Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 54439 |
|---|---|
| ensemblid | ENSG00000091009.8 |
| hgncid | 29243 |
| symbol | RBM27 |
| name | RNA binding motif protein 27 |
| refseq_nuc | NM_018989.2 |
| refseq_prot | NP_061862.1 |
| ensembl_nuc | ENST00000265271.7 |
| ensembl_prot | ENSP00000265271.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 146203605 |
| end | 146289223 |
| strand | + |
| ver | v1.2 |
| region | chr5:146203605-146289223 |
| region5000 | chr5:146198605-146294223 |
| regionname0 | RBM27_chr5_146203605_146289223 |
| regionname5000 | RBM27_chr5_146198605_146294223 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1060 | 270 | 71 | 48 | 106 | 10 | 33 | 84 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0002 | 0/0 | 1060 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0003 | 0/0 | 1060 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 3183 | 205 | 23 | 40 | 103 | 8 | 29 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| c0002 | 0/0 | 3183 | 62 | 48 | 8 | 0 | 2 | 4 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| c0003 | 0/0 | 3183 | 3 | 0 | 0 | 3 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| c0004 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| c0005 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 3355 | 109 | 22 | 16 | 48 | 5 | 17 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0002 | 0/1 | 3355 | 73 | 0 | 18 | 42 | 3 | 9 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0003 | 0/0 | 3356 | 17 | 16 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0004 | 0/0 | 3355 | 16 | 6 | 3 | 0 | 2 | 5 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0005 | 0/0 | 3356 | 8 | 6 | 2 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0006 | 0/0 | 3355 | 7 | 6 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0007 | 0/0 | 3355 | 7 | 0 | 0 | 7 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0008 | 0/0 | 3355 | 4 | 0 | 4 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0009 | 0/0 | 3355 | 3 | 3 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0010 | 0/0 | 3355 | 3 | 0 | 0 | 3 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0011 | 0/0 | 3355 | 3 | 3 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0012 | 0/0 | 3355 | 2 | 1 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0013 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0014 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0015 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0016 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0017 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0018 | 0/0 | 3355 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0019 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0020 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0021 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0022 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0023 | 0/0 | 3355 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0024 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0025 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0026 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0027 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0028 | 0/0 | 3355 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0029 | 0/0 | 3355 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0030 | 0/0 | 3355 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0031 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| t0032 | 0/0 | 3355 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3183 | 205 | 23 | 40 | 103 | 8 | 29 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002 | 0/0 | 3183 | 62 | 48 | 8 | 0 | 2 | 4 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0003 | 0/0 | 3183 | 3 | 0 | 0 | 3 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0002c0004 | 0/0 | 3183 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0003c0005 | 0/0 | 3183 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 6537 | 98 | 12 | 15 | 48 | 5 | 17 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0002 | 0/1 | 6537 | 70 | 0 | 18 | 39 | 3 | 9 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0006 | 0/0 | 6537 | 7 | 6 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0007 | 0/0 | 6537 | 7 | 0 | 0 | 7 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0008 | 0/0 | 6537 | 4 | 0 | 4 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0010 | 0/0 | 6537 | 3 | 0 | 0 | 3 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0011 | 0/0 | 6537 | 3 | 3 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0017 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0018 | 0/0 | 6537 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0019 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0020 | 0/0 | 6537 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0022 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0023 | 0/0 | 6537 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0025 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0027 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0028 | 0/0 | 6537 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0029 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0030 | 0/0 | 6537 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0031 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0001t0032 | 0/0 | 6537 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0001 | 0/0 | 6537 | 11 | 10 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0003 | 0/0 | 6538 | 17 | 16 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0004 | 0/0 | 6537 | 15 | 6 | 3 | 0 | 2 | 4 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0005 | 0/0 | 6538 | 8 | 6 | 2 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0009 | 0/0 | 6537 | 3 | 3 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0012 | 0/0 | 6537 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0013 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0014 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0015 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0016 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0021 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0024 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0002t0026 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0001c0003t0002 | 0/0 | 6537 | 3 | 0 | 0 | 3 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0002c0004t0004 | 0/0 | 6537 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| a0003c0005t0012 | 0/0 | 6537 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | copy fasta | chr5 | 146198605 | 146294223 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0006g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0006g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0007g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0007g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0008g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0008g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0010g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0010g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0010g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0011g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0017g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0018g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0019g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0020g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0022g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0023g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0025g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0027g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0028g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0029g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0030g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0031g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0001t0032g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0005g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0012g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0013g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0014g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0016g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0021g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0024g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0002t0026g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0003t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0003t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0001c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0002c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| a0003c0005t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0004 | g0025 | EUR | GBR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0191 | EUR | GBR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0019 | EUR | GBR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0240 | EUR | FIN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | FIN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00639 | hp2 | a0001 | c0002 | t0004 | g0017 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0026 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0248 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01069 | hp1 | a0001 | c0002 | t0005 | g0007 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01071 | hp1 | a0001 | c0002 | t0005 | g0001 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01099 | hp1 | a0001 | c0002 | t0004 | g0023 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01167 | hp1 | a0001 | c0002 | t0012 | g0005 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0038 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0136 | AMR | PUR | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01255 | hp2 | a0001 | c0002 | t0003 | g0036 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01346 | hp2 | a0001 | c0001 | t0028 | g0095 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01433 | hp2 | a0001 | c0001 | t0008 | g0113 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01496 | hp1 | a0001 | c0001 | t0020 | g0267 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0034 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01884 | hp2 | a0001 | c0002 | t0015 | g0010 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01891 | hp2 | a0001 | c0002 | t0003 | g0041 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01952 | hp2 | a0001 | c0001 | t0008 | g0081 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0085 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02040 | hp1 | a0001 | c0003 | t0002 | g0236 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0266 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02055 | hp2 | a0001 | c0001 | t0029 | g0135 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02135 | hp2 | a0001 | c0003 | t0002 | g0249 | EAS | KHV | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02145 | hp1 | a0001 | c0002 | t0009 | g0009 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0131 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CDX | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0060 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02273 | hp1 | a0001 | c0001 | t0008 | g0080 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0057 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0128 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02647 | hp1 | a0001 | c0002 | t0003 | g0043 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02647 | hp2 | a0001 | c0002 | t0003 | g0035 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02717 | hp1 | a0001 | c0002 | t0024 | g0264 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02717 | hp2 | a0001 | c0002 | t0026 | g0030 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02738 | hp2 | a0001 | c0002 | t0004 | g0016 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0018 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0001 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0138 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02886 | hp2 | a0001 | c0002 | t0003 | g0042 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02896 | hp2 | a0001 | c0002 | t0005 | g0268 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0052 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02922 | hp1 | a0001 | c0002 | t0003 | g0040 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0056 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02970 | hp2 | a0001 | c0001 | t0019 | g0083 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02976 | hp1 | a0001 | c0002 | t0005 | g0014 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03017 | hp2 | a0001 | c0002 | t0004 | g0022 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03098 | hp1 | a0001 | c0002 | t0005 | g0015 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0044 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0059 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03139 | hp2 | a0001 | c0001 | t0011 | g0002 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03209 | hp1 | a0001 | c0002 | t0014 | g0006 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03453 | hp1 | a0001 | c0002 | t0003 | g0037 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03453 | hp2 | a0001 | c0002 | t0003 | g0039 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0028 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0137 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0021 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03492 | hp2 | a0001 | c0002 | t0004 | g0024 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03516 | hp1 | a0001 | c0002 | t0003 | g0027 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0045 | AFR | ESN | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03579 | hp1 | a0001 | c0002 | t0016 | g0265 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03579 | hp2 | a0001 | c0002 | t0005 | g0008 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03654 | hp1 | a0001 | c0001 | t0030 | g0171 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03669 | hp1 | a0001 | c0001 | t0018 | g0164 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | PJL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03831 | hp1 | a0002 | c0004 | t0004 | g0020 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG04199 | hp1 | a0001 | c0001 | t0023 | g0119 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0002 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18522 | hp2 | a0001 | c0002 | t0009 | g0047 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | CHB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18747 | hp2 | a0001 | c0001 | t0007 | g0067 | EAS | CHB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0263 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18906 | hp2 | a0003 | c0005 | t0012 | g0046 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18940 | hp2 | a0001 | c0001 | t0017 | g0214 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18942 | hp1 | a0001 | c0001 | t0007 | g0066 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18944 | hp1 | a0001 | c0001 | t0007 | g0070 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18948 | hp1 | a0001 | c0001 | t0025 | g0168 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18949 | hp1 | a0001 | c0001 | t0032 | g0152 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18975 | hp2 | a0001 | c0001 | t0031 | g0241 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18985 | hp1 | a0001 | c0001 | t0010 | g0245 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18989 | hp2 | a0001 | c0001 | t0007 | g0065 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18991 | hp1 | a0001 | c0003 | t0002 | g0234 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18991 | hp2 | a0001 | c0001 | t0022 | g0127 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19005 | hp1 | a0001 | c0001 | t0007 | g0179 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19009 | hp2 | a0001 | c0001 | t0027 | g0146 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | LWK | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0262 | AFR | LWK | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19056 | hp1 | a0001 | c0001 | t0010 | g0246 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19079 | hp1 | a0001 | c0001 | t0010 | g0198 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0068 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19088 | hp1 | a0001 | c0001 | t0007 | g0064 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0032 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA19240 | hp2 | a0001 | c0002 | t0013 | g0011 | AFR | YRI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA20129 | hp1 | a0001 | c0002 | t0003 | g0033 | AFR | ASW | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0084 | AFR | ASW | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | TSI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0192 | EUR | TSI | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | GIH | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02109 | hp2 | a0001 | c0002 | t0021 | g0259 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02486 | hp1 | a0001 | c0002 | t0004 | g0058 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02486 | hp2 | a0001 | c0002 | t0009 | g0012 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0031 | AFR | ACB | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03471 | hp1 | a0001 | c0002 | t0005 | g0013 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| HG03471 | hp2 | a0001 | c0002 | t0003 | g0029 | AFR | MSL | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0226 | REF | REF | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0063 | REF | REF | RBM27_chr5_146198605_146294223 | RBM27 | chr5 | 146198605 | 146294223 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:146258493
|
A | G | 1 | a0003 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.1639A>G | p.Ile547Val | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/21 | 1800/6537 | 1639/3183 | 547/1060 | chr5 | 146258493 | ||
| chr5:146285957
|
C | A | 1 | a0002 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.3110C>A | p.Thr1037Asn | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 3271/6537 | 3110/3183 | 1037/1060 | chr5 | 146285957 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:146261779
|
T | C | 1 | a0001c0003 | 3 | HG02040.hp1 HG02135.hp2 NA18991.hp1 |
synonymous_variant | LOW | c.2163T>C | p.Pro721Pro | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/21 | 2324/6537 | 2163/3183 | 721/1060 | chr5 | 146261779 | ||
| chr5:146271034
|
A | G | 3 | a0001c0002a0002c0004a0003c0005 | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
synonymous_variant | LOW | c.2772A>G | p.Lys924Lys | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/21 | 2933/6537 | 2772/3183 | 924/1060 | chr5 | 146271034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:146203696
|
G | A | 5 | a0001c0002t0005a0001c0002t0009a0001c0002t0013others(2): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-70G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/21 | 70 | chr5 | 146203696 | |||||
| chr5:146203706
|
T | G | 1 | a0001c0001t0006 | 7 | HG01243.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-60T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/21 | 60 | chr5 | 146203706 | |||||
| chr5:146203714
|
A | C | 1 | a0001c0001t0032 | 1 | NA18949.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/21 | 52 | chr5 | 146203714 | |||||
| chr5:146203729
|
G | T | 1 | a0001c0001t0031 | 1 | NA18975.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/21 | 37 | chr5 | 146203729 | |||||
| chr5:146286081
|
T | C | 1 | a0001c0002t0016 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 51 | chr5 | 146286081 | |||||
| chr5:146286328
|
A | T | 1 | a0001c0001t0008 | 4 | HG01433.hp2 HG01952.hp2 HG01975.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*298A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 298 | chr5 | 146286328 | |||||
| chr5:146286354
|
T | C | 5 | a0001c0001t0002a0001c0001t0010a0001c0001t0017others(2): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*324T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 324 | chr5 | 146286354 | |||||
| chr5:146286530
|
A | AT | 2 | a0001c0002t0003a0001c0002t0005 | 25 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*515dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 516 | INFO_REALIGN_3_PRIME | chr5 | 146286530 | ||||
| chr5:146286699
|
A | G | 1 | a0001c0001t0030 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*669A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 669 | chr5 | 146286699 | |||||
| chr5:146286861
|
A | G | 1 | a0001c0001t0029 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*831A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 831 | chr5 | 146286861 | |||||
| chr5:146287042
|
A | G | 1 | a0001c0001t0028 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1012A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1012 | chr5 | 146287042 | |||||
| chr5:146287127
|
G | A | 1 | a0001c0001t0018 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1097G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1097 | chr5 | 146287127 | |||||
| chr5:146287147
|
G | A | 1 | a0001c0001t0019 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1117G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1117 | chr5 | 146287147 | |||||
| chr5:146287157
|
G | C | 1 | a0001c0002t0013 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1127G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1127 | chr5 | 146287157 | |||||
| chr5:146287255
|
G | A | 1 | a0001c0001t0007 | 7 | NA18747.hp2 NA18942.hp1 NA18944.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1225G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1225 | chr5 | 146287255 | |||||
| chr5:146287301
|
A | G | 1 | a0001c0001t0027 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1271A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1271 | chr5 | 146287301 | |||||
| chr5:146287318
|
G | A | 1 | a0001c0001t0010 | 3 | NA18985.hp1 NA19056.hp1 NA19079.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1288G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1288 | chr5 | 146287318 | |||||
| chr5:146287461
|
A | T | 1 | a0001c0001t0011 | 3 | HG02886.hp1 HG03139.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1431A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1431 | chr5 | 146287461 | |||||
| chr5:146287660
|
C | T | 1 | a0001c0002t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1630C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1630 | chr5 | 146287660 | |||||
| chr5:146287686
|
A | G | 2 | a0001c0002t0013a0001c0002t0015 | 2 | HG01884.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1656A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1656 | chr5 | 146287686 | |||||
| chr5:146287788
|
T | C | 2 | a0001c0002t0004a0002c0004t0004 | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1758T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1758 | chr5 | 146287788 | |||||
| chr5:146287839
|
A | G | 2 | a0001c0002t0004a0002c0004t0004 | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1809A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1809 | chr5 | 146287839 | |||||
| chr5:146287953
|
A | G | 1 | a0001c0001t0025 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1923A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 1923 | chr5 | 146287953 | |||||
| chr5:146288296
|
A | G | 2 | a0001c0002t0012a0003c0005t0012 | 2 | HG01167.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2266A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2266 | chr5 | 146288296 | |||||
| chr5:146288478
|
C | A | 6 | a0001c0001t0002a0001c0001t0010a0001c0001t0017others(3): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2448C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2448 | chr5 | 146288478 | |||||
| chr5:146288516
|
C | A | 1 | a0001c0002t0021 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2486C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2486 | chr5 | 146288516 | |||||
| chr5:146288690
|
A | G | 1 | a0001c0002t0014 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2660A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2660 | chr5 | 146288690 | |||||
| chr5:146288735
|
C | T | 6 | a0001c0001t0002a0001c0001t0010a0001c0001t0017others(3): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2705C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2705 | chr5 | 146288735 | |||||
| chr5:146288824
|
A | T | 6 | a0001c0002t0005a0001c0002t0009a0001c0002t0013others(3): Show | 15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*2794A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2794 | chr5 | 146288824 | |||||
| chr5:146288830
|
T | C | 1 | a0001c0001t0017 | 1 | NA18940.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2800T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2800 | chr5 | 146288830 | |||||
| chr5:146288917
|
A | G | 1 | a0001c0001t0023 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2887A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 2887 | chr5 | 146288917 | |||||
| chr5:146289060
|
A | G | 1 | a0001c0001t0022 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3030A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 3030 | chr5 | 146289060 | |||||
| chr5:146289128
|
A | G | 1 | a0001c0001t0020 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3098A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 3098 | chr5 | 146289128 | |||||
| chr5:146289162
|
A | G | 5 | a0001c0001t0002a0001c0001t0010a0001c0001t0017others(2): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*3132A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 21/21 | 3132 | chr5 | 146289162 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:146203845
|
C | G | 1 | a0001c0002t0005g0268 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.59+21C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146203845 | ||||||
| chr5:146204060
|
A | G | 85 | a0001c0001t0001g0004a0001c0001t0002g0184a0001c0001t0002g0185others(82): Show | 86 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.59+236A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204060 | ||||||
| chr5:146204169
|
G | A | 50 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(47): Show | 51 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.59+345G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204169 | ||||||
| chr5:146204263
|
A | G | 9 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+439A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204263 | ||||||
| chr5:146204310
|
G | A | 9 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+486G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204310 | ||||||
| chr5:146204528
|
GA | G | 138 | a0001c0001t0001g0004a0001c0001t0002g0181a0001c0001t0002g0182others(135): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.59+705delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204528 | ||||||
| chr5:146204554
|
T | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18982.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.59+730T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204554 | ||||||
| chr5:146204573
|
A | G | 9 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+749A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204573 | ||||||
| chr5:146204630
|
G | A | 138 | a0001c0001t0001g0004a0001c0001t0002g0181a0001c0001t0002g0182others(135): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.59+806G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204630 | ||||||
| chr5:146204767
|
A | G | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+943A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204767 | ||||||
| chr5:146204825
|
A | G | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.59+1001A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204825 | ||||||
| chr5:146204937
|
T | C | 1 | a0001c0001t0002g0184 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.59+1113T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146204937 | ||||||
| chr5:146205361
|
TAGA | T | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+1544_59+1546del others(3): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146205361 | |||||
| chr5:146205587
|
G | GT | 41 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0143others(38): Show | 42 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.59+1770dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146205587 | |||||
| chr5:146205628
|
G | A | 1 | a0001c0001t0001g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.59+1804G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146205628 | ||||||
| chr5:146205848
|
G | A | 10 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(7): Show | 10 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2024G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146205848 | ||||||
| chr5:146205998
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.59+2174C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146205998 | ||||||
| chr5:146206201
|
C | T | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.59+2377C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206201 | ||||||
| chr5:146206247
|
T | C | 1 | a0001c0001t0032g0152 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.59+2423T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206247 | ||||||
| chr5:146206248
|
C | T | 1 | a0001c0001t0032g0152 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.59+2424C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206248 | ||||||
| chr5:146206296
|
G | T | 9 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+2472G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206296 | ||||||
| chr5:146206302
|
T | TG | 4 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(1): Show | 4 | HG01361.hp2 HG03927.hp1 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2479dupG | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146206302 | |||||
| chr5:146206303
|
GT | G | 10 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(7): Show | 10 | HG01167.hp1 HG01496.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.59+2492delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146206303 | |||||
| chr5:146206304
|
T | G | 128 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(125): Show | 129 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.59+2480T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206304 | ||||||
| chr5:146206305
|
T | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.59+2481T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206305 | ||||||
| chr5:146206352
|
T | G | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.59+2528T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206352 | ||||||
| chr5:146206378
|
T | TC | 13 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+2556dupC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146206378 | |||||
| chr5:146206527
|
T | A | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.59+2703T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206527 | ||||||
| chr5:146206549
|
TA | T | 135 | a0001c0001t0001g0180a0001c0001t0002g0181a0001c0001t0002g0182others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.59+2736delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146206549 | |||||
| chr5:146206578
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG01257.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.59+2754T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206578 | ||||||
| chr5:146206746
|
A | G | 1 | a0001c0001t0002g0254 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.59+2922A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206746 | ||||||
| chr5:146206858
|
C | T | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+3034C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146206858 | ||||||
| chr5:146207010
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.59+3186T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207010 | ||||||
| chr5:146207315
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.59+3491G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207315 | ||||||
| chr5:146207454
|
T | G | 1 | a0001c0001t0001g0156 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.59+3630T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207454 | ||||||
| chr5:146207493
|
A | G | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.59+3669A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207493 | ||||||
| chr5:146207502
|
T | C | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.59+3678T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207502 | ||||||
| chr5:146207590
|
T | TC | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.59+3769dupC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207590 | |||||
| chr5:146207658
|
C | CT | 14 | a0001c0001t0001g0054a0001c0001t0001g0139a0001c0001t0001g0178others(11): Show | 14 | HG00099.hp1 HG00735.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.59+3852dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207658 | |||||
| chr5:146207658
|
CT | C | 42 | a0001c0001t0002g0185a0001c0001t0002g0186a0001c0001t0002g0187others(39): Show | 43 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.59+3852delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207658 | |||||
| chr5:146207722
|
T | A | 1 | a0001c0002t0003g0027 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.59+3898T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207722 | ||||||
| chr5:146207769
|
C | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.59+3945C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207769 | ||||||
| chr5:146207903
|
C | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+4079C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207903 | ||||||
| chr5:146207951
|
G | GT | 127 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(124): Show | 130 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.59+4150dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207951 | |||||
| chr5:146207951
|
G | GTT | 107 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(104): Show | 108 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.59+4149_59+4150dup others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207951 | |||||
| chr5:146207951
|
G | GTTT | 27 | a0001c0001t0002g0244a0001c0001t0002g0247a0001c0001t0002g0248others(24): Show | 27 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.59+4148_59+4150dup others(3): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207951 | |||||
| chr5:146207951
|
G | GTTTT | 5 | a0001c0002t0001g0038a0001c0002t0003g0036a0001c0002t0003g0037others(2): Show | 5 | HG01243.hp1 HG01255.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.59+4147_59+4150dup others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146207951 | |||||
| chr5:146207989
|
C | G | 1 | a0001c0001t0001g0123 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.59+4165C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146207989 | ||||||
| chr5:146208017
|
C | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.59+4193C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208017 | ||||||
| chr5:146208047
|
C | T | 2 | a0001c0002t0005g0014a0001c0002t0005g0015 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.59+4223C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208047 | ||||||
| chr5:146208060
|
A | C | 5 | a0001c0001t0002g0242a0001c0001t0002g0243a0001c0001t0002g0251others(2): Show | 5 | NA18975.hp2 NA18980.hp2 NA19064.hp2 others(2): Show |
intron_variant | MODIFIER | c.59+4236A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208060 | ||||||
| chr5:146208250
|
G | A | 9 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0069others(6): Show | 9 | NA18747.hp2 NA18942.hp1 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.59+4426G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208250 | ||||||
| chr5:146208458
|
C | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.59+4634C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208458 | ||||||
| chr5:146208486
|
G | C | 9 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+4662G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208486 | ||||||
| chr5:146208501
|
C | A | 1 | a0001c0001t0002g0191 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.59+4677C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208501 | ||||||
| chr5:146208508
|
G | A | 9 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59+4684G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208508 | ||||||
| chr5:146208683
|
T | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.59+4859T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208683 | ||||||
| chr5:146208920
|
G | A | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.59+5096G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146208920 | ||||||
| chr5:146209028
|
C | T | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+5204C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146209028 | ||||||
| chr5:146209951
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.59+6127A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146209951 | ||||||
| chr5:146209979
|
C | T | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.59+6155C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146209979 | ||||||
| chr5:146210170
|
T | C | 1 | a0001c0001t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.59+6346T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210170 | ||||||
| chr5:146210200
|
A | G | 8 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.59+6376A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210200 | ||||||
| chr5:146210322
|
A | G | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+6498A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210322 | ||||||
| chr5:146210331
|
A | G | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+6507A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210331 | ||||||
| chr5:146210415
|
C | T | 266 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.59+6591C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210415 | ||||||
| chr5:146210589
|
C | T | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01167.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.59+6765C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210589 | ||||||
| chr5:146210674
|
A | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.59+6850A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210674 | ||||||
| chr5:146210685
|
T | C | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.59+6861T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210685 | ||||||
| chr5:146210686
|
G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59+6862G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210686 | ||||||
| chr5:146210863
|
C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.59+7039C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210863 | ||||||
| chr5:146210878
|
C | T | 13 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+7054C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146210878 | ||||||
| chr5:146211066
|
A | G | 2 | a0001c0002t0001g0266a0001c0002t0016g0265 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.59+7242A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211066 | ||||||
| chr5:146211169
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.59+7345A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211169 | ||||||
| chr5:146211187
|
G | A | 13 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.59+7363G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211187 | ||||||
| chr5:146211317
|
A | G | 1 | a0001c0002t0003g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.59+7493A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211317 | ||||||
| chr5:146211464
|
C | CT | 29 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0116others(26): Show | 29 | HG00408.hp1 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.60-7491dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTT | 8 | a0001c0001t0001g0121a0001c0002t0001g0038a0001c0002t0003g0035others(5): Show | 8 | HG01243.hp1 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-7492_60-7491dup others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG01975.hp1 HG02273.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.60-7500_60-7491dup others(10): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0002g0221a0001c0001t0002g0222a0001c0001t0002g0247 | 3 | HG01255.hp1 HG01346.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.60-7501_60-7491dup others(11): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0002g0223 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.60-7502_60-7491dup others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0002g0188 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.60-7504_60-7491dup others(14): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0002g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.60-7506_60-7491dup others(16): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(12): Show |
4 | a0001c0001t0002g0224a0001c0001t0002g0225a0001c0001t0002g0226others(1): Show | 4 | HG01257.hp1 HG01496.hp2 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-7509_60-7491dup others(19): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(13): Show |
9 | a0001c0001t0002g0191a0001c0001t0002g0228a0001c0001t0002g0229others(6): Show | 9 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-7510_60-7491dup others(20): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(14): Show |
5 | a0001c0001t0002g0235a0001c0001t0002g0237a0001c0003t0002g0234others(2): Show | 5 | HG01981.hp2 HG02040.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-7511_60-7491dup others(21): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0002g0258 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.60-7512_60-7491dup others(22): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(17): Show |
1 | a0001c0001t0002g0238 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.60-7514_60-7491dup others(24): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(19): Show |
3 | a0001c0001t0002g0239a0001c0001t0002g0240a0001c0001t0002g0250 | 3 | HG00323.hp1 HG00642.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.60-7516_60-7491dup others(26): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
C | CTTTTTTT others(24): Show |
1 | a0001c0001t0002g0190 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.60-7491_60-7490ins others(31): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
CT | C | 63 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0072others(60): Show | 67 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.60-7491delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
CTTTTT | C | 41 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(38): Show | 41 | HG00438.hp2 HG02074.hp2 HG02132.hp1 others(38): Show |
intron_variant | MODIFIER | c.60-7495_60-7491del others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
CTTTTTT | C | 16 | a0001c0001t0002g0185a0001c0001t0002g0192a0001c0002t0004g0016others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-7496_60-7491del others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
CTTTTTTT others(3): Show |
C | 9 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.60-7500_60-7491del others(10): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211464
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-7502_60-7491del others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146211464 | |||||
| chr5:146211494
|
T | A | 1 | a0001c0001t0002g0215 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.60-7491T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211494 | ||||||
| chr5:146211574
|
T | C | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.60-7411T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211574 | ||||||
| chr5:146211575
|
G | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.60-7410G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211575 | ||||||
| chr5:146211576
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.60-7409G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211576 | ||||||
| chr5:146211680
|
C | T | 1 | a0001c0002t0024g0264 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.60-7305C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211680 | ||||||
| chr5:146211717
|
GTA | G | 3 | a0001c0002t0012g0005a0001c0002t0026g0030a0003c0005t0012g0046 | 3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-7267_60-7266del others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211717 | ||||||
| chr5:146211722
|
C | T | 3 | a0001c0002t0012g0005a0001c0002t0026g0030a0003c0005t0012g0046 | 3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-7263C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211722 | ||||||
| chr5:146211856
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.60-7129G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146211856 | ||||||
| chr5:146212061
|
T | TC | 8 | a0001c0001t0001g0054a0001c0001t0001g0122a0001c0001t0001g0126others(5): Show | 8 | HG00741.hp1 HG00741.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-6921dupC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146212061 | |||||
| chr5:146212202
|
C | T | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-6783C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212202 | ||||||
| chr5:146212203
|
G | A | 1 | a0001c0002t0009g0012 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.60-6782G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212203 | ||||||
| chr5:146212205
|
G | A | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-6780G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212205 | ||||||
| chr5:146212300
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0126 | 2 | NA18954.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.60-6685C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212300 | ||||||
| chr5:146212301
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.60-6684G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212301 | ||||||
| chr5:146212336
|
G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.60-6649G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212336 | ||||||
| chr5:146212433
|
C | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.60-6552C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212433 | ||||||
| chr5:146212518
|
T | A | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.60-6467T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212518 | ||||||
| chr5:146212594
|
T | C | 9 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0029others(6): Show | 9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-6391T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212594 | ||||||
| chr5:146212619
|
G | C | 1 | a0001c0002t0005g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.60-6366G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212619 | ||||||
| chr5:146212731
|
A | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.60-6254A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212731 | ||||||
| chr5:146212966
|
T | A | 13 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-6019T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146212966 | ||||||
| chr5:146213082
|
G | A | 1 | a0001c0001t0030g0171 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.60-5903G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213082 | ||||||
| chr5:146213105
|
G | T | 11 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(8): Show | 11 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.60-5880G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213105 | ||||||
| chr5:146213225
|
C | T | 1 | a0001c0001t0008g0113 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.60-5760C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213225 | ||||||
| chr5:146213239
|
A | G | 15 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0019others(12): Show | 15 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.60-5746A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213239 | ||||||
| chr5:146213622
|
G | A | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.60-5363G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213622 | ||||||
| chr5:146213771
|
A | G | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.60-5214A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146213771 | ||||||
| chr5:146214115
|
C | G | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.60-4870C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214115 | ||||||
| chr5:146214607
|
G | A | 2 | a0001c0001t0007g0064a0001c0001t0007g0065 | 2 | NA18989.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.60-4378G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214607 | ||||||
| chr5:146214652
|
T | C | 141 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(138): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.60-4333T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214652 | ||||||
| chr5:146214675
|
A | G | 3 | a0001c0002t0012g0005a0001c0002t0026g0030a0003c0005t0012g0046 | 3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.60-4310A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214675 | ||||||
| chr5:146214792
|
G | A | 13 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.60-4193G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214792 | ||||||
| chr5:146214918
|
C | T | 2 | a0001c0001t0001g0111a0001c0001t0001g0140 | 2 | HG02056.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.60-4067C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214918 | ||||||
| chr5:146214966
|
C | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.60-4019C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146214966 | ||||||
| chr5:146215086
|
A | G | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.60-3899A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215086 | ||||||
| chr5:146215088
|
C | T | 2 | a0001c0002t0001g0262a0001c0002t0001g0263 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.60-3897C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215088 | ||||||
| chr5:146215130
|
A | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0125 | 2 | HG02027.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.60-3855A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215130 | ||||||
| chr5:146215164
|
C | T | 1 | a0001c0002t0005g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.60-3821C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215164 | ||||||
| chr5:146215385
|
A | T | 9 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.60-3600A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215385 | ||||||
| chr5:146215440
|
A | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.60-3545A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215440 | ||||||
| chr5:146215552
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.60-3433T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215552 | ||||||
| chr5:146215595
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0112 | 2 | HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.60-3390G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215595 | ||||||
| chr5:146215736
|
A | C | 2 | a0001c0002t0012g0005a0003c0005t0012g0046 | 2 | HG01167.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.60-3249A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215736 | ||||||
| chr5:146215757
|
A | AT | 11 | a0001c0001t0001g0110a0001c0001t0001g0134a0001c0002t0001g0038others(8): Show | 11 | HG01243.hp1 HG01255.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.60-3215dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146215757 | |||||
| chr5:146215805
|
C | T | 1 | a0001c0002t0004g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.60-3180C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215805 | ||||||
| chr5:146215843
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.60-3142C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215843 | ||||||
| chr5:146215939
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.60-3046C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215939 | ||||||
| chr5:146215977
|
C | G | 2 | a0001c0002t0004g0017a0001c0002t0004g0026 | 2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.60-3008C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146215977 | ||||||
| chr5:146216031
|
A | C | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.60-2954A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216031 | ||||||
| chr5:146216088
|
G | T | 1 | a0001c0001t0001g0121 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.60-2897G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216088 | ||||||
| chr5:146216099
|
C | T | 18 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(15): Show | 18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.60-2886C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216099 | ||||||
| chr5:146216133
|
T | A | 1 | a0001c0001t0002g0224 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.60-2852T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216133 | ||||||
| chr5:146216245
|
C | T | 18 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(15): Show | 18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.60-2740C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216245 | ||||||
| chr5:146216274
|
C | T | 1 | a0001c0001t0011g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.60-2711C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216274 | ||||||
| chr5:146216511
|
G | T | 1 | a0001c0001t0002g0213 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.60-2474G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216511 | ||||||
| chr5:146216617
|
C | T | 55 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(52): Show | 56 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.60-2368C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216617 | ||||||
| chr5:146216627
|
C | T | 9 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0029others(6): Show | 9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.60-2358C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216627 | ||||||
| chr5:146216653
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.60-2332C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216653 | ||||||
| chr5:146216657
|
C | A | 1 | a0001c0001t0001g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.60-2328C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216657 | ||||||
| chr5:146216768
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.60-2217C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146216768 | ||||||
| chr5:146217059
|
C | T | 1 | a0001c0002t0005g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.60-1926C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217059 | ||||||
| chr5:146217069
|
C | T | 1 | a0001c0003t0002g0249 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.60-1916C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217069 | ||||||
| chr5:146217118
|
C | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.60-1867C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217118 | ||||||
| chr5:146217164
|
G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.60-1821G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217164 | ||||||
| chr5:146217169
|
G | C | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-1816G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217169 | ||||||
| chr5:146217256
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.60-1729C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217256 | ||||||
| chr5:146217262
|
C | T | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.60-1723C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217262 | ||||||
| chr5:146217360
|
A | AT | 3 | a0001c0001t0002g0215a0001c0001t0002g0239a0001c0001t0002g0240 | 3 | HG00323.hp1 HG00642.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.60-1624dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217360 | |||||
| chr5:146217464
|
G | GT | 40 | a0001c0001t0001g0054a0001c0001t0001g0061a0001c0001t0001g0086others(37): Show | 40 | HG00323.hp2 HG00408.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.60-1494dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
G | GTT | 8 | a0001c0001t0001g0093a0001c0001t0001g0115a0001c0001t0001g0125others(5): Show | 8 | HG01243.hp2 HG02027.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.60-1495_60-1494dup others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
G | GTTT | 5 | a0001c0001t0001g0180a0001c0002t0003g0027a0001c0002t0003g0031others(2): Show | 5 | HG02559.hp2 HG02647.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-1496_60-1494dup others(3): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
G | GTTTT | 6 | a0001c0002t0001g0049a0001c0002t0001g0050a0001c0002t0001g0051others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1497_60-1494dup others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
G | GTTTTTTT others(4): Show |
2 | a0001c0002t0003g0040a0001c0002t0003g0043 | 2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.60-1504_60-1494dup others(11): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
G | GTTTTTTT others(5): Show |
1 | a0001c0002t0003g0042 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.60-1505_60-1494dup others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
G | GTTTTTTT others(6): Show |
1 | a0001c0002t0003g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.60-1506_60-1494dup others(13): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
G | GTTTTTTT others(15): Show |
1 | a0001c0002t0003g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.60-1515_60-1494dup others(22): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
G | GTTTTTTT others(21): Show |
1 | a0001c0002t0003g0044 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.60-1494_60-1493ins others(28): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
GT | G | 49 | a0001c0001t0001g0172a0001c0001t0002g0193a0001c0001t0002g0209others(46): Show | 50 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.60-1494delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
GTT | G | 57 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(54): Show | 57 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(54): Show |
intron_variant | MODIFIER | c.60-1495_60-1494del others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217464
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.60-1505_60-1494del others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146217464 | |||||
| chr5:146217582
|
C | G | 1 | a0001c0002t0024g0264 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.60-1403C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217582 | ||||||
| chr5:146217612
|
A | T | 1 | a0001c0001t0002g0183 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.60-1373A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217612 | ||||||
| chr5:146217614
|
C | G | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.60-1371C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217614 | ||||||
| chr5:146217827
|
C | T | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.60-1158C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217827 | ||||||
| chr5:146217828
|
G | A | 1 | a0001c0001t0002g0239 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.60-1157G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217828 | ||||||
| chr5:146217896
|
T | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0112 | 2 | HG03710.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.60-1089T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146217896 | ||||||
| chr5:146218054
|
A | G | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.60-931A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218054 | ||||||
| chr5:146218068
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.60-917C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218068 | ||||||
| chr5:146218134
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.60-851A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218134 | ||||||
| chr5:146218153
|
G | GTA | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.60-822_60-821dupAT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr5 | 146218153 | |||||
| chr5:146218212
|
C | T | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-773C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218212 | ||||||
| chr5:146218329
|
T | C | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.60-656T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218329 | ||||||
| chr5:146218450
|
A | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.60-535A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218450 | ||||||
| chr5:146218521
|
C | G | 5 | a0001c0001t0002g0208a0001c0001t0002g0211a0001c0001t0002g0216others(2): Show | 5 | NA18948.hp2 NA18979.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-464C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218521 | ||||||
| chr5:146218595
|
T | G | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.60-390T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218595 | ||||||
| chr5:146218720
|
A | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.60-265A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 1/20 | chr5 | 146218720 | ||||||
| chr5:146219695
|
C | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.178+592C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146219695 | ||||||
| chr5:146219971
|
A | G | 2 | a0001c0002t0003g0028a0001c0002t0003g0044 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.178+868A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146219971 | ||||||
| chr5:146220204
|
G | A | 16 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(13): Show | 16 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.178+1101G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220204 | ||||||
| chr5:146220244
|
G | A | 3 | a0001c0002t0004g0016a0001c0002t0004g0019a0002c0004t0004g0020 | 3 | HG00140.hp2 HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.178+1141G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220244 | ||||||
| chr5:146220397
|
C | T | 13 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+1294C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220397 | ||||||
| chr5:146220461
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.178+1358C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220461 | ||||||
| chr5:146220474
|
C | CA | 6 | a0001c0001t0001g0122a0001c0002t0001g0048a0001c0002t0001g0049others(3): Show | 6 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.178+1387dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220474 | |||||
| chr5:146220474
|
CA | C | 118 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(115): Show | 119 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.178+1387delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220474 | |||||
| chr5:146220474
|
CAA | C | 6 | a0001c0001t0001g0091a0001c0002t0005g0001a0001c0002t0005g0007others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.178+1386_178+1387d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220474 | |||||
| chr5:146220487
|
AAAAT | A | 11 | a0001c0001t0002g0204a0001c0001t0002g0205a0001c0001t0002g0206others(8): Show | 11 | HG00438.hp2 HG02132.hp1 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.178+1386_178+1389d others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220487 | |||||
| chr5:146220488
|
AAAT | A | 59 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(56): Show | 59 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.178+1387_178+1389d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146220488 | |||||
| chr5:146220489
|
A | AT | 17 | a0001c0001t0001g0055a0001c0001t0001g0088a0001c0001t0001g0092others(14): Show | 17 | HG00323.hp2 HG01167.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.178+1386_178+1387i others(3): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220489 | ||||||
| chr5:146220489
|
A | T | 34 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(31): Show | 36 | HG00099.hp2 HG01069.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.178+1386A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220489 | ||||||
| chr5:146220490
|
AT | A | 21 | a0001c0001t0001g0106a0001c0001t0001g0130a0001c0001t0011g0002others(18): Show | 22 | HG00099.hp1 HG00140.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.178+1388delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220490 | ||||||
| chr5:146220491
|
T | A | 2 | a0001c0002t0003g0031a0001c0002t0003g0035 | 2 | HG02559.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.178+1388T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220491 | ||||||
| chr5:146220493
|
T | A | 4 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039others(1): Show | 4 | HG02559.hp2 HG02647.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.178+1390T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220493 | ||||||
| chr5:146220495
|
T | A | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.178+1392T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220495 | ||||||
| chr5:146220497
|
T | A | 1 | a0001c0002t0003g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.178+1394T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220497 | ||||||
| chr5:146220501
|
T | C | 13 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.178+1398T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220501 | ||||||
| chr5:146220535
|
G | A | 7 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.178+1432G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220535 | ||||||
| chr5:146220643
|
A | G | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.178+1540A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220643 | ||||||
| chr5:146220872
|
G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.178+1769G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146220872 | ||||||
| chr5:146221093
|
C | T | 6 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(3): Show | 6 | HG02109.hp2 HG02572.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.178+1990C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221093 | ||||||
| chr5:146221127
|
G | A | 7 | a0001c0001t0002g0191a0001c0001t0002g0225a0001c0001t0002g0226others(4): Show | 7 | HG00140.hp1 HG00741.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.178+2024G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221127 | ||||||
| chr5:146221141
|
C | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0090a0001c0001t0019g0083 | 3 | HG02615.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.178+2038C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221141 | ||||||
| chr5:146221147
|
C | CA | 9 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.178+2058dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146221147 | |||||
| chr5:146221167
|
A | G | 2 | a0001c0001t0002g0202a0001c0001t0002g0203 | 2 | NA18949.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.178+2064A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221167 | ||||||
| chr5:146221245
|
A | G | 8 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.178+2142A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221245 | ||||||
| chr5:146221520
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.179-1883A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221520 | ||||||
| chr5:146221779
|
A | G | 12 | a0001c0001t0001g0055a0001c0001t0001g0087a0001c0001t0001g0088others(9): Show | 12 | HG00323.hp2 HG01099.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-1624A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146221779 | ||||||
| chr5:146221885
|
TATA | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.179-1513_179-1511d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr5 | 146221885 | |||||
| chr5:146222017
|
A | T | 2 | a0001c0002t0004g0021a0001c0002t0004g0024 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.179-1386A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222017 | ||||||
| chr5:146222103
|
CT | C | 3 | a0001c0002t0001g0260a0001c0002t0001g0262a0001c0002t0001g0263 | 3 | HG02572.hp1 NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.179-1299delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222103 | ||||||
| chr5:146222180
|
A | C | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.179-1223A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222180 | ||||||
| chr5:146222185
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.179-1218C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222185 | ||||||
| chr5:146222216
|
G | A | 9 | a0001c0001t0020g0267a0001c0002t0001g0260a0001c0002t0001g0261others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.179-1187G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222216 | ||||||
| chr5:146222237
|
G | C | 1 | a0001c0001t0001g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.179-1166G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222237 | ||||||
| chr5:146222335
|
T | C | 55 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(52): Show | 56 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.179-1068T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222335 | ||||||
| chr5:146222362
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.179-1041A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222362 | ||||||
| chr5:146222438
|
C | T | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.179-965C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222438 | ||||||
| chr5:146222453
|
G | T | 3 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0151 | 3 | HG00408.hp2 HG02040.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.179-950G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222453 | ||||||
| chr5:146222584
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.179-819C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222584 | ||||||
| chr5:146222585
|
G | C | 3 | a0001c0001t0006g0131a0001c0001t0006g0136a0001c0001t0006g0137 | 3 | HG01243.hp2 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.179-818G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222585 | ||||||
| chr5:146222590
|
A | G | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.179-813A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222590 | ||||||
| chr5:146222857
|
A | T | 6 | a0001c0002t0009g0009a0001c0002t0009g0012a0001c0002t0009g0047others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.179-546A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222857 | ||||||
| chr5:146222936
|
T | A | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.179-467T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222936 | ||||||
| chr5:146222968
|
G | C | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.179-435G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146222968 | ||||||
| chr5:146223011
|
T | G | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.179-392T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146223011 | ||||||
| chr5:146223169
|
C | T | 12 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0029others(9): Show | 12 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.179-234C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146223169 | ||||||
| chr5:146223371
|
C | T | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.179-32C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 2/20 | chr5 | 146223371 | ||||||
| chr5:146223651
|
G | A | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.303+124G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223651 | ||||||
| chr5:146223716
|
T | G | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.303+189T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223716 | ||||||
| chr5:146223728
|
C | G | 8 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+201C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223728 | ||||||
| chr5:146223738
|
T | G | 1 | a0001c0001t0001g0148 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.303+211T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223738 | ||||||
| chr5:146223859
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.303+332T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223859 | ||||||
| chr5:146223976
|
T | A | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01167.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.303+449T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146223976 | ||||||
| chr5:146224040
|
A | G | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.303+513A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146224040 | ||||||
| chr5:146224354
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.303+827G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146224354 | ||||||
| chr5:146224498
|
A | G | 6 | a0001c0002t0003g0028a0001c0002t0003g0040a0001c0002t0003g0041others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.303+971A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146224498 | ||||||
| chr5:146224654
|
C | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.303+1127C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146224654 | ||||||
| chr5:146225072
|
G | A | 87 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(84): Show | 87 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.303+1545G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225072 | ||||||
| chr5:146225092
|
C | G | 1 | a0001c0001t0002g0203 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.303+1565C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225092 | ||||||
| chr5:146225199
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.303+1672C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225199 | ||||||
| chr5:146225567
|
G | GT | 14 | a0001c0001t0001g0111a0001c0001t0002g0257a0001c0002t0001g0048others(11): Show | 15 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.303+2057dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146225567 | |||||
| chr5:146225567
|
GT | G | 70 | a0001c0001t0001g0115a0001c0001t0001g0133a0001c0001t0002g0181others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.303+2057delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146225567 | |||||
| chr5:146225573
|
T | G | 2 | a0001c0002t0013g0011a0001c0002t0015g0010 | 2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.303+2046T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225573 | ||||||
| chr5:146225931
|
C | T | 55 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(52): Show | 56 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.303+2404C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146225931 | ||||||
| chr5:146226028
|
A | ATT | 74 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(71): Show | 74 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.303+2518_303+2519d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146226028 | |||||
| chr5:146226028
|
AT | A | 182 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(179): Show | 186 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.303+2519delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146226028 | |||||
| chr5:146226131
|
G | T | 18 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(15): Show | 18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.303+2604G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146226131 | ||||||
| chr5:146226159
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.303+2632C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146226159 | ||||||
| chr5:146226707
|
T | A | 81 | a0001c0001t0001g0111a0001c0001t0001g0117a0001c0001t0001g0140others(78): Show | 81 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.304-2239T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146226707 | ||||||
| chr5:146226787
|
C | G | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.304-2159C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146226787 | ||||||
| chr5:146227029
|
A | G | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-1917A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227029 | ||||||
| chr5:146227202
|
A | G | 3 | a0001c0002t0009g0012a0001c0002t0013g0011a0001c0002t0015g0010 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.304-1744A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227202 | ||||||
| chr5:146227429
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.304-1517A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227429 | ||||||
| chr5:146227692
|
T | G | 1 | a0001c0001t0002g0218 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.304-1254T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227692 | ||||||
| chr5:146227710
|
A | G | 18 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(15): Show | 18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-1236A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227710 | ||||||
| chr5:146227739
|
C | A | 87 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(84): Show | 87 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.304-1207C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227739 | ||||||
| chr5:146227898
|
C | G | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.304-1048C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227898 | ||||||
| chr5:146227909
|
C | G | 3 | a0001c0001t0001g0102a0001c0001t0008g0113a0001c0001t0023g0119 | 3 | HG01433.hp2 HG01943.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.304-1037C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227909 | ||||||
| chr5:146227971
|
A | T | 55 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(52): Show | 56 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.304-975A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227971 | ||||||
| chr5:146227975
|
A | G | 7 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.304-971A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146227975 | ||||||
| chr5:146228005
|
C | T | 34 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.304-941C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228005 | ||||||
| chr5:146228257
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.304-689A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228257 | ||||||
| chr5:146228278
|
C | CT | 6 | a0001c0001t0002g0207a0001c0001t0002g0253a0001c0002t0001g0266others(3): Show | 6 | HG02055.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.304-665dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146228278 | |||||
| chr5:146228280
|
TTC | T | 7 | a0001c0002t0001g0038a0001c0002t0003g0032a0001c0002t0003g0033others(4): Show | 7 | HG01243.hp1 HG01255.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-664_304-663del others(2): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146228280 | |||||
| chr5:146228281
|
TC | T | 39 | a0001c0001t0002g0194a0001c0001t0020g0267a0001c0002t0001g0048others(36): Show | 40 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.304-664delC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228281 | ||||||
| chr5:146228282
|
C | T | 96 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(93): Show | 96 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(93): Show |
intron_variant | MODIFIER | c.304-664C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228282 | ||||||
| chr5:146228316
|
G | A | 1 | a0001c0002t0003g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.304-630G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228316 | ||||||
| chr5:146228364
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.304-582C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228364 | ||||||
| chr5:146228368
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.304-578G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228368 | ||||||
| chr5:146228465
|
C | T | 1 | a0001c0002t0003g0029 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.304-481C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228465 | ||||||
| chr5:146228468
|
G | A | 6 | a0001c0002t0009g0009a0001c0002t0009g0012a0001c0002t0009g0047others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-478G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228468 | ||||||
| chr5:146228606
|
TTTTG | T | 3 | a0001c0002t0012g0005a0001c0002t0026g0030a0003c0005t0012g0046 | 3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.304-332_304-329del others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr5 | 146228606 | |||||
| chr5:146228625
|
A | G | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.304-321A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228625 | ||||||
| chr5:146228732
|
C | G | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.304-214C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228732 | ||||||
| chr5:146228748
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.304-198G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228748 | ||||||
| chr5:146228761
|
T | A | 1 | a0001c0001t0001g0143 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.304-185T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228761 | ||||||
| chr5:146228771
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.304-175A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 3/20 | chr5 | 146228771 | ||||||
| chr5:146229124
|
T | C | 1 | a0001c0001t0006g0084 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.395+87T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 4/20 | chr5 | 146229124 | ||||||
| chr5:146229263
|
G | T | 11 | a0001c0001t0001g0102a0001c0001t0001g0163a0001c0001t0001g0165others(8): Show | 11 | HG00741.hp2 HG01069.hp2 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.395+226G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 4/20 | chr5 | 146229263 | ||||||
| chr5:146229977
|
G | A | 12 | a0001c0002t0004g0017a0001c0002t0004g0021a0001c0002t0004g0022others(9): Show | 12 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.589+67G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 5/20 | chr5 | 146229977 | ||||||
| chr5:146230622
|
CTTTGTTT others(7): Show |
C | 3 | a0001c0002t0004g0016a0001c0002t0004g0019a0002c0004t0004g0020 | 3 | HG00140.hp2 HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.590-32_590-19delTG others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr5 | 146230622 | |||||
| chr5:146231138
|
C | T | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.850+221C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146231138 | ||||||
| chr5:146231356
|
C | T | 14 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0075others(11): Show | 14 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.850+439C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146231356 | ||||||
| chr5:146231510
|
A | AT | 8 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.850+601dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr5 | 146231510 | |||||
| chr5:146231763
|
G | A | 17 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG01978.hp2 HG02132.hp2 HG02976.hp2 others(14): Show |
intron_variant | MODIFIER | c.850+846G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146231763 | ||||||
| chr5:146232016
|
T | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.850+1099T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232016 | ||||||
| chr5:146232141
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.850+1224G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232141 | ||||||
| chr5:146232247
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.851-1203A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232247 | ||||||
| chr5:146232360
|
A | G | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.851-1090A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232360 | ||||||
| chr5:146232526
|
T | G | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.851-924T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232526 | ||||||
| chr5:146232701
|
T | G | 87 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(84): Show | 87 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.851-749T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232701 | ||||||
| chr5:146232714
|
G | A | 5 | a0001c0001t0002g0187a0001c0001t0002g0196a0001c0001t0002g0202others(2): Show | 5 | HG02074.hp2 NA18949.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.851-736G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232714 | ||||||
| chr5:146232939
|
A | G | 1 | a0001c0001t0001g0161 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.851-511A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146232939 | ||||||
| chr5:146233109
|
C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.851-341C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146233109 | ||||||
| chr5:146233130
|
A | G | 1 | a0001c0002t0001g0266 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.851-320A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146233130 | ||||||
| chr5:146233167
|
C | T | 6 | a0001c0002t0001g0038a0001c0002t0003g0032a0001c0002t0003g0033others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.851-283C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146233167 | ||||||
| chr5:146233259
|
A | G | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.851-191A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 6/20 | chr5 | 146233259 | ||||||
| chr5:146233961
|
C | G | 7 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1144+218C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146233961 | ||||||
| chr5:146234123
|
G | A | 6 | a0001c0001t0002g0187a0001c0001t0002g0196a0001c0001t0002g0197others(3): Show | 6 | HG02074.hp2 NA18949.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144+380G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234123 | ||||||
| chr5:146234280
|
T | A | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1144+537T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234280 | ||||||
| chr5:146234472
|
T | C | 4 | a0001c0001t0002g0196a0001c0001t0002g0202a0001c0001t0002g0203others(1): Show | 4 | HG02074.hp2 NA18949.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.1144+729T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234472 | ||||||
| chr5:146234519
|
T | TA | 265 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0055others(262): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1144+787dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146234519 | |||||
| chr5:146234631
|
G | T | 6 | a0001c0002t0003g0028a0001c0002t0003g0040a0001c0002t0003g0041others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1144+888G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234631 | ||||||
| chr5:146234813
|
C | G | 2 | a0001c0002t0003g0027a0001c0002t0003g0029 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1144+1070C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234813 | ||||||
| chr5:146234854
|
C | T | 1 | a0001c0001t0001g0121 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1144+1111C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146234854 | ||||||
| chr5:146235033
|
A | AAAAT | 19 | a0001c0001t0001g0074a0001c0001t0001g0094a0001c0001t0001g0098others(16): Show | 19 | HG01167.hp1 HG01361.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.1144+1330_1144+133 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | |||||
| chr5:146235033
|
A | AAAATAAA others(1): Show |
81 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0061others(78): Show | 83 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1144+1326_1144+133 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | |||||
| chr5:146235033
|
A | AAAATAAA others(5): Show |
43 | a0001c0001t0001g0004a0001c0001t0001g0055a0001c0001t0001g0069others(40): Show | 44 | HG00140.hp2 HG00621.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1144+1322_1144+133 others(16): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | |||||
| chr5:146235033
|
A | AAAATAAA others(9): Show |
7 | a0001c0001t0001g0091a0001c0001t0001g0108a0001c0001t0001g0157others(4): Show | 7 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1144+1318_1144+133 others(20): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | |||||
| chr5:146235033
|
AAAAT | A | 36 | a0001c0001t0001g0115a0001c0001t0002g0185a0001c0001t0002g0192others(33): Show | 37 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.1144+1330_1144+133 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | |||||
| chr5:146235033
|
AAAATAAA others(1): Show |
A | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1144+1326_1144+133 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235033 | |||||
| chr5:146235077
|
A | T | 5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0002t0004g0016others(2): Show | 5 | HG00140.hp2 HG01257.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1144+1334A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235077 | ||||||
| chr5:146235637
|
C | T | 2 | a0001c0001t0001g0091a0001c0001t0001g0108 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1145-1661C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235637 | ||||||
| chr5:146235655
|
T | TA | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1145-1641dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146235655 | |||||
| chr5:146235712
|
C | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1145-1586C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235712 | ||||||
| chr5:146235884
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1145-1414G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235884 | ||||||
| chr5:146235922
|
C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1145-1376C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146235922 | ||||||
| chr5:146236138
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1145-1160A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236138 | ||||||
| chr5:146236139
|
A | T | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1145-1159A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236139 | ||||||
| chr5:146236140
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1145-1158G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236140 | ||||||
| chr5:146236493
|
G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1145-805G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236493 | ||||||
| chr5:146236930
|
C | CT | 13 | a0001c0001t0002g0184a0001c0001t0002g0186a0001c0001t0002g0195others(10): Show | 13 | HG01884.hp2 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1145-344dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146236930 | |||||
| chr5:146236930
|
CT | C | 122 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(119): Show | 125 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1145-344delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr5 | 146236930 | |||||
| chr5:146236932
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1145-366T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236932 | ||||||
| chr5:146236945
|
T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1145-353T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236945 | ||||||
| chr5:146236954
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1145-344T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146236954 | ||||||
| chr5:146237024
|
C | T | 6 | a0001c0002t0001g0038a0001c0002t0003g0032a0001c0002t0003g0033others(3): Show | 6 | HG01243.hp1 HG01884.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.1145-274C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146237024 | ||||||
| chr5:146237130
|
G | T | 1 | a0001c0001t0001g0086 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1145-168G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146237130 | ||||||
| chr5:146237220
|
G | T | 1 | a0001c0001t0001g0103 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1145-78G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 7/20 | chr5 | 146237220 | ||||||
| chr5:146237591
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1279+159A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146237591 | ||||||
| chr5:146238041
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0086 | 2 | HG02257.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.1279+609G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238041 | ||||||
| chr5:146238081
|
T | C | 3 | a0001c0001t0006g0003a0001c0001t0006g0084a0001c0001t0006g0128 | 4 | HG02109.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+649T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238081 | ||||||
| chr5:146238144
|
G | A | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1279+712G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238144 | ||||||
| chr5:146238306
|
C | A | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+874C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238306 | ||||||
| chr5:146238337
|
C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+905C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238337 | ||||||
| chr5:146238534
|
C | T | 3 | a0001c0001t0006g0003a0001c0001t0006g0084a0001c0001t0006g0128 | 4 | HG02109.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+1102C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238534 | ||||||
| chr5:146238569
|
T | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1279+1137T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146238569 | ||||||
| chr5:146238657
|
A | AT | 5 | a0001c0001t0001g0126a0001c0001t0001g0174a0001c0002t0004g0016others(2): Show | 5 | HG02717.hp2 HG02738.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+1242dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146238657 | |||||
| chr5:146238657
|
AT | A | 93 | a0001c0001t0001g0092a0001c0001t0002g0181a0001c0001t0002g0182others(90): Show | 94 | HG00140.hp1 HG00438.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.1279+1242delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146238657 | |||||
| chr5:146239248
|
C | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1279+1816C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239248 | ||||||
| chr5:146239344
|
A | G | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279+1912A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239344 | ||||||
| chr5:146239467
|
C | CTTTTTT | 30 | a0001c0001t0020g0267a0001c0002t0001g0048a0001c0002t0001g0049others(27): Show | 31 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1279+2039_1279+204 others(10): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239467 | |||||
| chr5:146239467
|
CTTTTCT | C | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1279+2040_1279+204 others(10): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239467 | |||||
| chr5:146239470
|
T | TTTTTTTT others(1): Show |
7 | a0001c0002t0001g0263a0001c0002t0001g0266a0001c0002t0003g0027others(4): Show | 7 | HG02055.hp1 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1279+2039_1279+204 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239470 | |||||
| chr5:146239471
|
T | TTTTTTTC | 25 | a0001c0002t0001g0038a0001c0002t0001g0260a0001c0002t0001g0261others(22): Show | 25 | HG00140.hp2 HG01167.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1279+2039_1279+204 others(11): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239471 | ||||||
| chr5:146239472
|
C | CT | 6 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0165others(3): Show | 6 | HG01978.hp2 HG02145.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1279+2063dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239472 | |||||
| chr5:146239472
|
C | T | 34 | a0001c0002t0001g0038a0001c0002t0001g0260a0001c0002t0001g0261others(31): Show | 34 | HG00140.hp2 HG01167.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.1279+2040C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239472 | ||||||
| chr5:146239478
|
T | C | 1 | a0001c0002t0021g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1279+2046T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239478 | ||||||
| chr5:146239484
|
T | C | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1279+2052T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239484 | ||||||
| chr5:146239620
|
G | C | 13 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279+2188G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239620 | ||||||
| chr5:146239746
|
G | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+2314G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239746 | ||||||
| chr5:146239775
|
CT | C | 81 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(78): Show | 81 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1279+2362delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146239775 | |||||
| chr5:146239874
|
C | T | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+2442C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239874 | ||||||
| chr5:146239884
|
C | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1279+2452C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146239884 | ||||||
| chr5:146240164
|
A | T | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1279+2732A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240164 | ||||||
| chr5:146240182
|
C | T | 1 | a0001c0001t0001g0088 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279+2750C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240182 | ||||||
| chr5:146240290
|
T | TTCTG | 43 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0184others(40): Show | 43 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.1279+2861_1279+286 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240290 | |||||
| chr5:146240290
|
T | TTCTGTCT others(1): Show |
17 | a0001c0001t0002g0187a0001c0001t0002g0197a0001c0001t0002g0200others(14): Show | 17 | HG02027.hp1 HG02040.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.1279+2861_1279+286 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240290 | |||||
| chr5:146240290
|
T | TTCTGTCT others(5): Show |
1 | a0001c0001t0002g0254 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1279+2861_1279+286 others(16): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240290 | |||||
| chr5:146240290
|
TTCTA | T | 3 | a0001c0001t0002g0215a0001c0001t0002g0229a0001c0001t0002g0239 | 3 | HG00642.hp2 HG01192.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1279+2862_1279+286 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240290 | |||||
| chr5:146240294
|
A | ATCTG | 12 | a0001c0001t0001g0160a0001c0001t0001g0170a0001c0001t0001g0177others(9): Show | 13 | HG00140.hp2 HG00741.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1279+2898_1279+290 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240294 | |||||
| chr5:146240294
|
A | G | 75 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(72): Show | 75 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1279+2862A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240294 | ||||||
| chr5:146240294
|
ATCTG | A | 39 | a0001c0001t0001g0103a0001c0001t0001g0156a0001c0001t0006g0131others(36): Show | 40 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.1279+2898_1279+290 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240294 | |||||
| chr5:146240294
|
ATCTGTCT others(1): Show |
A | 5 | a0001c0001t0006g0137a0001c0002t0004g0057a0001c0002t0004g0058others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279+2894_1279+290 others(12): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146240294 | |||||
| chr5:146240378
|
G | A | 1 | a0001c0001t0007g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1279+2946G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240378 | ||||||
| chr5:146240408
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1279+2976C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240408 | ||||||
| chr5:146240489
|
G | A | 2 | a0001c0002t0001g0262a0001c0002t0001g0263 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1279+3057G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240489 | ||||||
| chr5:146240497
|
T | C | 12 | a0001c0002t0004g0017a0001c0002t0004g0021a0001c0002t0004g0022others(9): Show | 12 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279+3065T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240497 | ||||||
| chr5:146240527
|
A | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1279+3095A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240527 | ||||||
| chr5:146240603
|
G | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1279+3171G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240603 | ||||||
| chr5:146240880
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1279+3448G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240880 | ||||||
| chr5:146240953
|
T | C | 31 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(28): Show | 32 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.1279+3521T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146240953 | ||||||
| chr5:146241164
|
TA | T | 63 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1279+3740delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146241164 | |||||
| chr5:146241176
|
G | A | 1 | a0001c0002t0004g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1279+3744G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241176 | ||||||
| chr5:146241236
|
T | A | 6 | a0001c0002t0009g0009a0001c0002t0009g0012a0001c0002t0009g0047others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279+3804T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241236 | ||||||
| chr5:146241507
|
A | C | 1 | a0001c0001t0029g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1279+4075A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241507 | ||||||
| chr5:146241508
|
G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+4076G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241508 | ||||||
| chr5:146241530
|
A | G | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1279+4098A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241530 | ||||||
| chr5:146241616
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1279+4184G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241616 | ||||||
| chr5:146241655
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1279+4223C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146241655 | ||||||
| chr5:146242135
|
G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+4703G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242135 | ||||||
| chr5:146242224
|
C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+4792C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242224 | ||||||
| chr5:146242490
|
G | C | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1279+5058G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242490 | ||||||
| chr5:146242501
|
C | G | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279+5069C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242501 | ||||||
| chr5:146242657
|
G | T | 1 | a0001c0001t0001g0176 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1279+5225G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242657 | ||||||
| chr5:146242679
|
C | T | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1279+5247C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242679 | ||||||
| chr5:146242720
|
A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+5288A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242720 | ||||||
| chr5:146242755
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1279+5323G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242755 | ||||||
| chr5:146242799
|
T | C | 1 | a0001c0001t0002g0250 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1279+5367T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242799 | ||||||
| chr5:146242874
|
A | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1279+5442A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242874 | ||||||
| chr5:146242890
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279+5458T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242890 | ||||||
| chr5:146242909
|
T | C | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1279+5477T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146242909 | ||||||
| chr5:146243040
|
C | T | 1 | a0001c0002t0016g0265 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1279+5608C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243040 | ||||||
| chr5:146243170
|
G | A | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279+5738G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243170 | ||||||
| chr5:146243262
|
A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+5830A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243262 | ||||||
| chr5:146243458
|
T | C | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1279+6026T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243458 | ||||||
| chr5:146243511
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1279+6079A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243511 | ||||||
| chr5:146243524
|
A | T | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1279+6092A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243524 | ||||||
| chr5:146243658
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1279+6226A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243658 | ||||||
| chr5:146243721
|
T | G | 1 | a0001c0001t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1279+6289T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243721 | ||||||
| chr5:146243846
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1279+6414T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243846 | ||||||
| chr5:146243852
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1279+6420C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243852 | ||||||
| chr5:146243902
|
T | C | 1 | a0001c0002t0024g0264 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1279+6470T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146243902 | ||||||
| chr5:146244083
|
A | G | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1279+6651A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244083 | ||||||
| chr5:146244335
|
G | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1279+6903G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244335 | ||||||
| chr5:146244401
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1279+6969T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244401 | ||||||
| chr5:146244640
|
G | T | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1280-7071G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244640 | ||||||
| chr5:146244798
|
C | T | 1 | a0001c0001t0002g0183 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1280-6913C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244798 | ||||||
| chr5:146244838
|
A | T | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1280-6873A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244838 | ||||||
| chr5:146244909
|
T | C | 9 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0029others(6): Show | 9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1280-6802T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146244909 | ||||||
| chr5:146245109
|
C | G | 2 | a0001c0002t0001g0266a0001c0002t0016g0265 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1280-6602C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146245109 | ||||||
| chr5:146245409
|
C | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1280-6302C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146245409 | ||||||
| chr5:146245420
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0108 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1280-6291A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146245420 | ||||||
| chr5:146245924
|
G | C | 2 | a0001c0002t0009g0009a0001c0002t0014g0006 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1280-5787G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146245924 | ||||||
| chr5:146246073
|
CTGTT | C | 7 | a0001c0002t0001g0038a0001c0002t0003g0032a0001c0002t0003g0033others(4): Show | 7 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-5635_1280-563 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146246073 | |||||
| chr5:146246153
|
A | G | 267 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1280-5558A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246153 | ||||||
| chr5:146246159
|
A | G | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1280-5552A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246159 | ||||||
| chr5:146246239
|
T | C | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1280-5472T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246239 | ||||||
| chr5:146246249
|
T | G | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280-5462T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246249 | ||||||
| chr5:146246313
|
A | C | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1280-5398A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246313 | ||||||
| chr5:146246369
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1280-5342G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246369 | ||||||
| chr5:146246749
|
G | T | 3 | a0001c0001t0001g0158a0001c0001t0001g0172a0001c0001t0032g0152 | 3 | NA18949.hp1 NA19063.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.1280-4962G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246749 | ||||||
| chr5:146246775
|
G | A | 7 | a0001c0002t0004g0017a0001c0002t0004g0021a0001c0002t0004g0022others(4): Show | 7 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-4936G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246775 | ||||||
| chr5:146246864
|
G | GT | 11 | a0001c0001t0001g0079a0001c0001t0002g0210a0001c0001t0002g0215others(8): Show | 11 | HG01167.hp1 HG01192.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1280-4829dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146246864 | |||||
| chr5:146246864
|
G | T | 1 | a0001c0001t0001g0177 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1280-4847G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246864 | ||||||
| chr5:146246864
|
GT | G | 7 | a0001c0001t0002g0187a0001c0001t0002g0196a0001c0001t0002g0197others(4): Show | 7 | HG01257.hp1 HG02074.hp2 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.1280-4829delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146246864 | |||||
| chr5:146246967
|
A | G | 3 | a0001c0001t0007g0066a0001c0001t0007g0067a0001c0001t0007g0070 | 3 | NA18747.hp2 NA18942.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1280-4744A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146246967 | ||||||
| chr5:146247011
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1280-4700G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247011 | ||||||
| chr5:146247077
|
T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1280-4634T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247077 | ||||||
| chr5:146247250
|
T | G | 1 | a0001c0001t0002g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1280-4461T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247250 | ||||||
| chr5:146247377
|
C | G | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1280-4334C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247377 | ||||||
| chr5:146247379
|
T | C | 63 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1280-4332T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247379 | ||||||
| chr5:146247548
|
G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1280-4163G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247548 | ||||||
| chr5:146247739
|
C | T | 1 | a0001c0001t0029g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1280-3972C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247739 | ||||||
| chr5:146247819
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1280-3892T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247819 | ||||||
| chr5:146247943
|
A | G | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1280-3768A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146247943 | ||||||
| chr5:146248132
|
A | G | 34 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1280-3579A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248132 | ||||||
| chr5:146248190
|
C | G | 7 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0158others(4): Show | 7 | HG01257.hp2 HG01981.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-3521C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248190 | ||||||
| chr5:146248210
|
G | A | 2 | a0001c0001t0002g0226a0001c0001t0002g0228 | 2 | HG00741.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1280-3501G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248210 | ||||||
| chr5:146248234
|
G | GT | 130 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(127): Show | 131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1280-3460dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146248234 | |||||
| chr5:146248238
|
T | TG | 7 | a0001c0002t0001g0038a0001c0002t0003g0032a0001c0002t0003g0033others(4): Show | 7 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1280-3473_1280-347 others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248238 | ||||||
| chr5:146248359
|
G | A | 2 | a0001c0002t0001g0262a0001c0002t0001g0263 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1280-3352G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248359 | ||||||
| chr5:146248520
|
C | T | 3 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | NA18944.hp2 NA18954.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1280-3191C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248520 | ||||||
| chr5:146248535
|
G | A | 1 | a0001c0002t0001g0263 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1280-3176G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248535 | ||||||
| chr5:146248668
|
A | G | 2 | a0001c0002t0001g0262a0001c0002t0001g0263 | 2 | NA18906.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1280-3043A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248668 | ||||||
| chr5:146248743
|
G | A | 3 | a0001c0002t0012g0005a0001c0002t0026g0030a0003c0005t0012g0046 | 3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1280-2968G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248743 | ||||||
| chr5:146248801
|
G | T | 2 | a0001c0002t0003g0027a0001c0002t0003g0029 | 2 | HG03471.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1280-2910G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146248801 | ||||||
| chr5:146248867
|
CTTAA | C | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1280-2840_1280-283 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146248867 | |||||
| chr5:146249130
|
C | T | 2 | a0001c0002t0001g0038a0001c0002t0003g0033 | 2 | HG01243.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1280-2581C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249130 | ||||||
| chr5:146249184
|
T | C | 3 | a0001c0002t0005g0013a0001c0002t0005g0014a0001c0002t0005g0015 | 3 | HG02976.hp1 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1280-2527T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249184 | ||||||
| chr5:146249204
|
A | G | 18 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(15): Show | 18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1280-2507A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249204 | ||||||
| chr5:146249231
|
C | A | 1 | a0001c0001t0002g0191 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1280-2480C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249231 | ||||||
| chr5:146249460
|
T | C | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1280-2251T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249460 | ||||||
| chr5:146249515
|
G | A | 1 | a0001c0001t0002g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1280-2196G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249515 | ||||||
| chr5:146249547
|
C | T | 1 | a0001c0002t0015g0010 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1280-2164C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249547 | ||||||
| chr5:146249574
|
C | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0108 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1280-2137C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249574 | ||||||
| chr5:146249633
|
G | A | 1 | a0001c0001t0007g0070 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1280-2078G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249633 | ||||||
| chr5:146249683
|
C | CA | 21 | a0001c0001t0002g0187a0001c0001t0002g0196a0001c0001t0002g0202others(18): Show | 21 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1280-2010dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146249683 | |||||
| chr5:146249709
|
T | TA | 82 | a0001c0001t0001g0118a0001c0001t0001g0174a0001c0001t0002g0181others(79): Show | 82 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1280-1992dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146249709 | |||||
| chr5:146249822
|
G | T | 1 | a0001c0001t0001g0163 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1280-1889G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249822 | ||||||
| chr5:146249926
|
T | G | 1 | a0001c0001t0002g0199 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1280-1785T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146249926 | ||||||
| chr5:146250004
|
T | A | 1 | a0001c0002t0001g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1280-1707T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250004 | ||||||
| chr5:146250040
|
C | T | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1280-1671C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250040 | ||||||
| chr5:146250041
|
C | T | 266 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1280-1670C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250041 | ||||||
| chr5:146250257
|
G | A | 56 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(53): Show | 57 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1280-1454G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250257 | ||||||
| chr5:146250324
|
C | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1280-1387C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250324 | ||||||
| chr5:146250431
|
C | CA | 116 | a0001c0001t0001g0055a0001c0001t0001g0073a0001c0001t0001g0091others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.1280-1262dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250431 | |||||
| chr5:146250431
|
C | CAA | 22 | a0001c0001t0002g0193a0001c0001t0002g0196a0001c0001t0002g0204others(19): Show | 22 | HG00438.hp2 HG00741.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1280-1263_1280-126 others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250431 | |||||
| chr5:146250757
|
T | G | 9 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0029others(6): Show | 9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1280-954T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146250757 | ||||||
| chr5:146250770
|
C | CT | 43 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0106others(40): Show | 43 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(40): Show |
intron_variant | MODIFIER | c.1280-917dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250770 | |||||
| chr5:146250770
|
C | CTT | 6 | a0001c0001t0006g0131a0001c0001t0007g0070a0001c0002t0001g0266others(3): Show | 6 | HG02055.hp1 HG02145.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1280-918_1280-917d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250770 | |||||
| chr5:146250770
|
CT | C | 93 | a0001c0001t0001g0055a0001c0001t0001g0075a0001c0001t0001g0087others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.1280-917delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250770 | |||||
| chr5:146250770
|
CTT | C | 6 | a0001c0002t0001g0038a0001c0002t0003g0032a0001c0002t0003g0033others(3): Show | 6 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1280-918_1280-917d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146250770 | |||||
| chr5:146251053
|
GCGTGAGC others(2): Show |
G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1280-647_1280-639d others(11): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr5 | 146251053 | |||||
| chr5:146251129
|
G | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1280-582G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251129 | ||||||
| chr5:146251174
|
T | C | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1280-537T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251174 | ||||||
| chr5:146251352
|
G | T | 10 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(7): Show | 10 | NA18942.hp2 NA18951.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1280-359G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251352 | ||||||
| chr5:146251481
|
T | C | 1 | a0001c0002t0003g0041 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1280-230T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251481 | ||||||
| chr5:146251489
|
C | T | 3 | a0001c0001t0002g0194a0001c0001t0002g0206a0001c0001t0002g0213 | 3 | NA18952.hp1 NA18960.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1280-222C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251489 | ||||||
| chr5:146251592
|
T | G | 1 | a0001c0001t0029g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1280-119T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 8/20 | chr5 | 146251592 | ||||||
| chr5:146252092
|
A | G | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1444+217A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252092 | ||||||
| chr5:146252149
|
T | C | 1 | a0001c0001t0001g0153 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1444+274T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252149 | ||||||
| chr5:146252252
|
C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1444+377C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252252 | ||||||
| chr5:146252348
|
C | T | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1444+473C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252348 | ||||||
| chr5:146252793
|
C | G | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1444+918C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146252793 | ||||||
| chr5:146253102
|
A | G | 1 | a0001c0002t0009g0009 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1444+1227A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253102 | ||||||
| chr5:146253287
|
C | T | 9 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0029others(6): Show | 9 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1444+1412C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253287 | ||||||
| chr5:146253291
|
C | T | 1 | a0001c0002t0021g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1444+1416C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253291 | ||||||
| chr5:146253354
|
G | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1444+1479G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253354 | ||||||
| chr5:146253422
|
T | C | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1445-1521T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253422 | ||||||
| chr5:146253735
|
G | A | 4 | a0001c0002t0004g0057a0001c0002t0004g0058a0001c0002t0004g0059others(1): Show | 4 | HG02257.hp2 HG02280.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1445-1208G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253735 | ||||||
| chr5:146253811
|
T | C | 1 | a0001c0001t0002g0244 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1445-1132T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253811 | ||||||
| chr5:146253911
|
T | C | 12 | a0001c0002t0004g0017a0001c0002t0004g0021a0001c0002t0004g0022others(9): Show | 12 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1445-1032T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146253911 | ||||||
| chr5:146254041
|
T | A | 2 | a0001c0002t0001g0266a0001c0002t0016g0265 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1445-902T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254041 | ||||||
| chr5:146254143
|
G | T | 3 | a0001c0001t0006g0131a0001c0001t0006g0136a0001c0001t0006g0137 | 3 | HG01243.hp2 HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1445-800G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254143 | ||||||
| chr5:146254160
|
C | CAAAT | 6 | a0001c0002t0003g0028a0001c0002t0003g0040a0001c0002t0003g0041others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1445-782_1445-779d others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 146254160 | |||||
| chr5:146254431
|
AT | A | 90 | a0001c0001t0001g0099a0001c0001t0002g0181a0001c0001t0002g0182others(87): Show | 90 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1445-499delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 146254431 | |||||
| chr5:146254544
|
A | G | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1445-399A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254544 | ||||||
| chr5:146254556
|
GA | G | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1445-380delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr5 | 146254556 | |||||
| chr5:146254561
|
A | T | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1445-382A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254561 | ||||||
| chr5:146254579
|
A | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1445-364A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254579 | ||||||
| chr5:146254639
|
C | T | 1 | a0001c0002t0003g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1445-304C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254639 | ||||||
| chr5:146254659
|
T | G | 1 | a0001c0002t0005g0013 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1445-284T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254659 | ||||||
| chr5:146254723
|
C | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1445-220C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254723 | ||||||
| chr5:146254732
|
G | A | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1445-211G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254732 | ||||||
| chr5:146254741
|
C | A | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1445-202C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254741 | ||||||
| chr5:146254757
|
T | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1445-186T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 9/20 | chr5 | 146254757 | ||||||
| chr5:146255588
|
C | G | 29 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(26): Show | 30 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.1594+496C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255588 | ||||||
| chr5:146255657
|
C | A | 1 | a0001c0001t0017g0214 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+565C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255657 | ||||||
| chr5:146255660
|
C | G | 1 | a0001c0001t0017g0214 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+568C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255660 | ||||||
| chr5:146255665
|
C | G | 1 | a0001c0001t0017g0214 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+573C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255665 | ||||||
| chr5:146255666
|
C | A | 1 | a0001c0001t0017g0214 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+574C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255666 | ||||||
| chr5:146255667
|
A | T | 1 | a0001c0001t0017g0214 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+575A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255667 | ||||||
| chr5:146255668
|
C | G | 1 | a0001c0001t0017g0214 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+576C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255668 | ||||||
| chr5:146255670
|
A | T | 1 | a0001c0001t0017g0214 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1594+578A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255670 | ||||||
| chr5:146255710
|
G | GT | 4 | a0001c0001t0001g0098a0001c0001t0001g0114a0001c0001t0001g0126others(1): Show | 4 | HG02132.hp2 NA18954.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1594+625dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr5 | 146255710 | |||||
| chr5:146255852
|
C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1594+760C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146255852 | ||||||
| chr5:146256056
|
A | G | 34 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(31): Show | 34 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.1594+964A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256056 | ||||||
| chr5:146256103
|
A | G | 1 | a0001c0002t0004g0056 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1594+1011A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256103 | ||||||
| chr5:146256336
|
T | A | 1 | a0001c0001t0007g0068 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1594+1244T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256336 | ||||||
| chr5:146256357
|
A | G | 1 | a0001c0001t0002g0186 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1594+1265A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256357 | ||||||
| chr5:146256418
|
C | T | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1594+1326C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256418 | ||||||
| chr5:146256539
|
C | T | 1 | a0001c0002t0005g0015 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1594+1447C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256539 | ||||||
| chr5:146256872
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1595-1577A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146256872 | ||||||
| chr5:146257090
|
C | T | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1595-1359C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257090 | ||||||
| chr5:146257108
|
T | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1595-1341T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257108 | ||||||
| chr5:146257433
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1595-1016A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257433 | ||||||
| chr5:146257489
|
A | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1595-960A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257489 | ||||||
| chr5:146257506
|
C | T | 124 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(121): Show | 127 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1595-943C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146257506 | ||||||
| chr5:146257810
|
G | GT | 22 | a0001c0001t0001g0160a0001c0001t0002g0184a0001c0001t0002g0209others(19): Show | 23 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1595-627dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr5 | 146257810 | |||||
| chr5:146258445
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG01346.hp1 | splice_region_variant&intron_variant | LOW | c.1595-4A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 10/20 | chr5 | 146258445 | ||||||
| chr5:146258652
|
T | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1739+59T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146258652 | ||||||
| chr5:146258768
|
AT | A | 5 | a0001c0001t0001g0069a0001c0001t0002g0194a0001c0001t0002g0206others(2): Show | 5 | HG02273.hp1 NA18952.hp1 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1739+191delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146258768 | |||||
| chr5:146258768
|
ATT | A | 24 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(21): Show | 24 | HG01167.hp1 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.1739+190_1739+191d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146258768 | |||||
| chr5:146258792
|
G | A | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1739+199G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146258792 | ||||||
| chr5:146259077
|
A | C | 25 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0061others(22): Show | 25 | HG01361.hp1 HG01433.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.1739+484A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259077 | ||||||
| chr5:146259303
|
G | A | 3 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG00639.hp1 HG03491.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1739+710G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259303 | ||||||
| chr5:146259336
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1739+743A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259336 | ||||||
| chr5:146259504
|
C | CA | 19 | a0001c0001t0001g0124a0001c0001t0001g0143a0001c0001t0001g0147others(16): Show | 19 | HG01099.hp2 HG01891.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.1739+934dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259504 | |||||
| chr5:146259504
|
CA | C | 59 | a0001c0001t0001g0062a0001c0001t0001g0078a0001c0001t0001g0099others(56): Show | 59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1739+934delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259504 | |||||
| chr5:146259504
|
CAAAA | C | 7 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1739+931_1739+934d others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259504 | |||||
| chr5:146259528
|
G | T | 1 | a0001c0001t0002g0220 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1739+935G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259528 | ||||||
| chr5:146259546
|
A | G | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1739+953A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259546 | ||||||
| chr5:146259740
|
A | G | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1740-1005A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259740 | ||||||
| chr5:146259778
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1740-967C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259778 | ||||||
| chr5:146259803
|
G | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1740-942G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259803 | ||||||
| chr5:146259836
|
A | G | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1740-909A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259836 | ||||||
| chr5:146259895
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1740-850C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259895 | ||||||
| chr5:146259949
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1740-796C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259949 | ||||||
| chr5:146259974
|
C | T | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1740-771C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146259974 | ||||||
| chr5:146259979
|
C | CA | 46 | a0001c0001t0001g0055a0001c0001t0001g0069a0001c0001t0001g0073others(43): Show | 46 | HG00438.hp1 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.1740-738dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | |||||
| chr5:146259979
|
C | CAA | 29 | a0001c0001t0001g0054a0001c0001t0001g0107a0001c0001t0001g0111others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.1740-739_1740-738d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | |||||
| chr5:146259979
|
C | CAAA | 18 | a0001c0002t0001g0048a0001c0002t0001g0050a0001c0002t0001g0263others(15): Show | 18 | HG01255.hp2 HG02109.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1740-740_1740-738d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | |||||
| chr5:146259979
|
C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0100 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1740-752_1740-738d others(17): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | |||||
| chr5:146259979
|
CAAAA | C | 7 | a0001c0001t0002g0193a0001c0001t0002g0203a0001c0001t0002g0220others(4): Show | 7 | HG00741.hp1 HG01346.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.1740-741_1740-738d others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | |||||
| chr5:146259979
|
CAAAAA | C | 70 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(67): Show | 70 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.1740-742_1740-738d others(7): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146259979 | |||||
| chr5:146260083
|
G | A | 18 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(15): Show | 18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1740-662G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260083 | ||||||
| chr5:146260086
|
G | A | 14 | a0001c0001t0002g0193a0001c0001t0002g0204a0001c0001t0002g0205others(11): Show | 14 | HG00438.hp2 HG02040.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.1740-659G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260086 | ||||||
| chr5:146260115
|
A | T | 2 | a0001c0002t0001g0266a0001c0002t0016g0265 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1740-630A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260115 | ||||||
| chr5:146260268
|
C | A | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1740-477C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260268 | ||||||
| chr5:146260293
|
C | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1740-452C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260293 | ||||||
| chr5:146260309
|
AAAG | A | 28 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(25): Show | 29 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1740-430_1740-428d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr5 | 146260309 | |||||
| chr5:146260424
|
A | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1740-321A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260424 | ||||||
| chr5:146260535
|
T | A | 15 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(12): Show | 15 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1740-210T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260535 | ||||||
| chr5:146260652
|
A | G | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1740-93A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260652 | ||||||
| chr5:146260719
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1740-26C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 11/20 | chr5 | 146260719 | ||||||
| chr5:146261120
|
A | G | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1893+222A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261120 | ||||||
| chr5:146261221
|
G | A | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1894-289G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261221 | ||||||
| chr5:146261246
|
G | A | 14 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(11): Show | 15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1894-264G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261246 | ||||||
| chr5:146261270
|
G | A | 1 | a0001c0002t0021g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1894-240G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261270 | ||||||
| chr5:146261294
|
C | T | 7 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1894-216C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261294 | ||||||
| chr5:146261493
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1894-17G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 12/20 | chr5 | 146261493 | ||||||
| chr5:146261936
|
A | T | 1 | a0001c0001t0001g0061 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2190+130A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146261936 | ||||||
| chr5:146262170
|
C | A | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2190+364C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262170 | ||||||
| chr5:146262292
|
T | TTTG | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2190+488_2190+489i others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr5 | 146262292 | |||||
| chr5:146262444
|
T | C | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2190+638T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262444 | ||||||
| chr5:146262445
|
G | A | 1 | a0001c0001t0002g0231 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2190+639G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262445 | ||||||
| chr5:146262544
|
C | T | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2190+738C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262544 | ||||||
| chr5:146262548
|
G | A | 4 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2190+742G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262548 | ||||||
| chr5:146262636
|
C | A | 1 | a0001c0002t0003g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2190+830C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262636 | ||||||
| chr5:146262746
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2191-745A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262746 | ||||||
| chr5:146262890
|
C | CT | 7 | a0001c0002t0001g0260a0001c0002t0001g0262a0001c0002t0001g0263others(4): Show | 7 | HG02559.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2191-586dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr5 | 146262890 | |||||
| chr5:146262890
|
CT | C | 5 | a0001c0001t0001g0073a0001c0001t0001g0092a0001c0001t0001g0102others(2): Show | 5 | HG01099.hp1 HG01433.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.2191-586delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr5 | 146262890 | |||||
| chr5:146262935
|
C | G | 1 | a0001c0001t0030g0171 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2191-556C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146262935 | ||||||
| chr5:146263072
|
C | T | 3 | a0001c0002t0004g0016a0001c0002t0004g0019a0002c0004t0004g0020 | 3 | HG00140.hp2 HG02738.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2191-419C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263072 | ||||||
| chr5:146263074
|
G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2191-417G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263074 | ||||||
| chr5:146263086
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2191-405G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263086 | ||||||
| chr5:146263362
|
C | T | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2191-129C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263362 | ||||||
| chr5:146263485
|
G | A | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
splice_region_variant&intron_variant | LOW | c.2191-6G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 13/20 | chr5 | 146263485 | ||||||
| chr5:146263814
|
T | G | 1 | a0001c0001t0001g0176 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2331+183T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146263814 | ||||||
| chr5:146263844
|
C | G | 6 | a0001c0001t0002g0209a0001c0001t0002g0242a0001c0001t0002g0243others(3): Show | 6 | HG03688.hp2 NA18975.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.2331+213C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146263844 | ||||||
| chr5:146263999
|
C | T | 7 | a0001c0002t0004g0017a0001c0002t0004g0021a0001c0002t0004g0022others(4): Show | 7 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2331+368C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146263999 | ||||||
| chr5:146264000
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2331+369G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264000 | ||||||
| chr5:146264105
|
C | CA | 29 | a0001c0001t0001g0105a0001c0001t0001g0130a0001c0001t0001g0134others(26): Show | 29 | HG01167.hp1 HG01243.hp1 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.2331+487dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 146264105 | |||||
| chr5:146264206
|
A | G | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2331+575A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264206 | ||||||
| chr5:146264364
|
G | A | 3 | a0001c0002t0012g0005a0001c0002t0026g0030a0003c0005t0012g0046 | 3 | HG01167.hp1 HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2331+733G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264364 | ||||||
| chr5:146264654
|
TA | T | 25 | a0001c0001t0001g0062a0001c0001t0001g0124a0001c0001t0001g0163others(22): Show | 26 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.2331+1044delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 146264654 | |||||
| chr5:146264654
|
TAA | T | 108 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(105): Show | 108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.2331+1043_2331+104 others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 146264654 | |||||
| chr5:146264654
|
TAAA | T | 6 | a0001c0001t0020g0267a0001c0002t0003g0031a0001c0002t0003g0035others(3): Show | 6 | HG01496.hp1 HG02559.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.2331+1042_2331+104 others(7): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr5 | 146264654 | |||||
| chr5:146264655
|
A | T | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2331+1024A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264655 | ||||||
| chr5:146264761
|
A | G | 1 | a0001c0002t0003g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2331+1130A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264761 | ||||||
| chr5:146264883
|
A | T | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2331+1252A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264883 | ||||||
| chr5:146264964
|
C | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2331+1333C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146264964 | ||||||
| chr5:146265044
|
T | C | 1 | a0001c0002t0026g0030 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2331+1413T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265044 | ||||||
| chr5:146265100
|
A | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2331+1469A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265100 | ||||||
| chr5:146265159
|
T | C | 1 | a0001c0001t0002g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2331+1528T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265159 | ||||||
| chr5:146265194
|
A | G | 1 | a0001c0002t0004g0025 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2331+1563A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265194 | ||||||
| chr5:146265266
|
G | T | 1 | a0001c0002t0003g0039 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2331+1635G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265266 | ||||||
| chr5:146265826
|
T | C | 1 | a0001c0002t0004g0056 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2332-1823T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265826 | ||||||
| chr5:146265900
|
C | T | 1 | a0001c0001t0001g0130 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2332-1749C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146265900 | ||||||
| chr5:146266163
|
G | A | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2332-1486G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266163 | ||||||
| chr5:146266187
|
C | T | 2 | a0001c0001t0001g0089a0001c0001t0001g0107 | 2 | HG02165.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2332-1462C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266187 | ||||||
| chr5:146266318
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2332-1331A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266318 | ||||||
| chr5:146266808
|
G | A | 1 | a0001c0002t0009g0047 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2332-841G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266808 | ||||||
| chr5:146266866
|
G | A | 2 | a0001c0002t0001g0266a0001c0002t0016g0265 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2332-783G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146266866 | ||||||
| chr5:146267271
|
G | T | 1 | a0001c0001t0001g0103 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2332-378G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146267271 | ||||||
| chr5:146267410
|
C | A | 7 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2332-239C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146267410 | ||||||
| chr5:146267588
|
C | T | 37 | a0001c0001t0001g0055a0001c0001t0001g0073a0001c0001t0001g0075others(34): Show | 38 | HG00323.hp2 HG01099.hp2 HG01433.hp2 others(35): Show |
intron_variant | MODIFIER | c.2332-61C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146267588 | ||||||
| chr5:146267617
|
G | T | 1 | a0001c0001t0022g0127 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2332-32G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 14/20 | chr5 | 146267617 | ||||||
| chr5:146267930
|
AC | A | 7 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2451+163delC | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146267930 | ||||||
| chr5:146268245
|
C | CT | 83 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(80): Show | 83 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.2451+491dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr5 | 146268245 | |||||
| chr5:146268392
|
G | A | 2 | a0001c0001t0001g0123a0001c0002t0026g0030 | 2 | HG02717.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2451+624G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268392 | ||||||
| chr5:146268702
|
C | A | 1 | a0001c0001t0011g0002 | 2 | HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2452-505C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268702 | ||||||
| chr5:146268734
|
A | G | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2452-473A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268734 | ||||||
| chr5:146268740
|
T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2452-467T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268740 | ||||||
| chr5:146268782
|
C | G | 1 | a0001c0001t0008g0113 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2452-425C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268782 | ||||||
| chr5:146268894
|
A | C | 5 | a0001c0002t0004g0056a0001c0002t0004g0057a0001c0002t0004g0058others(2): Show | 5 | HG02257.hp2 HG02280.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.2452-313A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146268894 | ||||||
| chr5:146269026
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2452-181G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 15/20 | chr5 | 146269026 | ||||||
| chr5:146269411
|
A | G | 1 | a0001c0003t0002g0236 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2527-9A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 16/20 | chr5 | 146269411 | ||||||
| chr5:146269415
|
C | T | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
splice_region_variant&intron_variant | LOW | c.2527-5C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 16/20 | chr5 | 146269415 | ||||||
| chr5:146269742
|
C | CT | 29 | a0001c0001t0001g0111a0001c0001t0001g0126a0001c0001t0001g0156others(26): Show | 30 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.2691+182dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr5 | 146269742 | |||||
| chr5:146269742
|
C | CTT | 16 | a0001c0002t0003g0039a0001c0002t0004g0016a0001c0002t0004g0017others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2691+181_2691+182d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr5 | 146269742 | |||||
| chr5:146269742
|
CT | C | 7 | a0001c0001t0001g0092a0001c0001t0001g0102a0001c0001t0002g0240others(4): Show | 7 | HG00323.hp1 HG01433.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.2691+182delT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr5 | 146269742 | |||||
| chr5:146269742
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2691+172_2691+182d others(13): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr5 | 146269742 | |||||
| chr5:146269772
|
A | T | 1 | a0001c0001t0029g0135 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2691+188A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146269772 | ||||||
| chr5:146269868
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2691+284C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146269868 | ||||||
| chr5:146270002
|
C | T | 7 | a0001c0001t0007g0064a0001c0001t0007g0065a0001c0001t0007g0066others(4): Show | 7 | NA18747.hp2 NA18942.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.2691+418C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270002 | ||||||
| chr5:146270108
|
C | G | 63 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2691+524C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270108 | ||||||
| chr5:146270329
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2692-625A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270329 | ||||||
| chr5:146270337
|
TTAC | T | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2692-616_2692-614d others(5): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270337 | ||||||
| chr5:146270609
|
T | C | 266 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(263): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.2692-345T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270609 | ||||||
| chr5:146270737
|
C | T | 2 | a0001c0002t0001g0266a0001c0002t0016g0265 | 2 | HG02055.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2692-217C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270737 | ||||||
| chr5:146270821
|
A | G | 8 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2692-133A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270821 | ||||||
| chr5:146270893
|
T | G | 14 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(11): Show | 15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2692-61T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 17/20 | chr5 | 146270893 | ||||||
| chr5:146271081
|
G | A | 3 | a0001c0002t0009g0012a0001c0002t0013g0011a0001c0002t0015g0010 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2796+23G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271081 | ||||||
| chr5:146271136
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2796+78C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271136 | ||||||
| chr5:146271324
|
T | C | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2797-159T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271324 | ||||||
| chr5:146271360
|
A | G | 4 | a0001c0002t0001g0260a0001c0002t0001g0262a0001c0002t0001g0263others(1): Show | 4 | HG02109.hp2 HG02572.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-123A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271360 | ||||||
| chr5:146271369
|
G | A | 63 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2797-114G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271369 | ||||||
| chr5:146271449
|
T | C | 18 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(15): Show | 18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2797-34T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 18/20 | chr5 | 146271449 | ||||||
| chr5:146271903
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2988+229G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146271903 | ||||||
| chr5:146271904
|
C | T | 14 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(11): Show | 15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2988+230C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146271904 | ||||||
| chr5:146272128
|
A | G | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2988+454A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146272128 | ||||||
| chr5:146272156
|
C | G | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2988+482C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146272156 | ||||||
| chr5:146272416
|
T | C | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.2988+742T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146272416 | ||||||
| chr5:146272591
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2988+917G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146272591 | ||||||
| chr5:146272722
|
CA | C | 20 | a0001c0001t0001g0094a0001c0001t0001g0098a0001c0001t0001g0099others(17): Show | 20 | HG01167.hp1 HG01167.hp2 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.2988+1063delA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146272722 | |||||
| chr5:146273101
|
C | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2988+1427C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273101 | ||||||
| chr5:146273194
|
C | T | 1 | a0001c0001t0006g0136 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2988+1520C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273194 | ||||||
| chr5:146273290
|
A | G | 13 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(10): Show | 14 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2988+1616A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273290 | ||||||
| chr5:146273369
|
T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+1695T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273369 | ||||||
| chr5:146273541
|
A | C | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.2988+1867A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273541 | ||||||
| chr5:146273821
|
T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+2147T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273821 | ||||||
| chr5:146273990
|
T | C | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2988+2316T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273990 | ||||||
| chr5:146273991
|
G | A | 1 | a0001c0002t0003g0031 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2988+2317G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273991 | ||||||
| chr5:146273995
|
T | G | 6 | a0001c0002t0003g0028a0001c0002t0003g0040a0001c0002t0003g0041others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2988+2321T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146273995 | ||||||
| chr5:146274217
|
T | TA | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01167.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2988+2544dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146274217 | |||||
| chr5:146274222
|
C | CT | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2988+2559dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146274222 | |||||
| chr5:146274403
|
C | T | 7 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2988+2729C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274403 | ||||||
| chr5:146274466
|
G | T | 1 | a0001c0002t0001g0266 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2988+2792G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274466 | ||||||
| chr5:146274608
|
T | C | 1 | a0001c0002t0016g0265 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2988+2934T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274608 | ||||||
| chr5:146274644
|
T | C | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2988+2970T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274644 | ||||||
| chr5:146274695
|
C | A | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2988+3021C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274695 | ||||||
| chr5:146274732
|
C | T | 3 | a0001c0002t0009g0012a0001c0002t0013g0011a0001c0002t0015g0010 | 3 | HG01884.hp2 HG02486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2988+3058C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274732 | ||||||
| chr5:146274782
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2988+3108A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274782 | ||||||
| chr5:146274789
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0108 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2988+3115A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146274789 | ||||||
| chr5:146275032
|
T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+3358T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146275032 | ||||||
| chr5:146275050
|
A | G | 4 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2988+3376A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146275050 | ||||||
| chr5:146275146
|
A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+3472A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146275146 | ||||||
| chr5:146275304
|
C | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+3630C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146275304 | ||||||
| chr5:146276189
|
C | T | 1 | a0001c0001t0001g0107 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2988+4515C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146276189 | ||||||
| chr5:146276414
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2988+4740G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146276414 | ||||||
| chr5:146276524
|
C | T | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+4850C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146276524 | ||||||
| chr5:146276890
|
A | C | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2988+5216A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146276890 | ||||||
| chr5:146277116
|
T | C | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2988+5442T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277116 | ||||||
| chr5:146277181
|
A | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2988+5507A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277181 | ||||||
| chr5:146277212
|
C | A | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2988+5538C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277212 | ||||||
| chr5:146277241
|
T | C | 1 | a0003c0005t0012g0046 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2988+5567T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277241 | ||||||
| chr5:146277359
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2988+5685G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277359 | ||||||
| chr5:146277491
|
T | C | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2988+5817T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277491 | ||||||
| chr5:146277517
|
A | AT | 32 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0078others(29): Show | 33 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.2988+5866dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146277517 | |||||
| chr5:146277667
|
C | T | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2988+5993C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277667 | ||||||
| chr5:146277735
|
T | C | 2 | a0001c0002t0001g0050a0001c0002t0001g0051 | 2 | HG02615.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.2988+6061T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277735 | ||||||
| chr5:146277824
|
C | T | 1 | a0001c0002t0004g0018 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2988+6150C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277824 | ||||||
| chr5:146277825
|
G | A | 2 | a0001c0002t0004g0022a0001c0002t0004g0023 | 2 | HG01099.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.2988+6151G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277825 | ||||||
| chr5:146277967
|
A | G | 7 | a0001c0002t0009g0009a0001c0002t0009g0012a0001c0002t0009g0047others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2988+6293A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146277967 | ||||||
| chr5:146278040
|
T | C | 92 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(89): Show | 93 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.2988+6366T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278040 | ||||||
| chr5:146278089
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2988+6415A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278089 | ||||||
| chr5:146278130
|
A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2988+6456A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278130 | ||||||
| chr5:146278402
|
A | G | 7 | a0001c0002t0001g0038a0001c0002t0003g0032a0001c0002t0003g0033others(4): Show | 7 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.2989-6220A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278402 | ||||||
| chr5:146278505
|
C | A | 148 | a0001c0001t0001g0004a0001c0001t0001g0053a0001c0001t0001g0054others(145): Show | 152 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.2989-6117C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278505 | ||||||
| chr5:146278655
|
T | C | 3 | a0001c0002t0003g0031a0001c0002t0003g0035a0001c0002t0003g0039 | 3 | HG02559.hp2 HG02647.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2989-5967T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278655 | ||||||
| chr5:146278687
|
T | C | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2989-5935T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278687 | ||||||
| chr5:146278869
|
T | C | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2989-5753T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278869 | ||||||
| chr5:146278885
|
C | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2989-5737C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146278885 | ||||||
| chr5:146279174
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2989-5448G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279174 | ||||||
| chr5:146279178
|
G | A | 2 | a0001c0002t0012g0005a0003c0005t0012g0046 | 2 | HG01167.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2989-5444G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279178 | ||||||
| chr5:146279231
|
C | T | 2 | a0001c0002t0003g0042a0001c0002t0003g0043 | 2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2989-5391C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279231 | ||||||
| chr5:146279235
|
G | A | 2 | a0001c0001t0001g0091a0001c0001t0001g0108 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2989-5387G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279235 | ||||||
| chr5:146279292
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2989-5330A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279292 | ||||||
| chr5:146279318
|
G | A | 1 | a0001c0002t0001g0048 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2989-5304G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279318 | ||||||
| chr5:146279452
|
C | T | 1 | a0001c0001t0002g0209 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2989-5170C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279452 | ||||||
| chr5:146279460
|
C | CA | 7 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2989-5152dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146279460 | |||||
| chr5:146279470
|
A | C | 1 | a0001c0001t0002g0237 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.2989-5152A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279470 | ||||||
| chr5:146279562
|
C | T | 1 | a0001c0001t0002g0192 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2989-5060C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279562 | ||||||
| chr5:146279637
|
A | G | 14 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(11): Show | 15 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2989-4985A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279637 | ||||||
| chr5:146279679
|
C | T | 16 | a0001c0002t0004g0016a0001c0002t0004g0017a0001c0002t0004g0018others(13): Show | 16 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.2989-4943C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279679 | ||||||
| chr5:146279807
|
C | CA | 11 | a0001c0001t0001g0079a0001c0001t0001g0093a0001c0001t0001g0109others(8): Show | 11 | HG00642.hp2 HG01891.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.2989-4796dupA | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146279807 | |||||
| chr5:146279860
|
T | G | 1 | a0001c0002t0001g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2989-4762T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279860 | ||||||
| chr5:146279982
|
G | A | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2989-4640G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146279982 | ||||||
| chr5:146280057
|
A | AT | 18 | a0001c0001t0001g0166a0001c0001t0001g0174a0001c0001t0020g0267others(15): Show | 18 | HG01167.hp2 HG01243.hp1 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.2989-4551dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146280057 | |||||
| chr5:146280058
|
T | A | 1 | a0001c0001t0011g0138 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2989-4564T>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280058 | ||||||
| chr5:146280092
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2989-4530C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280092 | ||||||
| chr5:146280283
|
C | T | 1 | a0001c0002t0016g0265 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2989-4339C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280283 | ||||||
| chr5:146280354
|
C | T | 1 | a0001c0002t0001g0261 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2989-4268C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280354 | ||||||
| chr5:146280442
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2989-4180C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280442 | ||||||
| chr5:146280664
|
C | T | 1 | a0001c0002t0001g0260 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2989-3958C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280664 | ||||||
| chr5:146280850
|
T | TTTTA | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2989-3752_2989-374 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146280850 | |||||
| chr5:146280883
|
A | G | 1 | a0001c0002t0021g0259 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2989-3739A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280883 | ||||||
| chr5:146280899
|
T | C | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2989-3723T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280899 | ||||||
| chr5:146280951
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2989-3671G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146280951 | ||||||
| chr5:146281017
|
C | T | 1 | a0001c0002t0012g0005 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2989-3605C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281017 | ||||||
| chr5:146281134
|
C | T | 5 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(2): Show | 5 | HG02615.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2989-3488C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281134 | ||||||
| chr5:146281142
|
C | T | 18 | a0001c0002t0001g0038a0001c0002t0003g0027a0001c0002t0003g0028others(15): Show | 18 | HG01243.hp1 HG01255.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.2989-3480C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281142 | ||||||
| chr5:146281375
|
A | ATGTC | 7 | a0001c0002t0009g0009a0001c0002t0009g0012a0001c0002t0009g0047others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2989-3245_2989-324 others(8): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146281375 | |||||
| chr5:146281817
|
G | T | 79 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(76): Show | 79 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.2989-2805G>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281817 | ||||||
| chr5:146281986
|
A | C | 1 | a0001c0001t0001g0126 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2989-2636A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146281986 | ||||||
| chr5:146282000
|
C | CT | 113 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0107others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.2989-2601dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146282000 | |||||
| chr5:146282000
|
C | CTT | 32 | a0001c0001t0002g0196a0001c0001t0002g0252a0001c0001t0002g0256others(29): Show | 32 | HG01243.hp1 HG01255.hp2 HG01496.hp1 others(29): Show |
intron_variant | MODIFIER | c.2989-2602_2989-260 others(6): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr5 | 146282000 | |||||
| chr5:146282065
|
G | A | 14 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0076others(11): Show | 14 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2989-2557G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282065 | ||||||
| chr5:146282243
|
T | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.2989-2379T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282243 | ||||||
| chr5:146282249
|
G | A | 1 | a0001c0001t0002g0248 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2989-2373G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282249 | ||||||
| chr5:146282257
|
C | T | 63 | a0001c0002t0001g0038a0001c0002t0001g0048a0001c0002t0001g0049others(60): Show | 64 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.2989-2365C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282257 | ||||||
| chr5:146282280
|
A | G | 2 | a0001c0002t0004g0021a0001c0002t0004g0024 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2989-2342A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282280 | ||||||
| chr5:146282612
|
A | G | 6 | a0001c0002t0003g0028a0001c0002t0003g0040a0001c0002t0003g0041others(3): Show | 6 | HG01891.hp2 HG02647.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2989-2010A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282612 | ||||||
| chr5:146282682
|
GACTTGAG others(14): Show |
G | 1 | a0001c0001t0001g0150 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.2989-1939_2989-191 others(25): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282682 | ||||||
| chr5:146282862
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2989-1760G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282862 | ||||||
| chr5:146282982
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2989-1640T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146282982 | ||||||
| chr5:146283070
|
A | T | 1 | a0001c0002t0024g0264 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2989-1552A>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283070 | ||||||
| chr5:146283222
|
C | T | 7 | a0001c0002t0009g0009a0001c0002t0009g0012a0001c0002t0009g0047others(4): Show | 7 | HG01884.hp2 HG02145.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2989-1400C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283222 | ||||||
| chr5:146283478
|
A | C | 8 | a0001c0002t0001g0048a0001c0002t0001g0049a0001c0002t0001g0050others(5): Show | 8 | HG01167.hp1 HG02615.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2989-1144A>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283478 | ||||||
| chr5:146283690
|
C | T | 7 | a0001c0002t0001g0260a0001c0002t0001g0261a0001c0002t0001g0262others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.2989-932C>T | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283690 | ||||||
| chr5:146283909
|
A | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2989-713A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283909 | ||||||
| chr5:146283914
|
A | G | 7 | a0001c0002t0005g0001a0001c0002t0005g0007a0001c0002t0005g0008others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2989-708A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146283914 | ||||||
| chr5:146284082
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0129 | 2 | HG01192.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2989-540G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284082 | ||||||
| chr5:146284295
|
C | G | 1 | a0001c0001t0002g0232 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2989-327C>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284295 | ||||||
| chr5:146284296
|
C | A | 142 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2989-326C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284296 | ||||||
| chr5:146284334
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2989-288G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284334 | ||||||
| chr5:146284576
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2989-46G>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 19/20 | chr5 | 146284576 | ||||||
| chr5:146285173
|
C | A | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3099+441C>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285173 | ||||||
| chr5:146285468
|
A | G | 78 | a0001c0001t0002g0181a0001c0001t0002g0182a0001c0001t0002g0183others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.3100-479A>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285468 | ||||||
| chr5:146285560
|
T | G | 1 | a0001c0001t0020g0267 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3100-387T>G | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285560 | ||||||
| chr5:146285582
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3100-365T>C | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285582 | ||||||
| chr5:146285791
|
C | CT | 38 | a0001c0001t0001g0165a0001c0001t0001g0174a0001c0001t0002g0196others(35): Show | 39 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.3100-142dupT | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr5 | 146285791 | |||||
| chr5:146285791
|
C | CTT | 19 | a0001c0002t0003g0028a0001c0002t0003g0040a0001c0002t0003g0041others(16): Show | 19 | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.3100-143_3100-142d others(4): Show |
RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr5 | 146285791 | |||||
| chr5:146285815
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3100-132G>A | RBM27 | ENSG00000091009.8 | transcript | ENST00000265271.7 | protein_coding | 20/20 | chr5 | 146285815 |