Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr9 | 74492335 | 74698177 |
| a0002 | 0/0 | 459 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0003 | 0/0 | 459 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1380 | 194 | 67 | 37 | 64 | 6 | 18 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| c0002 | 0/0 | 1380 | 29 | 2 | 8 | 15 | 2 | 2 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| c0003 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| c0004 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| c0005 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 8202 | 64 | 10 | 16 | 23 | 6 | 9 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0002 | 0/0 | 8203 | 18 | 1 | 2 | 13 | 0 | 2 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0003 | 0/0 | 8202 | 12 | 1 | 1 | 7 | 1 | 2 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0004 | 0/0 | 8202 | 11 | 4 | 4 | 2 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0005 | 0/0 | 8203 | 8 | 0 | 0 | 8 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0006 | 0/1 | 8203 | 8 | 1 | 5 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0007 | 0/0 | 8202 | 7 | 6 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0008 | 0/0 | 8203 | 5 | 0 | 0 | 5 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0009 | 0/0 | 8203 | 5 | 0 | 2 | 3 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0010 | 0/0 | 8202 | 4 | 4 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0011 | 0/0 | 8202 | 4 | 0 | 3 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0012 | 0/0 | 8202 | 4 | 3 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0013 | 0/0 | 8199 | 4 | 4 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0014 | 0/0 | 8199 | 4 | 4 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0015 | 0/0 | 8202 | 3 | 3 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0016 | 1/0 | 8202 | 3 | 2 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0017 | 0/0 | 8202 | 3 | 3 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0018 | 0/0 | 8202 | 3 | 2 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0019 | 0/0 | 8202 | 3 | 3 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0020 | 0/0 | 8202 | 2 | 2 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0021 | 0/0 | 8202 | 2 | 2 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0022 | 0/0 | 8203 | 2 | 0 | 2 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0023 | 0/0 | 8202 | 2 | 0 | 1 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0024 | 0/0 | 8202 | 2 | 0 | 0 | 1 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0025 | 0/0 | 8203 | 2 | 0 | 0 | 2 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0026 | 0/0 | 8203 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0027 | 0/0 | 8202 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0028 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0029 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0030 | 0/0 | 8203 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0031 | 0/0 | 8203 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0032 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0033 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0034 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0035 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0036 | 0/0 | 8203 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0037 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0038 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0039 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0040 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0041 | 0/0 | 8202 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0042 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0043 | 0/0 | 8202 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0044 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0045 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0046 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0047 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0048 | 0/0 | 8202 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0049 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0050 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0051 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0052 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0053 | 0/0 | 8202 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0054 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0055 | 0/0 | 8203 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0056 | 0/0 | 8199 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0057 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0058 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0059 | 0/0 | 8199 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0060 | 0/0 | 8202 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0061 | 0/0 | 8203 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0062 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0063 | 0/0 | 8182 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0064 | 0/0 | 8202 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0065 | 0/0 | 8203 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| t0066 | 0/0 | 8202 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1380 | 194 | 67 | 37 | 64 | 6 | 18 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002 | 0/0 | 1380 | 29 | 2 | 8 | 15 | 2 | 2 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0005 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0002c0003 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0003c0004 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | 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 | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0002 | 0/0 | 9582 | 14 | 1 | 2 | 9 | 0 | 2 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0003 | 0/0 | 9581 | 3 | 1 | 0 | 0 | 1 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0004 | 0/0 | 9581 | 10 | 4 | 3 | 2 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0005 | 0/0 | 9582 | 5 | 0 | 0 | 5 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0006 | 0/1 | 9582 | 7 | 1 | 4 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0007 | 0/0 | 9581 | 7 | 6 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0008 | 0/0 | 9582 | 5 | 0 | 0 | 5 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0009 | 0/0 | 9582 | 4 | 0 | 1 | 3 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0010 | 0/0 | 9581 | 4 | 4 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0011 | 0/0 | 9581 | 3 | 0 | 2 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0012 | 0/0 | 9581 | 4 | 3 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0013 | 0/0 | 9578 | 4 | 4 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0014 | 0/0 | 9578 | 4 | 4 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0015 | 0/0 | 9581 | 3 | 3 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0016 | 1/0 | 9581 | 3 | 2 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0017 | 0/0 | 9581 | 3 | 3 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0018 | 0/0 | 9581 | 3 | 2 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0019 | 0/0 | 9581 | 3 | 3 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0020 | 0/0 | 9581 | 2 | 2 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0021 | 0/0 | 9581 | 2 | 2 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0022 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0024 | 0/0 | 9581 | 2 | 0 | 0 | 1 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0025 | 0/0 | 9582 | 2 | 0 | 0 | 2 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0026 | 0/0 | 9582 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0027 | 0/0 | 9581 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0028 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0029 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0031 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0032 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0033 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0034 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0035 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0036 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0037 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0038 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0039 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0040 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0041 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0042 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0043 | 0/0 | 9581 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0044 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0045 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0046 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0047 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0048 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0049 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0050 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0051 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0052 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0053 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0054 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0055 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0056 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0057 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0059 | 0/0 | 9578 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0062 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0063 | 0/0 | 9561 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0064 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0001t0066 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0001 | 0/0 | 9581 | 3 | 0 | 1 | 0 | 2 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0002 | 0/0 | 9582 | 4 | 0 | 0 | 4 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0003 | 0/0 | 9581 | 9 | 0 | 1 | 7 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0004 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0005 | 0/0 | 9582 | 3 | 0 | 0 | 3 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0009 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0011 | 0/0 | 9581 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0022 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0023 | 0/0 | 9581 | 2 | 0 | 1 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0058 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0060 | 0/0 | 9581 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0061 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0002t0065 | 0/0 | 9582 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0001c0005t0006 | 0/0 | 9582 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0002c0003t0001 | 0/0 | 9581 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| a0003c0004t0030 | 0/0 | 9582 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | copy fasta | chr9 | 74492335 | 74698177 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0131 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0188 | 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 |
| a0001c0001t0001g0196 | 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 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0055 | 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 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0002g0165 | 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 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0009g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0009g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0009g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0010g0003 | 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 |
| a0001c0001t0010g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0010g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0011g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0011g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0011g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0012g0158 | 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 |
| a0001c0001t0012g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0012g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0013g0050 | 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 |
| a0001c0001t0013g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0014g0018 | 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 |
| a0001c0001t0015g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0015g0110 | 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 |
| a0001c0001t0016g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0016g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0016g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0017g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0017g0106 | 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 |
| a0001c0001t0018g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0018g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0018g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0019g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0019g0089 | 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 |
| a0001c0001t0020g0137 | 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 |
| a0001c0001t0021g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0021g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0022g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0024g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0024g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0025g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0025g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0026g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0027g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0028g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0029g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0031g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0032g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0033g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0034g0067 | 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 |
| a0001c0001t0036g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0037g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0038g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0039g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0040g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0041g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0042g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0043g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0044g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0045g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0046g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0047g0086 | 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 |
| a0001c0001t0049g0104 | 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 |
| a0001c0001t0051g0204 | 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 |
| a0001c0001t0053g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0054g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0055g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0056g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0057g0036 | 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 |
| a0001c0001t0062g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0063g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0064g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0001t0066g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0002g0217 | 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 |
| a0001c0002t0003g0040 | 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 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0002t0003g0215 | 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 |
| a0001c0002t0005g0076 | 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 |
| a0001c0002t0011g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0022g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0023g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0023g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0058g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0060g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0061g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0002t0065g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0001c0005t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0002c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| a0003c0004t0030g0013 | 0/0 | 1 | 1 | 0 | 0 | 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 | g0046 | EUR | GBR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00323 | hp1 | a0001 | c0001 | t0027 | g0081 | EUR | FIN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | FIN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00408 | hp2 | a0001 | c0001 | t0025 | g0218 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00597 | hp1 | a0001 | c0001 | t0008 | g0077 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00609 | hp1 | a0001 | c0001 | t0025 | g0053 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00609 | hp2 | a0001 | c0002 | t0003 | g0164 | EAS | CHS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00738 | hp1 | a0001 | c0002 | t0003 | g0215 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0180 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0064 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0125 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01081 | hp1 | a0001 | c0002 | t0061 | g0044 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0101 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01106 | hp2 | a0001 | c0001 | t0011 | g0171 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01109 | hp1 | a0001 | c0001 | t0041 | g0059 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01168 | hp1 | a0001 | c0005 | t0006 | g0219 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01168 | hp2 | a0001 | c0001 | t0018 | g0017 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01175 | hp2 | a0001 | c0002 | t0023 | g0216 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01192 | hp1 | a0001 | c0001 | t0036 | g0149 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01243 | hp1 | a0001 | c0001 | t0066 | g0181 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01243 | hp2 | a0001 | c0001 | t0012 | g0214 | AMR | PUR | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01255 | hp1 | a0001 | c0001 | t0007 | g0099 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01256 | hp1 | a0001 | c0001 | t0031 | g0123 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01256 | hp2 | a0001 | c0001 | t0006 | g0083 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01433 | hp2 | a0001 | c0002 | t0011 | g0120 | AMR | CLM | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01496 | hp1 | a0001 | c0001 | t0064 | g0100 | 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 | g0170 | EUR | IBS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0151 | EUR | IBS | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01884 | hp1 | a0001 | c0001 | t0056 | g0221 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01891 | hp1 | a0001 | c0001 | t0040 | g0021 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01891 | hp2 | a0001 | c0001 | t0042 | g0154 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01975 | hp1 | a0001 | c0001 | t0022 | g0071 | 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 | g0072 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01981 | hp1 | a0001 | c0001 | t0011 | g0178 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02004 | hp1 | a0001 | c0001 | t0009 | g0075 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02080 | hp1 | a0001 | c0001 | t0009 | g0022 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02080 | hp2 | a0001 | c0001 | t0024 | g0175 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02135 | hp1 | a0001 | c0001 | t0045 | g0062 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02135 | hp2 | a0001 | c0001 | t0044 | g0186 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02148 | hp1 | a0001 | c0002 | t0022 | g0025 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0156 | 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 | g0061 | EAS | CDX | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02257 | hp1 | a0001 | c0001 | t0018 | g0029 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02258 | hp2 | a0001 | c0001 | t0057 | g0036 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02280 | hp1 | a0001 | c0001 | t0038 | g0161 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02280 | hp2 | a0001 | c0002 | t0058 | g0108 | 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 | g0140 | AMR | PEL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0020 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02451 | hp2 | a0001 | c0001 | t0019 | g0090 | AFR | ACB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02523 | hp2 | a0001 | c0001 | t0029 | g0056 | EAS | KHV | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02572 | hp2 | a0001 | c0001 | t0010 | g0159 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02622 | hp1 | a0001 | c0001 | t0012 | g0213 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02622 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02630 | hp2 | a0001 | c0001 | t0014 | g0009 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02647 | hp1 | a0001 | c0001 | t0054 | g0162 | 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 | g0043 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0095 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02723 | hp1 | a0001 | c0001 | t0016 | g0098 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0225 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02809 | hp1 | a0001 | c0001 | t0007 | g0136 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0157 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02886 | hp1 | a0001 | c0001 | t0010 | g0003 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0014 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02895 | hp1 | a0001 | c0001 | t0020 | g0138 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02895 | hp2 | a0001 | c0001 | t0021 | g0002 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0007 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02896 | hp2 | a0001 | c0001 | t0013 | g0109 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02897 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02897 | hp2 | a0001 | c0001 | t0020 | g0137 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02965 | hp1 | a0001 | c0002 | t0060 | g0015 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02965 | hp2 | a0001 | c0001 | t0013 | g0050 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02970 | hp1 | a0001 | c0001 | t0017 | g0106 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG02970 | hp2 | a0003 | c0004 | t0030 | g0013 | 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 | g0038 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03017 | hp1 | a0001 | c0001 | t0043 | g0047 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0023 | 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 | g0006 | AFR | GWD | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03098 | hp1 | a0001 | c0001 | t0013 | g0035 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03098 | hp2 | a0001 | c0001 | t0051 | g0204 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03130 | hp1 | a0001 | c0001 | t0019 | g0085 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03195 | hp2 | a0001 | c0001 | t0015 | g0110 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03209 | hp1 | a0001 | c0001 | t0013 | g0051 | 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 | g0089 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03225 | hp2 | a0001 | c0001 | t0012 | g0158 | 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 | g0111 | 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 | g0155 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03516 | hp2 | a0001 | c0001 | t0046 | g0093 | AFR | ESN | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03579 | hp1 | a0001 | c0001 | t0047 | g0086 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0222 | AFR | MSL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG03927 | hp2 | a0001 | c0001 | t0024 | g0094 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | STU | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04115 | hp2 | a0001 | c0001 | t0011 | g0208 | 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 | g0034 | SAS | BEB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04199 | hp1 | a0001 | c0001 | t0026 | g0185 | SAS | STU | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04199 | hp2 | a0001 | c0002 | t0003 | g0122 | SAS | STU | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0210 | 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 | g0041 | EAS | CHB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | CHB | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18906 | hp1 | a0001 | c0001 | t0014 | g0019 | AFR | YRI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18939 | hp1 | a0001 | c0002 | t0003 | g0045 | 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 | g0165 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0091 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18947 | hp2 | a0001 | c0001 | t0034 | g0067 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18952 | hp1 | a0001 | c0001 | t0009 | g0070 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18960 | hp1 | a0001 | c0001 | t0028 | g0189 | 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 | a0002 | 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 | g0129 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18969 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18969 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18983 | hp1 | a0001 | c0001 | t0037 | g0183 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18999 | hp1 | a0001 | c0001 | t0033 | g0078 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19001 | hp1 | a0001 | c0001 | t0063 | g0198 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19001 | hp2 | a0001 | c0001 | t0039 | g0032 | 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 | g0202 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0168 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19010 | hp1 | a0001 | c0001 | t0049 | g0104 | 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 | g0088 | AFR | LWK | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | LWK | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19054 | hp1 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19054 | hp2 | a0001 | c0001 | t0008 | g0197 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0055 | 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 | g0030 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19064 | hp2 | a0001 | c0001 | t0008 | g0130 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0040 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19076 | hp1 | a0001 | c0001 | t0062 | g0103 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19078 | hp1 | a0001 | c0001 | t0008 | g0105 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19082 | hp1 | a0001 | c0002 | t0003 | g0163 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19087 | hp1 | a0001 | c0002 | t0005 | g0076 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19087 | hp2 | a0001 | c0001 | t0053 | g0173 | EAS | JPT | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19240 | hp1 | a0001 | c0001 | t0017 | g0096 | AFR | YRI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA19240 | hp2 | a0001 | c0001 | t0016 | g0028 | AFR | YRI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0169 | EUR | TSI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | USA | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| HG06807 | hp2 | a0001 | c0001 | t0055 | g0016 | AFR | USA | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | USA | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | USA | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0102 | REF | REF | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0016 | g0206 | REF | REF | RORB_chr9_74492335_74698177 | RORB | chr9 | 74492335 | 74698177 |
| 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 | a0002 | 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 | a0003 | 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 |
| 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 |
| 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 | a0001c0001t0025a0001c0002t0065 | 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 | a0001c0001t0002a0001c0001t0009a0001c0001t0025others(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 | a0001c0001t0005a0001c0001t0008a0001c0001t0028others(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 | a0001c0001t0003a0001c0001t0022a0001c0001t0057others(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 | a0001c0001t0013a0001c0001t0014a0001c0001t0055others(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 | a0001c0001t0005a0001c0001t0008a0001c0001t0028others(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 | a0001c0001t0008a0001c0001t0032a0001c0001t0033others(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 | a0001c0001t0017a0001c0001t0019a0001c0001t0051others(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 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(27): Show | 72 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(69): 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 | a0001c0001t0015a0001c0001t0054 | 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 | a0001c0001t0003a0001c0001t0031a0001c0002t0003others(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 | a0001c0001t0005a0001c0001t0008a0001c0001t0028others(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 | a0001c0001t0003a0001c0001t0022a0001c0001t0050others(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 | a0001c0001t0003a0001c0001t0022a0001c0001t0038others(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 | a0001c0001t0013a0001c0001t0014a0001c0001t0056others(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 | a0001c0001t0017a0001c0001t0019a0001c0001t0052 | 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 | a0001c0001t0013a0001c0001t0015a0001c0001t0038others(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 | a0001c0001t0010a0001c0001t0040 | 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(39): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(39): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(151): 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 | a0001c0001t0046a0001c0002t0058 | 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 | a0001c0001t0002a0001c0001t0004a0001c0001t0025others(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 | a0001c0001t0001a0001c0001t0006a0001c0001t0009others(31): Show | 112 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(109): 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(71): Show | 221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): 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 | a0001c0001t0005a0001c0001t0008a0001c0001t0017others(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 | a0001c0001t0017a0001c0001t0019a0001c0001t0051others(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 | a0001c0001t0046a0001c0002t0058 | 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 | a0001c0001t0011a0001c0002t0011 | 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 | a0001c0001t0010a0001c0001t0038 | 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 | a0001c0001t0014a0001c0001t0017a0001c0001t0019others(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 | a0001c0001t0037a0001c0001t0062 | 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(71): Show | 221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
3_prime_UTR_variant | MODIFIER | c.*7515T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 10/10 | 7515 | chr9 | 74693133 |
| 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0001g0220a0001c0005t0006g0219 | 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 | a0001c0001t0025g0218 | 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 | a0001c0002t0002g0217 | 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 | a0001c0001t0001g0004 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0007g0007others(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 | a0001c0001t0005g0010 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0007g0212a0001c0001t0010g0003a0001c0001t0012g0211others(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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0007g0012a0001c0001t0015g0014a0001c0002t0060g0015others(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 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 173 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(170): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0040g0021 | 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 | a0001c0002t0003g0163a0001c0002t0003g0164 | 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 | 99 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(96): Show | 100 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(97): 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 | a0001c0001t0013g0109a0001c0001t0015g0110a0001c0001t0021g0111others(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 | a0001c0001t0007g0212a0001c0001t0010g0003a0001c0001t0012g0211others(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 | a0001c0001t0054g0162 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0001g0011a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0001g0160a0001c0001t0010g0159a0001c0001t0038g0161 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0002t0058g0108 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0001g0160a0001c0001t0010g0159a0001c0001t0038g0161 | 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 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020 | 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 | a0001c0001t0021g0111 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0107 | 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 | a0001c0001t0006g0210 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0054g0162 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0007g0212a0001c0001t0010g0003a0001c0001t0012g0211others(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 | a0001c0001t0001g0135 | 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 | a0001c0001t0007g0012 | 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 | a0001c0001t0009g0022 | 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 | a0001c0001t0004g0157 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0017g0106 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0003g0023 | 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 | a0001c0001t0009g0024 | 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 | a0001c0001t0007g0212a0001c0001t0010g0003a0001c0001t0012g0211others(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 | a0001c0001t0001g0011a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0014g0009 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0207a0001c0001t0011g0208 | 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 | a0001c0001t0001g0112a0001c0001t0001g0113 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0002t0003g0026a0001c0002t0004g0027a0001c0002t0022g0025 | 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 | a0001c0001t0002g0165a0001c0001t0002g0166 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0114 | 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 | a0001c0001t0016g0028a0001c0001t0018g0029 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0054g0162 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0008g0105 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0049g0104 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0002t0065g0030 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0001g0031 | 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0002g0166 | 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 | a0001c0001t0062g0103 | 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 | 2 | a0001c0001t0006g0101a0001c0001t0006g0102 | 2 | HG01106.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.7+10610G>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74508593 | ||||||
| chr9:74508638
|
T | A | 46 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0172others(43): 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 | a0001c0001t0014g0009a0001c0001t0039g0032 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0054g0162 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0010g0225 | 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 | a0001c0001t0007g0212a0001c0001t0010g0003a0001c0001t0012g0211others(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 | a0001c0001t0010g0225 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0001g0160a0001c0001t0010g0159a0001c0001t0038g0161 | 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 | a0001c0001t0005g0168 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0005g0033 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 173 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(170): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0170a0001c0001t0011g0171a0001c0002t0001g0169 | 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 | a0001c0001t0007g0012a0001c0001t0015g0014a0001c0002t0060g0015others(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 | a0001c0001t0001g0172 | 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 | a0001c0001t0014g0009 | 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 | a0001c0001t0064g0100 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0160a0001c0001t0001g0223a0001c0001t0004g0222others(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 | a0001c0001t0007g0212a0001c0001t0010g0003a0001c0001t0012g0211others(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 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0003g0151others(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 | a0001c0001t0010g0225 | 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 | a0001c0001t0007g0212a0001c0001t0010g0003a0001c0001t0012g0211others(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 | a0001c0001t0011g0171 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0112a0001c0001t0001g0113 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0007g0099a0001c0001t0016g0098a0001c0001t0064g0100 | 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 | a0001c0001t0001g0155 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0006g0101 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0005 | 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 | 99 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(96): Show | 100 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(97): 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0013g0035a0001c0001t0057g0036 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0001g0097a0001c0001t0017g0096 | 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 | a0001c0001t0004g0095 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0053g0173 | 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 | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(169): Show | 173 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(170): 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0016g0098 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0018g0029 | 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0001g0160a0001c0001t0010g0159a0001c0001t0038g0161 | 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 | a0001c0001t0002g0037 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0005g0010 | 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 | a0001c0001t0007g0038 | 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 | a0001c0001t0024g0094 | 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0004g0174 | 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 | a0001c0001t0004g0092a0001c0001t0046g0093 | 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 | a0001c0001t0001g0160a0001c0001t0001g0223a0001c0001t0004g0222others(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 | a0001c0001t0024g0175 | 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 | a0001c0001t0002g0039 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | 158 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 158 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(155): 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 | a0001c0001t0008g0091 | 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 | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.7+23890C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74521873 | ||||||
| chr9:74521980
|
C | A | 57 | a0001c0001t0001g0042a0001c0001t0001g0167a0001c0001t0001g0170others(54): 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 | 57 | a0001c0001t0001g0042a0001c0001t0001g0167a0001c0001t0001g0170others(54): 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 | 58 | a0001c0001t0001g0042a0001c0001t0001g0167a0001c0001t0001g0170others(55): 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 | a0001c0001t0001g0160a0001c0001t0001g0223a0001c0001t0004g0222others(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 | a0001c0001t0013g0050a0001c0001t0013g0051 | 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 | a0001c0001t0008g0091 | 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 | a0001c0001t0001g0160a0001c0001t0001g0223a0001c0001t0004g0222others(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 | a0001c0001t0010g0003a0001c0001t0021g0002 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | 57 | a0001c0001t0001g0042a0001c0001t0001g0167a0001c0001t0001g0170others(54): 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0117others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0055g0016 | 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 | a0001c0001t0001g0203 | 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 | a0001c0001t0019g0089a0001c0001t0019g0090 | 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 | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): 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 | a0001c0001t0049g0104 | 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 | 137 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0058others(134): Show | 138 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(135): 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0039g0032 | 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 | 21 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0187others(18): 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 | a0001c0001t0051g0204 | 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 | 57 | a0001c0001t0001g0042a0001c0001t0001g0167a0001c0001t0001g0170others(54): 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 | a0001c0002t0003g0049 | 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 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0011g0178 | 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 | a0001c0001t0001g0087a0001c0001t0018g0088a0001c0001t0047g0086 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0019g0085a0001c0001t0019g0089a0001c0001t0019g0090 | 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 | 84 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(81): Show | 84 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(81): 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0013g0035 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0031 | 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 | a0001c0002t0002g0048 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0016g0028a0001c0001t0018g0029 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0005g0202a0001c0001t0053g0173 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | 84 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(81): Show | 84 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.7+31144C>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74529127 | ||||||
| chr9:74529284
|
A | G | 78 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(75): Show | 78 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(75): 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 | a0001c0001t0016g0028a0001c0001t0018g0029 | 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 | a0001c0001t0006g0180 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0051g0204 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0007g0012a0001c0001t0015g0014a0001c0001t0016g0028others(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 | a0001c0001t0039g0032 | 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 | a0001c0002t0003g0040 | 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 | a0001c0001t0001g0006a0001c0001t0007g0136a0001c0001t0020g0137others(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 | a0001c0001t0013g0050a0001c0001t0013g0051a0001c0001t0014g0018others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0043g0047 | 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 | a0001c0001t0024g0175 | 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 | a0001c0002t0002g0048 | 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 | a0001c0001t0041g0059 | 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 | a0001c0001t0001g0114a0001c0001t0001g0117a0001c0002t0009g0116 | 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 | a0001c0002t0002g0048 | 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 | a0001c0002t0002g0048 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0002t0058g0108 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0001g0160a0001c0001t0010g0159a0001c0001t0038g0161 | 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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0054g0162 | 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0055g0016 | 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 | a0001c0001t0024g0175 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0014g0009 | 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 | a0001c0001t0007g0012a0001c0001t0015g0014a0001c0001t0016g0028others(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 | a0001c0001t0049g0104 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0051g0204 | 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0001g0160a0001c0001t0010g0159a0001c0001t0038g0161 | 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 | a0001c0002t0003g0041 | 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 | a0001c0002t0001g0169 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0139 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0036g0149 | 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 | a0001c0001t0016g0028a0001c0001t0018g0029 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0049g0104 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(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 | a0001c0001t0016g0028a0001c0001t0018g0029 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | 62 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0172others(59): Show | 62 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.7+40566T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74538549 | ||||||
| chr9:74538728
|
C | CA | 126 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(123): Show | 126 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(123): 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 | a0001c0001t0001g0176a0001c0001t0001g0187a0001c0001t0001g0188others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0140 | 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0001t0012g0158 | 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 | 61 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0172others(58): Show | 61 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.7+41062C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74539045 | ||||||
| chr9:74539084
|
G | A | 217 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): 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 | a0001c0001t0001g0203 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(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 | a0001c0001t0010g0225 | 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 | a0001c0001t0001g0042a0001c0001t0001g0134a0001c0001t0007g0212others(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 | a0001c0001t0001g0223a0001c0001t0003g0023a0001c0001t0004g0222others(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 | 80 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(77): Show | 81 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(78): 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 | a0001c0001t0001g0113a0001c0001t0001g0132a0001c0001t0001g0148others(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 | 121 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 121 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(118): 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0006g0101 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0052others(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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): 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 | a0001c0001t0001g0087a0001c0001t0018g0088a0001c0001t0047g0086 | 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 | a0001c0001t0016g0028a0001c0001t0018g0029 | 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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0002g0065others(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 | 23 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0176others(20): 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 | a0001c0001t0001g0006a0001c0001t0001g0113a0001c0001t0001g0139others(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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(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 | a0001c0001t0001g0112a0001c0001t0001g0132a0001c0001t0001g0140others(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 | a0001c0001t0004g0222a0001c0001t0057g0036 | 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0014g0020a0001c0001t0018g0017 | 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 | a0001c0001t0014g0018a0001c0001t0014g0019 | 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 | a0001c0001t0013g0051 | 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 | a0001c0001t0013g0050 | 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 | 33 | a0001c0001t0001g0042a0001c0001t0001g0134a0001c0001t0001g0170others(30): Show | 34 | HG00140.hp2 HG01074.hp2 HG01081.hp1 others(31): 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 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0052g0147 | 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 | a0001c0001t0019g0089 | 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 | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0080others(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 | a0001c0001t0001g0004a0001c0001t0001g0139a0001c0001t0001g0140others(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 | a0001c0001t0008g0077 | 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 | a0001c0002t0003g0215a0001c0002t0023g0216 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0012g0158 | 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 | a0001c0001t0066g0181 | 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 | a0001c0002t0001g0046 | 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 | a0001c0001t0001g0172a0001c0001t0001g0192 | 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 | a0001c0001t0002g0055 | 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 | 217 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.7+45077A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74543060 | ||||||
| chr9:74543232
|
C | T | 217 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(214): Show | 218 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(215): 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0001g0042a0001c0001t0001g0134a0001c0001t0007g0212others(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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | 221 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(218): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): 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 | a0001c0001t0001g0139 | 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 | 51 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0001g0172others(48): Show | 51 | HG00140.hp1 HG00140.hp2 HG01070.hp2 others(48): 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 | a0001c0001t0014g0009 | 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 | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(195): 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 | a0001c0001t0001g0182 | 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(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 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0052others(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 | a0001c0001t0001g0160a0001c0001t0010g0159a0001c0001t0038g0161 | 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 | a0001c0001t0001g0069a0001c0001t0001g0156a0001c0001t0003g0152others(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 | 44 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0001g0167others(41): Show | 44 | HG00140.hp1 HG00140.hp2 HG00738.hp2 others(41): 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 | a0001c0001t0001g0172a0001c0001t0001g0188a0001c0001t0001g0207others(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 | a0001c0002t0060g0015a0003c0004t0030g0013 | 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 | a0001c0001t0049g0104 | 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 | a0001c0001t0002g0039 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | 206 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): 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 | a0001c0002t0060g0015a0003c0004t0030g0013 | 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 | a0001c0002t0060g0015a0003c0004t0030g0013 | 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 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0042others(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 | a0001c0002t0060g0015a0003c0004t0030g0013 | 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 | a0001c0002t0060g0015a0003c0004t0030g0013 | 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 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0042others(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 | a0001c0001t0012g0158 | 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 | a0001c0002t0001g0046 | 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 | a0001c0001t0054g0162 | 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 | a0001c0001t0064g0100 | 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 | a0001c0001t0010g0225 | 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 | a0001c0001t0001g0058a0001c0001t0008g0091 | 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 | 127 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(124): Show | 127 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(124): 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 | a0001c0001t0054g0162 | 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 | a0001c0001t0064g0100 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0004g0092a0001c0001t0013g0109a0001c0001t0015g0110others(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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0112others(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 | a0001c0001t0005g0033 | 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 | a0001c0001t0012g0158a0003c0004t0030g0013 | 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 | a0001c0001t0007g0012 | 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 | a0001c0001t0017g0106 | 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 | 83 | a0001c0001t0001g0004a0001c0001t0001g0068a0001c0001t0001g0134others(80): Show | 83 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(80): 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 | a0001c0001t0012g0158a0003c0004t0030g0013 | 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 | 83 | a0001c0001t0001g0004a0001c0001t0001g0068a0001c0001t0001g0134others(80): Show | 83 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(80): 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 | a0001c0001t0017g0096 | 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 | a0001c0001t0005g0033 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0112others(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 | 138 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(135): Show | 138 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(135): 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 | a0001c0001t0007g0012 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0002t0065g0030a0003c0004t0030g0013 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0004g0157 | 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 | 134 | a0001c0001t0001g0004a0001c0001t0001g0068a0001c0001t0001g0112others(131): Show | 134 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(131): 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 | a0001c0001t0001g0006a0001c0001t0054g0162 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0054g0162 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0001g0052a0001c0001t0001g0203a0001c0001t0002g0055others(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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.7+51536G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74549519 | ||||||
| chr9:74549521
|
G | A | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0034g0067 | 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 | a0001c0001t0019g0085 | 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 | a0001c0002t0065g0030 | 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 | a0001c0001t0025g0218 | 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 | a0001c0001t0005g0168a0001c0001t0008g0197a0001c0001t0063g0198 | 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 | a0001c0001t0001g0172a0001c0001t0001g0196a0001c0001t0002g0166others(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 | a0001c0001t0001g0167a0001c0001t0001g0176a0001c0001t0001g0182others(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 | a0001c0001t0037g0183 | 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 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0193others(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 | a0001c0001t0001g0207a0001c0001t0066g0181 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0209a0001c0001t0018g0029 | 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 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0148others(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 | a0001c0001t0001g0140a0001c0001t0001g0156a0001c0001t0001g0223others(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 | a0001c0001t0001g0006a0001c0001t0002g0054a0001c0001t0007g0012others(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 | a0001c0001t0001g0131a0001c0001t0003g0023a0001c0001t0007g0099others(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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(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 | a0001c0001t0001g0034a0001c0001t0001g0132a0001c0001t0001g0134others(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 | 17 | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0133others(14): Show | 17 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(14): 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 | a0001c0001t0006g0101 | 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 | a0001c0001t0001g0135a0001c0001t0004g0124 | 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 | a0001c0001t0014g0009 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0001g0031a0001c0001t0032g0061 | 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 | a0001c0001t0001g0107a0001c0001t0001g0170a0001c0001t0002g0066others(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 | a0001c0001t0008g0105a0001c0001t0031g0123a0001c0002t0002g0048 | 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 | a0001c0001t0001g0011a0001c0001t0001g0058a0001c0001t0001g0097others(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 | a0001c0001t0001g0069a0001c0001t0008g0091a0001c0001t0009g0070others(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 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0002g0037others(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 | a0001c0001t0053g0173a0001c0002t0003g0040 | 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0018g0088others(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 | a0001c0001t0009g0075a0001c0001t0034g0067 | 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 | a0001c0001t0029g0056 | 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 | a0001c0001t0024g0094 | 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 | a0001c0001t0024g0094a0001c0001t0043g0047 | 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 | 142 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(139): Show | 142 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(139): 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0112others(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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0013g0109a0001c0001t0015g0110a0001c0001t0015g0142others(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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0019g0085 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0072a0001c0001t0002g0039a0001c0001t0002g0060others(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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0079a0001c0001t0033g0078 | 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 | a0001c0001t0032g0061 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0002t0061g0044 | 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 | a0001c0001t0013g0109a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0002t0004g0027a0001c0002t0022g0025 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0012g0158 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0064g0100 | 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 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0002g0037others(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 | a0001c0001t0004g0092 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0012g0158a0003c0004t0030g0013 | 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 | a0001c0002t0003g0049 | 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 | a0001c0001t0012g0158a0003c0004t0030g0013 | 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 | a0001c0001t0003g0151 | 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 | a0001c0001t0011g0208 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0136others(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 | a0001c0001t0051g0204 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0017g0106 | 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 | a0001c0002t0003g0041 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0024g0094 | 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 | 73 | a0001c0001t0001g0004a0001c0001t0001g0068a0001c0001t0001g0115others(70): Show | 73 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(70): 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 | a0001c0001t0004g0057 | 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 | a0001c0001t0001g0034a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0008g0105 | 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 | a0001c0001t0038g0161 | 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0112others(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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0002g0073 | 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 | a0001c0001t0008g0105 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0012g0158a0001c0001t0051g0204a0003c0004t0030g0013 | 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 | a0001c0001t0004g0157a0001c0001t0010g0143a0001c0001t0010g0225others(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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0013g0109a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0002g0165 | 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 | a0001c0001t0064g0100 | 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 | a0001c0001t0015g0014 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0001c0001t0007g0012 | 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 | 14 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0187others(11): 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 | a0001c0001t0001g0112a0001c0001t0001g0113 | 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 | a0001c0001t0014g0019 | 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 | a0001c0002t0023g0043 | 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 | a0001c0002t0023g0043 | 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 | a0001c0002t0003g0215 | 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 | 141 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(138): Show | 141 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(138): 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0004g0095a0001c0001t0041g0059 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0017g0106 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0112others(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 | a0001c0001t0013g0109a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0004g0092 | 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 | a0001c0001t0007g0012 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0004g0174 | 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 | a0001c0001t0008g0197 | 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 | a0001c0002t0002g0048 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0031g0123a0001c0002t0001g0121a0001c0002t0003g0122others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0016g0028a0001c0001t0018g0029a0001c0001t0046g0093 | 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 | a0001c0002t0002g0048 | 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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0136others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0016g0028a0001c0001t0018g0029a0001c0001t0046g0093 | 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 | a0001c0001t0063g0198 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0051g0204 | 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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0006g0083 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.7+64972T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562955 | ||||||
| chr9:74562956
|
C | T | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.7+64973C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74562956 | ||||||
| chr9:74563118
|
G | A | 223 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0034a0001c0001t0001g0072others(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 | a0001c0001t0001g0148a0001c0001t0001g0172a0001c0001t0001g0176others(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 | a0001c0001t0001g0042a0001c0002t0023g0043 | 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 | a0001c0001t0055g0016 | 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 | a0001c0001t0001g0182a0001c0001t0002g0165a0001c0001t0002g0166 | 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 | a0001c0001t0051g0204 | 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 | a0001c0002t0002g0048a0001c0002t0005g0001 | 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 | a0001c0001t0045g0062 | 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 | a0001c0001t0006g0101a0001c0001t0006g0180a0001c0001t0026g0185others(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 | a0001c0002t0003g0040 | 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 | a0001c0001t0013g0109a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0029g0056 | 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 | a0001c0001t0049g0104 | 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 | a0001c0001t0038g0161a0001c0001t0051g0204 | 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 | a0001c0001t0009g0022 | 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 | a0001c0001t0062g0103 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0007g0212 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0013g0109a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0019g0089 | 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 | a0001c0002t0003g0122 | 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 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0017g0096 | 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 | a0001c0001t0016g0028a0001c0001t0018g0029a0001c0001t0046g0093 | 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 | a0001c0001t0014g0009 | 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 | a0001c0001t0001g0132 | 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 | a0001c0002t0022g0025 | 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 | a0001c0001t0001g0042a0001c0001t0002g0118a0001c0001t0039g0032others(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 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(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 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0003g0151others(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 | 2 | a0001c0001t0006g0102a0001c0001t0006g0210 | 2 | HG04204.hp1 homoSapiens_chm13v2.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 | a0001c0001t0038g0161 | 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 | a0001c0001t0038g0161 | 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 | a0001c0001t0007g0012 | 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 | a0001c0001t0001g0042a0001c0002t0003g0049a0001c0002t0023g0043 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0042a0001c0002t0003g0026a0001c0002t0003g0040others(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 | a0003c0004t0030g0013 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0007g0012 | 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 | a0001c0001t0003g0023 | 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 | a0001c0001t0056g0221 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0007g0038 | 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 | a0001c0001t0002g0084 | 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 | a0001c0001t0012g0158a0001c0001t0013g0109a0001c0001t0015g0110others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0064g0100 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0004g0092 | 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 | a0001c0002t0002g0048 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0001g0072a0001c0001t0001g0153a0001c0001t0003g0151others(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 | a0001c0001t0001g0209a0001c0001t0003g0023a0001c0001t0004g0126others(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 | a0001c0001t0001g0068a0001c0001t0010g0159 | 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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0016g0028others(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 | a0001c0001t0001g0201 | 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 | a0001c0001t0007g0099a0001c0001t0016g0098 | 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 | a0001c0001t0031g0123a0001c0002t0001g0121a0001c0002t0003g0122others(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 | a0001c0001t0012g0158a0003c0004t0030g0013 | 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 | a0001c0002t0003g0122 | 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0129 | 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 | 182 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(179): Show | 183 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(180): 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 | a0001c0001t0001g0107a0001c0001t0001g0131a0001c0001t0006g0083others(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 | a0001c0001t0001g0042a0001c0002t0003g0049 | 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 | a0001c0002t0003g0215 | 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 | 73 | a0001c0001t0001g0004a0001c0001t0001g0068a0001c0001t0001g0115others(70): Show | 73 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(70): 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 | a0001c0001t0056g0221 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0036g0149 | 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 | 6 | a0001c0001t0006g0101a0001c0001t0006g0102a0001c0001t0006g0180others(3): Show | 6 | HG01070.hp2 HG01106.hp1 HG04199.hp1 others(3): 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0043g0047 | 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0112others(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 | a0001c0001t0053g0173 | 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 | a0001c0005t0006g0219 | 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 | a0001c0001t0039g0032 | 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 | a0001c0001t0004g0092 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0001t0054g0162 | 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 | a0001c0001t0013g0035a0001c0001t0013g0050a0001c0001t0013g0051others(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 | a0001c0001t0004g0124 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0107others(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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0150 | 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 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0136others(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 | a0001c0002t0060g0015 | 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 | 188 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(185): Show | 189 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(186): 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0008g0077 | 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 | a0001c0001t0008g0077 | 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 | a0001c0001t0005g0010 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0001t0042g0154 | 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 | a0001c0002t0003g0215 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0031 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0107others(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 | 73 | a0001c0001t0001g0004a0001c0001t0001g0068a0001c0001t0001g0115others(70): Show | 73 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(70): 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 | a0001c0001t0001g0207a0001c0001t0011g0208 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0001g0052 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | 69 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-51245C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74579037 | ||||||
| chr9:74579039
|
C | G | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0001t0001g0006a0001c0001t0020g0137a0001c0001t0020g0138 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0056g0221 | 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 | a0001c0001t0029g0056 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0107others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0034g0067 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0006g0210 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0004g0157 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0177 | 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 | a0001c0001t0025g0053a0001c0001t0025g0218a0001c0002t0065g0030 | 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 | a0001c0001t0006g0064 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0107others(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 | a0001c0001t0017g0096 | 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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): 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 | a0001c0001t0011g0171 | 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 | a0001c0002t0060g0015 | 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 | a0001c0005t0006g0219 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0017g0106 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0112a0001c0001t0001g0113 | 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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0010g0159 | 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 | a0001c0001t0064g0100 | 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 | a0001c0001t0002g0037 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0007g0012a0001c0001t0056g0221 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0001g0132a0001c0001t0001g0135 | 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 | a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.8-46117G>A | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74584165 | ||||||
| chr9:74584241
|
C | T | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0001t0024g0094 | 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 | a0001c0001t0062g0103 | 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 | a0001c0001t0004g0124 | 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 | 69 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): 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 | a0001c0001t0001g0042a0001c0001t0039g0032a0001c0001t0043g0047others(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 | 69 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): 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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0017g0106 | 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 | a0001c0001t0018g0029 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0068others(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 | a0001c0001t0001g0203a0001c0001t0007g0212a0001c0001t0012g0211others(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 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0058others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0069others(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 |
67 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0134others(64): Show | 67 | HG00140.hp2 HG00408.hp2 HG00609.hp1 others(64): 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 | a0001c0001t0001g0087a0001c0001t0001g0148a0001c0001t0001g0209others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0010g0159 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0025g0053a0001c0001t0025g0218a0001c0002t0065g0030 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0004g0157others(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 | a0001c0001t0001g0155 | 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 | a0001c0001t0001g0134a0001c0001t0001g0184 | 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 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0136others(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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(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 | 210 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0001g0034a0001c0001t0007g0012a0001c0001t0007g0038others(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 | a0001c0001t0001g0107a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0134others(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 |
54 | a0001c0001t0001g0052a0001c0001t0001g0079a0001c0001t0001g0097others(51): Show | 54 | HG00140.hp2 HG00738.hp1 HG00738.hp2 others(51): 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 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(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 | a0001c0001t0001g0069a0001c0001t0001g0201a0001c0001t0005g0010others(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 | a0001c0001t0001g0209a0001c0001t0010g0159a0001c0001t0018g0029others(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 | a0001c0001t0004g0095a0001c0002t0003g0163 | 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 | a0001c0001t0001g0006a0001c0001t0020g0137a0001c0001t0020g0138 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0004g0174a0001c0001t0005g0168a0001c0001t0063g0198 | 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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0064g0100 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0004g0057 | 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 | a0001c0001t0005g0190a0001c0001t0005g0202a0001c0001t0028g0189 | 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 | a0001c0001t0001g0172 | 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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0003g0023 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0027g0081 | 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 | a0001c0002t0060g0015 | 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 | a0001c0002t0003g0215 | 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 | a0001c0002t0003g0215 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0002t0003g0215 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(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 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0136others(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 | a0001c0001t0001g0069a0001c0001t0002g0082 | 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 | a0001c0001t0017g0106 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0007g0012a0001c0001t0056g0221 | 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 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0011g0178 | 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 | a0001c0001t0004g0125a0001c0001t0004g0126 | 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 | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(207): 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 | a0001c0001t0009g0070 | 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 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0052g0147 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0079a0001c0001t0033g0078 | 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 | a0001c0001t0014g0009a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | a0001c0001t0014g0018 | 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 | a0001c0001t0004g0095 | 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 | a0001c0002t0061g0044 | 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 | a0001c0001t0010g0143a0001c0001t0010g0225 | 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 | a0001c0001t0042g0154 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0001t0001g0072a0001c0001t0002g0039a0001c0001t0002g0073others(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 | a0001c0002t0002g0048 | 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 | a0001c0001t0053g0173 | 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 | a0001c0001t0001g0177a0001c0001t0035g0146a0001c0002t0003g0215 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0004g0157 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0001t0064g0100 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0004g0157others(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 | a0001c0001t0004g0092 | 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 | a0001c0001t0007g0012 | 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 | a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | a0001c0001t0010g0003 | 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 | a0001c0001t0002g0066a0001c0001t0002g0074a0001c0001t0002g0084others(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 | 66 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0139others(63): Show | 66 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(63): 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(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 | a0001c0001t0002g0066a0001c0001t0002g0074a0001c0001t0002g0084others(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 | a0001c0002t0005g0076 | 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 | a0001c0001t0004g0174 | 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 | a0001c0001t0064g0100 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | 69 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): 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 | a0001c0001t0007g0099a0001c0001t0016g0098 | 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 | 64 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(61): Show | 64 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(61): 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 | a0001c0001t0056g0221 | 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 | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0004a0001c0001t0048g0144 | 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 | a0001c0001t0013g0109a0001c0001t0015g0110a0001c0001t0015g0142others(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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0013g0050a0001c0001t0013g0051 | 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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0014g0019a0001c0001t0014g0020 | 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 | a0001c0002t0060g0015 | 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 | 69 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): Show |
intron_variant | MODIFIER | c.8-33870C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74596412 | ||||||
| chr9:74596577
|
C | T | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): 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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0017g0106 | 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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0107others(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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0107others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | 167 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(164): Show | 168 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(165): 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(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 | a0001c0001t0016g0028a0001c0001t0046g0093 | 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 | a0001c0001t0009g0022 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0018g0029others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0002t0060g0015 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0107others(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 | a0001c0002t0003g0215 | 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 | a0001c0001t0056g0221 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0016g0098 | 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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | 166 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(164): 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 | a0001c0001t0041g0059 | 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 | a0001c0001t0001g0182a0001c0001t0002g0165a0001c0001t0002g0166 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0004g0095 | 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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0017g0106 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0097a0001c0001t0007g0012 | 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 | a0001c0001t0001g0182 | 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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0016g0028others(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 | a0001c0001t0004g0157 | 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 | a0001c0001t0013g0035a0001c0001t0013g0050a0001c0001t0013g0051others(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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0004g0157others(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 | a0001c0001t0004g0092 | 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 | a0001c0001t0012g0158a0003c0004t0030g0013 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0008g0130 | 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 | a0001c0002t0003g0049 | 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 | 212 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(209): Show | 213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): 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 | a0001c0001t0066g0181 | 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 | a0001c0001t0014g0018a0001c0001t0014g0019a0001c0001t0014g0020 | 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 | a0001c0001t0012g0158 | 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 | 69 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0054g0162 | 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 | 69 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0056g0221 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | 162 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(159): Show | 163 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(160): 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 | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(162): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): 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 | a0001c0001t0031g0123a0001c0001t0041g0059a0001c0002t0001g0121others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0097others(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 | a0001c0002t0003g0215 | 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 | a0001c0001t0007g0099a0001c0001t0016g0098 | 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 | a0001c0001t0017g0096 | 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 | a0001c0001t0003g0023 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0097others(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 | a0001c0001t0001g0087 | 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 | a0001c0001t0001g0150 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0049g0104 | 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 | a0001c0001t0029g0056 | 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 | a0001c0001t0064g0100 | 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 | a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0004g0157a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0038g0161 | 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 | a0001c0001t0004g0157 | 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 | a0001c0001t0001g0072 | 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 | a0001c0001t0017g0096 | 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 | 30 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0176others(27): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(161): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): 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 | a0001c0001t0010g0143a0001c0001t0010g0225 | 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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0051g0204 | 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 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0042others(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 | 44 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0115others(41): Show | 44 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(41): 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 | 28 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0176others(25): 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 | a0001c0001t0003g0151a0001c0001t0010g0143a0001c0001t0010g0225others(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 | a0001c0001t0004g0157 | 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 | a0001c0002t0060g0015 | 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 | a0001c0002t0060g0015 | 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 | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(162): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): 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 | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(160): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.8-21313C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74608969 | ||||||
| chr9:74609088
|
T | C | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(161): Show | 165 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(162): 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 | a0001c0001t0004g0095 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0004g0157 | 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 | a0001c0001t0002g0039 | 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 | a0001c0001t0004g0174a0001c0001t0005g0168a0001c0001t0063g0198 | 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 | 74 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(71): Show | 74 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(71): 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 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0112others(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 | 69 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0016g0028others(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 | a0001c0001t0031g0123a0001c0002t0001g0121 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0097others(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 | a0001c0001t0021g0002 | 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 | a0001c0001t0064g0100 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0010g0159 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0005g0190a0001c0001t0005g0202a0001c0001t0028g0189 | 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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0010g0143others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0002t0003g0215 | 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 | 163 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(160): Show | 164 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(161): 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 | a0001c0001t0001g0207a0001c0001t0011g0208 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0010g0143others(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 | a0001c0002t0003g0049 | 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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0004g0157a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | a0001c0001t0013g0035a0001c0001t0013g0050a0001c0001t0013g0051others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0119a0001c0001t0007g0212a0001c0001t0012g0211others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0005g0033 | 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 | a0001c0001t0066g0181 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0010g0159 | 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 | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(162): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0097others(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 | a0001c0001t0004g0125a0001c0001t0004g0126a0001c0001t0004g0174others(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 | 14 | a0001c0001t0001g0172a0001c0001t0001g0176a0001c0001t0001g0187others(11): 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 | a0001c0001t0004g0157a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0001g0223a0001c0001t0004g0222a0001c0001t0004g0224others(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 | a0001c0001t0004g0057a0001c0001t0006g0063a0001c0001t0006g0064others(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 | 69 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(66): Show | 69 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(66): 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 | a0001c0001t0001g0112a0001c0001t0001g0113 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | 165 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(162): Show | 166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): 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 | a0001c0001t0001g0097a0001c0001t0007g0012 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0014g0009 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0001g0107a0001c0001t0001g0129a0001c0001t0001g0131others(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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0001g0182 | 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 | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(153): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.8-13193delT | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617088 | ||||||
| chr9:74617089
|
T | C | 55 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0097others(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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0002t0003g0215 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.8-12949T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617333 | ||||||
| chr9:74617578
|
A | G | 1 | a0001c0001t0006g0102 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.8-12704A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74617578 | ||||||
| chr9:74617602
|
G | A | 1 | a0001c0001t0004g0157 | 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 | a0001c0001t0001g0058a0001c0001t0008g0091 | 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 | 160 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(157): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0068a0001c0001t0001g0160 | 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 | a0001c0002t0022g0025 | 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 | a0001c0001t0009g0022a0001c0002t0002g0217 | 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 | a0001c0001t0001g0031a0001c0001t0001g0203a0001c0001t0002g0055others(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 | a0001c0001t0001g0006a0001c0001t0020g0137a0001c0001t0020g0138 | 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 | a0001c0001t0004g0157 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0011g0208 | 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 | a0001c0001t0039g0032 | 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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0112others(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 | a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | a0001c0001t0019g0085a0001c0001t0019g0089a0001c0001t0019g0090 | 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 | a0001c0001t0013g0109a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0004g0092 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0001g0179a0001c0001t0011g0178 | 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 | a0001c0001t0001g0134a0001c0001t0001g0139a0001c0001t0001g0177others(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 | a0001c0002t0003g0215 | 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 | a0001c0001t0002g0118a0001c0001t0008g0105 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0107others(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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0053g0173 | 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 | 71 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(68): Show | 71 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(68): 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 | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): 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 | a0001c0001t0001g0172a0001c0001t0001g0192 | 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 | a0001c0001t0056g0221 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0042others(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 | a0001c0001t0007g0099a0001c0001t0016g0098 | 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 | a0001c0001t0001g0097a0001c0001t0007g0012a0001c0001t0056g0221 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0097others(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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.8-8778A>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621504 | ||||||
| chr9:74621505
|
A | G | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.8-8777A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74621505 | ||||||
| chr9:74621575
|
G | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0012g0158a0001c0001t0013g0109a0001c0001t0015g0110others(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 | a0001c0001t0001g0042a0001c0001t0039g0032a0001c0001t0043g0047others(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 | a0001c0001t0004g0157a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0042a0001c0001t0039g0032a0001c0001t0043g0047others(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 | a0001c0001t0007g0012 | 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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0016g0028others(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 | 71 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0034others(68): Show | 71 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(68): 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 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0068others(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 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0058others(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 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0087others(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 | a0001c0001t0018g0017 | 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0001g0006 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0004g0092 | 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 | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.8-7105T>C | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623177 | ||||||
| chr9:74623187
|
A | G | 160 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(157): Show | 161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0007g0099a0001c0001t0016g0098 | 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 | a0001c0001t0024g0094 | 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 | a0001c0001t0024g0094 | 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 | a0001c0001t0004g0157a0001c0001t0051g0204a0001c0002t0060g0015 | 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 | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(180): Show | 184 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(181): 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 | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.8-6640A>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74623642 | ||||||
| chr9:74623944
|
T | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): 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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0010g0143others(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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0107others(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 | a0001c0001t0004g0124 | 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 | a0001c0001t0039g0032 | 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 | a0001c0001t0021g0111 | 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 | a0001c0002t0003g0045 | 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 | 159 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(156): Show | 160 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(157): 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 | a0001c0001t0001g0199 | 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 | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(207): 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 | a0001c0001t0001g0068a0001c0001t0001g0160 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0097others(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 | a0001c0001t0007g0038 | 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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0097others(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 | a0001c0001t0053g0173 | 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 | a0001c0002t0003g0215 | 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 | a0001c0001t0001g0068a0001c0001t0001g0160a0001c0001t0010g0143others(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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0007g0012 | 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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): Show |
intron_variant | MODIFIER | c.8-4361T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74625921 | ||||||
| chr9:74625929
|
T | G | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0004g0092 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | 70 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0134others(67): Show | 70 | HG00140.hp2 HG00738.hp2 HG01070.hp2 others(67): 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 | a0001c0001t0013g0035a0001c0001t0013g0050a0001c0001t0013g0051others(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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0018g0029others(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 | 108 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0068others(105): Show | 109 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(106): 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0052others(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 | a0001c0001t0051g0204 | 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 | a0001c0001t0006g0180 | 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 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0072others(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 | a0001c0001t0012g0158a0003c0004t0030g0013 | 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 | a0001c0001t0001g0069 | 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0002g0037a0001c0001t0049g0104 | 2 | HG03704.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.8-2106T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74628176 | ||||||
| chr9:74628186
|
C | T | 224 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(221): Show | 225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.8-2096C>T | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74628186 | ||||||
| chr9:74628275
|
G | T | 1 | a0001c0001t0004g0124 | 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 | a0001c0001t0001g0006a0001c0001t0020g0137a0001c0001t0020g0138 | 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 | a0001c0001t0012g0158 | 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 | a0001c0002t0058g0108 | 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 | a0001c0001t0044g0186 | 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 | a0001c0001t0032g0061 | 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 | a0001c0001t0025g0053a0001c0001t0025g0218 | 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 | a0001c0001t0001g0068a0001c0001t0010g0143a0001c0001t0010g0159others(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 | a0001c0001t0001g0006a0001c0001t0001g0034a0001c0001t0001g0042others(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 | 210 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 211 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.8-744T>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 1/9 | chr9 | 74629538 | ||||||
| chr9:74629866
|
T | C | 206 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(203): Show | 207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0068a0001c0001t0010g0143a0001c0001t0010g0225others(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 | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): 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 | a0001c0001t0001g0132 | 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 | 9 | a0001c0001t0006g0063a0001c0001t0006g0064a0001c0001t0006g0083others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(6): 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 | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): 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 | a0001c0001t0001g0068a0001c0001t0010g0143a0001c0001t0010g0225others(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 | 61 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(58): Show | 61 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.93+468delA | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 74630826 | |||||
| chr9:74630835
|
AG | A | 134 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(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 | a0001c0001t0001g0068a0001c0001t0004g0157a0001c0001t0010g0143others(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 | a0001c0001t0001g0058a0001c0001t0002g0066a0001c0001t0002g0074others(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 | 61 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(58): Show | 61 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(58): 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 | a0001c0001t0004g0157 | 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 | a0001c0002t0060g0015 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0002t0005g0076 | 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 | a0001c0001t0051g0204 | 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 | a0001c0001t0013g0050a0001c0001t0013g0051a0001c0001t0055g0016 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0012g0158a0003c0004t0030g0013 | 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0031others(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 | a0001c0001t0010g0143a0001c0001t0010g0225a0001c0001t0014g0009others(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 | a0001c0002t0023g0216 | 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 | a0001c0001t0008g0105 | 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 | a0001c0001t0001g0209 | 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 | a0001c0001t0002g0039a0001c0001t0002g0073a0001c0001t0009g0075others(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 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0003g0151others(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 | a0001c0001t0001g0119 | 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 | 62 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(59): Show | 62 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(59): 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0001g0011a0001c0001t0001g0052a0001c0001t0001g0058others(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 | 59 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(56): Show | 59 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(56): 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 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0087others(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 | a0001c0001t0001g0006a0001c0001t0020g0137a0001c0001t0020g0138 | 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 | a0001c0001t0001g0160a0001c0001t0013g0109a0001c0001t0015g0110others(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 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0034others(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 | a0001c0001t0013g0050a0001c0001t0013g0051 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | 62 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(59): Show | 62 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(59): 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 | a0001c0001t0001g0068a0001c0001t0007g0212a0001c0001t0010g0143others(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 | a0001c0001t0004g0157 | 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 | a0001c0001t0001g0068a0001c0001t0007g0212a0001c0001t0010g0143others(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 | a0001c0001t0051g0204 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0001g0080a0001c0001t0001g0097a0001c0001t0007g0012others(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 | 36 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(33): Show | 36 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(33): 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 | 31 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0001g0172others(28): 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 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0087others(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 | a0001c0001t0018g0017 | 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 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0087others(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 | 63 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(60): Show | 63 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(60): 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 | a0001c0001t0066g0181 | 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 | a0001c0002t0002g0048a0001c0002t0002g0127a0001c0002t0002g0128others(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 | a0001c0001t0014g0018 | 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 | a0001c0002t0003g0045 | 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 | a0001c0001t0017g0096 | 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 | a0001c0001t0001g0031a0001c0001t0001g0203a0001c0001t0002g0055others(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 | a0001c0002t0003g0049a0001c0002t0023g0043a0001c0002t0023g0216 | 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 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0001g0170others(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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0001g0042a0001c0001t0066g0181 | 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 | a0001c0001t0001g0160a0001c0001t0013g0109a0001c0001t0015g0110others(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 | a0001c0001t0054g0162 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | 123 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0052others(120): Show | 124 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(121): 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 | a0001c0001t0010g0003a0001c0001t0051g0204 | 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 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0001g0170others(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 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0001g0170others(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 | a0001c0001t0025g0218 | 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 | a0001c0001t0010g0003a0001c0001t0051g0204 | 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 | a0001c0001t0009g0070 | 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 | a0001c0001t0010g0003a0001c0001t0051g0204 | 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 | a0001c0001t0042g0154 | 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 | a0001c0001t0007g0007a0001c0001t0007g0008a0001c0001t0007g0136others(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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0097others(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 | a0001c0001t0001g0052a0001c0001t0001g0058a0001c0001t0001g0170others(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 | a0001c0001t0066g0181 | 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 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0007g0212others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0004g0125a0001c0001t0004g0126 | 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 | a0001c0001t0012g0214 | 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 | a0001c0001t0038g0161 | 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 | 186 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(183): Show | 187 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(184): 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0097others(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 | 209 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 210 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(207): 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 | a0001c0001t0001g0200 | 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 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0001g0069a0001c0001t0001g0072a0001c0001t0001g0079others(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 | a0001c0001t0010g0003a0001c0001t0051g0204 | 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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0018g0029others(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 | a0001c0001t0004g0174 | 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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): 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 | a0001c0001t0012g0158 | 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 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0220others(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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0068a0001c0001t0004g0057a0001c0001t0007g0007others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0007g0038 | 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 | a0001c0002t0003g0041a0001c0002t0003g0163a0001c0002t0003g0164 | 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 | 53 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0115others(50): Show | 53 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(50): 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 | a0001c0001t0001g0160a0001c0001t0013g0109a0001c0001t0015g0014others(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 | a0001c0001t0029g0056a0001c0002t0003g0041a0001c0002t0003g0163others(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 | a0001c0001t0001g0097 | 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 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0140others(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 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0003g0151others(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 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0018g0029others(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 | a0001c0001t0001g0034 | 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 | a0001c0001t0002g0066a0001c0001t0002g0074 | 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 | a0001c0001t0004g0057 | 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 | a0001c0001t0001g0068a0001c0001t0004g0057a0001c0001t0004g0157others(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 | a0001c0001t0010g0003a0001c0001t0051g0204 | 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 | a0001c0001t0007g0007a0001c0001t0007g0008 | 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 | a0001c0001t0016g0028a0001c0001t0046g0093 | 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 | a0001c0001t0054g0162 | 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 | a0001c0001t0041g0059 | 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 | a0001c0001t0004g0124 | 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 | a0001c0001t0001g0068a0001c0001t0004g0057a0001c0001t0004g0157others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0031g0123 | 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 | a0001c0002t0001g0169a0001c0002t0003g0122 | 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 | a0001c0001t0006g0064 | 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 | a0001c0001t0051g0204 | 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 | a0001c0001t0016g0028a0001c0001t0046g0093 | 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 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(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 | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(175): Show | 179 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(176): 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0017g0096 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0002t0011g0120 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0001g0160a0001c0001t0013g0109a0001c0001t0015g0014others(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 | a0001c0001t0013g0035 | 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 | a0001c0001t0012g0214 | 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 | a0001c0001t0014g0009 | 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 | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(204): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): 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 | a0001c0001t0001g0160a0001c0001t0013g0109a0001c0001t0015g0014others(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 | a0001c0002t0003g0026a0001c0002t0003g0040a0001c0002t0003g0045others(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 | a0001c0001t0001g0069a0001c0001t0002g0082a0001c0001t0027g0081 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0068a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0220others(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 | a0001c0001t0001g0160a0001c0001t0013g0109a0001c0001t0015g0014others(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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0097others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0002g0084 | 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 | a0001c0001t0001g0170a0001c0001t0007g0212a0001c0001t0011g0171others(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 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0004g0174 | 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 | 205 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0004g0092others(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 | a0001c0001t0004g0157 | 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 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0002t0060g0015 | 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 | a0001c0001t0025g0053 | 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 | a0001c0001t0001g0203a0001c0001t0003g0023 | 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 | a0001c0002t0001g0046a0001c0002t0001g0121a0001c0002t0002g0048others(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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0097others(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 | a0001c0001t0001g0052 | 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 | a0001c0001t0001g0052a0001c0001t0001g0203a0001c0001t0003g0023others(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 | a0001c0001t0005g0168a0001c0001t0063g0198 | 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 | a0001c0001t0001g0119a0001c0001t0001g0133a0001c0001t0001g0134others(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 | a0003c0004t0030g0013 | 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 | a0001c0001t0001g0052a0001c0001t0001g0203a0001c0001t0003g0023others(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 | a0001c0001t0004g0157 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0037g0183 | 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 | a0001c0001t0001g0058a0001c0001t0008g0077a0001c0001t0008g0091others(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 | a0001c0002t0003g0122 | 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 | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): 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 | a0001c0001t0001g0052a0001c0001t0001g0203a0001c0001t0003g0023others(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 | a0001c0001t0010g0159a0001c0001t0017g0096 | 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 | a0001c0001t0045g0062 | 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 | a0001c0001t0001g0160a0001c0001t0013g0109a0001c0001t0015g0014others(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 | a0001c0001t0013g0035 | 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 | a0001c0001t0016g0028a0001c0001t0046g0093 | 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 | a0001c0002t0001g0046 | 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 | a0001c0001t0054g0162 | 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0097others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0097others(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 | a0001c0001t0009g0024 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0064g0100 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0068 | 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 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0177others(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 | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(169): Show | 172 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(169): 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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): 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 | a0001c0001t0001g0058a0001c0001t0001g0115a0001c0001t0001g0170others(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 | a0001c0001t0005g0168a0001c0001t0063g0198 | 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 | a0001c0001t0009g0075 | 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 | a0001c0001t0001g0006a0001c0001t0001g0135a0001c0001t0005g0010others(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 | a0001c0001t0001g0004a0001c0001t0001g0031a0001c0001t0001g0034others(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 | 33 | a0001c0001t0001g0011a0001c0001t0001g0150a0001c0001t0001g0167others(30): 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 | 20 | a0001c0001t0001g0160a0001c0001t0004g0095a0001c0001t0006g0063others(17): Show | 20 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(17): 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 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0087others(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 | a0001c0001t0012g0158a0001c0002t0060g0015 | 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 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0177others(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 | a0001c0001t0001g0115a0001c0001t0002g0037a0001c0001t0002g0039others(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 | a0001c0001t0001g0034a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0001g0034a0001c0001t0001g0112a0001c0001t0001g0113others(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 | a0001c0001t0001g0006 | 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0018g0029others(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 | a0001c0001t0016g0028a0001c0001t0046g0093 | 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 | a0001c0001t0016g0028a0001c0001t0046g0093 | 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 | a0001c0001t0066g0181 | 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 | a0001c0001t0025g0218 | 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 | a0001c0001t0002g0037 | 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 | a0001c0001t0016g0028a0001c0001t0046g0093 | 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 | a0001c0001t0001g0160a0001c0001t0013g0109a0001c0001t0015g0014others(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 | a0001c0001t0016g0028a0001c0001t0046g0093 | 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 | a0001c0001t0001g0072 | 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 | a0001c0002t0003g0041 | 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 | a0001c0001t0001g0119a0001c0001t0001g0133 | 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 | 218 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(215): Show | 219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0058a0001c0001t0001g0115a0001c0001t0001g0170others(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 | a0001c0001t0004g0124 | 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 | a0001c0001t0001g0052a0001c0001t0001g0203a0001c0001t0003g0023others(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 | a0001c0001t0016g0028a0001c0001t0046g0093 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0072a0001c0001t0001g0114a0001c0001t0001g0117others(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 | a0001c0001t0011g0208 | 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 | a0001c0001t0001g0058a0001c0001t0001g0115a0001c0001t0001g0170others(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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.638-3198C>G | RORB | ENSG00000198963.11 | transcript | ENST00000376896.8 | protein_coding | 4/9 | chr9 | 74657419 | ||||||
| chr9:74657433
|
G | A | 6 | a0001c0001t0004g0095a0001c0001t0006g0101a0001c0001t0006g0102others(3): Show | 6 | HG01070.hp2 HG01106.hp1 HG02698.hp2 others(3): 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 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0177others(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 | a0001c0001t0001g0058a0001c0001t0001g0115a0001c0001t0001g0170others(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 | a0001c0001t0001g0006a0001c0001t0020g0137a0001c0001t0020g0138 | 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 | a0001c0001t0001g0179a0001c0001t0011g0178 | 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 | a0001c0001t0009g0024 | 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 | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(208): Show | 212 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(209): 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 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0001g0160a0001c0001t0013g0109a0001c0001t0015g0014others(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 | a0001c0001t0001g0058a0001c0001t0001g0115a0001c0001t0002g0037others(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 | a0001c0001t0001g0052a0001c0001t0001g0068a0001c0001t0001g0177others(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 | 48 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0140others(45): Show | 48 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(45): 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0097others(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 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0001g0131 | 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 | 49 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0140others(46): Show | 49 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(46): 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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0220others(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 | a0001c0001t0001g0177a0001c0001t0001g0179a0001c0001t0001g0220others(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 | a0001c0001t0001g0207 | 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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0155others(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 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0069others(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 | a0001c0001t0001g0153 | 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 | a0001c0002t0002g0217a0001c0002t0009g0116 | 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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | 60 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0011others(57): Show | 60 | HG00408.hp1 HG01070.hp2 HG01071.hp1 others(57): 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 | a0001c0001t0007g0038a0001c0001t0007g0212a0001c0001t0012g0211others(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 | a0001c0001t0007g0212a0001c0001t0012g0211a0001c0001t0012g0213others(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 | a0001c0001t0029g0056 | 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 | a0001c0001t0001g0131a0001c0001t0015g0014a0001c0001t0015g0110others(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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0097others(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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0007g0012others(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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0001g0068a0001c0001t0007g0212a0001c0001t0012g0211others(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 | a0001c0001t0013g0109 | 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0097others(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 | a0001c0001t0045g0062 | 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 | a0001c0001t0001g0177 | 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 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(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 | a0001c0001t0001g0177 | 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 | a0001c0001t0005g0033a0001c0001t0005g0168a0001c0001t0005g0190others(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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(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 | a0001c0001t0001g0058a0001c0001t0001g0069a0001c0001t0001g0072others(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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(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 | a0001c0001t0004g0222a0001c0001t0004g0224a0001c0001t0015g0014others(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 | a0001c0001t0001g0097a0001c0001t0002g0060a0001c0001t0002g0066others(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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0001t0001g0068a0001c0001t0007g0212a0001c0001t0012g0211others(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 | a0001c0001t0001g0150 | 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 | a0001c0001t0001g0005a0001c0001t0001g0068a0001c0001t0001g0087others(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 | a0001c0001t0012g0158a0001c0001t0046g0093 | 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 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0001t0001g0005a0001c0001t0001g0068a0001c0001t0001g0087others(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 | a0001c0001t0006g0101a0001c0001t0006g0180a0001c0001t0026g0185 | 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 | a0001c0001t0012g0158a0001c0001t0046g0093 | 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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0002t0003g0164 | 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 | a0001c0001t0012g0158a0001c0001t0046g0093 | 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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0068others(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 | a0001c0002t0058g0108 | 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 | a0001c0001t0015g0014a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0011g0208 | 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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0134others(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 | a0001c0001t0057g0036 | 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 | a0001c0001t0013g0035a0001c0001t0013g0050a0001c0001t0013g0051others(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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0024g0094a0001c0001t0024g0175 | 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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0034others(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 | a0001c0002t0002g0048a0001c0002t0002g0127a0001c0002t0002g0128 | 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 | a0001c0001t0037g0183 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0054g0162 | 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 | a0001c0001t0012g0211a0001c0001t0012g0213a0001c0001t0012g0214others(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 | a0001c0001t0002g0039a0001c0001t0002g0073a0001c0001t0009g0075 | 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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0001t0013g0035a0001c0001t0013g0050a0001c0001t0013g0051others(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 | a0001c0001t0018g0017a0001c0001t0018g0029a0001c0001t0018g0088 | 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 | a0001c0001t0015g0014a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0015g0014a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0007g0038 | 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 | a0001c0001t0007g0038 | 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 | a0001c0001t0003g0023a0001c0001t0003g0151a0001c0001t0003g0152others(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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0024g0175 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 | a0001c0002t0060g0015 | 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 | a0001c0002t0001g0121 | 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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0005g0168 | 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 | a0001c0001t0002g0055a0001c0001t0003g0023a0001c0001t0003g0151others(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 | a0001c0001t0001g0031a0001c0001t0001g0058a0001c0001t0001g0134others(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 | a0001c0001t0006g0063a0001c0001t0006g0064 | 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 | a0001c0001t0001g0031a0001c0001t0001g0034a0001c0001t0001g0042others(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 | a0001c0001t0001g0042 | 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 | a0001c0002t0058g0108 | 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 | a0001c0001t0018g0017a0001c0001t0018g0029a0001c0001t0018g0088 | 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 | a0001c0001t0049g0104 | 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 | a0001c0002t0003g0122 | 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0004g0174 | 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 | a0001c0001t0012g0214 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0044g0186 | 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 | a0001c0001t0006g0101 | 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 | a0001c0002t0002g0127a0001c0002t0002g0128 | 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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0002t0058g0108 | 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 | a0001c0001t0021g0002a0001c0001t0021g0111 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0013g0035a0001c0001t0013g0050a0001c0001t0013g0051others(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 | a0001c0001t0056g0221 | 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 | a0001c0001t0006g0210 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0024g0094 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0003g0023a0001c0001t0022g0071a0001c0002t0003g0026others(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 | a0001c0001t0017g0106 | 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 | a0001c0001t0054g0162 | 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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0155others(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 | a0001c0001t0056g0221 | 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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 | a0001c0001t0038g0161 | 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 | a0001c0001t0028g0189 | 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 | a0001c0001t0013g0035a0001c0001t0013g0050a0001c0001t0013g0051others(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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0015g0014a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0004g0092 | 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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0003c0004t0030g0013 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 | a0001c0002t0058g0108 | 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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0041g0059 | 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 | a0001c0001t0003g0151 | 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 | a0001c0002t0058g0108 | 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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 | 216 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 217 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(214): 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 | a0001c0001t0018g0017 | 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 | a0001c0002t0058g0108 | 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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0001t0001g0182 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0024g0094 | 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 | a0001c0001t0012g0211a0001c0001t0012g0213a0001c0001t0012g0214others(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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0003g0023a0001c0001t0003g0151a0001c0001t0003g0152others(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 | a0001c0001t0010g0225 | 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 | a0001c0001t0018g0017a0001c0001t0018g0029a0001c0001t0018g0088 | 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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0001t0006g0083 | 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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0001g0203 | 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 | a0001c0001t0001g0011a0001c0001t0003g0023a0001c0001t0017g0096others(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 | a0001c0001t0001g0140a0001c0001t0001g0192a0001c0001t0004g0057others(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 | a0001c0001t0012g0211a0001c0001t0012g0213a0001c0001t0012g0214others(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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0038g0161 | 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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0004g0157a0001c0001t0007g0038 | 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 | a0003c0004t0030g0013 | 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 | a0001c0002t0060g0015 | 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 | a0001c0001t0001g0052 | 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 | a0001c0002t0058g0108 | 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 | a0001c0002t0060g0015 | 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0054g0162 | 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 | a0001c0001t0024g0175 | 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 | a0001c0001t0002g0082 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(219): Show | 223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): 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 | a0001c0001t0009g0024a0001c0001t0028g0189 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0002t0058g0108 | 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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0003c0004t0030g0013 | 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 | a0001c0001t0012g0211a0001c0001t0012g0213a0001c0001t0012g0214others(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 | a0001c0002t0058g0108 | 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0015g0014a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0002g0118a0001c0001t0025g0053a0001c0001t0025g0218others(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 | a0001c0001t0044g0186 | 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 | a0001c0001t0001g0006a0001c0001t0001g0068a0001c0001t0020g0137others(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 | a0001c0001t0003g0023a0001c0002t0003g0026a0001c0002t0003g0040others(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 | a0001c0002t0058g0108 | 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 | a0003c0004t0030g0013 | 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 | a0001c0001t0034g0067 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0015g0014a0001c0001t0015g0110a0001c0001t0015g0142others(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 | a0001c0001t0001g0119 | 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 | a0001c0001t0001g0134a0001c0001t0001g0177a0001c0001t0001g0179others(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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0012g0211a0001c0001t0012g0213a0001c0001t0012g0214 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0007g0099 | 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 | a0001c0001t0012g0211a0001c0001t0012g0213a0001c0001t0012g0214 | 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 | a0001c0001t0012g0211a0001c0001t0012g0213a0001c0001t0012g0214 | 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 | a0001c0001t0005g0168 | 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 | a0001c0001t0001g0072a0001c0001t0001g0114a0001c0001t0001g0117others(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 | a0001c0001t0004g0125a0001c0001t0004g0126 | 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 | a0001c0002t0003g0026a0001c0002t0003g0040a0001c0002t0003g0045others(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 | a0001c0001t0046g0093 | 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 | a0001c0001t0021g0002a0001c0001t0021g0111 | 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 | a0001c0001t0051g0204 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0001g0042a0001c0001t0066g0181 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0002g0037 | 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 | a0001c0001t0054g0162 | 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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0018g0017a0001c0001t0018g0029a0001c0001t0018g0088 | 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 | a0001c0001t0013g0035a0001c0001t0013g0050a0001c0001t0013g0051others(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 | a0001c0001t0002g0037a0001c0001t0002g0039a0001c0001t0002g0054others(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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0005g0010a0001c0001t0005g0033a0001c0001t0005g0168others(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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 | a0001c0001t0046g0093 | 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 | a0001c0001t0001g0097a0001c0001t0001g0134a0001c0001t0001g0177others(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 | a0001c0002t0060g0015 | 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 | a0001c0001t0003g0023a0001c0001t0003g0151a0001c0001t0003g0152others(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 | a0001c0001t0001g0117a0001c0001t0001g0192a0001c0001t0002g0065others(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 | a0001c0001t0017g0096a0001c0001t0017g0106a0001c0001t0017g0141others(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 |