0001g0059 a0001c0001t0008g0078 a0001c0001t0008g0092 others(1): Show |
4 | HG00597.hp1 HG02155.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.637+8569A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74651384 | |||||||
| chr9:74651436 | G | A | 1 | a0001c0002t0003g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.637+8621G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74651436 | |||||||
| chr9:74651534 | CA | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.637+8733delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74651534 | ||||||
| chr9:74651534 | CAA | C | 17 | a0001c0001t0001g0053 a0001c0001t0001g0202 a0001c0001t0003g0024 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.637+8732_637+8733d others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74651534 | ||||||
| chr9:74651551 | A | G | 2 | a0001c0001t0010g0160 a0001c0001t0017g0097 |
2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.637+8736A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74651551 | |||||||
| chr9:74651688 | T | G | 1 | a0001c0001t0045g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.637+8873T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74651688 | |||||||
| chr9:74651784 | T | G | 7 | a0001c0001t0001g0161 a0001c0001t0013g0110 a0001c0001t0015g0015 others(4): Show |
7 | HG01891.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.638-8833T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74651784 | |||||||
| chr9:74652001 | T | A | 1 | a0001c0001t0013g0036 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.638-8616T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74652001 | |||||||
| chr9:74652240 | C | T | 2 | a0001c0001t0016g0029 a0001c0001t0046g0094 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-8377C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74652240 | |||||||
| chr9:74652279 | G | T | 1 | a0001c0002t0001g0047 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.638-8338G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74652279 | |||||||
| chr9:74652381 | T | C | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.638-8236T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74652381 | |||||||
| chr9:74652385 | C | T | 39 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0098 others(36): Show |
40 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.638-8232C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74652385 | |||||||
| chr9:74652603 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-8014G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74652603 | |||||||
| chr9:74652704 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0098 others(12): Show |
15 | HG01109.hp1 HG01884.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.638-7913C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74652704 | |||||||
| chr9:74653285 | T | A | 1 | a0001c0001t0009g0025 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.638-7332T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74653285 | |||||||
| chr9:74653310 | T | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-7307T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74653310 | |||||||
| chr9:74653678 | G | T | 1 | a0001c0001t0064g0101 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.638-6939G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74653678 | |||||||
| chr9:74653724 | G | A | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-6893G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74653724 | |||||||
| chr9:74653724 | G | C | 1 | a0001c0001t0001g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.638-6893G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74653724 | |||||||
| chr9:74653750 | G | T | 48 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0178 others(45): Show |
48 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.638-6867G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74653750 | |||||||
| chr9:74653804 | GTCTA | G | 170 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(167): Show |
171 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.638-6808_638-6805d others(6): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74653804 | ||||||
| chr9:74653951 | C | T | 216 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.638-6666C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74653951 | |||||||
| chr9:74654144 | T | C | 30 | a0001c0001t0001g0059 a0001c0001t0001g0117 a0001c0001t0001g0171 others(27): Show |
30 | HG00597.hp1 HG01106.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.638-6473T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74654144 | |||||||
| chr9:74654205 | G | A | 2 | a0001c0001t0005g0169 a0001c0001t0063g0197 |
2 | NA19001.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.638-6412G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74654205 | |||||||
| chr9:74654319 | T | G | 1 | a0001c0001t0009g0070 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.638-6298T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74654319 | |||||||
| chr9:74654333 | G | GGA | 4 | a0001c0001t0001g0007 a0001c0001t0001g0136 a0001c0001t0005g0011 others(1): Show |
4 | HG03041.hp2 NA18747.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-6246_638-6245d others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74654333 | ||||||
| chr9:74654333 | GGA | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0032 a0001c0001t0001g0035 others(41): Show |
44 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.638-6246_638-6245d others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74654333 | ||||||
| chr9:74654333 | GGAGA | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0151 others(29): Show |
33 | HG00408.hp1 HG01243.hp2 HG02040.hp1 others(30): Show |
intron_variant | MODIFIER | c.638-6248_638-6245d others(6): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74654333 | ||||||
| chr9:74654333 | GGAGAGA | G | 19 | a0001c0001t0001g0161 a0001c0001t0004g0096 a0001c0001t0006g0062 others(16): Show |
19 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.638-6250_638-6245d others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74654333 | ||||||
| chr9:74654333 | GGAGAGAG others(1): Show |
G | 51 | a0001c0001t0001g0006 a0001c0001t0001g0059 a0001c0001t0001g0088 others(48): Show |
52 | HG00140.hp1 HG00597.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.638-6252_638-6245d others(10): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74654333 | ||||||
| chr9:74654333 | GGAGAGAG others(3): Show |
G | 2 | a0001c0001t0012g0159 a0001c0002t0060g0016 |
2 | HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.638-6254_638-6245d others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74654333 | ||||||
| chr9:74654333 | GGAGAGAG others(5): Show |
G | 47 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0178 others(44): Show |
47 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.638-6256_638-6245d others(14): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74654333 | ||||||
| chr9:74654333 | GGAGAGAG others(9): Show |
G | 11 | a0001c0001t0001g0117 a0001c0001t0002g0038 a0001c0001t0002g0040 others(8): Show |
11 | HG01433.hp1 HG01975.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.638-6260_638-6245d others(18): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74654333 | ||||||
| chr9:74654513 | C | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG01081.hp2 HG01192.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-6104C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74654513 | |||||||
| chr9:74654680 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0113 a0001c0001t0001g0114 others(1): Show |
4 | HG01081.hp2 HG01192.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-5937C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74654680 | |||||||
| chr9:74654751 | C | T | 1 | a0001c0001t0001g0007 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.638-5866C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74654751 | |||||||
| chr9:74654785 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0018g0030 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-5832G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74654785 | |||||||
| chr9:74654846 | A | G | 2 | a0001c0001t0016g0029 a0001c0001t0046g0094 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-5771A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74654846 | |||||||
| chr9:74654945 | A | G | 2 | a0001c0001t0016g0029 a0001c0001t0046g0094 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-5672A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74654945 | |||||||
| chr9:74655608 | C | T | 1 | a0001c0001t0066g0182 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.638-5009C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74655608 | |||||||
| chr9:74655829 | C | T | 1 | a0001c0001t0025g0217 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.638-4788C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74655829 | |||||||
| chr9:74655861 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.638-4756A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74655861 | |||||||
| chr9:74656023 | A | G | 2 | a0001c0001t0016g0029 a0001c0001t0046g0094 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-4594A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656023 | |||||||
| chr9:74656123 | A | T | 7 | a0001c0001t0001g0161 a0001c0001t0013g0110 a0001c0001t0015g0015 others(4): Show |
7 | HG01891.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.638-4494A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656123 | |||||||
| chr9:74656411 | A | G | 2 | a0001c0001t0016g0029 a0001c0001t0046g0094 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-4206A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656411 | |||||||
| chr9:74656429 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.638-4188G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656429 | |||||||
| chr9:74656443 | A | C | 1 | a0001c0002t0003g0042 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.638-4174A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656443 | |||||||
| chr9:74656473 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0134 |
2 | HG00323.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.638-4144C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656473 | |||||||
| chr9:74656596 | T | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.638-4021T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656596 | |||||||
| chr9:74656660 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-3957C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656660 | |||||||
| chr9:74656795 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-3822C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656795 | |||||||
| chr9:74656862 | A | T | 29 | a0001c0001t0001g0059 a0001c0001t0001g0117 a0001c0001t0001g0171 others(26): Show |
29 | HG00597.hp1 HG01106.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.638-3755A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74656862 | |||||||
| chr9:74657056 | T | C | 1 | a0001c0001t0004g0125 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.638-3561T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657056 | |||||||
| chr9:74657069 | C | T | 17 | a0001c0001t0001g0053 a0001c0001t0001g0202 a0001c0001t0003g0024 others(14): Show |
17 | HG00408.hp2 HG00609.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.638-3548C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657069 | |||||||
| chr9:74657146 | A | G | 2 | a0001c0001t0016g0029 a0001c0001t0046g0094 |
2 | HG03516.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.638-3471A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657146 | |||||||
| chr9:74657192 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.638-3425C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657192 | |||||||
| chr9:74657211 | A | AATTT | 4 | a0001c0001t0001g0071 a0001c0001t0001g0115 a0001c0001t0001g0118 others(1): Show |
4 | HG01261.hp2 HG01978.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.638-3382_638-3379d others(6): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74657211 | ||||||
| chr9:74657315 | T | C | 1 | a0001c0001t0011g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.638-3302T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657315 | |||||||
| chr9:74657380 | G | A | 30 | a0001c0001t0001g0059 a0001c0001t0001g0117 a0001c0001t0001g0171 others(27): Show |
30 | HG00597.hp1 HG01106.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.638-3237G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657380 | |||||||
| chr9:74657419 | C | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.638-3198C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657419 | |||||||
| chr9:74657433 | G | A | 5 | a0001c0001t0004g0096 a0001c0001t0006g0102 a0001c0001t0006g0181 others(2): Show |
5 | HG01070.hp2 HG01106.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-3184G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657433 | |||||||
| chr9:74657451 | G | C | 40 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0178 others(37): Show |
40 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.638-3166G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657451 | |||||||
| chr9:74657519 | C | T | 30 | a0001c0001t0001g0059 a0001c0001t0001g0117 a0001c0001t0001g0171 others(27): Show |
30 | HG00597.hp1 HG01106.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.638-3098C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657519 | |||||||
| chr9:74657521 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0020g0138 a0001c0001t0020g0139 |
3 | HG02895.hp1 HG02897.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.638-3096T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657521 | |||||||
| chr9:74657528 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0011g0179 |
2 | HG00140.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.638-3089C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657528 | |||||||
| chr9:74657614 | C | G | 1 | a0001c0001t0009g0025 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.638-3003C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657614 | |||||||
| chr9:74657804 | G | A | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.638-2813G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657804 | |||||||
| chr9:74657897 | C | T | 38 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0035 others(35): Show |
38 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.638-2720C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657897 | |||||||
| chr9:74657998 | C | T | 7 | a0001c0001t0001g0161 a0001c0001t0013g0110 a0001c0001t0015g0015 others(4): Show |
7 | HG01891.hp1 HG02886.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.638-2619C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657998 | |||||||
| chr9:74658004 | C | CA | 36 | a0001c0001t0001g0059 a0001c0001t0001g0117 a0001c0001t0002g0038 others(33): Show |
36 | HG00408.hp2 HG00597.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.638-2589dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74658004 | ||||||
| chr9:74658004 | C | CAA | 37 | a0001c0001t0001g0053 a0001c0001t0001g0067 a0001c0001t0001g0178 others(34): Show |
37 | HG00140.hp2 HG00609.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.638-2590_638-2589d others(4): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74658004 | ||||||
| chr9:74658004 | CA | C | 46 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(43): Show |
47 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.638-2589delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74658004 | ||||||
| chr9:74658004 | CAAAAAA | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0098 others(37): Show |
41 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.638-2594_638-2589d others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74658004 | ||||||
| chr9:74658004 | CAAAAAAA others(3): Show |
C | 37 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0035 others(34): Show |
37 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.638-2598_638-2589d others(12): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74658004 | ||||||
| chr9:74658004 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0132 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.638-2599_638-2589d others(13): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74658004 | ||||||
| chr9:74658380 | C | A | 47 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0012 others(44): Show |
48 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.638-2237C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74658380 | |||||||
| chr9:74658388 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.638-2229C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74658388 | |||||||
| chr9:74658502 | AC | A | 25 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0219 others(22): Show |
25 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.638-2114delC | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74658502 | |||||||
| chr9:74658516 | T | C | 25 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0219 others(22): Show |
25 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.638-2101T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74658516 | |||||||
| chr9:74658517 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.638-2100C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74658517 | |||||||
| chr9:74658915 | A | G | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-1702A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74658915 | |||||||
| chr9:74658992 | C | T | 4 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(1): Show |
4 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-1625C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74658992 | |||||||
| chr9:74658994 | T | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0156 others(17): Show |
20 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.638-1623T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74658994 | |||||||
| chr9:74659099 | A | G | 38 | a0001c0001t0001g0032 a0001c0001t0001g0059 a0001c0001t0001g0068 others(35): Show |
38 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.638-1518A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659099 | |||||||
| chr9:74659100 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.638-1517C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659100 | |||||||
| chr9:74659149 | G | A | 2 | a0001c0002t0002g0216 a0001c0002t0009g0116 |
2 | HG01975.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.638-1468G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659149 | |||||||
| chr9:74659196 | G | A | 48 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0043 others(45): Show |
48 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.638-1421G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659196 | |||||||
| chr9:74659481 | C | CTTGTT | 30 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(27): Show |
30 | HG00408.hp2 HG00609.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.638-1117_638-1113d others(7): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74659481 | ||||||
| chr9:74659508 | C | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(55): Show |
59 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.638-1109C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659508 | |||||||
| chr9:74659511 | T | C | 7 | a0001c0001t0007g0039 a0001c0001t0007g0213 a0001c0001t0012g0210 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.638-1106T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659511 | |||||||
| chr9:74659593 | C | G | 5 | a0001c0001t0007g0213 a0001c0001t0012g0210 a0001c0001t0012g0211 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-1024C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659593 | |||||||
| chr9:74659636 | G | A | 1 | a0001c0001t0029g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.638-981G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659636 | |||||||
| chr9:74659667 | G | GT | 5 | a0001c0001t0001g0132 a0001c0001t0015g0015 a0001c0001t0015g0111 others(2): Show |
5 | HG02886.hp2 HG03195.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-941dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74659667 | ||||||
| chr9:74659689 | G | T | 23 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0098 others(20): Show |
23 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.638-928G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659689 | |||||||
| chr9:74659785 | T | G | 27 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(24): Show |
27 | HG00408.hp2 HG00609.hp1 HG01433.hp1 others(24): Show |
intron_variant | MODIFIER | c.638-832T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659785 | |||||||
| chr9:74659918 | A | T | 23 | a0001c0001t0003g0152 a0001c0001t0003g0153 a0001c0001t0007g0013 others(20): Show |
23 | HG00140.hp1 HG00609.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.638-699A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659918 | |||||||
| chr9:74659923 | G | T | 32 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(29): Show |
32 | HG00408.hp2 HG00609.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.638-694G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659923 | |||||||
| chr9:74659994 | T | TA | 150 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(147): Show |
151 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.638-622dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr9 | 74659994 | ||||||
| chr9:74659996 | G | A | 5 | a0001c0001t0001g0067 a0001c0001t0007g0213 a0001c0001t0012g0210 others(2): Show |
5 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-621G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74659996 | |||||||
| chr9:74660208 | G | A | 1 | a0001c0001t0013g0110 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.638-409G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74660208 | |||||||
| chr9:74660379 | A | G | 1 | a0001c0001t0050g0145 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.638-238A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74660379 | |||||||
| chr9:74660513 | C | A | 21 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0098 others(18): Show |
21 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.638-104C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74660513 | |||||||
| chr9:74660795 | C | T | 1 | a0001c0001t0045g0061 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.759+57C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74660795 | |||||||
| chr9:74660901 | G | T | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.759+163G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74660901 | |||||||
| chr9:74660997 | G | T | 146 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(143): Show |
147 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.759+259G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74660997 | |||||||
| chr9:74661165 | T | A | 60 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0043 others(57): Show |
61 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.759+427T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661165 | |||||||
| chr9:74661253 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.759+515T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661253 | |||||||
| chr9:74661489 | C | T | 17 | a0001c0001t0005g0034 a0001c0001t0005g0169 a0001c0001t0005g0189 others(14): Show |
18 | HG00597.hp1 HG01256.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.759+751C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661489 | |||||||
| chr9:74661627 | T | C | 60 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0043 others(57): Show |
61 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.760-847T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661627 | |||||||
| chr9:74661636 | C | CT | 72 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0001t0001g0071 others(69): Show |
73 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.760-812dupT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 74661636 | ||||||
| chr9:74661636 | C | CTT | 10 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0043 others(7): Show |
10 | HG01175.hp1 HG02074.hp1 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.760-813_760-812dup others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 74661636 | ||||||
| chr9:74661636 | C | CTTT | 5 | a0001c0001t0004g0221 a0001c0001t0004g0223 a0001c0001t0015g0015 others(2): Show |
5 | HG02258.hp2 HG02886.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.760-814_760-812dup others(3): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 74661636 | ||||||
| chr9:74661636 | CT | C | 15 | a0001c0001t0001g0098 a0001c0001t0002g0060 a0001c0001t0002g0066 others(12): Show |
15 | HG01255.hp1 HG01884.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.760-812delT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 74661636 | ||||||
| chr9:74661636 | CTT | C | 24 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(21): Show |
24 | HG00408.hp2 HG00609.hp1 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.760-813_760-812del others(2): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 74661636 | ||||||
| chr9:74661705 | C | T | 5 | a0001c0001t0001g0067 a0001c0001t0007g0213 a0001c0001t0012g0210 others(2): Show |
5 | HG01243.hp2 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.760-769C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661705 | |||||||
| chr9:74661714 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.760-760G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661714 | |||||||
| chr9:74661790 | GC | G | 84 | a0001c0001t0001g0006 a0001c0001t0001g0067 a0001c0001t0001g0088 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.760-677delC | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 74661790 | ||||||
| chr9:74661795 | C | G | 2 | a0001c0001t0012g0159 a0001c0001t0046g0094 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.760-679C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661795 | |||||||
| chr9:74661864 | G | C | 145 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(142): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.760-610G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661864 | |||||||
| chr9:74661879 | C | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0067 a0001c0001t0001g0088 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.760-595C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661879 | |||||||
| chr9:74661913 | G | A | 3 | a0001c0001t0006g0102 a0001c0001t0006g0181 a0001c0001t0026g0186 |
3 | HG01070.hp2 HG01106.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.760-561G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661913 | |||||||
| chr9:74661928 | AGCCACCG others(1): Show |
A | 2 | a0001c0001t0012g0159 a0001c0001t0046g0094 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.760-542_760-535del others(8): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 74661928 | ||||||
| chr9:74661940 | C | T | 32 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(29): Show |
32 | HG00408.hp2 HG00609.hp1 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.760-534C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74661940 | |||||||
| chr9:74662111 | A | G | 1 | a0001c0002t0003g0165 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.760-363A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74662111 | |||||||
| chr9:74662205 | A | G | 2 | a0001c0001t0012g0159 a0001c0001t0046g0094 |
2 | HG03225.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.760-269A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 5/9 | chr9 | 74662205 | |||||||
| chr9:74662778 | T | G | 21 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0067 others(18): Show |
21 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.892+172T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74662778 | |||||||
| chr9:74662901 | C | G | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.892+295C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74662901 | |||||||
| chr9:74663088 | C | A | 4 | a0001c0001t0015g0015 a0001c0001t0015g0111 a0001c0001t0015g0142 others(1): Show |
4 | HG02647.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.892+482C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74663088 | |||||||
| chr9:74663274 | A | G | 1 | a0001c0001t0011g0207 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.892+668A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74663274 | |||||||
| chr9:74663335 | A | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0135 others(22): Show |
25 | HG00140.hp2 HG00323.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.892+729A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74663335 | |||||||
| chr9:74663417 | A | G | 1 | a0001c0001t0059g0205 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.892+811A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74663417 | |||||||
| chr9:74663489 | C | T | 1 | a0001c0001t0057g0037 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.892+883C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74663489 | |||||||
| chr9:74663630 | C | A | 13 | a0001c0001t0013g0036 a0001c0001t0013g0051 a0001c0001t0013g0052 others(10): Show |
13 | HG01168.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.892+1024C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74663630 | |||||||
| chr9:74663980 | C | G | 57 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(54): Show |
58 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.892+1374C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74663980 | |||||||
| chr9:74664164 | A | G | 2 | a0001c0001t0024g0095 a0001c0001t0024g0176 |
2 | HG02080.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.893-1324A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74664164 | |||||||
| chr9:74664451 | A | AC | 9 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(6): Show |
9 | HG01891.hp2 HG02451.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.893-1036dupC | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 74664451 | ||||||
| chr9:74664890 | C | T | 20 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(17): Show |
20 | HG00140.hp2 HG00323.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.893-598C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74664890 | |||||||
| chr9:74665019 | G | A | 101 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(98): Show |
102 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.893-469G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74665019 | |||||||
| chr9:74665229 | A | G | 162 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0035 others(159): Show |
163 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.893-259A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74665229 | |||||||
| chr9:74665235 | G | A | 3 | a0001c0002t0002g0049 a0001c0002t0002g0129 a0001c0002t0002g0130 |
3 | NA18977.hp2 NA19062.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.893-253G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74665235 | |||||||
| chr9:74665382 | T | C | 1 | a0001c0001t0037g0184 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.893-106T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74665382 | |||||||
| chr9:74665430 | A | T | 32 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(29): Show |
33 | HG00597.hp1 HG01243.hp2 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.893-58A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 6/9 | chr9 | 74665430 | |||||||
| chr9:74665867 | C | T | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1000+272C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74665867 | |||||||
| chr9:74665895 | A | G | 13 | a0001c0001t0012g0210 a0001c0001t0012g0211 a0001c0001t0012g0212 others(10): Show |
13 | HG01243.hp2 HG01891.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1000+300A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74665895 | |||||||
| chr9:74665914 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0002g0072 a0001c0001t0009g0070 |
3 | HG01433.hp1 HG02004.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1000+319C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74665914 | |||||||
| chr9:74666040 | A | G | 36 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(33): Show |
36 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1000+445A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666040 | |||||||
| chr9:74666144 | A | G | 10 | a0001c0001t0013g0036 a0001c0001t0013g0051 a0001c0001t0013g0052 others(7): Show |
10 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1000+549A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666144 | |||||||
| chr9:74666145 | C | T | 3 | a0001c0001t0018g0018 a0001c0001t0018g0030 a0001c0001t0018g0089 |
3 | HG01168.hp2 HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1000+550C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666145 | |||||||
| chr9:74666152 | T | G | 5 | a0001c0001t0015g0015 a0001c0001t0015g0111 a0001c0001t0015g0142 others(2): Show |
5 | HG02258.hp2 HG02647.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000+557T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666152 | |||||||
| chr9:74666169 | C | T | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1000+574C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666169 | |||||||
| chr9:74666241 | A | C | 102 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(99): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1000+646A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666241 | |||||||
| chr9:74666376 | G | A | 6 | a0001c0001t0015g0015 a0001c0001t0015g0111 a0001c0001t0015g0142 others(3): Show |
6 | HG02258.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1000+781G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666376 | |||||||
| chr9:74666398 | C | T | 1 | a0001c0001t0007g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1000+803C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666398 | |||||||
| chr9:74666399 | T | C | 1 | a0001c0001t0007g0039 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1000+804T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666399 | |||||||
| chr9:74666458 | T | TA | 21 | a0001c0001t0003g0024 a0001c0001t0003g0152 a0001c0001t0003g0153 others(18): Show |
21 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.1000+875dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 74666458 | ||||||
| chr9:74666620 | G | A | 120 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(117): Show |
121 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1000+1025G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666620 | |||||||
| chr9:74666637 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1000+1042T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74666637 | |||||||
| chr9:74667026 | C | T | 1 | a0001c0001t0017g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1001-765C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74667026 | |||||||
| chr9:74667052 | C | G | 1 | a0001c0001t0024g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1001-739C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74667052 | |||||||
| chr9:74667323 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1001-468A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74667323 | |||||||
| chr9:74667492 | A | T | 9 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(6): Show |
9 | HG01891.hp2 HG02451.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1001-299A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74667492 | |||||||
| chr9:74667554 | A | G | 30 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(27): Show |
30 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1001-237A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 7/9 | chr9 | 74667554 | |||||||
| chr9:74668011 | T | C | 20 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(17): Show |
20 | HG00140.hp2 HG00323.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.1111+110T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74668011 | |||||||
| chr9:74668027 | T | A | 9 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(6): Show |
9 | HG01891.hp2 HG02451.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1111+126T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74668027 | |||||||
| chr9:74668478 | T | C | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1111+577T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74668478 | |||||||
| chr9:74668814 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1111+913T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74668814 | |||||||
| chr9:74668973 | G | A | 120 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(117): Show |
121 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1111+1072G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74668973 | |||||||
| chr9:74669183 | T | A | 52 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(49): Show |
53 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1111+1282T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74669183 | |||||||
| chr9:74669237 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1111+1336G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74669237 | |||||||
| chr9:74669356 | G | A | 1 | a0001c0001t0005g0169 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1111+1455G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74669356 | |||||||
| chr9:74669479 | C | CA | 22 | a0001c0001t0002g0056 a0001c0001t0003g0024 a0001c0001t0003g0152 others(19): Show |
22 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.1111+1595dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 74669479 | ||||||
| chr9:74669479 | CA | C | 69 | a0001c0001t0001g0032 a0001c0001t0001g0059 a0001c0001t0001g0135 others(66): Show |
70 | HG00140.hp2 HG00323.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.1111+1595delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr9 | 74669479 | ||||||
| chr9:74669489 | A | T | 2 | a0001c0001t0006g0062 a0001c0001t0006g0063 |
2 | HG01071.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1111+1588A>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74669489 | |||||||
| chr9:74669643 | G | C | 24 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0043 others(21): Show |
24 | HG00323.hp2 HG00597.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.1111+1742G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74669643 | |||||||
| chr9:74669670 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1111+1769C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74669670 | |||||||
| chr9:74669733 | G | A | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1111+1832G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74669733 | |||||||
| chr9:74669950 | T | A | 3 | a0001c0001t0018g0018 a0001c0001t0018g0030 a0001c0001t0018g0089 |
3 | HG01168.hp2 HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1112-1839T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74669950 | |||||||
| chr9:74670110 | A | G | 1 | a0001c0001t0049g0105 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1112-1679A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74670110 | |||||||
| chr9:74670192 | T | C | 1 | a0001c0002t0003g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1112-1597T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74670192 | |||||||
| chr9:74670311 | C | T | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1112-1478C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74670311 | |||||||
| chr9:74670370 | C | A | 1 | a0001c0001t0004g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1112-1419C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74670370 | |||||||
| chr9:74670501 | G | T | 1 | a0001c0001t0012g0212 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1112-1288G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74670501 | |||||||
| chr9:74670760 | T | C | 1 | a0001c0001t0017g0141 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1112-1029T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74670760 | |||||||
| chr9:74671134 | G | A | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1112-655G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74671134 | |||||||
| chr9:74671259 | C | T | 1 | a0001c0001t0044g0187 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1112-530C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74671259 | |||||||
| chr9:74671263 | T | G | 1 | a0001c0001t0006g0102 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1112-526T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74671263 | |||||||
| chr9:74671316 | T | A | 1 | a0001c0001t0002g0065 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1112-473T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74671316 | |||||||
| chr9:74671500 | A | G | 1 | a0001c0002t0003g0026 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1112-289A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74671500 | |||||||
| chr9:74671726 | G | A | 2 | a0001c0002t0002g0129 a0001c0002t0002g0130 |
2 | NA19062.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1112-63G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 8/9 | chr9 | 74671726 | |||||||
| chr9:74671960 | A | C | 121 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(118): Show |
122 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1224+59A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74671960 | |||||||
| chr9:74672028 | T | C | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1224+127T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74672028 | |||||||
| chr9:74672494 | G | T | 2 | a0001c0001t0021g0003 a0001c0001t0021g0112 |
2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1224+593G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74672494 | |||||||
| chr9:74672692 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1224+791A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74672692 | |||||||
| chr9:74673404 | G | A | 23 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(20): Show |
23 | HG00140.hp2 HG00323.hp1 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.1224+1503G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74673404 | |||||||
| chr9:74674001 | C | T | 13 | a0001c0001t0013g0036 a0001c0001t0013g0051 a0001c0001t0013g0052 others(10): Show |
13 | HG01168.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1224+2100C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674001 | |||||||
| chr9:74674007 | A | G | 1 | a0001c0001t0056g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1224+2106A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674007 | |||||||
| chr9:74674119 | G | C | 1 | a0001c0001t0006g0209 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1224+2218G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674119 | |||||||
| chr9:74674161 | T | C | 18 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(15): Show |
19 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1224+2260T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674161 | |||||||
| chr9:74674374 | G | A | 1 | a0001c0001t0024g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1224+2473G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674374 | |||||||
| chr9:74674382 | G | T | 20 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(17): Show |
21 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1224+2481G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674382 | |||||||
| chr9:74674402 | C | T | 14 | a0001c0001t0003g0024 a0001c0001t0022g0069 a0001c0002t0003g0026 others(11): Show |
14 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1224+2501C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674402 | |||||||
| chr9:74674412 | G | A | 1 | a0001c0001t0017g0107 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1224+2511G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674412 | |||||||
| chr9:74674507 | T | A | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1224+2606T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674507 | |||||||
| chr9:74674598 | A | C | 8 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(5): Show |
8 | HG02451.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1224+2697A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674598 | |||||||
| chr9:74674606 | T | C | 5 | a0001c0001t0001g0006 a0001c0001t0001g0088 a0001c0001t0001g0156 others(2): Show |
5 | HG01884.hp2 HG03195.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1224+2705T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674606 | |||||||
| chr9:74674614 | G | C | 1 | a0001c0001t0056g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1224+2713G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674614 | |||||||
| chr9:74674634 | C | T | 10 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(7): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224+2733C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674634 | |||||||
| chr9:74674685 | A | G | 1 | a0001c0001t0038g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1224+2784A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674685 | |||||||
| chr9:74674839 | T | C | 1 | a0001c0001t0028g0188 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1224+2938T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674839 | |||||||
| chr9:74674860 | G | C | 10 | a0001c0001t0013g0036 a0001c0001t0013g0051 a0001c0001t0013g0052 others(7): Show |
10 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224+2959G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74674860 | |||||||
| chr9:74675036 | GA | G | 20 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(17): Show |
21 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1224+3144delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 74675036 | ||||||
| chr9:74675053 | G | A | 20 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(17): Show |
21 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(18): Show |
intron_variant | MODIFIER | c.1224+3152G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74675053 | |||||||
| chr9:74675139 | T | C | 4 | a0001c0001t0015g0015 a0001c0001t0015g0111 a0001c0001t0015g0142 others(1): Show |
4 | HG02647.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1224+3238T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74675139 | |||||||
| chr9:74675172 | G | A | 1 | a0001c0001t0004g0093 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1224+3271G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74675172 | |||||||
| chr9:74675301 | G | GA | 102 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(99): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.1224+3410dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 74675301 | ||||||
| chr9:74675607 | T | G | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1224+3706T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74675607 | |||||||
| chr9:74675715 | G | T | 18 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(15): Show |
19 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1224+3814G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74675715 | |||||||
| chr9:74675736 | G | A | 8 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(5): Show |
8 | HG02451.hp2 HG02970.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1224+3835G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74675736 | |||||||
| chr9:74675894 | G | C | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1224+3993G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74675894 | |||||||
| chr9:74675932 | A | G | 121 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(118): Show |
122 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1224+4031A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74675932 | |||||||
| chr9:74675945 | C | G | 1 | a0001c0001t0041g0074 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1224+4044C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74675945 | |||||||
| chr9:74676076 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1224+4175G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74676076 | |||||||
| chr9:74676145 | A | G | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1224+4244A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74676145 | |||||||
| chr9:74676450 | G | A | 10 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(7): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224+4549G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74676450 | |||||||
| chr9:74676451 | C | A | 10 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(7): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1224+4550C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74676451 | |||||||
| chr9:74676464 | G | A | 214 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(211): Show |
216 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.1224+4563G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74676464 | |||||||
| chr9:74676609 | G | A | 1 | a0001c0001t0018g0018 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1224+4708G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74676609 | |||||||
| chr9:74677257 | C | T | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1224+5356C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74677257 | |||||||
| chr9:74677373 | T | G | 99 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(96): Show |
100 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.1224+5472T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74677373 | |||||||
| chr9:74677518 | A | G | 1 | a0001c0001t0001g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1224+5617A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74677518 | |||||||
| chr9:74677795 | C | T | 18 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(15): Show |
19 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1224+5894C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74677795 | |||||||
| chr9:74677998 | A | G | 1 | a0001c0001t0024g0095 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1224+6097A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74677998 | |||||||
| chr9:74678033 | G | A | 13 | a0001c0001t0012g0210 a0001c0001t0012g0211 a0001c0001t0012g0212 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1224+6132G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74678033 | |||||||
| chr9:74678206 | G | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1224+6305G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74678206 | |||||||
| chr9:74678255 | G | A | 14 | a0001c0001t0003g0024 a0001c0001t0003g0152 a0001c0001t0003g0153 others(11): Show |
14 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.1224+6354G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74678255 | |||||||
| chr9:74678524 | A | G | 1 | a0001c0001t0010g0224 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1224+6623A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74678524 | |||||||
| chr9:74678771 | C | T | 3 | a0001c0001t0018g0018 a0001c0001t0018g0030 a0001c0001t0018g0089 |
3 | HG01168.hp2 HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1225-6692C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74678771 | |||||||
| chr9:74678800 | C | T | 30 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(27): Show |
30 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1225-6663C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74678800 | |||||||
| chr9:74678947 | G | A | 1 | a0001c0001t0006g0084 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1225-6516G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74678947 | |||||||
| chr9:74678973 | A | G | 30 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(27): Show |
30 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1225-6490A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74678973 | |||||||
| chr9:74679031 | CA | C | 116 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(113): Show |
117 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1225-6420delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 74679031 | ||||||
| chr9:74679038 | A | C | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1225-6425A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679038 | |||||||
| chr9:74679058 | C | A | 23 | a0001c0001t0001g0012 a0001c0001t0003g0024 a0001c0001t0017g0097 others(20): Show |
23 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.1225-6405C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679058 | |||||||
| chr9:74679058 | C | CA | 22 | a0001c0001t0001g0149 a0001c0001t0001g0193 a0001c0001t0004g0058 others(19): Show |
23 | HG00597.hp1 HG01074.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.1225-6394dupA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 74679058 | ||||||
| chr9:74679062 | A | C | 13 | a0001c0001t0012g0210 a0001c0001t0012g0211 a0001c0001t0012g0212 others(10): Show |
13 | HG01243.hp2 HG02451.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.1225-6401A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679062 | |||||||
| chr9:74679078 | C | A | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1225-6385C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679078 | |||||||
| chr9:74679146 | C | A | 1 | a0001c0001t0038g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1225-6317C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679146 | |||||||
| chr9:74679255 | G | C | 18 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(15): Show |
18 | HG00140.hp2 HG00323.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1225-6208G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679255 | |||||||
| chr9:74679414 | T | G | 2 | a0001c0001t0004g0158 a0001c0001t0007g0039 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1225-6049T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679414 | |||||||
| chr9:74679422 | C | T | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1225-6041C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679422 | |||||||
| chr9:74679439 | T | C | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1225-6024T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679439 | |||||||
| chr9:74679463 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1225-6000G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679463 | |||||||
| chr9:74679476 | A | C | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1225-5987A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679476 | |||||||
| chr9:74679486 | A | G | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1225-5977A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679486 | |||||||
| chr9:74679499 | G | C | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1225-5964G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679499 | |||||||
| chr9:74679590 | C | T | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1225-5873C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679590 | |||||||
| chr9:74679755 | G | A | 1 | a0001c0001t0024g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1225-5708G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679755 | |||||||
| chr9:74679758 | C | G | 1 | a0001c0001t0002g0083 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1225-5705C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679758 | |||||||
| chr9:74679872 | C | T | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1225-5591C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679872 | |||||||
| chr9:74679934 | G | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.1225-5529G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679934 | |||||||
| chr9:74679974 | G | A | 2 | a0001c0001t0009g0025 a0001c0001t0028g0188 |
2 | NA18960.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1225-5489G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74679974 | |||||||
| chr9:74680148 | C | G | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1225-5315C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74680148 | |||||||
| chr9:74680268 | G | A | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1225-5195G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74680268 | |||||||
| chr9:74680379 | T | G | 30 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(27): Show |
30 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.1225-5084T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74680379 | |||||||
| chr9:74680414 | A | C | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1225-5049A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74680414 | |||||||
| chr9:74680471 | A | G | 14 | a0001c0001t0012g0210 a0001c0001t0012g0211 a0001c0001t0012g0212 others(11): Show |
14 | HG01243.hp2 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1225-4992A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74680471 | |||||||
| chr9:74680820 | T | G | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1225-4643T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74680820 | |||||||
| chr9:74680937 | C | T | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1225-4526C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74680937 | |||||||
| chr9:74681021 | C | T | 4 | a0001c0001t0015g0015 a0001c0001t0015g0111 a0001c0001t0015g0142 others(1): Show |
4 | HG02647.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-4442C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74681021 | |||||||
| chr9:74681245 | T | C | 4 | a0001c0001t0002g0119 a0001c0001t0025g0054 a0001c0001t0025g0217 others(1): Show |
4 | HG00408.hp2 HG00609.hp1 HG02040.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-4218T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74681245 | |||||||
| chr9:74681290 | A | G | 1 | a0001c0001t0044g0187 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1225-4173A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74681290 | |||||||
| chr9:74681581 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0067 a0001c0001t0020g0138 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-3882T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74681581 | |||||||
| chr9:74681743 | G | T | 12 | a0001c0001t0003g0024 a0001c0002t0003g0026 a0001c0002t0003g0041 others(9): Show |
12 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1225-3720G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74681743 | |||||||
| chr9:74681974 | C | T | 1 | a0001c0002t0058g0109 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1225-3489C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74681974 | |||||||
| chr9:74682384 | G | A | 1 | a0002c0004t0030g0014 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1225-3079G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682384 | |||||||
| chr9:74682399 | G | A | 1 | a0001c0001t0034g0064 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1225-3064G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682399 | |||||||
| chr9:74682642 | G | A | 46 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(43): Show |
47 | HG00597.hp1 HG01168.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.1225-2821G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682642 | |||||||
| chr9:74682733 | T | A | 4 | a0001c0001t0015g0015 a0001c0001t0015g0111 a0001c0001t0015g0142 others(1): Show |
4 | HG02647.hp1 HG02886.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-2730T>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682733 | |||||||
| chr9:74682744 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1225-2719T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682744 | |||||||
| chr9:74682758 | T | G | 17 | a0001c0001t0001g0135 a0001c0001t0001g0178 a0001c0001t0001g0180 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1225-2705T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682758 | |||||||
| chr9:74682771 | C | T | 36 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(33): Show |
37 | HG00597.hp1 HG01168.hp2 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.1225-2692C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682771 | |||||||
| chr9:74682774 | A | G | 3 | a0001c0001t0012g0210 a0001c0001t0012g0211 a0001c0001t0012g0212 |
3 | HG01243.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1225-2689A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682774 | |||||||
| chr9:74682830 | G | C | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1225-2633G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682830 | |||||||
| chr9:74682963 | C | T | 1 | a0001c0001t0007g0100 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1225-2500C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74682963 | |||||||
| chr9:74683096 | C | G | 3 | a0001c0001t0012g0210 a0001c0001t0012g0211 a0001c0001t0012g0212 |
3 | HG01243.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1225-2367C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74683096 | |||||||
| chr9:74683201 | C | T | 3 | a0001c0001t0012g0210 a0001c0001t0012g0211 a0001c0001t0012g0212 |
3 | HG01243.hp2 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1225-2262C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74683201 | |||||||
| chr9:74683479 | C | A | 1 | a0001c0001t0005g0169 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1225-1984C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74683479 | |||||||
| chr9:74683510 | A | G | 7 | a0001c0001t0001g0071 a0001c0001t0001g0115 a0001c0001t0001g0118 others(4): Show |
7 | HG00323.hp2 HG00738.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1225-1953A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74683510 | |||||||
| chr9:74683532 | C | G | 2 | a0001c0001t0004g0126 a0001c0001t0004g0127 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1225-1931C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74683532 | |||||||
| chr9:74683760 | G | A | 4 | a0001c0002t0003g0026 a0001c0002t0003g0041 a0001c0002t0003g0046 others(1): Show |
4 | NA18939.hp1 NA18965.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1225-1703G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74683760 | |||||||
| chr9:74683872 | G | T | 1 | a0001c0001t0046g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1225-1591G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74683872 | |||||||
| chr9:74683954 | A | G | 2 | a0001c0001t0021g0003 a0001c0001t0021g0112 |
2 | HG02895.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1225-1509A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74683954 | |||||||
| chr9:74684102 | C | T | 1 | a0001c0001t0051g0203 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1225-1361C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684102 | |||||||
| chr9:74684128 | T | C | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1225-1335T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684128 | |||||||
| chr9:74684163 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0066g0182 |
2 | HG01175.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1225-1300C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684163 | |||||||
| chr9:74684189 | C | G | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1225-1274C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684189 | |||||||
| chr9:74684254 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1225-1209A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684254 | |||||||
| chr9:74684336 | G | C | 1 | a0001c0001t0054g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1225-1127G>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684336 | |||||||
| chr9:74684375 | T | C | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1225-1088T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684375 | |||||||
| chr9:74684470 | A | ATCACAGT others(318): Show |
3 | a0001c0001t0018g0018 a0001c0001t0018g0030 a0001c0001t0018g0089 |
3 | HG01168.hp2 HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1225-979_1225-978i others(327): Show |
RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 74684470 | ||||||
| chr9:74684539 | A | G | 10 | a0001c0001t0013g0036 a0001c0001t0013g0051 a0001c0001t0013g0052 others(7): Show |
10 | HG02451.hp1 HG02622.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1225-924A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684539 | |||||||
| chr9:74684588 | TA | T | 29 | a0001c0001t0002g0038 a0001c0001t0002g0040 a0001c0001t0002g0055 others(26): Show |
29 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.1225-872delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 74684588 | ||||||
| chr9:74684657 | T | G | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1225-806T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684657 | |||||||
| chr9:74684667 | A | C | 19 | a0001c0001t0005g0011 a0001c0001t0005g0034 a0001c0001t0005g0169 others(16): Show |
20 | HG00597.hp1 HG01256.hp1 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1225-796A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684667 | |||||||
| chr9:74684681 | A | G | 11 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(8): Show |
11 | HG01884.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1225-782A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684681 | |||||||
| chr9:74684731 | G | A | 1 | a0001c0001t0046g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1225-732G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684731 | |||||||
| chr9:74684824 | G | A | 26 | a0001c0001t0001g0098 a0001c0001t0001g0135 a0001c0001t0001g0178 others(23): Show |
26 | HG00140.hp2 HG00323.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1225-639G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684824 | |||||||
| chr9:74684861 | C | G | 1 | a0001c0002t0060g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1225-602C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74684861 | |||||||
| chr9:74685003 | T | C | 16 | a0001c0001t0003g0024 a0001c0001t0003g0152 a0001c0001t0003g0153 others(13): Show |
16 | HG00609.hp2 HG00738.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1225-460T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | chr9 | 74685003 | |||||||
| chr9:74685269 | C | CG | 10 | a0001c0001t0001g0118 a0001c0001t0001g0193 a0001c0001t0002g0065 others(7): Show |
10 | HG00597.hp1 HG01261.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.1225-187dupG | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 74685269 | ||||||
| chr9:74685356 | TC | T | 10 | a0001c0001t0017g0097 a0001c0001t0017g0107 a0001c0001t0017g0141 others(7): Show |
10 | HG01884.hp1 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1225-105delC | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 74685356 |