| geneid | 155435 |
|---|---|
| ensemblid | ENSG00000184863.11 |
| hgncid | 27223 |
| symbol | RBM33 |
| name | RNA binding motif protein 33 |
| refseq_nuc | NM_053043.3 |
| refseq_prot | NP_444271.2 |
| ensembl_nuc | ENST00000401878.8 |
| ensembl_prot | ENSP00000384160.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 155644661 |
| end | 155781480 |
| strand | + |
| ver | v1.2 |
| region | chr7:155644661-155781480 |
| region5000 | chr7:155639661-155786480 |
| regionname0 | RBM33_chr7_155644661_155781480 |
| regionname5000 | RBM33_chr7_155639661_155786480 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1170 | 152 | 63 | 13 | 64 | 2 | 10 | 52 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002 | 1/1 | 1170 | 144 | 23 | 36 | 56 | 7 | 20 | 43 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0003 | 0/0 | 1170 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0004 | 0/0 | 1170 | 3 | 0 | 0 | 1 | 0 | 2 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0005 | 0/0 | 1170 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0006 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0007 | 0/0 | 1166 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0008 | 0/0 | 1170 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 3513 | 127 | 23 | 26 | 54 | 6 | 17 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0002 | 0/0 | 3513 | 90 | 21 | 8 | 53 | 1 | 7 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0003 | 0/0 | 3513 | 31 | 14 | 4 | 9 | 1 | 3 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0004 | 0/0 | 3513 | 20 | 19 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0005 | 1/0 | 3513 | 16 | 0 | 10 | 1 | 1 | 3 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0006 | 0/0 | 3513 | 4 | 4 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0007 | 0/0 | 3513 | 3 | 2 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0008 | 0/0 | 3513 | 2 | 2 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0009 | 0/0 | 3513 | 2 | 0 | 0 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0010 | 0/0 | 3513 | 2 | 0 | 0 | 1 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0011 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0012 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0013 | 0/0 | 3501 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0014 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0015 | 0/0 | 3513 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0016 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0017 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0018 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| c0019 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 6667 | 28 | 1 | 5 | 15 | 1 | 6 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0002 | 0/0 | 6667 | 24 | 2 | 5 | 8 | 2 | 7 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0003 | 0/0 | 6656 | 12 | 3 | 3 | 6 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0004 | 0/0 | 6656 | 12 | 3 | 2 | 4 | 2 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0005 | 0/0 | 6656 | 12 | 11 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0006 | 0/0 | 6667 | 12 | 0 | 1 | 8 | 0 | 3 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0007 | 0/0 | 6656 | 11 | 1 | 2 | 6 | 1 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0008 | 0/0 | 6667 | 8 | 0 | 2 | 5 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0009 | 0/0 | 6656 | 7 | 0 | 1 | 3 | 2 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0010 | 0/0 | 6656 | 7 | 0 | 0 | 7 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0011 | 0/0 | 6667 | 6 | 0 | 0 | 6 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0012 | 0/0 | 6667 | 6 | 0 | 0 | 6 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0013 | 0/0 | 6656 | 5 | 0 | 0 | 5 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0014 | 1/0 | 6656 | 5 | 0 | 3 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0015 | 0/0 | 6667 | 4 | 0 | 0 | 4 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0016 | 0/0 | 6656 | 4 | 0 | 2 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0017 | 0/0 | 6668 | 4 | 0 | 0 | 2 | 0 | 2 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0018 | 0/0 | 6667 | 4 | 0 | 3 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0019 | 0/0 | 6656 | 3 | 3 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0020 | 0/0 | 6667 | 3 | 0 | 0 | 3 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0021 | 0/0 | 6656 | 3 | 3 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0022 | 0/0 | 6656 | 3 | 2 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0023 | 0/0 | 6656 | 3 | 3 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0024 | 0/0 | 6667 | 3 | 2 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0025 | 0/0 | 6656 | 3 | 3 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0026 | 0/0 | 6667 | 3 | 0 | 2 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0027 | 0/0 | 6667 | 3 | 0 | 1 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0028 | 0/0 | 6667 | 3 | 0 | 0 | 3 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0029 | 0/0 | 6667 | 3 | 0 | 0 | 3 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0030 | 0/0 | 6656 | 2 | 1 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0031 | 0/0 | 6669 | 2 | 2 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0032 | 0/0 | 6664 | 2 | 2 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0033 | 0/0 | 6656 | 2 | 0 | 2 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0034 | 0/0 | 6656 | 2 | 2 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0035 | 0/0 | 6657 | 2 | 1 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0036 | 0/0 | 6657 | 2 | 1 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0037 | 0/0 | 6667 | 2 | 0 | 0 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0038 | 0/0 | 6667 | 2 | 0 | 1 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0039 | 0/0 | 6656 | 2 | 0 | 0 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0040 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0041 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0042 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0043 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0044 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0045 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0046 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0047 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0048 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0049 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0050 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0051 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0052 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0053 | 0/0 | 6658 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0054 | 0/0 | 6653 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0055 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0056 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0057 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0058 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0059 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0060 | 0/0 | 6667 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0061 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0062 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0063 | 0/0 | 6667 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0064 | 0/0 | 6667 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0065 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0066 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0067 | 0/0 | 6667 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0068 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0069 | 0/0 | 6656 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0070 | 0/0 | 6656 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0071 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0072 | 0/0 | 6667 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0073 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0074 | 0/0 | 6667 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0075 | 0/1 | 6667 | 1 | 0 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0076 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0077 | 0/0 | 6657 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0078 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0079 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0080 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0081 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0082 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0083 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0084 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0085 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0086 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0087 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0088 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0089 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0090 | 0/0 | 6668 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0091 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0092 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0093 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0094 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0095 | 0/0 | 6657 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0096 | 0/0 | 6656 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0097 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0098 | 0/0 | 6667 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0099 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0100 | 0/0 | 6668 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0101 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0102 | 0/0 | 6667 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0103 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0104 | 0/0 | 6656 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0105 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0106 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0107 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0108 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0109 | 0/0 | 6656 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0110 | 0/0 | 6668 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0111 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0112 | 0/0 | 6656 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0113 | 0/0 | 6656 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0114 | 0/0 | 6656 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0115 | 0/0 | 6667 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0116 | 0/0 | 6656 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0117 | 0/0 | 6656 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0118 | 0/0 | 6668 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0119 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0120 | 0/0 | 6667 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| t0121 | 0/0 | 6684 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 3513 | 90 | 21 | 8 | 53 | 1 | 7 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003 | 0/0 | 3513 | 31 | 14 | 4 | 9 | 1 | 3 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0004 | 0/0 | 3513 | 20 | 19 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0006 | 0/0 | 3513 | 4 | 4 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0008 | 0/0 | 3513 | 2 | 2 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0009 | 0/0 | 3513 | 2 | 0 | 0 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0011 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0017 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0018 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001 | 0/1 | 3513 | 127 | 23 | 26 | 54 | 6 | 17 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0005 | 1/0 | 3513 | 16 | 0 | 10 | 1 | 1 | 3 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0019 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0003c0007 | 0/0 | 3513 | 3 | 2 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0004c0010 | 0/0 | 3513 | 2 | 0 | 0 | 1 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0004c0015 | 0/0 | 3513 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0005c0012 | 0/0 | 3513 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0006c0014 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0007c0013 | 0/0 | 3501 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0008c0016 | 0/0 | 3513 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0006 | 0/0 | 10179 | 12 | 0 | 1 | 8 | 0 | 3 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0007 | 0/0 | 10168 | 10 | 1 | 1 | 6 | 1 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0010 | 0/0 | 10168 | 6 | 0 | 0 | 6 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0011 | 0/0 | 10179 | 6 | 0 | 0 | 6 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0012 | 0/0 | 10179 | 6 | 0 | 0 | 6 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0023 | 0/0 | 10168 | 3 | 3 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0024 | 0/0 | 10179 | 3 | 2 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0025 | 0/0 | 10168 | 3 | 3 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0027 | 0/0 | 10179 | 3 | 0 | 1 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0028 | 0/0 | 10179 | 2 | 0 | 0 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0029 | 0/0 | 10179 | 3 | 0 | 0 | 3 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0031 | 0/0 | 10181 | 2 | 2 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0036 | 0/0 | 10169 | 2 | 1 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0037 | 0/0 | 10179 | 2 | 0 | 0 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0038 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0039 | 0/0 | 10168 | 2 | 0 | 0 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0045 | 0/0 | 10168 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0053 | 0/0 | 10170 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0081 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0082 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0089 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0090 | 0/0 | 10180 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0101 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0102 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0103 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0104 | 0/0 | 10168 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0105 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0106 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0107 | 0/0 | 10180 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0108 | 0/0 | 10180 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0111 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0112 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0113 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0114 | 0/0 | 10168 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0115 | 0/0 | 10179 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0116 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0117 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0118 | 0/0 | 10180 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0119 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0002t0120 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0005 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0007 | 0/0 | 10168 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0008 | 0/0 | 10179 | 7 | 0 | 2 | 4 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0009 | 0/0 | 10168 | 6 | 0 | 1 | 3 | 1 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0019 | 0/0 | 10168 | 3 | 3 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0046 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0047 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0048 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0049 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0050 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0051 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0052 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0085 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0088 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0096 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0098 | 0/0 | 10179 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0099 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0003t0100 | 0/0 | 10180 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0004t0005 | 0/0 | 10168 | 11 | 10 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0004t0021 | 0/0 | 10168 | 3 | 3 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0004t0041 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0004t0042 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0004t0043 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0004t0080 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0004t0083 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0004t0084 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0006t0087 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0006t0092 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0006t0093 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0006t0094 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0008t0086 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0008t0091 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0009t0010 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0009t0028 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0011t0097 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0017t0055 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0001c0018t0079 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0001 | 0/0 | 10179 | 24 | 1 | 5 | 14 | 1 | 3 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0002 | 0/0 | 10179 | 24 | 2 | 5 | 8 | 2 | 7 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0003 | 0/0 | 10168 | 11 | 3 | 3 | 5 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0004 | 0/0 | 10168 | 12 | 3 | 2 | 4 | 2 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0013 | 0/0 | 10168 | 5 | 0 | 0 | 5 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0015 | 0/0 | 10179 | 4 | 0 | 0 | 4 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0016 | 0/0 | 10168 | 4 | 0 | 2 | 2 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0017 | 0/0 | 10180 | 3 | 0 | 0 | 2 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0020 | 0/0 | 10179 | 3 | 0 | 0 | 3 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0030 | 0/0 | 10168 | 2 | 1 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0032 | 0/0 | 10176 | 2 | 2 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0033 | 0/0 | 10168 | 2 | 0 | 2 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0034 | 0/0 | 10168 | 2 | 2 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0035 | 0/0 | 10169 | 2 | 1 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0040 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0044 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0054 | 0/0 | 10165 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0056 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0057 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0058 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0059 | 0/0 | 10168 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0060 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0062 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0063 | 0/0 | 10179 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0064 | 0/0 | 10179 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0065 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0066 | 0/0 | 10168 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0067 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0068 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0069 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0070 | 0/0 | 10168 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0071 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0072 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0073 | 0/0 | 10179 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0074 | 0/0 | 10179 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0075 | 0/1 | 10179 | 1 | 0 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0076 | 0/0 | 10180 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0077 | 0/0 | 10169 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0078 | 0/0 | 10180 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0109 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0001t0121 | 0/0 | 10196 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0005t0001 | 0/0 | 10179 | 2 | 0 | 0 | 0 | 0 | 2 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0005t0014 | 1/0 | 10168 | 5 | 0 | 3 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0005t0018 | 0/0 | 10179 | 4 | 0 | 3 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0005t0026 | 0/0 | 10179 | 3 | 0 | 2 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0005t0038 | 0/0 | 10179 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0005t0110 | 0/0 | 10180 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0002c0019t0003 | 0/0 | 10168 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0003c0007t0022 | 0/0 | 10168 | 3 | 2 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0004c0010t0001 | 0/0 | 10179 | 2 | 0 | 0 | 1 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0004c0015t0017 | 0/0 | 10180 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0005c0012t0008 | 0/0 | 10179 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0006c0014t0095 | 0/0 | 10169 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0007c0013t0009 | 0/0 | 10156 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| a0008c0016t0061 | 0/0 | 10168 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | copy fasta | chr7 | 155639661 | 155786480 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0006g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0010g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0010g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0010g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0010g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0010g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0011g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0011g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0011g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0011g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0011g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0011g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0012g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0012g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0012g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0012g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0012g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0023g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0023g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0023g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0024g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0024g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0024g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0025g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0025g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0025g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0027g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0027g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0027g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0028g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0028g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0029g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0029g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0029g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0031g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0031g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0036g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0036g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0037g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0037g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0038g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0039g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0039g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0045g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0053g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0081g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0082g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0089g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0090g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0101g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0102g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0103g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0104g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0105g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0106g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0107g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0108g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0111g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0112g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0113g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0114g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0115g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0116g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0117g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0118g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0119g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0002t0120g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0007g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0008g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0008g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0008g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0008g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0009g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0009g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0009g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0009g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0009g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0019g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0019g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0019g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0046g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0047g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0048g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0049g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0050g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0051g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0052g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0085g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0088g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0096g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0098g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0099g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0003t0100g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0021g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0021g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0021g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0041g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0042g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0043g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0080g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0083g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0004t0084g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0006t0087g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0006t0092g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0006t0093g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0006t0094g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0008t0086g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0008t0091g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0009t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0009t0028g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0011t0097g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0017t0055g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0001c0018t0079g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0013g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0013g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0013g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0013g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0015g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0015g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0015g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0016g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0016g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0016g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0016g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0017g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0017g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0017g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0020g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0020g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0020g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0030g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0030g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0032g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0032g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0033g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0033g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0034g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0034g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0035g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0035g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0040g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0044g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0054g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0056g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0057g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0058g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0059g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0060g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0062g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0063g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0064g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0065g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0066g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0067g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0068g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0069g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0070g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0071g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0072g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0073g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0074g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0075g0286 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0076g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0077g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0078g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0109g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0001t0121g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0014g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0014g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0014g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0014g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0014g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0018g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0018g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0018g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0018g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0026g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0026g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0026g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0038g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0005t0110g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0002c0019t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0003c0007t0022g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0003c0007t0022g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0003c0007t0022g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0004c0010t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0004c0010t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0004c0015t0017g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0005c0012t0008g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0006c0014t0095g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0007c0013t0009g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| a0008c0016t0061g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0001 | t0002 | g0110 | EUR | GBR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00140 | hp2 | a0001 | c0002 | t0007 | g0169 | EUR | GBR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00280 | hp1 | a0007 | c0013 | t0009 | g0265 | EUR | FIN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00280 | hp2 | a0002 | c0005 | t0026 | g0205 | EUR | FIN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00323 | hp1 | a0002 | c0001 | t0004 | g0119 | EUR | FIN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00323 | hp2 | a0001 | c0003 | t0009 | g0270 | EUR | FIN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00423 | hp1 | a0002 | c0001 | t0001 | g0062 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00423 | hp2 | a0001 | c0002 | t0010 | g0216 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00544 | hp1 | a0001 | c0002 | t0007 | g0179 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00544 | hp2 | a0002 | c0001 | t0062 | g0020 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00558 | hp1 | a0002 | c0001 | t0002 | g0114 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00558 | hp2 | a0001 | c0002 | t0029 | g0207 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00621 | hp1 | a0002 | c0001 | t0121 | g0069 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00621 | hp2 | a0001 | c0002 | t0011 | g0177 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00639 | hp1 | a0001 | c0004 | t0005 | g0135 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00639 | hp2 | a0002 | c0005 | t0018 | g0192 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00642 | hp1 | a0001 | c0002 | t0024 | g0160 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00642 | hp2 | a0002 | c0001 | t0002 | g0100 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00673 | hp1 | a0001 | c0002 | t0007 | g0222 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00673 | hp2 | a0002 | c0001 | t0002 | g0123 | EAS | CHS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00733 | hp1 | a0001 | c0002 | t0107 | g0276 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00733 | hp2 | a0002 | c0001 | t0002 | g0108 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00735 | hp1 | a0003 | c0007 | t0022 | g0291 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00735 | hp2 | a0002 | c0001 | t0004 | g0126 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00738 | hp1 | a0002 | c0001 | t0002 | g0109 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00738 | hp2 | a0001 | c0002 | t0006 | g0233 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00741 | hp1 | a0002 | c0001 | t0001 | g0058 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG00741 | hp2 | a0002 | c0001 | t0016 | g0247 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01070 | hp1 | a0002 | c0001 | t0033 | g0054 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01070 | hp2 | a0001 | c0002 | t0108 | g0277 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01071 | hp1 | a0002 | c0001 | t0001 | g0055 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01071 | hp2 | a0002 | c0001 | t0033 | g0021 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01099 | hp1 | a0002 | c0001 | t0003 | g0041 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01099 | hp2 | a0001 | c0002 | t0007 | g0228 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01175 | hp1 | a0002 | c0001 | t0067 | g0057 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01175 | hp2 | a0002 | c0001 | t0060 | g0288 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01243 | hp1 | a0002 | c0001 | t0001 | g0056 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01243 | hp2 | a0001 | c0003 | t0007 | g0213 | AMR | PUR | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01255 | hp1 | a0001 | c0002 | t0045 | g0198 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01255 | hp2 | a0002 | c0001 | t0030 | g0301 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01257 | hp1 | a0002 | c0001 | t0001 | g0072 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01257 | hp2 | a0002 | c0005 | t0014 | g0170 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01258 | hp1 | a0002 | c0001 | t0072 | g0248 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01258 | hp2 | a0002 | c0001 | t0001 | g0053 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01346 | hp1 | a0002 | c0001 | t0003 | g0074 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01346 | hp2 | a0002 | c0005 | t0026 | g0194 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01496 | hp1 | a0002 | c0005 | t0018 | g0206 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01496 | hp2 | a0002 | c0001 | t0002 | g0116 | AMR | CLM | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01517 | hp1 | a0002 | c0001 | t0002 | g0040 | EUR | IBS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01517 | hp2 | a0002 | c0001 | t0001 | g0105 | EUR | IBS | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01884 | hp1 | a0001 | c0004 | t0041 | g0083 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01884 | hp2 | a0002 | c0001 | t0109 | g0299 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01891 | hp1 | a0001 | c0002 | t0025 | g0006 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01891 | hp2 | a0002 | c0001 | t0003 | g0039 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01928 | hp1 | a0002 | c0005 | t0014 | g0211 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01928 | hp2 | a0001 | c0003 | t0008 | g0002 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01934 | hp1 | a0002 | c0001 | t0003 | g0067 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01934 | hp2 | a0002 | c0005 | t0014 | g0189 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01943 | hp1 | a0002 | c0005 | t0110 | g0196 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01943 | hp2 | a0001 | c0003 | t0009 | g0263 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01952 | hp1 | a0002 | c0005 | t0018 | g0195 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01952 | hp2 | a0002 | c0001 | t0004 | g0102 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01978 | hp1 | a0001 | c0002 | t0027 | g0234 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01978 | hp2 | a0002 | c0001 | t0066 | g0287 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01981 | hp1 | a0002 | c0001 | t0078 | g0117 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG01981 | hp2 | a0001 | c0002 | t0114 | g0218 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02004 | hp1 | a0002 | c0001 | t0016 | g0038 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02004 | hp2 | a0002 | c0005 | t0038 | g0193 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02040 | hp1 | a0002 | c0001 | t0020 | g0029 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02040 | hp2 | a0001 | c0002 | t0028 | g0200 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02055 | hp1 | a0002 | c0001 | t0040 | g0303 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02055 | hp2 | a0001 | c0003 | t0051 | g0281 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02056 | hp1 | a0001 | c0002 | t0012 | g0235 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02056 | hp2 | a0002 | c0001 | t0065 | g0063 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02071 | hp1 | a0002 | c0001 | t0013 | g0061 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02071 | hp2 | a0001 | c0002 | t0011 | g0163 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02074 | hp1 | a0002 | c0001 | t0017 | g0019 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02074 | hp2 | a0001 | c0002 | t0113 | g0203 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02080 | hp1 | a0001 | c0002 | t0028 | g0208 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02080 | hp2 | a0002 | c0001 | t0004 | g0147 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02132 | hp1 | a0001 | c0002 | t0010 | g0183 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02132 | hp2 | a0004 | c0010 | t0001 | g0043 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02135 | hp1 | a0001 | c0002 | t0120 | g0220 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02135 | hp2 | a0002 | c0001 | t0013 | g0050 | EAS | KHV | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02145 | hp1 | a0002 | c0001 | t0001 | g0026 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02145 | hp2 | a0001 | c0003 | t0050 | g0253 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02165 | hp1 | a0002 | c0001 | t0015 | g0051 | EAS | CDX | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02165 | hp2 | a0002 | c0001 | t0001 | g0031 | EAS | CDX | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02257 | hp1 | a0001 | c0017 | t0055 | g0142 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02257 | hp2 | a0002 | c0001 | t0034 | g0113 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02258 | hp1 | a0001 | c0004 | t0005 | g0133 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02258 | hp2 | a0001 | c0002 | t0053 | g0090 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02273 | hp1 | a0002 | c0001 | t0002 | g0127 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02273 | hp2 | a0001 | c0003 | t0008 | g0002 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02280 | hp1 | a0001 | c0002 | t0090 | g0091 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02280 | hp2 | a0002 | c0001 | t0071 | g0122 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02300 | hp1 | a0002 | c0005 | t0026 | g0224 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02300 | hp2 | a0002 | c0001 | t0059 | g0300 | AMR | PEL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02451 | hp1 | a0001 | c0004 | t0043 | g0081 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02451 | hp2 | a0001 | c0002 | t0031 | g0092 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02572 | hp1 | a0001 | c0006 | t0093 | g0166 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02572 | hp2 | a0001 | c0003 | t0046 | g0254 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02602 | hp1 | a0002 | c0001 | t0002 | g0246 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02602 | hp2 | a0002 | c0001 | t0001 | g0034 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02615 | hp1 | a0001 | c0002 | t0007 | g0226 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02615 | hp2 | a0002 | c0001 | t0002 | g0118 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02630 | hp1 | a0001 | c0004 | t0005 | g0137 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02630 | hp2 | a0001 | c0002 | t0102 | g0154 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02647 | hp1 | a0001 | c0003 | t0047 | g0282 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02647 | hp2 | a0001 | c0004 | t0084 | g0141 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02683 | hp1 | a0002 | c0001 | t0002 | g0111 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02683 | hp2 | a0001 | c0002 | t0006 | g0173 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02717 | hp1 | a0001 | c0002 | t0023 | g0157 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02717 | hp2 | a0001 | c0003 | t0005 | g0256 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02723 | hp1 | a0001 | c0002 | t0101 | g0161 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02723 | hp2 | a0002 | c0001 | t0003 | g0047 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02738 | hp1 | a0001 | c0002 | t0036 | g0274 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02738 | hp2 | a0002 | c0001 | t0035 | g0250 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02809 | hp1 | a0001 | c0002 | t0025 | g0007 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02809 | hp2 | a0002 | c0001 | t0054 | g0294 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02818 | hp1 | a0001 | c0004 | t0005 | g0131 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02818 | hp2 | a0001 | c0006 | t0094 | g0164 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02886 | hp1 | a0001 | c0002 | t0089 | g0093 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02886 | hp2 | a0002 | c0001 | t0004 | g0101 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02895 | hp1 | a0001 | c0002 | t0024 | g0155 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02895 | hp2 | a0002 | c0001 | t0076 | g0097 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02896 | hp1 | a0001 | c0003 | t0019 | g0252 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02896 | hp2 | a0001 | c0003 | t0099 | g0084 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02897 | hp1 | a0001 | c0002 | t0024 | g0153 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02897 | hp2 | a0001 | c0003 | t0019 | g0255 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02922 | hp1 | a0001 | c0004 | t0021 | g0149 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02922 | hp2 | a0001 | c0003 | t0088 | g0284 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02965 | hp1 | a0001 | c0003 | t0049 | g0283 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02965 | hp2 | a0001 | c0004 | t0005 | g0132 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02970 | hp1 | a0001 | c0003 | t0048 | g0280 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02970 | hp2 | a0002 | c0001 | t0032 | g0297 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02976 | hp1 | a0002 | c0001 | t0030 | g0302 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02976 | hp2 | a0001 | c0002 | t0081 | g0089 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03041 | hp1 | a0001 | c0002 | t0025 | g0005 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03041 | hp2 | a0002 | c0001 | t0044 | g0292 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03098 | hp1 | a0001 | c0004 | t0021 | g0151 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03098 | hp2 | a0002 | c0001 | t0068 | g0099 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03130 | hp1 | a0001 | c0003 | t0052 | g0279 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03130 | hp2 | a0001 | c0008 | t0091 | g0086 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03139 | hp1 | a0001 | c0004 | t0042 | g0082 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03139 | hp2 | a0001 | c0004 | t0005 | g0134 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03195 | hp1 | a0001 | c0002 | t0023 | g0156 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03195 | hp2 | a0003 | c0007 | t0022 | g0289 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03209 | hp1 | a0001 | c0002 | t0103 | g0158 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03209 | hp2 | a0001 | c0002 | t0082 | g0088 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03225 | hp1 | a0002 | c0001 | t0003 | g0293 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03225 | hp2 | a0001 | c0002 | t0031 | g0094 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03491 | hp1 | a0002 | c0001 | t0070 | g0095 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03491 | hp2 | a0002 | c0005 | t0001 | g0024 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03492 | hp1 | a0002 | c0005 | t0001 | g0023 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03492 | hp2 | a0002 | c0001 | t0004 | g0249 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03516 | hp1 | a0006 | c0014 | t0095 | g0271 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03516 | hp2 | a0001 | c0004 | t0080 | g0136 | AFR | ESN | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03540 | hp1 | a0002 | c0001 | t0004 | g0296 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03540 | hp2 | a0001 | c0006 | t0087 | g0165 | AFR | GWD | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03579 | hp1 | a0001 | c0008 | t0086 | g0087 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03579 | hp2 | a0001 | c0004 | t0005 | g0152 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03654 | hp1 | a0001 | c0002 | t0006 | g0175 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03654 | hp2 | a0001 | c0002 | t0104 | g0171 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03669 | hp1 | a0002 | c0001 | t0002 | g0129 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03669 | hp2 | a0001 | c0003 | t0009 | g0259 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03688 | hp1 | a0004 | c0010 | t0001 | g0044 | SAS | STU | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03688 | hp2 | a0002 | c0001 | t0002 | g0121 | SAS | STU | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03710 | hp1 | a0002 | c0001 | t0001 | g0066 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03710 | hp2 | a0001 | c0002 | t0115 | g0238 | SAS | PJL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03831 | hp1 | a0002 | c0001 | t0064 | g0070 | SAS | BEB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03831 | hp2 | a0001 | c0003 | t0008 | g0268 | SAS | BEB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03834 | hp1 | a0001 | c0003 | t0098 | g0264 | SAS | BEB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03834 | hp2 | a0002 | c0001 | t0002 | g0143 | SAS | BEB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03927 | hp1 | a0001 | c0002 | t0006 | g0217 | SAS | BEB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03927 | hp2 | a0004 | c0015 | t0017 | g0065 | SAS | BEB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03942 | hp1 | a0002 | c0001 | t0002 | g0103 | SAS | BEB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03942 | hp2 | a0002 | c0005 | t0014 | g0223 | SAS | BEB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG04115 | hp1 | a0001 | c0002 | t0007 | g0215 | SAS | STU | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG04115 | hp2 | a0002 | c0001 | t0017 | g0076 | SAS | STU | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG04204 | hp1 | a0002 | c0001 | t0001 | g0009 | SAS | STU | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG04204 | hp2 | a0002 | c0001 | t0002 | g0124 | SAS | STU | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG04228 | hp1 | a0002 | c0001 | t0077 | g0033 | SAS | STU | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG04228 | hp2 | a0002 | c0001 | t0063 | g0027 | SAS | STU | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18522 | hp1 | a0002 | c0001 | t0032 | g0298 | AFR | YRI | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18522 | hp2 | a0001 | c0003 | t0085 | g0272 | AFR | YRI | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18906 | hp1 | a0001 | c0004 | t0005 | g0140 | AFR | YRI | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18906 | hp2 | a0008 | c0016 | t0061 | g0048 | AFR | YRI | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18940 | hp1 | a0001 | c0002 | t0007 | g0212 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18940 | hp2 | a0002 | c0001 | t0058 | g0046 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18941 | hp1 | a0001 | c0002 | t0007 | g0186 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18941 | hp2 | a0002 | c0001 | t0001 | g0015 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18949 | hp1 | a0002 | c0019 | t0003 | g0014 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18949 | hp2 | a0001 | c0002 | t0118 | g0236 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18951 | hp1 | a0001 | c0002 | t0010 | g0172 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18951 | hp2 | a0002 | c0001 | t0004 | g0144 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18953 | hp1 | a0001 | c0002 | t0112 | g0178 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18953 | hp2 | a0002 | c0001 | t0003 | g0042 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18956 | hp1 | a0001 | c0002 | t0029 | g0176 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18956 | hp2 | a0002 | c0001 | t0016 | g0004 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18957 | hp1 | a0002 | c0001 | t0002 | g0278 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18957 | hp2 | a0001 | c0002 | t0011 | g0239 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18960 | hp1 | a0002 | c0001 | t0013 | g0071 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18960 | hp2 | a0001 | c0009 | t0028 | g0242 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18961 | hp1 | a0001 | c0002 | t0006 | g0174 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18961 | hp2 | a0002 | c0001 | t0001 | g0022 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18962 | hp1 | a0002 | c0001 | t0001 | g0145 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18962 | hp2 | a0001 | c0002 | t0012 | g0230 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18966 | hp1 | a0002 | c0001 | t0015 | g0028 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18966 | hp2 | a0001 | c0002 | t0037 | g0201 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18970 | hp1 | a0001 | c0002 | t0117 | g0001 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18970 | hp2 | a0002 | c0001 | t0001 | g0011 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18974 | hp1 | a0001 | c0002 | t0027 | g0199 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18974 | hp2 | a0002 | c0001 | t0002 | g0096 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18979 | hp1 | a0001 | c0003 | t0008 | g0266 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18979 | hp2 | a0002 | c0001 | t0056 | g0068 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0010 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18980 | hp2 | a0001 | c0002 | t0010 | g0187 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18981 | hp1 | a0002 | c0001 | t0016 | g0080 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18981 | hp2 | a0001 | c0002 | t0006 | g0219 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18983 | hp1 | a0001 | c0002 | t0119 | g0191 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18983 | hp2 | a0001 | c0003 | t0009 | g0262 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18984 | hp1 | a0002 | c0001 | t0003 | g0037 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18984 | hp2 | a0001 | c0002 | t0010 | g0184 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18988 | hp1 | a0002 | c0001 | t0002 | g0049 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18988 | hp2 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18989 | hp1 | a0002 | c0001 | t0069 | g0107 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18989 | hp2 | a0001 | c0003 | t0100 | g0077 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18990 | hp1 | a0001 | c0002 | t0037 | g0243 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18990 | hp2 | a0002 | c0001 | t0003 | g0064 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18994 | hp1 | a0002 | c0005 | t0018 | g0225 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18994 | hp2 | a0002 | c0001 | t0002 | g0128 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18995 | hp1 | a0001 | c0002 | t0011 | g0241 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18995 | hp2 | a0002 | c0001 | t0001 | g0012 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18998 | hp1 | a0001 | c0002 | t0011 | g0232 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18998 | hp2 | a0001 | c0002 | t0012 | g0209 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18999 | hp1 | a0002 | c0001 | t0001 | g0025 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18999 | hp2 | a0001 | c0002 | t0006 | g0180 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19004 | hp1 | a0002 | c0001 | t0013 | g0060 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19004 | hp2 | a0001 | c0002 | t0029 | g0162 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19006 | hp1 | a0002 | c0001 | t0004 | g0003 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19006 | hp2 | a0002 | c0001 | t0057 | g0013 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19009 | hp1 | a0002 | c0001 | t0013 | g0073 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19009 | hp2 | a0001 | c0002 | t0038 | g0214 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19010 | hp1 | a0001 | c0002 | t0006 | g0237 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19010 | hp2 | a0001 | c0003 | t0008 | g0269 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19011 | hp1 | a0001 | c0002 | t0006 | g0181 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19011 | hp2 | a0001 | c0003 | t0008 | g0258 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19030 | hp1 | a0001 | c0004 | t0005 | g0139 | AFR | LWK | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19030 | hp2 | a0002 | c0001 | t0035 | g0120 | AFR | LWK | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19043 | hp1 | a0001 | c0004 | t0021 | g0148 | AFR | LWK | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19043 | hp2 | a0001 | c0004 | t0005 | g0138 | AFR | LWK | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19055 | hp1 | a0001 | c0002 | t0039 | g0227 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19055 | hp2 | a0002 | c0001 | t0017 | g0052 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19056 | hp1 | a0001 | c0002 | t0010 | g0185 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19056 | hp2 | a0002 | c0001 | t0020 | g0030 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19058 | hp1 | a0002 | c0001 | t0020 | g0032 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19058 | hp2 | a0001 | c0002 | t0012 | g0231 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19060 | hp1 | a0001 | c0002 | t0007 | g0244 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19060 | hp2 | a0002 | c0001 | t0003 | g0018 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19062 | hp1 | a0001 | c0003 | t0096 | g0078 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19062 | hp2 | a0001 | c0002 | t0027 | g0197 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19065 | hp1 | a0002 | c0001 | t0001 | g0036 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19065 | hp2 | a0001 | c0009 | t0010 | g0240 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19066 | hp1 | a0001 | c0002 | t0011 | g0210 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0075 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19067 | hp1 | a0001 | c0003 | t0008 | g0257 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19067 | hp2 | a0001 | c0002 | t0039 | g0167 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19074 | hp1 | a0001 | c0003 | t0009 | g0260 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19074 | hp2 | a0002 | c0001 | t0003 | g0016 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19079 | hp1 | a0001 | c0002 | t0111 | g0182 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19079 | hp2 | a0002 | c0001 | t0015 | g0059 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19080 | hp1 | a0001 | c0002 | t0012 | g0001 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19080 | hp2 | a0002 | c0001 | t0002 | g0146 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19081 | hp1 | a0001 | c0002 | t0006 | g0190 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19081 | hp2 | a0002 | c0001 | t0002 | g0125 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19082 | hp1 | a0001 | c0002 | t0012 | g0229 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19082 | hp2 | a0002 | c0001 | t0004 | g0106 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19084 | hp1 | a0001 | c0002 | t0106 | g0202 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19084 | hp2 | a0001 | c0003 | t0009 | g0261 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19085 | hp1 | a0001 | c0002 | t0116 | g0188 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19085 | hp2 | a0002 | c0001 | t0015 | g0045 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19087 | hp1 | a0005 | c0012 | t0008 | g0267 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19087 | hp2 | a0001 | c0002 | t0007 | g0168 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19091 | hp1 | a0001 | c0002 | t0006 | g0273 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA19091 | hp2 | a0002 | c0001 | t0001 | g0035 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA20129 | hp1 | a0001 | c0002 | t0023 | g0159 | AFR | ASW | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA20129 | hp2 | a0002 | c0001 | t0002 | g0295 | AFR | ASW | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA20752 | hp1 | a0002 | c0001 | t0004 | g0245 | EUR | TSI | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA20752 | hp2 | a0002 | c0001 | t0074 | g0285 | EUR | TSI | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02109 | hp1 | a0001 | c0003 | t0019 | g0251 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02109 | hp2 | a0002 | c0001 | t0004 | g0098 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02486 | hp1 | a0003 | c0007 | t0022 | g0290 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02486 | hp2 | a0001 | c0006 | t0092 | g0304 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02559 | hp1 | a0002 | c0001 | t0073 | g0115 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG02559 | hp2 | a0001 | c0004 | t0083 | g0150 | AFR | ACB | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03471 | hp1 | a0002 | c0001 | t0034 | g0112 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG03471 | hp2 | a0001 | c0002 | t0105 | g0008 | AFR | MSL | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG06807 | hp1 | a0001 | c0004 | t0005 | g0130 | AFR | USA | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| HG06807 | hp2 | a0001 | c0002 | t0036 | g0275 | AFR | USA | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18955 | hp1 | a0001 | c0002 | t0006 | g0221 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA18955 | hp2 | a0002 | c0001 | t0001 | g0017 | EAS | JPT | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA21309 | hp1 | a0001 | c0011 | t0097 | g0085 | AFR | LWK | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| NA21309 | hp2 | a0001 | c0018 | t0079 | g0079 | AFR | LWK | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0075 | g0286 | REF | REF | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| homoSapiens_grch38 | hp1 | a0002 | c0005 | t0014 | g0204 | REF | REF | RBM33_chr7_155639661_155786480 | RBM33 | chr7 | 155639661 | 155786480 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:155738386
|
A | G | 5 | a0001a0003a0005others(2): Show | 158 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(155): Show |
missense_variant | MODERATE | c.1720A>G | p.Thr574Ala | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/18 | 1936/10168 | 1720/3513 | 574/1170 | chr7 | 155738386 | ||
| chr7:155739798
|
TCCGCACC others(5): Show |
T | 1 | a0007 | 1 | HG00280.hp1 | disruptive_inframe_deletion | MODERATE | c.1838_1849delACCAGC others(6): Show |
p.His613_Pro616del | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/18 | 2054/10168 | 1838/3513 | 613/1170 | INFO_REALIGN_3_PRIME | chr7 | 155739798 | |
| chr7:155741853
|
T | C | 1 | a0006 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2084T>C | p.Met695Thr | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/18 | 2300/10168 | 2084/3513 | 695/1170 | chr7 | 155741853 | ||
| chr7:155741936
|
A | G | 1 | a0004 | 3 | HG02132.hp2 HG03688.hp1 HG03927.hp2 |
missense_variant | MODERATE | c.2167A>G | p.Ser723Gly | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/18 | 2383/10168 | 2167/3513 | 723/1170 | chr7 | 155741936 | ||
| chr7:155742044
|
G | T | 1 | a0003 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
missense_variant | MODERATE | c.2275G>T | p.Val759Leu | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/18 | 2491/10168 | 2275/3513 | 759/1170 | chr7 | 155742044 | ||
| chr7:155763966
|
C | T | 1 | a0005 | 1 | NA19087.hp1 | missense_variant | MODERATE | c.3134C>T | p.Ser1045Leu | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/18 | 3350/10168 | 3134/3513 | 1045/1170 | chr7 | 155763966 | ||
| chr7:155764008
|
C | T | 1 | a0008 | 1 | NA18906.hp2 | missense_variant | MODERATE | c.3176C>T | p.Pro1059Leu | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/18 | 3392/10168 | 3176/3513 | 1059/1170 | chr7 | 155764008 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:155665209
|
G | A | 1 | a0001c0011 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.78G>A | p.Ala26Ala | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/18 | 294/10168 | 78/3513 | 26/1170 | chr7 | 155665209 | ||
| chr7:155680794
|
C | T | 1 | a0002c0019 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.453C>T | p.His151His | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/18 | 669/10168 | 453/3513 | 151/1170 | chr7 | 155680794 | ||
| chr7:155711226
|
A | T | 10 | a0001c0004a0001c0006a0001c0017others(7): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
synonymous_variant | LOW | c.972A>T | p.Pro324Pro | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/18 | 1188/10168 | 972/3513 | 324/1170 | chr7 | 155711226 | ||
| chr7:155711347
|
C | T | 2 | a0001c0004a0001c0018 | 21 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(18): Show |
synonymous_variant | LOW | c.1093C>T | p.Leu365Leu | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/18 | 1309/10168 | 1093/3513 | 365/1170 | chr7 | 155711347 | ||
| chr7:155718404
|
G | A | 1 | a0001c0008 | 2 | HG03130.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.1221G>A | p.Pro407Pro | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/18 | 1437/10168 | 1221/3513 | 407/1170 | chr7 | 155718404 | ||
| chr7:155738260
|
T | C | 10 | a0001c0002a0001c0003a0001c0006others(7): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
synonymous_variant | LOW | c.1594T>C | p.Leu532Leu | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/18 | 1810/10168 | 1594/3513 | 532/1170 | chr7 | 155738260 | ||
| chr7:155738358
|
C | A | 1 | a0004c0015 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.1692C>A | p.Gly564Gly | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/18 | 1908/10168 | 1692/3513 | 564/1170 | chr7 | 155738358 | ||
| chr7:155739894
|
C | T | 2 | a0001c0006a0006c0014 | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.1917C>T | p.His639His | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/18 | 2133/10168 | 1917/3513 | 639/1170 | chr7 | 155739894 | ||
| chr7:155741959
|
C | G | 4 | a0001c0003a0001c0011a0005c0012others(1): Show | 34 | HG00280.hp1 HG00323.hp2 HG01243.hp2 others(31): Show |
synonymous_variant | LOW | c.2190C>G | p.Pro730Pro | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/18 | 2406/10168 | 2190/3513 | 730/1170 | chr7 | 155741959 | ||
| chr7:155763958
|
C | T | 1 | a0001c0018 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.3126C>T | p.His1042His | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/18 | 3342/10168 | 3126/3513 | 1042/1170 | chr7 | 155763958 | ||
| chr7:155766514
|
G | A | 1 | a0001c0009 | 2 | NA18960.hp2 NA19065.hp2 |
synonymous_variant | LOW | c.3234G>A | p.Arg1078Arg | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/18 | 3450/10168 | 3234/3513 | 1078/1170 | chr7 | 155766514 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:155644661
|
G | GGGCGCGG others(10): Show |
1 | a0002c0001t0121 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-215_-199dupGGCGCG others(11): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 198 | INFO_REALIGN_3_PRIME | chr7 | 155644661 | ||||
| chr7:155644702
|
C | A | 2 | a0002c0001t0030a0002c0001t0040 | 3 | HG01255.hp2 HG02055.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-175C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 175 | chr7 | 155644702 | |||||
| chr7:155644704
|
T | A | 2 | a0002c0001t0030a0002c0001t0040 | 3 | HG01255.hp2 HG02055.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-173T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 173 | chr7 | 155644704 | |||||
| chr7:155644705
|
C | A | 3 | a0001c0004t0041a0001c0004t0042a0001c0004t0043 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
5_prime_UTR_variant | MODIFIER | c.-172C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 172 | chr7 | 155644705 | |||||
| chr7:155644707
|
T | C | 1 | a0002c0001t0044 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-170T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 170 | chr7 | 155644707 | |||||
| chr7:155644721
|
G | A | 2 | a0002c0001t0030a0002c0001t0040 | 3 | HG01255.hp2 HG02055.hp1 HG02976.hp1 |
5_prime_UTR_variant | MODIFIER | c.-156G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 156 | chr7 | 155644721 | |||||
| chr7:155644737
|
G | A | 1 | a0001c0002t0045 | 1 | HG01255.hp1 | 5_prime_UTR_variant | MODIFIER | c.-140G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 140 | chr7 | 155644737 | |||||
| chr7:155644781
|
T | C | 102 | a0001c0002t0023a0001c0002t0024a0001c0002t0025others(99): Show | 225 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(222): Show |
5_prime_UTR_variant | MODIFIER | c.-96T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 96 | chr7 | 155644781 | |||||
| chr7:155644802
|
C | A | 8 | a0001c0003t0019a0001c0003t0046a0001c0003t0047others(5): Show | 10 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-75C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 75 | chr7 | 155644802 | |||||
| chr7:155644842
|
G | GA | 2 | a0001c0002t0031a0001c0002t0053 | 3 | HG02258.hp2 HG02451.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-35_-34insA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 34 | chr7 | 155644842 | |||||
| chr7:155644843
|
T | G | 2 | a0001c0002t0031a0001c0002t0053 | 3 | HG02258.hp2 HG02451.hp2 HG03225.hp2 |
5_prime_UTR_variant | MODIFIER | c.-34T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 34 | chr7 | 155644843 | |||||
| chr7:155644845
|
G | C | 1 | a0001c0002t0037 | 2 | NA18966.hp2 NA18990.hp1 |
5_prime_UTR_variant | MODIFIER | c.-32G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/18 | 32 | chr7 | 155644845 | |||||
| chr7:155775262
|
C | G | 78 | a0001c0002t0006a0001c0002t0007a0001c0002t0010others(75): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*221C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 221 | chr7 | 155775262 | |||||
| chr7:155775319
|
A | C | 1 | a0001c0003t0052 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*278A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 278 | chr7 | 155775319 | |||||
| chr7:155775396
|
C | T | 3 | a0001c0004t0042a0001c0004t0043a0002c0001t0109 | 3 | HG01884.hp2 HG02451.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*355C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 355 | chr7 | 155775396 | |||||
| chr7:155775514
|
C | T | 1 | a0001c0002t0120 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*473C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 473 | chr7 | 155775514 | |||||
| chr7:155775744
|
G | C | 1 | a0001c0002t0112 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 703 | chr7 | 155775744 | |||||
| chr7:155775749
|
C | T | 1 | a0001c0002t0119 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*708C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 708 | chr7 | 155775749 | |||||
| chr7:155775856
|
A | T | 35 | a0001c0002t0006a0001c0002t0007a0001c0002t0010others(32): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*815A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 815 | chr7 | 155775856 | |||||
| chr7:155775860
|
G | GT | 9 | a0001c0003t0050a0001c0003t0051a0001c0003t0100others(6): Show | 12 | HG01981.hp1 HG02055.hp1 HG02055.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*826dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 827 | INFO_REALIGN_3_PRIME | chr7 | 155775860 | ||||
| chr7:155776018
|
TGGC | T | 2 | a0002c0001t0032a0002c0001t0054 | 3 | HG02809.hp2 HG02970.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*978_*980delGGC | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 978 | chr7 | 155776018 | |||||
| chr7:155776266
|
A | G | 1 | a0001c0003t0099 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 1225 | chr7 | 155776266 | |||||
| chr7:155776322
|
C | G | 8 | a0001c0003t0008a0001c0003t0009a0001c0003t0096others(5): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1281C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 1281 | chr7 | 155776322 | |||||
| chr7:155776461
|
A | G | 1 | a0006c0014t0095 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1420A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 1420 | chr7 | 155776461 | |||||
| chr7:155776473
|
C | T | 35 | a0001c0002t0006a0001c0002t0007a0001c0002t0010others(32): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1432C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 1432 | chr7 | 155776473 | |||||
| chr7:155776548
|
C | A | 1 | a0001c0018t0079 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1507C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 1507 | chr7 | 155776548 | |||||
| chr7:155776630
|
T | TG | 4 | a0001c0006t0092a0001c0006t0093a0001c0006t0094others(1): Show | 4 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1590dupG | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 1591 | INFO_REALIGN_3_PRIME | chr7 | 155776630 | ||||
| chr7:155776714
|
G | A | 1 | a0001c0004t0080 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1673G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 1673 | chr7 | 155776714 | |||||
| chr7:155777048
|
C | CT | 8 | a0001c0002t0031a0001c0002t0053a0001c0002t0089others(5): Show | 11 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2020dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 2021 | INFO_REALIGN_3_PRIME | chr7 | 155777048 | ||||
| chr7:155777107
|
T | A | 3 | a0001c0004t0042a0001c0004t0043a0002c0001t0109 | 3 | HG01884.hp2 HG02451.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2066T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 2066 | chr7 | 155777107 | |||||
| chr7:155777198
|
G | A | 2 | a0001c0002t0081a0001c0002t0082 | 2 | HG02976.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2157G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 2157 | chr7 | 155777198 | |||||
| chr7:155777233
|
G | A | 2 | a0001c0004t0021a0001c0004t0083 | 4 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2192G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 2192 | chr7 | 155777233 | |||||
| chr7:155777289
|
G | A | 104 | a0001c0002t0006a0001c0002t0007a0001c0002t0010others(101): Show | 228 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*2248G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 2248 | chr7 | 155777289 | |||||
| chr7:155777351
|
C | T | 1 | a0001c0003t0052 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2310C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 2310 | chr7 | 155777351 | |||||
| chr7:155777490
|
A | G | 1 | a0002c0001t0034 | 2 | HG02257.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2449A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 2449 | chr7 | 155777490 | |||||
| chr7:155777539
|
T | C | 1 | a0001c0017t0055 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2498T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 2498 | chr7 | 155777539 | |||||
| chr7:155777883
|
G | A | 5 | a0002c0001t0013a0002c0001t0015a0002c0001t0020others(2): Show | 14 | HG00621.hp1 HG02040.hp1 HG02071.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2842G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 2842 | chr7 | 155777883 | |||||
| chr7:155778535
|
C | T | 4 | a0001c0002t0012a0001c0002t0039a0001c0002t0117others(1): Show | 10 | HG02056.hp1 HG03130.hp2 NA18962.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3494C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 3494 | chr7 | 155778535 | |||||
| chr7:155778720
|
T | C | 2 | a0001c0003t0096a0001c0003t0100 | 2 | NA18989.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3679T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 3679 | chr7 | 155778720 | |||||
| chr7:155778908
|
C | T | 4 | a0001c0003t0088a0001c0006t0087a0001c0006t0093others(1): Show | 4 | HG02572.hp1 HG02818.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3867C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 3867 | chr7 | 155778908 | |||||
| chr7:155778909
|
A | G | 78 | a0001c0002t0006a0001c0002t0007a0001c0002t0010others(75): Show | 155 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*3868A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 3868 | chr7 | 155778909 | |||||
| chr7:155778968
|
TC | T | 1 | a0001c0002t0025 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3929delC | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 3929 | INFO_REALIGN_3_PRIME | chr7 | 155778968 | ||||
| chr7:155778975
|
C | T | 6 | a0001c0003t0047a0001c0003t0048a0001c0003t0049others(3): Show | 6 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3934C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 3934 | chr7 | 155778975 | |||||
| chr7:155778998
|
A | G | 1 | a0002c0001t0073 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3957A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 3957 | chr7 | 155778998 | |||||
| chr7:155779090
|
GT | G | 1 | a0003c0007t0022 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4056delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4056 | INFO_REALIGN_3_PRIME | chr7 | 155779090 | ||||
| chr7:155779106
|
C | T | 1 | a0001c0006t0092 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4065C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4065 | chr7 | 155779106 | |||||
| chr7:155779115
|
C | T | 38 | a0001c0002t0031a0001c0002t0053a0001c0002t0089others(35): Show | 66 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*4074C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4074 | chr7 | 155779115 | |||||
| chr7:155779198
|
A | AT | 7 | a0001c0002t0025a0001c0002t0036a0001c0002t0081others(4): Show | 10 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4171dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4172 | INFO_REALIGN_3_PRIME | chr7 | 155779198 | ||||
| chr7:155779261
|
A | G | 25 | a0001c0002t0029a0001c0002t0116a0001c0003t0008others(22): Show | 40 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4220A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4220 | chr7 | 155779261 | |||||
| chr7:155779262
|
T | G | 25 | a0001c0002t0029a0001c0002t0116a0001c0003t0008others(22): Show | 40 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*4221T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4221 | chr7 | 155779262 | |||||
| chr7:155779282
|
T | A | 1 | a0002c0001t0057 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4241T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4241 | chr7 | 155779282 | |||||
| chr7:155779296
|
C | G | 1 | a0003c0007t0022 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4255C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4255 | chr7 | 155779296 | |||||
| chr7:155779312
|
T | C | 10 | a0001c0002t0023a0001c0002t0024a0001c0002t0031others(7): Show | 15 | HG00642.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4271T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4271 | chr7 | 155779312 | |||||
| chr7:155779413
|
T | C | 3 | a0001c0002t0036a0001c0002t0107a0001c0002t0108 | 4 | HG00733.hp1 HG01070.hp2 HG02738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4372T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4372 | chr7 | 155779413 | |||||
| chr7:155779415
|
G | A | 1 | a0001c0002t0081 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4374G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4374 | chr7 | 155779415 | |||||
| chr7:155779573
|
T | G | 1 | a0002c0001t0066 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4532T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4532 | chr7 | 155779573 | |||||
| chr7:155779814
|
G | A | 1 | a0002c0001t0074 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4773G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4773 | chr7 | 155779814 | |||||
| chr7:155779914
|
C | T | 1 | a0001c0002t0045 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4873C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4873 | chr7 | 155779914 | |||||
| chr7:155780012
|
T | C | 9 | a0001c0003t0008a0001c0003t0009a0001c0003t0096others(6): Show | 20 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*4971T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 4971 | chr7 | 155780012 | |||||
| chr7:155780182
|
G | A | 2 | a0001c0006t0092a0006c0014t0095 | 2 | HG02486.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5141G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5141 | chr7 | 155780182 | |||||
| chr7:155780239
|
C | T | 6 | a0001c0002t0023a0001c0002t0024a0001c0002t0101others(3): Show | 10 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5198C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5198 | chr7 | 155780239 | |||||
| chr7:155780241
|
C | T | 1 | a0001c0003t0100 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5200C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5200 | chr7 | 155780241 | |||||
| chr7:155780289
|
C | T | 1 | a0001c0002t0108 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5248C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5248 | chr7 | 155780289 | |||||
| chr7:155780357
|
C | T | 6 | a0001c0002t0010a0001c0002t0011a0001c0002t0028others(3): Show | 17 | HG00423.hp2 HG00621.hp2 HG02040.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*5316C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5316 | chr7 | 155780357 | |||||
| chr7:155780462
|
G | A | 1 | a0001c0002t0114 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5421G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5421 | chr7 | 155780462 | |||||
| chr7:155780553
|
T | C | 1 | a0001c0004t0083 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5512T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5512 | chr7 | 155780553 | |||||
| chr7:155780606
|
C | A | 1 | a0002c0001t0059 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5565C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5565 | chr7 | 155780606 | |||||
| chr7:155780736
|
G | T | 3 | a0001c0004t0042a0001c0004t0043a0002c0001t0109 | 3 | HG01884.hp2 HG02451.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5695G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5695 | chr7 | 155780736 | |||||
| chr7:155780739
|
G | A | 1 | a0001c0002t0101 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5698G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5698 | chr7 | 155780739 | |||||
| chr7:155780778
|
T | TACCACTC others(4): Show |
12 | a0001c0002t0027a0001c0002t0028a0001c0002t0102others(9): Show | 18 | HG00280.hp2 HG01175.hp1 HG01175.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*5741_*5751dupACTC others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5752 | INFO_REALIGN_3_PRIME | chr7 | 155780778 | ||||
| chr7:155780778
|
T | TACCTCTC others(4): Show |
1 | a0002c0001t0072 | 1 | HG01258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5740_*5741insTCTC others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5741 | INFO_REALIGN_3_PRIME | chr7 | 155780778 | ||||
| chr7:155780782
|
A | ACTCCATC others(4): Show |
39 | a0001c0002t0006a0001c0002t0011a0001c0002t0012others(36): Show | 125 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(122): Show |
3_prime_UTR_variant | MODIFIER | c.*5745_*5755dupCATC others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5756 | INFO_REALIGN_3_PRIME | chr7 | 155780782 | ||||
| chr7:155780782
|
A | T | 4 | a0001c0002t0117a0001c0003t0050a0002c0001t0016others(1): Show | 7 | HG00741.hp2 HG01258.hp1 HG02004.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5741A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5741 | chr7 | 155780782 | |||||
| chr7:155780786
|
C | CATCACCT others(4): Show |
10 | a0001c0002t0024a0001c0002t0031a0001c0002t0090others(7): Show | 15 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5747_*5757dupTCAC others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5758 | INFO_REALIGN_3_PRIME | chr7 | 155780786 | ||||
| chr7:155780797
|
A | C | 1 | a0002c0001t0064 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5756A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5756 | chr7 | 155780797 | |||||
| chr7:155780848
|
A | G | 2 | a0002c0001t0063a0002c0001t0070 | 2 | HG03491.hp1 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5807A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 5807 | chr7 | 155780848 | |||||
| chr7:155781058
|
C | T | 1 | a0001c0006t0094 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6017C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 6017 | chr7 | 155781058 | |||||
| chr7:155781059
|
G | T | 3 | a0001c0004t0042a0001c0004t0043a0002c0001t0109 | 3 | HG01884.hp2 HG02451.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6018G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 6018 | chr7 | 155781059 | |||||
| chr7:155781109
|
G | A | 1 | a0002c0001t0033 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6068G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 6068 | chr7 | 155781109 | |||||
| chr7:155781132
|
G | A | 1 | a0001c0002t0104 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6091G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 6091 | chr7 | 155781132 | |||||
| chr7:155781157
|
T | C | 5 | a0001c0003t0046a0001c0003t0050a0001c0004t0042others(2): Show | 5 | HG02145.hp2 HG02559.hp2 HG02572.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6116T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 6116 | chr7 | 155781157 | |||||
| chr7:155781239
|
T | C | 2 | a0001c0002t0103a0002c0001t0071 | 2 | HG02280.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6198T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 6198 | chr7 | 155781239 | |||||
| chr7:155781261
|
T | C | 3 | a0001c0003t0088a0001c0006t0087a0002c0001t0068 | 3 | HG02922.hp2 HG03098.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6220T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 6220 | chr7 | 155781261 | |||||
| chr7:155781308
|
C | T | 1 | a0002c0001t0069 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6267C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 18/18 | 6267 | chr7 | 155781308 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:155644942
|
G | T | 1 | a0001c0006t0092g0304 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43+23G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155644942 | ||||||
| chr7:155644971
|
G | T | 3 | a0002c0001t0030g0301a0002c0001t0030g0302a0002c0001t0040g0303 | 3 | HG01255.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.43+52G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155644971 | ||||||
| chr7:155645031
|
C | T | 1 | a0002c0001t0059g0300 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.43+112C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645031 | ||||||
| chr7:155645051
|
C | T | 8 | a0002c0001t0002g0295a0002c0001t0003g0293a0002c0001t0004g0296others(5): Show | 8 | HG01884.hp2 HG02809.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.43+132C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645051 | ||||||
| chr7:155645071
|
C | T | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.43+152C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645071 | ||||||
| chr7:155645184
|
A | C | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.43+265A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645184 | ||||||
| chr7:155645247
|
C | T | 4 | a0002c0001t0060g0288a0002c0001t0066g0287a0002c0001t0074g0285others(1): Show | 4 | HG01175.hp2 HG01978.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.43+328C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645247 | ||||||
| chr7:155645253
|
C | A | 2 | a0002c0001t0004g0003a0002c0001t0016g0004 | 2 | NA18956.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.43+334C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645253 | ||||||
| chr7:155645537
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.43+618A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645537 | ||||||
| chr7:155645613
|
C | A | 4 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+694C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645613 | ||||||
| chr7:155645614
|
T | C | 69 | a0002c0001t0001g0009a0002c0001t0001g0010a0002c0001t0001g0011others(66): Show | 69 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.43+695T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645614 | ||||||
| chr7:155645970
|
T | C | 2 | a0001c0003t0096g0078a0001c0003t0100g0077 | 2 | NA18989.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.43+1051T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155645970 | ||||||
| chr7:155646356
|
G | C | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.43+1437G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646356 | ||||||
| chr7:155646407
|
A | G | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.43+1488A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646407 | ||||||
| chr7:155646511
|
G | A | 1 | a0002c0001t0016g0080 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.43+1592G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646511 | ||||||
| chr7:155646556
|
C | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.43+1637C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646556 | ||||||
| chr7:155646595
|
T | G | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.43+1676T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646595 | ||||||
| chr7:155646651
|
T | C | 1 | a0002c0001t0001g0009 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.43+1732T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646651 | ||||||
| chr7:155646730
|
G | C | 1 | a0001c0003t0099g0084 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.43+1811G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646730 | ||||||
| chr7:155646743
|
C | G | 2 | a0002c0001t0060g0288a0002c0001t0066g0287 | 2 | HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.43+1824C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646743 | ||||||
| chr7:155646792
|
C | T | 5 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.43+1873C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646792 | ||||||
| chr7:155646852
|
C | T | 1 | a0002c0001t0017g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.43+1933C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646852 | ||||||
| chr7:155646906
|
A | G | 1 | a0002c0001t0002g0278 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.43+1987A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646906 | ||||||
| chr7:155646937
|
G | A | 1 | a0001c0011t0097g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.43+2018G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155646937 | ||||||
| chr7:155647059
|
A | G | 1 | a0002c0001t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.43+2140A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647059 | ||||||
| chr7:155647083
|
A | G | 8 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(5): Show | 8 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+2164A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647083 | ||||||
| chr7:155647191
|
A | G | 1 | a0001c0002t0006g0273 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.43+2272A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647191 | ||||||
| chr7:155647272
|
A | G | 34 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(31): Show | 35 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.43+2353A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647272 | ||||||
| chr7:155647343
|
G | A | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+2424G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647343 | ||||||
| chr7:155647630
|
C | T | 6 | a0002c0001t0002g0246a0002c0001t0004g0245a0002c0001t0004g0249others(3): Show | 6 | HG00741.hp2 HG01258.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.43+2711C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647630 | ||||||
| chr7:155647700
|
G | A | 155 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(152): Show | 155 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.43+2781G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647700 | ||||||
| chr7:155647767
|
G | T | 1 | a0001c0004t0005g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.43+2848G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647767 | ||||||
| chr7:155647863
|
G | A | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.43+2944G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647863 | ||||||
| chr7:155647864
|
G | A | 1 | a0001c0008t0091g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.43+2945G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647864 | ||||||
| chr7:155647865
|
C | G | 1 | a0001c0008t0091g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.43+2946C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647865 | ||||||
| chr7:155647973
|
C | G | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+3054C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155647973 | ||||||
| chr7:155648002
|
A | C | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.43+3083A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155648002 | ||||||
| chr7:155648095
|
T | G | 1 | a0002c0001t0001g0010 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.43+3176T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155648095 | ||||||
| chr7:155648139
|
A | G | 1 | a0001c0002t0007g0244 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.43+3220A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155648139 | ||||||
| chr7:155648340
|
C | T | 1 | a0001c0002t0037g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.43+3421C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155648340 | ||||||
| chr7:155648418
|
TC | T | 4 | a0001c0002t0011g0239a0001c0002t0011g0241a0001c0009t0010g0240others(1): Show | 4 | NA18957.hp2 NA18960.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+3501delC | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155648418 | |||||
| chr7:155648438
|
G | T | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.43+3519G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155648438 | ||||||
| chr7:155648503
|
C | T | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+3584C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155648503 | ||||||
| chr7:155648536
|
T | C | 6 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.43+3617T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155648536 | ||||||
| chr7:155648623
|
CT | C | 155 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(152): Show | 155 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.43+3715delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155648623 | |||||
| chr7:155648769
|
A | G | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43+3850A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155648769 | ||||||
| chr7:155649047
|
C | A | 1 | a0002c0001t0044g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.43+4128C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155649047 | ||||||
| chr7:155649199
|
G | A | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+4280G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155649199 | ||||||
| chr7:155649211
|
A | G | 4 | a0001c0004t0021g0148a0001c0004t0021g0149a0001c0004t0021g0151others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.43+4292A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155649211 | ||||||
| chr7:155649309
|
C | T | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.43+4390C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155649309 | ||||||
| chr7:155649465
|
A | G | 1 | a0002c0001t0013g0073 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.43+4546A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155649465 | ||||||
| chr7:155649666
|
T | C | 1 | a0002c0001t0001g0011 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.43+4747T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155649666 | ||||||
| chr7:155649977
|
C | T | 2 | a0002c0001t0002g0146a0002c0001t0004g0147 | 2 | HG02080.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.43+5058C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155649977 | ||||||
| chr7:155650011
|
T | C | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.43+5092T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155650011 | ||||||
| chr7:155650156
|
G | A | 155 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(152): Show | 155 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.43+5237G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155650156 | ||||||
| chr7:155650241
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.43+5322A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155650241 | ||||||
| chr7:155650539
|
GACTT | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.43+5624_43+5627del others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155650539 | |||||
| chr7:155650585
|
C | A | 1 | a0001c0002t0029g0162 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.43+5666C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155650585 | ||||||
| chr7:155650675
|
T | C | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.43+5756T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155650675 | ||||||
| chr7:155650779
|
C | T | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.43+5860C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155650779 | ||||||
| chr7:155651125
|
G | A | 1 | a0002c0001t0001g0012 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.43+6206G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155651125 | ||||||
| chr7:155651370
|
T | G | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.43+6451T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155651370 | ||||||
| chr7:155651582
|
C | CA | 153 | a0001c0002t0007g0168a0001c0002t0011g0163a0001c0002t0036g0274others(150): Show | 154 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.43+6683dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155651582 | |||||
| chr7:155651582
|
C | CAA | 18 | a0001c0003t0005g0256a0001c0003t0008g0257a0001c0003t0019g0251others(15): Show | 18 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.43+6682_43+6683dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155651582 | |||||
| chr7:155651756
|
T | C | 156 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.43+6837T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155651756 | ||||||
| chr7:155651820
|
T | C | 1 | a0001c0002t0007g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.43+6901T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155651820 | ||||||
| chr7:155651893
|
C | T | 1 | a0002c0001t0017g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.43+6974C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155651893 | ||||||
| chr7:155652019
|
C | T | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43+7100C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652019 | ||||||
| chr7:155652207
|
C | G | 16 | a0001c0002t0006g0233a0001c0002t0006g0237a0001c0002t0007g0168others(13): Show | 16 | HG00738.hp2 HG01099.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.43+7288C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652207 | ||||||
| chr7:155652321
|
A | G | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+7402A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652321 | ||||||
| chr7:155652341
|
T | C | 156 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.43+7422T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652341 | ||||||
| chr7:155652359
|
A | G | 218 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(215): Show | 219 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.43+7440A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652359 | ||||||
| chr7:155652514
|
A | G | 1 | a0002c0001t0002g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.43+7595A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652514 | ||||||
| chr7:155652565
|
G | A | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+7646G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652565 | ||||||
| chr7:155652612
|
A | C | 156 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.43+7693A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652612 | ||||||
| chr7:155652624
|
T | C | 1 | a0002c0001t0070g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.43+7705T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652624 | ||||||
| chr7:155652824
|
T | C | 1 | a0002c0001t0003g0293 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.43+7905T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652824 | ||||||
| chr7:155652832
|
G | A | 1 | a0002c0001t0002g0096 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.43+7913G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652832 | ||||||
| chr7:155652906
|
A | T | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.43+7987A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155652906 | ||||||
| chr7:155653052
|
A | G | 3 | a0001c0002t0007g0226a0001c0006t0092g0304a0006c0014t0095g0271 | 3 | HG02486.hp2 HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.43+8133A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653052 | ||||||
| chr7:155653093
|
A | G | 1 | a0002c0005t0018g0225 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.43+8174A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653093 | ||||||
| chr7:155653105
|
A | G | 138 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081others(135): Show | 138 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.43+8186A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653105 | ||||||
| chr7:155653152
|
A | G | 1 | a0001c0008t0086g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.43+8233A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653152 | ||||||
| chr7:155653345
|
G | T | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.43+8426G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653345 | ||||||
| chr7:155653508
|
G | A | 3 | a0002c0001t0002g0246a0002c0001t0004g0245a0002c0001t0016g0247 | 3 | HG00741.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.43+8589G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653508 | ||||||
| chr7:155653530
|
C | T | 1 | a0002c0001t0002g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.43+8611C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653530 | ||||||
| chr7:155653577
|
C | T | 1 | a0002c0005t0026g0224 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.43+8658C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653577 | ||||||
| chr7:155653582
|
G | GGA | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.43+8665_43+8666dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155653582 | |||||
| chr7:155653625
|
T | G | 5 | a0001c0002t0081g0089a0001c0002t0082g0088a0003c0007t0022g0289others(2): Show | 5 | HG00735.hp1 HG02486.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+8706T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653625 | ||||||
| chr7:155653705
|
T | C | 1 | a0001c0004t0005g0130 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.43+8786T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653705 | ||||||
| chr7:155653772
|
C | T | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.43+8853C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653772 | ||||||
| chr7:155653898
|
A | G | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43+8979A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653898 | ||||||
| chr7:155653911
|
C | A | 8 | a0002c0001t0001g0012a0002c0001t0001g0015a0002c0001t0001g0017others(5): Show | 8 | HG02074.hp1 NA18941.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.43+8992C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653911 | ||||||
| chr7:155653985
|
A | T | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.43+9066A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155653985 | ||||||
| chr7:155654072
|
A | G | 18 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(15): Show | 18 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.43+9153A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654072 | ||||||
| chr7:155654272
|
T | C | 156 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.43+9353T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654272 | ||||||
| chr7:155654385
|
T | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.43+9466T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654385 | ||||||
| chr7:155654437
|
G | A | 1 | a0002c0005t0014g0170 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.43+9518G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654437 | ||||||
| chr7:155654486
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.43+9567A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654486 | ||||||
| chr7:155654620
|
T | G | 1 | a0002c0001t0062g0020 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.43+9701T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654620 | ||||||
| chr7:155654628
|
A | G | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.43+9709A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654628 | ||||||
| chr7:155654635
|
T | C | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.43+9716T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654635 | ||||||
| chr7:155654831
|
G | A | 1 | a0001c0002t0007g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+9912G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654831 | ||||||
| chr7:155654845
|
A | T | 5 | a0001c0002t0081g0089a0001c0002t0082g0088a0003c0007t0022g0289others(2): Show | 5 | HG00735.hp1 HG02486.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.43+9926A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654845 | ||||||
| chr7:155654860
|
A | G | 1 | a0002c0001t0002g0127 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.43+9941A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155654860 | ||||||
| chr7:155655026
|
A | T | 63 | a0002c0001t0001g0104a0002c0001t0001g0105a0002c0001t0001g0145others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.43+10107A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155655026 | ||||||
| chr7:155655165
|
C | T | 155 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(152): Show | 155 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.44-10010C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155655165 | ||||||
| chr7:155655338
|
G | C | 5 | a0002c0001t0004g0098a0002c0001t0030g0301a0002c0001t0030g0302others(2): Show | 5 | HG01255.hp2 HG02055.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-9837G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155655338 | ||||||
| chr7:155655339
|
C | CT | 5 | a0001c0004t0005g0138a0001c0004t0005g0139a0001c0004t0005g0140others(2): Show | 5 | HG02647.hp2 NA18906.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-9828dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155655339 | |||||
| chr7:155655482
|
C | T | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.44-9693C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155655482 | ||||||
| chr7:155655534
|
C | CT | 48 | a0001c0002t0006g0217a0001c0002t0006g0219a0001c0002t0006g0221others(45): Show | 49 | HG00280.hp1 HG00423.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.44-9616dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155655534 | |||||
| chr7:155655534
|
C | CTT | 64 | a0001c0002t0101g0161a0001c0003t0005g0256a0001c0003t0008g0268others(61): Show | 64 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.44-9617_44-9616dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155655534 | |||||
| chr7:155655534
|
C | CTTT | 85 | a0001c0002t0031g0092a0001c0002t0053g0090a0001c0002t0090g0091others(82): Show | 85 | HG00544.hp2 HG00639.hp1 HG00673.hp2 others(82): Show |
intron_variant | MODIFIER | c.44-9618_44-9616dup others(3): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155655534 | |||||
| chr7:155655534
|
C | CTTTT | 31 | a0001c0002t0031g0094a0001c0002t0081g0089a0001c0002t0082g0088others(28): Show | 31 | HG00423.hp1 HG00621.hp1 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.44-9619_44-9616dup others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155655534 | |||||
| chr7:155655705
|
G | T | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-9470G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155655705 | ||||||
| chr7:155655846
|
A | G | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.44-9329A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155655846 | ||||||
| chr7:155655883
|
G | A | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.44-9292G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155655883 | ||||||
| chr7:155656028
|
G | A | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.44-9147G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155656028 | ||||||
| chr7:155656031
|
T | A | 1 | a0001c0017t0055g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.44-9144T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155656031 | ||||||
| chr7:155656301
|
C | A | 1 | a0002c0001t0002g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.44-8874C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155656301 | ||||||
| chr7:155656323
|
C | T | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-8852C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155656323 | ||||||
| chr7:155656356
|
G | A | 1 | a0001c0002t0025g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.44-8819G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155656356 | ||||||
| chr7:155656375
|
A | AG | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.44-8798dupG | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155656375 | |||||
| chr7:155656655
|
A | G | 1 | a0001c0002t0081g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.44-8520A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155656655 | ||||||
| chr7:155656657
|
C | T | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.44-8518C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155656657 | ||||||
| chr7:155656909
|
A | G | 14 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-8266A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155656909 | ||||||
| chr7:155656963
|
G | GT | 6 | a0001c0002t0024g0160a0002c0001t0004g0126a0002c0001t0013g0073others(3): Show | 6 | HG00642.hp1 HG00735.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.44-8199dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155656963 | |||||
| chr7:155657240
|
G | A | 217 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(214): Show | 218 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.44-7935G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657240 | ||||||
| chr7:155657246
|
T | C | 1 | a0001c0002t0104g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.44-7929T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657246 | ||||||
| chr7:155657259
|
G | A | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.44-7916G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657259 | ||||||
| chr7:155657289
|
C | T | 199 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(196): Show | 200 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.44-7886C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657289 | ||||||
| chr7:155657418
|
T | C | 1 | a0001c0003t0008g0258 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.44-7757T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657418 | ||||||
| chr7:155657470
|
G | A | 13 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(10): Show | 13 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.44-7705G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657470 | ||||||
| chr7:155657735
|
C | T | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-7440C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657735 | ||||||
| chr7:155657873
|
AC | A | 133 | a0002c0001t0001g0009a0002c0001t0001g0010a0002c0001t0001g0011others(130): Show | 133 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.44-7301delC | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657873 | ||||||
| chr7:155657890
|
C | T | 4 | a0002c0001t0001g0053a0002c0001t0001g0055a0002c0001t0001g0072others(1): Show | 4 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-7285C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657890 | ||||||
| chr7:155657990
|
A | G | 1 | a0001c0003t0007g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.44-7185A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155657990 | ||||||
| chr7:155658140
|
C | G | 1 | a0001c0002t0023g0159 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.44-7035C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658140 | ||||||
| chr7:155658180
|
T | C | 4 | a0001c0004t0005g0138a0001c0004t0005g0139a0001c0004t0005g0140others(1): Show | 4 | HG02647.hp2 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-6995T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658180 | ||||||
| chr7:155658240
|
A | G | 158 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(155): Show | 158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.44-6935A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658240 | ||||||
| chr7:155658297
|
G | A | 217 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(214): Show | 218 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.44-6878G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658297 | ||||||
| chr7:155658307
|
T | G | 1 | a0002c0001t0017g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.44-6868T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658307 | ||||||
| chr7:155658384
|
A | AT | 55 | a0001c0002t0006g0233a0001c0002t0006g0237a0001c0002t0007g0168others(52): Show | 55 | HG00323.hp1 HG00558.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.44-6770dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155658384 | |||||
| chr7:155658412
|
G | A | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-6763G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658412 | ||||||
| chr7:155658454
|
C | G | 4 | a0001c0002t0036g0274a0001c0002t0036g0275a0001c0002t0107g0276others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-6721C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658454 | ||||||
| chr7:155658558
|
G | A | 1 | a0001c0002t0029g0207 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.44-6617G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658558 | ||||||
| chr7:155658589
|
C | T | 8 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(5): Show | 8 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-6586C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658589 | ||||||
| chr7:155658694
|
C | T | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.44-6481C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658694 | ||||||
| chr7:155658804
|
C | G | 1 | a0002c0001t0015g0051 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.44-6371C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155658804 | ||||||
| chr7:155659446
|
A | G | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.44-5729A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155659446 | ||||||
| chr7:155659524
|
T | C | 1 | a0002c0001t0001g0022 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.44-5651T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155659524 | ||||||
| chr7:155659527
|
A | T | 2 | a0001c0003t0019g0252a0001c0003t0019g0255 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.44-5648A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155659527 | ||||||
| chr7:155659611
|
G | A | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.44-5564G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155659611 | ||||||
| chr7:155659666
|
C | T | 197 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(194): Show | 198 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.44-5509C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155659666 | ||||||
| chr7:155659746
|
A | G | 1 | a0002c0001t0078g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.44-5429A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155659746 | ||||||
| chr7:155659799
|
CG | C | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.44-5374delG | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155659799 | |||||
| chr7:155659901
|
G | C | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.44-5274G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155659901 | ||||||
| chr7:155660011
|
A | G | 1 | a0002c0001t0002g0124 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.44-5164A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660011 | ||||||
| chr7:155660050
|
G | A | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.44-5125G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660050 | ||||||
| chr7:155660216
|
G | C | 2 | a0001c0003t0005g0256a0001c0003t0099g0084 | 2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.44-4959G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660216 | ||||||
| chr7:155660275
|
A | G | 1 | a0002c0001t0001g0145 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.44-4900A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660275 | ||||||
| chr7:155660350
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-4825A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660350 | ||||||
| chr7:155660365
|
C | T | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-4810C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660365 | ||||||
| chr7:155660368
|
C | T | 158 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(155): Show | 158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.44-4807C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660368 | ||||||
| chr7:155660428
|
A | C | 2 | a0001c0003t0009g0270a0007c0013t0009g0265 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.44-4747A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660428 | ||||||
| chr7:155660437
|
G | A | 158 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(155): Show | 158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.44-4738G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660437 | ||||||
| chr7:155660446
|
A | G | 1 | a0002c0001t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.44-4729A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660446 | ||||||
| chr7:155660472
|
C | T | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.44-4703C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660472 | ||||||
| chr7:155660586
|
G | A | 167 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(164): Show | 167 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.44-4589G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660586 | ||||||
| chr7:155660607
|
A | T | 1 | a0002c0005t0018g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.44-4568A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660607 | ||||||
| chr7:155660967
|
T | C | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-4208T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155660967 | ||||||
| chr7:155661024
|
G | A | 5 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0101g0161others(2): Show | 5 | HG02630.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-4151G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661024 | ||||||
| chr7:155661039
|
A | G | 155 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(152): Show | 155 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.44-4136A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661039 | ||||||
| chr7:155661083
|
CTG | C | 7 | a0001c0003t0019g0251a0001c0003t0046g0254a0001c0003t0047g0282others(4): Show | 7 | HG02055.hp2 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-4079_44-4078del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661083 | |||||
| chr7:155661096
|
T | G | 4 | a0001c0003t0005g0256a0001c0003t0019g0252a0001c0003t0019g0255others(1): Show | 4 | HG02717.hp2 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-4079T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661096 | ||||||
| chr7:155661097
|
G | GT | 5 | a0001c0003t0050g0253a0002c0001t0002g0116a0002c0001t0030g0301others(2): Show | 5 | HG01255.hp2 HG01496.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-4078_44-4077ins others(1): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661097 | ||||||
| chr7:155661097
|
G | T | 4 | a0001c0003t0005g0256a0001c0003t0019g0252a0001c0003t0019g0255others(1): Show | 4 | HG02717.hp2 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-4078G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661097 | ||||||
| chr7:155661097
|
GGT | G | 74 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(71): Show | 74 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.44-4045_44-4044del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661097 | |||||
| chr7:155661097
|
GGTGT | G | 12 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0031g0094others(9): Show | 12 | HG00733.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.44-4047_44-4044del others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661097 | |||||
| chr7:155661097
|
GGTGTGT | G | 8 | a0001c0002t0023g0156a0001c0002t0024g0153a0001c0002t0024g0155others(5): Show | 8 | HG00642.hp1 HG02451.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.44-4049_44-4044del others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661097 | |||||
| chr7:155661097
|
GGTGTGTG others(3): Show |
G | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.44-4053_44-4044del others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661097 | |||||
| chr7:155661118
|
G | A | 1 | a0001c0002t0082g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-4057G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661118 | ||||||
| chr7:155661120
|
G | A | 1 | a0001c0002t0082g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44-4055G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661120 | ||||||
| chr7:155661122
|
G | A | 5 | a0001c0002t0081g0089a0001c0002t0082g0088a0002c0001t0030g0301others(2): Show | 5 | HG01255.hp2 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-4053G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661122 | ||||||
| chr7:155661122
|
GTGTGTGT others(3): Show |
G | 1 | a0006c0014t0095g0271 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.44-4051_44-4042del others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661122 | |||||
| chr7:155661124
|
G | A | 11 | a0001c0002t0053g0090a0001c0002t0081g0089a0001c0002t0082g0088others(8): Show | 11 | HG01255.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.44-4051G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661124 | ||||||
| chr7:155661126
|
G | A | 36 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(33): Show | 36 | HG00639.hp1 HG01255.hp2 HG01952.hp2 others(33): Show |
intron_variant | MODIFIER | c.44-4049G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661126 | ||||||
| chr7:155661128
|
G | A | 110 | a0001c0002t0007g0168a0001c0002t0025g0005a0001c0002t0025g0006others(107): Show | 110 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.44-4047G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661128 | ||||||
| chr7:155661130
|
G | A | 182 | a0001c0002t0006g0233a0001c0002t0006g0237a0001c0002t0007g0168others(179): Show | 183 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.44-4045G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661130 | ||||||
| chr7:155661130
|
G | GTGTGTAT others(3): Show |
1 | a0002c0001t0073g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.44-4044_44-4043ins others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661130 | |||||
| chr7:155661132
|
A | G | 9 | a0001c0003t0019g0252a0001c0003t0019g0255a0002c0001t0002g0114others(6): Show | 9 | HG00323.hp1 HG00558.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.44-4043A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661132 | ||||||
| chr7:155661141
|
TATA | T | 5 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(2): Show | 5 | HG01891.hp1 HG02486.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.44-4033_44-4031del others(3): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661141 | ||||||
| chr7:155661142
|
A | T | 3 | a0001c0004t0005g0137a0001c0004t0021g0151a0001c0004t0083g0150 | 3 | HG02559.hp2 HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.44-4033A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661142 | ||||||
| chr7:155661143
|
TA | T | 4 | a0001c0002t0031g0094a0001c0002t0105g0008a0001c0003t0019g0251others(1): Show | 4 | HG02109.hp1 HG03225.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-4031delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661143 | ||||||
| chr7:155661143
|
TATA | T | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.44-4031_44-4029del others(3): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661143 | ||||||
| chr7:155661144
|
A | AT | 3 | a0001c0003t0046g0254a0001c0003t0050g0253a0001c0004t0021g0148 | 3 | HG02145.hp2 HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.44-4030dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661144 | |||||
| chr7:155661144
|
A | T | 30 | a0001c0002t0011g0232a0001c0002t0012g0001a0001c0002t0012g0229others(27): Show | 30 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.44-4031A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661144 | ||||||
| chr7:155661145
|
TA | T | 3 | a0001c0002t0031g0092a0001c0002t0053g0090a0006c0014t0095g0271 | 3 | HG02258.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.44-4029delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661145 | ||||||
| chr7:155661146
|
A | ATATATAT others(8): Show |
1 | a0002c0001t0004g0119 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.44-4028_44-4027ins others(15): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATATAT others(5): Show |
3 | a0002c0001t0001g0011a0002c0001t0001g0022a0002c0001t0001g0025 | 3 | NA18961.hp2 NA18970.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.44-4028_44-4027ins others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATATAT others(6): Show |
1 | a0002c0001t0057g0013 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.44-4028_44-4027ins others(13): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATATAT others(7): Show |
1 | a0002c0001t0002g0123 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.44-4028_44-4027ins others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATATAT others(3): Show |
7 | a0002c0001t0002g0103a0002c0001t0002g0121a0002c0001t0002g0124others(4): Show | 7 | HG01258.hp1 HG02738.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-4028_44-4027ins others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATATAT others(5): Show |
12 | a0002c0001t0002g0114a0002c0001t0002g0116a0002c0001t0002g0127others(9): Show | 12 | HG00558.hp1 HG00735.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.44-4028_44-4027ins others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATATAT others(6): Show |
2 | a0002c0001t0004g0003a0002c0001t0016g0004 | 2 | NA18956.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.44-4028_44-4027ins others(13): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATATTT others(1): Show |
21 | a0002c0001t0001g0015a0002c0001t0001g0026a0002c0001t0001g0056others(18): Show | 21 | HG00642.hp2 HG00741.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.44-4028_44-4027ins others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATATTT others(3): Show |
4 | a0001c0017t0055g0142a0003c0007t0022g0289a0003c0007t0022g0290others(1): Show | 4 | HG00735.hp1 HG02257.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-4028_44-4027ins others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATATTT others(5): Show |
6 | a0002c0001t0001g0145a0002c0001t0002g0108a0002c0001t0002g0109others(3): Show | 6 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.44-4028_44-4027ins others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATTTT | 43 | a0002c0001t0001g0009a0002c0001t0001g0012a0002c0001t0001g0031others(40): Show | 43 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.44-4028_44-4027ins others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATATTTTT others(1): Show |
7 | a0002c0001t0002g0096a0002c0001t0002g0146a0002c0001t0004g0147others(4): Show | 7 | HG02080.hp2 HG02132.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-4028_44-4027ins others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | ATTTT | 7 | a0002c0001t0004g0101a0002c0001t0004g0102a0002c0001t0015g0051others(4): Show | 7 | HG01952.hp2 HG02165.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-4019_44-4016dup others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661146
|
A | T | 58 | a0001c0002t0007g0212a0001c0002t0007g0222a0001c0002t0007g0228others(55): Show | 58 | HG00639.hp1 HG00673.hp1 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.44-4029A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661146 | ||||||
| chr7:155661146
|
AT | A | 26 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0102g0154others(23): Show | 27 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.44-4016delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661146 | |||||
| chr7:155661148
|
T | A | 4 | a0001c0002t0036g0274a0001c0002t0036g0275a0001c0002t0107g0276others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.44-4027T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661148 | ||||||
| chr7:155661149
|
T | A | 2 | a0001c0003t0047g0282a0001c0003t0051g0281 | 2 | HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.44-4026T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661149 | ||||||
| chr7:155661401
|
CTTTCTTT others(3): Show |
C | 2 | a0001c0006t0092g0304a0006c0014t0095g0271 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.44-3761_44-3752del others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155661401 | |||||
| chr7:155661441
|
T | C | 1 | a0002c0001t0063g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.44-3734T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661441 | ||||||
| chr7:155661463
|
A | T | 2 | a0002c0001t0001g0010a0002c0001t0003g0042 | 2 | NA18953.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.44-3712A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661463 | ||||||
| chr7:155661589
|
G | A | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.44-3586G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661589 | ||||||
| chr7:155661596
|
C | T | 1 | a0001c0002t0027g0234 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.44-3579C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661596 | ||||||
| chr7:155661628
|
G | A | 2 | a0001c0002t0010g0172a0001c0002t0038g0214 | 2 | NA18951.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.44-3547G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661628 | ||||||
| chr7:155661740
|
T | C | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-3435T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661740 | ||||||
| chr7:155661813
|
T | A | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.44-3362T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661813 | ||||||
| chr7:155661976
|
A | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.44-3199A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155661976 | ||||||
| chr7:155662364
|
T | G | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.44-2811T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662364 | ||||||
| chr7:155662375
|
T | C | 7 | a0001c0003t0005g0256a0001c0003t0047g0282a0001c0003t0048g0280others(4): Show | 7 | HG02055.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-2800T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662375 | ||||||
| chr7:155662413
|
C | T | 1 | a0001c0002t0081g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.44-2762C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662413 | ||||||
| chr7:155662485
|
G | A | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.44-2690G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662485 | ||||||
| chr7:155662519
|
G | C | 1 | a0001c0003t0051g0281 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.44-2656G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662519 | ||||||
| chr7:155662585
|
T | C | 3 | a0004c0010t0001g0043a0004c0010t0001g0044a0004c0015t0017g0065 | 3 | HG02132.hp2 HG03688.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.44-2590T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662585 | ||||||
| chr7:155662716
|
A | C | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.44-2459A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662716 | ||||||
| chr7:155662780
|
C | T | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-2395C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662780 | ||||||
| chr7:155662863
|
G | C | 14 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-2312G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662863 | ||||||
| chr7:155662889
|
C | G | 1 | a0002c0001t0059g0300 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.44-2286C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155662889 | ||||||
| chr7:155663197
|
TTTTC | T | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-1966_44-1963del others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155663197 | |||||
| chr7:155663209
|
C | CT | 134 | a0001c0002t0024g0153a0001c0002t0024g0160a0001c0017t0055g0142others(131): Show | 134 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.44-1954dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155663209 | |||||
| chr7:155663359
|
C | T | 18 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(15): Show | 18 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-1816C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155663359 | ||||||
| chr7:155663567
|
G | A | 17 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(14): Show | 18 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.44-1608G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155663567 | ||||||
| chr7:155663722
|
C | T | 1 | a0002c0001t0001g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.44-1453C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155663722 | ||||||
| chr7:155663754
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.44-1421A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155663754 | ||||||
| chr7:155663957
|
C | T | 14 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.44-1218C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155663957 | ||||||
| chr7:155664051
|
A | T | 1 | a0002c0005t0014g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.44-1124A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664051 | ||||||
| chr7:155664224
|
T | C | 218 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(215): Show | 219 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.44-951T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664224 | ||||||
| chr7:155664231
|
TTA | T | 59 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(56): Show | 60 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.44-932_44-931delAT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155664231 | |||||
| chr7:155664239
|
A | ATG | 3 | a0002c0001t0002g0116a0002c0001t0004g0126a0002c0001t0059g0300 | 3 | HG00735.hp2 HG01496.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.44-935_44-934insGT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155664239 | |||||
| chr7:155664239
|
A | G | 1 | a0001c0002t0028g0200 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.44-936A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664239 | ||||||
| chr7:155664241
|
A | ATG | 7 | a0002c0001t0002g0295a0002c0001t0004g0296a0002c0001t0032g0297others(4): Show | 7 | HG01884.hp2 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.44-933_44-932insGT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155664241 | |||||
| chr7:155664241
|
A | G | 152 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(149): Show | 152 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.44-934A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664241 | ||||||
| chr7:155664243
|
A | G | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.44-932A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664243 | ||||||
| chr7:155664265
|
AT | A | 167 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(164): Show | 167 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.44-899delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155664265 | |||||
| chr7:155664296
|
T | C | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.44-879T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664296 | ||||||
| chr7:155664321
|
T | A | 2 | a0002c0001t0060g0288a0002c0001t0066g0287 | 2 | HG01175.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.44-854T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664321 | ||||||
| chr7:155664323
|
C | A | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.44-852C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664323 | ||||||
| chr7:155664362
|
C | G | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.44-813C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664362 | ||||||
| chr7:155664416
|
G | A | 218 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(215): Show | 219 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.44-759G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664416 | ||||||
| chr7:155664427
|
A | AT | 13 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(10): Show | 13 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.44-735dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155664427 | |||||
| chr7:155664480
|
G | A | 14 | a0002c0001t0001g0031a0002c0001t0013g0050a0002c0001t0013g0060others(11): Show | 14 | HG00621.hp1 HG02040.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.44-695G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664480 | ||||||
| chr7:155664481
|
A | G | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.44-694A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664481 | ||||||
| chr7:155664523
|
C | T | 1 | a0001c0008t0091g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.44-652C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664523 | ||||||
| chr7:155664703
|
G | A | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.44-472G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664703 | ||||||
| chr7:155664819
|
G | C | 1 | a0001c0002t0115g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.44-356G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664819 | ||||||
| chr7:155664835
|
C | A | 1 | a0001c0004t0005g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.44-340C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155664835 | ||||||
| chr7:155664917
|
G | GT | 193 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(190): Show | 194 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.44-247dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 155664917 | |||||
| chr7:155665014
|
T | G | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.44-161T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155665014 | ||||||
| chr7:155665042
|
A | G | 1 | a0005c0012t0008g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.44-133A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155665042 | ||||||
| chr7:155665094
|
A | T | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.44-81A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 1/17 | chr7 | 155665094 | ||||||
| chr7:155665276
|
C | T | 1 | a0002c0001t0004g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.122+23C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665276 | ||||||
| chr7:155665320
|
G | A | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.122+67G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665320 | ||||||
| chr7:155665422
|
A | G | 1 | a0002c0001t0001g0145 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.122+169A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665422 | ||||||
| chr7:155665457
|
G | A | 5 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0101g0161others(2): Show | 5 | HG02630.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.122+204G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665457 | ||||||
| chr7:155665544
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.122+291A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665544 | ||||||
| chr7:155665554
|
C | A | 2 | a0002c0001t0002g0116a0002c0001t0004g0126 | 2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.122+301C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665554 | ||||||
| chr7:155665679
|
G | A | 1 | a0002c0001t0016g0080 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.122+426G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665679 | ||||||
| chr7:155665759
|
A | T | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.122+506A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665759 | ||||||
| chr7:155665810
|
A | G | 1 | a0002c0001t0001g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.122+557A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665810 | ||||||
| chr7:155665893
|
C | A | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.122+640C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665893 | ||||||
| chr7:155665897
|
A | G | 2 | a0002c0001t0001g0105a0002c0001t0078g0117 | 2 | HG01517.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.122+644A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155665897 | ||||||
| chr7:155666122
|
A | G | 1 | a0002c0001t0003g0041 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.122+869A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155666122 | ||||||
| chr7:155666135
|
A | G | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.122+882A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155666135 | ||||||
| chr7:155666196
|
A | G | 1 | a0002c0001t0002g0040 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.122+943A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155666196 | ||||||
| chr7:155666367
|
A | C | 1 | a0001c0003t0098g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.122+1114A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155666367 | ||||||
| chr7:155666453
|
T | C | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.122+1200T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155666453 | ||||||
| chr7:155666599
|
A | T | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.122+1346A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155666599 | ||||||
| chr7:155666681
|
C | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.122+1428C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155666681 | ||||||
| chr7:155667044
|
T | A | 1 | a0001c0003t0019g0251 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.122+1791T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667044 | ||||||
| chr7:155667089
|
C | T | 1 | a0001c0002t0023g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.122+1836C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667089 | ||||||
| chr7:155667107
|
C | T | 4 | a0002c0001t0060g0288a0002c0001t0066g0287a0002c0001t0074g0285others(1): Show | 4 | HG01175.hp2 HG01978.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.122+1854C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667107 | ||||||
| chr7:155667135
|
C | G | 1 | a0001c0002t0082g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.122+1882C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667135 | ||||||
| chr7:155667159
|
T | C | 16 | a0002c0001t0001g0010a0002c0001t0001g0031a0002c0001t0003g0042others(13): Show | 16 | HG00621.hp1 HG02040.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.122+1906T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667159 | ||||||
| chr7:155667587
|
C | T | 3 | a0002c0001t0003g0039a0002c0001t0003g0067a0002c0001t0003g0293 | 3 | HG01891.hp2 HG01934.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.122+2334C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667587 | ||||||
| chr7:155667605
|
C | T | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.122+2352C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667605 | ||||||
| chr7:155667754
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.122+2501A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667754 | ||||||
| chr7:155667811
|
C | T | 1 | a0002c0001t0015g0051 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.122+2558C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667811 | ||||||
| chr7:155667837
|
A | T | 1 | a0001c0003t0008g0269 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.122+2584A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667837 | ||||||
| chr7:155667974
|
A | G | 1 | a0002c0001t0001g0058 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.122+2721A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155667974 | ||||||
| chr7:155668253
|
G | C | 2 | a0001c0002t0006g0173a0001c0002t0007g0215 | 2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.122+3000G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155668253 | ||||||
| chr7:155668470
|
T | C | 1 | a0001c0002t0024g0160 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.122+3217T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155668470 | ||||||
| chr7:155668493
|
G | A | 8 | a0002c0001t0001g0012a0002c0001t0001g0015a0002c0001t0001g0017others(5): Show | 8 | HG02074.hp1 NA18941.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.122+3240G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155668493 | ||||||
| chr7:155668684
|
G | A | 2 | a0001c0003t0047g0282a0001c0003t0051g0281 | 2 | HG02055.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.122+3431G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155668684 | ||||||
| chr7:155668827
|
G | T | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.122+3574G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155668827 | ||||||
| chr7:155668865
|
A | C | 4 | a0001c0004t0005g0138a0001c0004t0005g0139a0001c0004t0005g0140others(1): Show | 4 | HG02647.hp2 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.122+3612A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155668865 | ||||||
| chr7:155668871
|
A | T | 134 | a0002c0001t0001g0009a0002c0001t0001g0010a0002c0001t0001g0011others(131): Show | 134 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.122+3618A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155668871 | ||||||
| chr7:155668908
|
A | C | 135 | a0001c0017t0055g0142a0002c0001t0001g0009a0002c0001t0001g0010others(132): Show | 135 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.122+3655A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155668908 | ||||||
| chr7:155669217
|
C | T | 1 | a0001c0004t0005g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.123-3650C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155669217 | ||||||
| chr7:155669256
|
C | T | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.123-3611C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155669256 | ||||||
| chr7:155669288
|
A | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.123-3579A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155669288 | ||||||
| chr7:155669477
|
C | T | 1 | a0002c0001t0078g0117 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.123-3390C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155669477 | ||||||
| chr7:155669478
|
G | A | 2 | a0001c0004t0041g0083a0001c0004t0043g0081 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.123-3389G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155669478 | ||||||
| chr7:155669837
|
G | A | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.123-3030G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155669837 | ||||||
| chr7:155669893
|
T | C | 9 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(6): Show | 9 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-2974T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155669893 | ||||||
| chr7:155670042
|
A | G | 4 | a0001c0003t0019g0252a0001c0003t0019g0255a0001c0003t0046g0254others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.123-2825A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155670042 | ||||||
| chr7:155670055
|
T | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.123-2812T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155670055 | ||||||
| chr7:155670172
|
G | A | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.123-2695G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155670172 | ||||||
| chr7:155670347
|
C | T | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.123-2520C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155670347 | ||||||
| chr7:155670674
|
C | T | 138 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081others(135): Show | 138 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.123-2193C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155670674 | ||||||
| chr7:155670696
|
T | A | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.123-2171T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155670696 | ||||||
| chr7:155670937
|
C | T | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.123-1930C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155670937 | ||||||
| chr7:155670994
|
C | CTTTTTTT others(5): Show |
9 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(6): Show | 9 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.123-1872_123-1871i others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 155670994 | |||||
| chr7:155671094
|
A | G | 156 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.123-1773A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155671094 | ||||||
| chr7:155671235
|
A | G | 1 | a0001c0002t0104g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.123-1632A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155671235 | ||||||
| chr7:155671290
|
C | A | 63 | a0002c0001t0001g0104a0002c0001t0001g0105a0002c0001t0001g0145others(60): Show | 63 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.123-1577C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155671290 | ||||||
| chr7:155671327
|
G | T | 2 | a0001c0002t0006g0237a0001c0002t0118g0236 | 2 | NA18949.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.123-1540G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155671327 | ||||||
| chr7:155672007
|
AATTGCAA others(7): Show |
A | 1 | a0002c0001t0002g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.123-857_123-844del others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 155672007 | |||||
| chr7:155672090
|
G | A | 1 | a0001c0002t0006g0174 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.123-777G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155672090 | ||||||
| chr7:155672196
|
T | G | 1 | a0001c0003t0007g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.123-671T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155672196 | ||||||
| chr7:155672343
|
GA | G | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.123-523delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155672343 | ||||||
| chr7:155672395
|
C | T | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.123-472C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155672395 | ||||||
| chr7:155672728
|
C | G | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.123-139C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155672728 | ||||||
| chr7:155672744
|
C | CA | 10 | a0001c0002t0006g0174a0001c0002t0007g0212a0001c0002t0007g0222others(7): Show | 10 | HG00673.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.123-102dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 155672744 | |||||
| chr7:155672744
|
C | CAAA | 12 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.123-104_123-102dup others(3): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 155672744 | |||||
| chr7:155672744
|
CA | C | 32 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0024g0153others(29): Show | 33 | HG00642.hp1 HG00733.hp1 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.123-102delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 155672744 | |||||
| chr7:155672744
|
CAAA | C | 158 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(155): Show | 158 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.123-104_123-102del others(3): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 155672744 | |||||
| chr7:155672823
|
C | T | 1 | a0001c0004t0005g0131 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.123-44C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 2/17 | chr7 | 155672823 | ||||||
| chr7:155673154
|
T | C | 8 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+239T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673154 | ||||||
| chr7:155673183
|
CAT | C | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+270_171+271del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673183 | |||||
| chr7:155673300
|
C | G | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+385C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673300 | ||||||
| chr7:155673313
|
C | T | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+398C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673313 | ||||||
| chr7:155673402
|
T | TTG | 5 | a0001c0002t0006g0221a0001c0002t0011g0239a0001c0002t0011g0241others(2): Show | 5 | NA18955.hp1 NA18957.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+525_171+526dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673402 | |||||
| chr7:155673402
|
TTG | T | 61 | a0001c0002t0006g0174a0001c0002t0006g0180a0001c0002t0006g0181others(58): Show | 61 | HG00544.hp1 HG00642.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.171+525_171+526del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673402 | |||||
| chr7:155673402
|
TTGTG | T | 23 | a0001c0002t0006g0175a0001c0002t0006g0217a0001c0002t0006g0233others(20): Show | 23 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.171+523_171+526del others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673402 | |||||
| chr7:155673402
|
TTGTGTG | T | 173 | a0001c0002t0006g0237a0001c0002t0012g0001a0001c0002t0012g0229others(170): Show | 174 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.171+521_171+526del others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673402 | |||||
| chr7:155673402
|
TTGTGTGT others(1): Show |
T | 5 | a0001c0002t0006g0173a0001c0002t0007g0215a0002c0001t0002g0129others(2): Show | 5 | HG02683.hp2 HG03669.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+519_171+526del others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673402 | |||||
| chr7:155673402
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0003t0007g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.171+517_171+526del others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673402 | |||||
| chr7:155673402
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0002t0036g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.171+515_171+526del others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673402 | |||||
| chr7:155673405
|
T | TGG | 16 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.171+491_171+492ins others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673405 | |||||
| chr7:155673407
|
T | G | 5 | a0001c0008t0086g0087a0001c0008t0091g0086a0003c0007t0022g0289others(2): Show | 5 | HG00735.hp1 HG02486.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+492T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673407 | ||||||
| chr7:155673409
|
T | G | 22 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(19): Show | 22 | HG00642.hp1 HG01891.hp1 HG02451.hp1 others(19): Show |
intron_variant | MODIFIER | c.171+494T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673409 | ||||||
| chr7:155673411
|
T | G | 14 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0099g0084others(11): Show | 14 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.171+496T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673411 | ||||||
| chr7:155673413
|
T | G | 181 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0002t0105g0008others(178): Show | 182 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.171+498T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673413 | ||||||
| chr7:155673414
|
G | A | 1 | a0001c0002t0010g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.171+499G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673414 | ||||||
| chr7:155673415
|
T | G | 129 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(126): Show | 129 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.171+500T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673415 | ||||||
| chr7:155673417
|
T | G | 18 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(15): Show | 18 | HG00642.hp1 HG02486.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.171+502T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673417 | ||||||
| chr7:155673421
|
T | G | 20 | a0001c0002t0023g0156a0001c0002t0105g0008a0001c0003t0008g0002others(17): Show | 21 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.171+506T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673421 | ||||||
| chr7:155673477
|
C | CGT | 3 | a0001c0002t0024g0153a0001c0002t0024g0155a0001c0002t0024g0160 | 3 | HG00642.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.171+567_171+568dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673477 | |||||
| chr7:155673482
|
G | GTA | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.171+576_171+577dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673482 | |||||
| chr7:155673488
|
A | G | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.171+573A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673488 | ||||||
| chr7:155673489
|
T | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.171+574T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673489 | ||||||
| chr7:155673491
|
T | TACCCACA others(387): Show |
1 | a0001c0003t0051g0281 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.171+578_171+579ins others(394): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673491 | |||||
| chr7:155673494
|
A | C | 11 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+579A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673494 | ||||||
| chr7:155673497
|
C | CATAT | 14 | a0001c0003t0005g0256a0001c0003t0009g0263a0001c0003t0019g0251others(11): Show | 14 | HG01943.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.171+586_171+589dup others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673497 | |||||
| chr7:155673499
|
TATATACA others(125): Show |
T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.171+610_171+741del | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673499 | |||||
| chr7:155673505
|
C | T | 1 | a0003c0007t0022g0291 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.171+590C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673505 | ||||||
| chr7:155673511
|
C | T | 143 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(140): Show | 143 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.171+596C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673511 | ||||||
| chr7:155673512
|
A | G | 6 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(3): Show | 6 | HG02647.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+597A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673512 | ||||||
| chr7:155673513
|
C | T | 6 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(3): Show | 6 | HG02647.hp1 HG02922.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+598C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673513 | ||||||
| chr7:155673525
|
T | C | 1 | a0002c0001t0001g0062 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.171+610T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673525 | ||||||
| chr7:155673530
|
A | G | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.171+615A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673530 | ||||||
| chr7:155673531
|
CAT | C | 17 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(14): Show | 18 | HG01928.hp2 HG01943.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.171+622_171+623del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673531 | |||||
| chr7:155673533
|
T | TATACATA others(279): Show |
7 | a0001c0003t0008g0268a0001c0003t0009g0259a0001c0003t0009g0270others(4): Show | 7 | HG00280.hp1 HG00323.hp2 HG03669.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+621_171+622ins others(286): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673533 | |||||
| chr7:155673533
|
T | TATACATA others(277): Show |
1 | a0001c0003t0098g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.171+621_171+622ins others(284): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673533 | |||||
| chr7:155673533
|
TATATACA others(25): Show |
T | 2 | a0001c0006t0092g0304a0006c0014t0095g0271 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.171+646_171+677del others(32): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673533 | |||||
| chr7:155673546
|
A | G | 1 | a0001c0003t0049g0283 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.171+631A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673546 | ||||||
| chr7:155673547
|
C | T | 1 | a0001c0003t0049g0283 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.171+632C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673547 | ||||||
| chr7:155673550
|
G | GTA | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.171+644_171+645dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673550 | |||||
| chr7:155673550
|
GTATATAT others(27): Show |
G | 1 | a0001c0002t0036g0274 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.171+678_171+711del others(34): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673550 | |||||
| chr7:155673559
|
TACACACA others(29): Show |
T | 3 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0102g0154 | 3 | HG02630.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.171+650_171+685del others(36): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673559 | |||||
| chr7:155673559
|
TACACACA others(61): Show |
T | 2 | a0001c0002t0101g0161a0001c0002t0103g0158 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.171+650_171+717del others(68): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673559 | |||||
| chr7:155673564
|
A | G | 31 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(28): Show | 32 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.171+649A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673564 | ||||||
| chr7:155673565
|
C | CAT | 181 | a0001c0002t0006g0173a0001c0002t0006g0217a0001c0002t0006g0233others(178): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.171+654_171+655dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673565 | |||||
| chr7:155673565
|
C | CATATATA others(63): Show |
1 | a0001c0002t0007g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.171+655_171+656ins others(70): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673565 | |||||
| chr7:155673567
|
TATACATA others(57): Show |
T | 5 | a0001c0004t0005g0138a0001c0004t0005g0139a0001c0004t0005g0140others(2): Show | 5 | HG00673.hp2 HG02647.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+656_171+719del others(64): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673567 | |||||
| chr7:155673579
|
C | G | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+664C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673579 | ||||||
| chr7:155673582
|
GTA | G | 43 | a0001c0002t0011g0232a0001c0002t0012g0001a0001c0002t0012g0229others(40): Show | 44 | HG00280.hp1 HG00323.hp2 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.171+678_171+679del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673582 | |||||
| chr7:155673582
|
GTATA | G | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.171+676_171+679del others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673582 | |||||
| chr7:155673584
|
A | ATATATAT others(87): Show |
1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.171+677_171+678ins others(94): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673584 | |||||
| chr7:155673584
|
A | ATATATAT others(119): Show |
1 | a0001c0003t0019g0251 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.171+677_171+678ins others(126): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673584 | |||||
| chr7:155673584
|
A | ATATATAT others(183): Show |
2 | a0001c0003t0019g0252a0001c0003t0019g0255 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.171+677_171+678ins others(190): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673584 | |||||
| chr7:155673584
|
A | ATATATAT others(215): Show |
2 | a0001c0003t0046g0254a0001c0003t0050g0253 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.171+677_171+678ins others(222): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673584 | |||||
| chr7:155673584
|
A | ATATATAT others(279): Show |
1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.171+677_171+678ins others(286): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673584 | |||||
| chr7:155673584
|
ATATATAT others(57): Show |
A | 6 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.171+678_171+741del others(64): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673584 | |||||
| chr7:155673586
|
ATATATAT others(55): Show |
A | 140 | a0001c0004t0005g0130a0001c0004t0005g0132a0001c0004t0005g0133others(137): Show | 140 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.171+722_171+783del others(62): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673586 | |||||
| chr7:155673588
|
ATATATAC others(53): Show |
A | 3 | a0001c0004t0005g0131a0001c0017t0055g0142a0002c0001t0001g0012 | 3 | HG02257.hp1 HG02818.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.171+680_171+739del others(60): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673588 | |||||
| chr7:155673591
|
TATACACA others(59): Show |
T | 3 | a0001c0002t0023g0156a0001c0002t0024g0153a0001c0002t0024g0155 | 3 | HG02895.hp1 HG02897.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.171+678_171+743del others(66): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673591 | |||||
| chr7:155673593
|
T | C | 3 | a0001c0002t0012g0231a0001c0003t0051g0281a0001c0018t0079g0079 | 3 | HG02055.hp2 NA19058.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.171+678T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673593 | ||||||
| chr7:155673598
|
A | G | 31 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(28): Show | 32 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.171+683A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673598 | ||||||
| chr7:155673599
|
C | T | 2 | a0001c0002t0012g0231a0001c0018t0079g0079 | 2 | NA19058.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.171+684C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673599 | ||||||
| chr7:155673601
|
T | C | 1 | a0001c0002t0024g0160 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.171+686T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673601 | ||||||
| chr7:155673605
|
C | A | 1 | a0001c0004t0042g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.171+690C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673605 | ||||||
| chr7:155673616
|
GTA | G | 6 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(3): Show | 6 | HG01891.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+710_171+711del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673616 | |||||
| chr7:155673618
|
ATATATAT others(23): Show |
A | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.171+742_171+771del others(30): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673618 | |||||
| chr7:155673625
|
T | C | 3 | a0001c0002t0024g0160a0001c0003t0009g0270a0007c0013t0009g0265 | 3 | HG00280.hp1 HG00323.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.171+710T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673625 | ||||||
| chr7:155673630
|
A | G | 31 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(28): Show | 32 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.171+715A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673630 | ||||||
| chr7:155673631
|
C | T | 1 | a0001c0002t0024g0160 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.171+716C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673631 | ||||||
| chr7:155673631
|
CAT | C | 3 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0102g0154 | 3 | HG02630.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.171+720_171+721del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673631 | |||||
| chr7:155673631
|
CATATACA others(57): Show |
C | 7 | a0002c0001t0001g0015a0002c0001t0001g0017a0002c0001t0001g0075others(4): Show | 7 | HG00735.hp1 HG02486.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+742_171+805del others(64): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673631 | |||||
| chr7:155673632
|
A | G | 1 | a0001c0008t0091g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.171+717A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673632 | ||||||
| chr7:155673633
|
TATACATA others(21): Show |
T | 4 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081others(1): Show | 4 | HG01884.hp1 HG02451.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+722_171+749del others(28): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673633 | |||||
| chr7:155673643
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.171+728C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673643 | ||||||
| chr7:155673648
|
G | GTA | 29 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(26): Show | 30 | HG00673.hp2 HG01928.hp2 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.171+740_171+741dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673648 | |||||
| chr7:155673648
|
G | GTATATAT others(27): Show |
1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.171+741_171+742ins others(34): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673648 | |||||
| chr7:155673648
|
G | GTATATAT others(153): Show |
2 | a0001c0003t0048g0280a0001c0003t0052g0279 | 2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.171+741_171+742ins others(160): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673648 | |||||
| chr7:155673650
|
ATATATAC others(21): Show |
A | 1 | a0001c0002t0024g0160 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.171+742_171+769del others(28): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673650 | |||||
| chr7:155673655
|
T | C | 1 | a0002c0001t0054g0294 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.171+740T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673655 | ||||||
| chr7:155673655
|
T | TATACACG others(223): Show |
1 | a0001c0003t0047g0282 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.171+741_171+742ins others(230): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673655 | |||||
| chr7:155673655
|
T | TATACACG others(255): Show |
1 | a0001c0003t0049g0283 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.171+741_171+742ins others(262): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673655 | |||||
| chr7:155673657
|
C | T | 2 | a0001c0002t0101g0161a0001c0002t0103g0158 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.171+742C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673657 | ||||||
| chr7:155673660
|
A | G | 27 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(24): Show | 28 | HG01928.hp2 HG01943.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.171+745A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673660 | ||||||
| chr7:155673661
|
C | CAT | 3 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0102g0154 | 3 | HG02630.hp2 HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.171+750_171+751dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673661 | |||||
| chr7:155673661
|
C | T | 3 | a0001c0003t0047g0282a0001c0003t0049g0283a0001c0003t0051g0281 | 3 | HG02055.hp2 HG02647.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.171+746C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673661 | ||||||
| chr7:155673663
|
T | C | 5 | a0001c0002t0023g0156a0001c0002t0024g0153a0001c0002t0024g0155others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+748T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673663 | ||||||
| chr7:155673678
|
G | GTATATAT others(29): Show |
3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.171+771_171+772ins others(36): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673678 | |||||
| chr7:155673678
|
GTA | G | 5 | a0001c0002t0023g0156a0001c0002t0024g0153a0001c0002t0024g0155others(2): Show | 5 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+772_171+773del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673678 | |||||
| chr7:155673687
|
T | C | 14 | a0001c0002t0024g0160a0001c0002t0025g0005a0001c0002t0025g0006others(11): Show | 14 | HG00280.hp1 HG00323.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.171+772T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673687 | ||||||
| chr7:155673687
|
T | TAC | 6 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0102g0154others(3): Show | 6 | HG02055.hp2 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+778_171+779dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673687 | |||||
| chr7:155673687
|
T | TACACGCA others(505): Show |
1 | a0001c0003t0008g0266 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.171+776_171+777ins others(512): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673687 | |||||
| chr7:155673687
|
T | TACACGCA others(347): Show |
1 | a0001c0003t0099g0084 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.171+776_171+777ins others(354): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673687 | |||||
| chr7:155673689
|
C | CACGCATA others(405): Show |
2 | a0001c0003t0008g0257a0001c0003t0009g0260 | 2 | NA19067.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.171+776_171+777ins others(412): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673689 | |||||
| chr7:155673689
|
C | CACGCATA others(469): Show |
1 | a0001c0003t0009g0263 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.171+776_171+777ins others(476): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673689 | |||||
| chr7:155673691
|
CACATATA others(5): Show |
C | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.171+780_171+791del others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673691 | |||||
| chr7:155673692
|
A | G | 18 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0258others(15): Show | 19 | HG01928.hp2 HG02109.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.171+777A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673692 | ||||||
| chr7:155673694
|
A | G | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+779A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673694 | ||||||
| chr7:155673695
|
T | C | 4 | a0001c0003t0008g0257a0001c0003t0009g0260a0001c0003t0009g0263others(1): Show | 4 | HG01943.hp2 NA18974.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+780T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673695 | ||||||
| chr7:155673695
|
T | TATACATA others(213): Show |
1 | a0001c0003t0008g0258 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.171+783_171+784ins others(220): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673695 | |||||
| chr7:155673695
|
T | TATACATA others(439): Show |
1 | a0005c0012t0008g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.171+783_171+784ins others(446): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673695 | |||||
| chr7:155673695
|
T | TATACATA others(279): Show |
1 | a0001c0003t0005g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.171+783_171+784ins others(286): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673695 | |||||
| chr7:155673695
|
T | TATACATA others(373): Show |
1 | a0001c0003t0008g0002 | 2 | HG01928.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.171+783_171+784ins others(380): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673695 | |||||
| chr7:155673695
|
T | TATACATA others(405): Show |
1 | a0001c0003t0008g0269 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.171+783_171+784ins others(412): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673695 | |||||
| chr7:155673695
|
T | TATACATA others(437): Show |
2 | a0001c0003t0009g0261a0001c0003t0009g0262 | 2 | NA18983.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.171+783_171+784ins others(444): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673695 | |||||
| chr7:155673699
|
T | C | 1 | a0001c0003t0008g0266 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.171+784T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673699 | ||||||
| chr7:155673701
|
CAT | C | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+788_171+789del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673701 | |||||
| chr7:155673717
|
TATATACA others(19): Show |
T | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.171+804_171+829del others(26): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673717 | |||||
| chr7:155673719
|
T | C | 2 | a0001c0002t0024g0160a0001c0002t0102g0154 | 2 | HG00642.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.171+804T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673719 | ||||||
| chr7:155673720
|
A | G | 2 | a0001c0002t0024g0160a0001c0002t0102g0154 | 2 | HG00642.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.171+805A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673720 | ||||||
| chr7:155673721
|
T | TAC | 3 | a0001c0004t0021g0148a0001c0004t0021g0151a0001c0004t0083g0150 | 3 | HG02559.hp2 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.171+814_171+815dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673721 | |||||
| chr7:155673721
|
TAC | T | 5 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+814_171+815del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673721 | |||||
| chr7:155673722
|
A | G | 2 | a0001c0002t0024g0160a0001c0002t0102g0154 | 2 | HG00642.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.171+807A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673722 | ||||||
| chr7:155673724
|
A | G | 2 | a0001c0002t0024g0160a0001c0002t0102g0154 | 2 | HG00642.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.171+809A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673724 | ||||||
| chr7:155673725
|
CACACATA others(21): Show |
C | 2 | a0001c0002t0024g0160a0001c0002t0102g0154 | 2 | HG00642.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.171+813_171+840del others(28): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673725 | |||||
| chr7:155673726
|
A | G | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.171+811A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673726 | ||||||
| chr7:155673728
|
A | G | 5 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+813A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673728 | ||||||
| chr7:155673730
|
A | G | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.171+815A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673730 | ||||||
| chr7:155673745
|
C | T | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.171+830C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673745 | ||||||
| chr7:155673749
|
T | C | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.171+834T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673749 | ||||||
| chr7:155673750
|
A | G | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.171+835A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673750 | ||||||
| chr7:155673751
|
T | C | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.171+836T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673751 | ||||||
| chr7:155673753
|
T | C | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.171+838T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673753 | ||||||
| chr7:155673754
|
A | ACGCG | 25 | a0001c0003t0050g0253a0001c0003t0085g0272a0001c0004t0005g0130others(22): Show | 25 | HG00140.hp1 HG00639.hp1 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.171+843_171+846dup others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673754 | |||||
| chr7:155673754
|
A | G | 9 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0081g0089others(6): Show | 9 | HG02055.hp2 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+839A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673754 | ||||||
| chr7:155673757
|
C | T | 4 | a0001c0002t0024g0153a0001c0002t0024g0155a0001c0002t0101g0161others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+842C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673757 | ||||||
| chr7:155673759
|
CGCAT | C | 10 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(7): Show | 10 | HG00323.hp2 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.171+847_171+850del others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673759 | |||||
| chr7:155673760
|
G | A | 2 | a0001c0004t0021g0148a0002c0001t0002g0108 | 2 | HG00733.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.171+845G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673760 | ||||||
| chr7:155673760
|
G | GCGCGCA | 3 | a0001c0004t0005g0152a0003c0007t0022g0289a0003c0007t0022g0290 | 3 | HG02486.hp1 HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.171+846_171+847ins others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673760 | |||||
| chr7:155673760
|
GCATGCGC others(11): Show |
G | 1 | a0001c0002t0082g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.171+848_171+865del others(18): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673760 | |||||
| chr7:155673761
|
CAT | C | 5 | a0001c0002t0102g0154a0001c0003t0008g0258a0001c0003t0046g0254others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+847_171+848del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673761 | ||||||
| chr7:155673762
|
A | G | 156 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0266others(153): Show | 157 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.171+847A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673762 | ||||||
| chr7:155673762
|
ATG | A | 5 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0006t0087g0165others(2): Show | 5 | HG02572.hp1 HG02717.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+848_171+849del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673762 | ||||||
| chr7:155673763
|
T | C | 197 | a0001c0002t0023g0156a0001c0002t0024g0153a0001c0002t0024g0155others(194): Show | 198 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.171+848T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673763 | ||||||
| chr7:155673764
|
G | A | 1 | a0001c0002t0024g0160 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.171+849G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673764 | ||||||
| chr7:155673764
|
G | GCA | 8 | a0001c0004t0005g0139a0001c0004t0041g0083a0001c0004t0043g0081others(5): Show | 8 | HG01071.hp2 HG01099.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.171+850_171+851ins others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673764 | |||||
| chr7:155673764
|
G | GCACACAC others(3): Show |
2 | a0002c0001t0001g0022a0002c0001t0015g0059 | 2 | NA18961.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.171+850_171+851ins others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673764 | |||||
| chr7:155673766
|
G | A | 130 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0024g0160others(127): Show | 130 | HG00323.hp1 HG00423.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.171+851G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673766 | ||||||
| chr7:155673768
|
G | A | 36 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0024g0160others(33): Show | 36 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.171+853G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673768 | ||||||
| chr7:155673768
|
G | GCA | 3 | a0001c0002t0007g0168a0001c0002t0036g0274a0001c0002t0107g0276 | 3 | HG00733.hp1 HG02738.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.171+885_171+886dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCACA | 41 | a0001c0002t0006g0174a0001c0002t0006g0175a0001c0002t0006g0237others(38): Show | 41 | HG00558.hp2 HG00673.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.171+883_171+886dup others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCACACA | 43 | a0001c0002t0006g0180a0001c0002t0006g0181a0001c0002t0006g0219others(40): Show | 43 | HG00140.hp1 HG00544.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.171+881_171+886dup others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCACACAC others(1): Show |
15 | a0001c0002t0007g0169a0001c0002t0045g0198a0002c0001t0001g0012others(12): Show | 15 | HG00140.hp2 HG00423.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+879_171+886dup others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCACACAC others(3): Show |
8 | a0002c0001t0001g0066a0002c0001t0013g0061a0002c0001t0017g0019others(5): Show | 8 | HG00621.hp1 HG02071.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.171+877_171+886dup others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCACACAC others(5): Show |
11 | a0002c0001t0001g0009a0002c0001t0001g0010a0002c0001t0001g0058others(8): Show | 11 | HG00741.hp1 HG02132.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.171+875_171+886dup others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCACACAC others(7): Show |
3 | a0002c0001t0003g0042a0002c0001t0054g0294a0002c0001t0062g0020 | 3 | HG00544.hp2 HG02809.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.171+873_171+886dup others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCACACAC others(9): Show |
2 | a0002c0001t0001g0011a0002c0001t0076g0097 | 2 | HG02895.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.171+871_171+886dup others(16): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCACACAC others(13): Show |
1 | a0002c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.171+867_171+886dup others(20): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCGCA | 9 | a0001c0002t0007g0226a0001c0002t0007g0228a0001c0002t0010g0172others(6): Show | 9 | HG00735.hp1 HG01099.hp2 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+854_171+855ins others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCGCACA | 20 | a0001c0002t0006g0173a0001c0002t0006g0273a0001c0002t0007g0215others(17): Show | 20 | HG00423.hp2 HG00621.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.171+854_171+855ins others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCGCACAC others(1): Show |
9 | a0001c0003t0019g0251a0001c0017t0055g0142a0002c0001t0002g0096others(6): Show | 9 | HG01255.hp2 HG02080.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+854_171+855ins others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCGCACAC others(3): Show |
16 | a0001c0002t0006g0217a0002c0001t0001g0105a0002c0001t0002g0123others(13): Show | 16 | HG00673.hp2 HG01517.hp2 HG01952.hp2 others(13): Show |
intron_variant | MODIFIER | c.171+854_171+855ins others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCGCACAC others(5): Show |
7 | a0002c0001t0002g0114a0002c0001t0002g0129a0002c0001t0002g0278others(4): Show | 7 | HG00558.hp1 HG02257.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+854_171+855ins others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCGCACAC others(7): Show |
8 | a0002c0001t0002g0118a0002c0001t0004g0119a0002c0001t0004g0126others(5): Show | 8 | HG00323.hp1 HG00735.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+854_171+855ins others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
G | GCGCACAC others(9): Show |
3 | a0002c0001t0002g0127a0002c0001t0060g0288a0002c0001t0066g0287 | 3 | HG01175.hp2 HG01978.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.171+854_171+855ins others(16): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673768
|
GCACACAC others(5): Show |
G | 1 | a0001c0003t0008g0266 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.171+875_171+886del others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673768 | |||||
| chr7:155673770
|
A | G | 16 | a0001c0002t0081g0089a0001c0003t0009g0270a0001c0003t0019g0252others(13): Show | 16 | HG00323.hp2 HG02258.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.171+855A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673770 | ||||||
| chr7:155673772
|
A | G | 13 | a0001c0002t0081g0089a0001c0003t0009g0270a0001c0003t0019g0252others(10): Show | 13 | HG00323.hp2 HG02258.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.171+857A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673772 | ||||||
| chr7:155673774
|
A | G | 5 | a0001c0002t0081g0089a0001c0003t0046g0254a0001c0018t0079g0079others(2): Show | 5 | HG02486.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+859A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673774 | ||||||
| chr7:155673776
|
A | G | 2 | a0001c0002t0081g0089a0001c0018t0079g0079 | 2 | HG02976.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.171+861A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673776 | ||||||
| chr7:155673778
|
A | G | 1 | a0001c0002t0081g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.171+863A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673778 | ||||||
| chr7:155673780
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.171+865A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673780 | ||||||
| chr7:155673789
|
CACACACA | C | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+875_171+881del others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673789 | ||||||
| chr7:155673798
|
A | C | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+883A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673798 | ||||||
| chr7:155673800
|
A | C | 24 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(21): Show | 25 | HG00323.hp2 HG01928.hp2 HG01943.hp2 others(22): Show |
intron_variant | MODIFIER | c.171+885A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673800 | ||||||
| chr7:155673801
|
C | CACACACA others(4): Show |
1 | a0002c0001t0063g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.171+886_171+887ins others(11): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673801 | ||||||
| chr7:155673805
|
T | C | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.171+890T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673805 | ||||||
| chr7:155673939
|
A | AGTT | 3 | a0001c0002t0081g0089a0002c0001t0002g0100a0002c0001t0002g0103 | 3 | HG00642.hp2 HG02976.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.171+1025_171+1027d others(5): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673939 | |||||
| chr7:155673939
|
A | AGTTGTTG others(3): Show |
1 | a0002c0001t0002g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.171+1027_171+1028i others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673939 | |||||
| chr7:155673940
|
G | GT | 30 | a0001c0002t0006g0173a0001c0002t0006g0219a0001c0002t0006g0221others(27): Show | 30 | HG00423.hp2 HG00621.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.171+1057dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTT | 8 | a0001c0002t0006g0237a0001c0002t0007g0168a0001c0002t0007g0228others(5): Show | 8 | HG01099.hp2 HG01978.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.171+1056_171+1057d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTT | 7 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(4): Show | 7 | HG02109.hp1 HG02145.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(4): Show |
1 | a0002c0001t0002g0123 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.171+1027_171+1028i others(13): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(5): Show |
4 | a0002c0001t0002g0049a0002c0001t0002g0124a0002c0001t0003g0037others(1): Show | 4 | HG04204.hp2 NA18984.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(6): Show |
2 | a0002c0001t0069g0107a0002c0019t0003g0014 | 2 | NA18949.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.171+1027_171+1028i others(15): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(10): Show |
1 | a0002c0001t0002g0108 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.171+1027_171+1028i others(19): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(8): Show |
3 | a0002c0001t0002g0096a0002c0001t0003g0047a0002c0001t0034g0112 | 3 | HG02723.hp2 HG03471.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.171+1027_171+1028i others(17): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(11): Show |
1 | a0002c0001t0003g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.171+1027_171+1028i others(20): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(9): Show |
6 | a0002c0001t0001g0105a0002c0001t0002g0121a0002c0001t0003g0293others(3): Show | 6 | HG01517.hp2 HG02257.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(18): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(10): Show |
13 | a0002c0001t0001g0022a0002c0001t0001g0031a0002c0001t0002g0110others(10): Show | 13 | HG00140.hp1 HG01891.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(19): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(11): Show |
15 | a0002c0001t0001g0011a0002c0001t0001g0012a0002c0001t0002g0109others(12): Show | 15 | HG00738.hp1 HG01496.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(20): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(12): Show |
13 | a0002c0001t0001g0015a0002c0001t0001g0025a0002c0001t0001g0034others(10): Show | 13 | HG00621.hp1 HG00735.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(21): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(13): Show |
9 | a0002c0001t0001g0017a0002c0001t0001g0036a0002c0001t0002g0129others(6): Show | 9 | HG02040.hp1 HG02071.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(22): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(14): Show |
7 | a0002c0001t0002g0127a0002c0001t0004g0296a0002c0001t0015g0051others(4): Show | 7 | HG02056.hp2 HG02165.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(23): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(15): Show |
5 | a0002c0001t0001g0026a0002c0001t0001g0072a0002c0001t0002g0040others(2): Show | 5 | HG00741.hp2 HG01099.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(24): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(17): Show |
4 | a0002c0001t0001g0053a0002c0001t0002g0125a0002c0001t0004g0098others(1): Show | 4 | HG01258.hp2 HG02109.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(26): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(18): Show |
4 | a0002c0001t0001g0009a0002c0001t0001g0062a0002c0001t0002g0278others(1): Show | 4 | HG00423.hp1 HG03492.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(27): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(19): Show |
2 | a0002c0001t0001g0010a0002c0001t0033g0054 | 2 | HG01070.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.171+1027_171+1028i others(28): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(20): Show |
3 | a0002c0001t0001g0055a0002c0001t0002g0114a0002c0001t0004g0119 | 3 | HG00323.hp1 HG00558.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.171+1027_171+1028i others(29): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(23): Show |
2 | a0002c0001t0015g0059a0002c0001t0033g0021 | 2 | HG01071.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.171+1027_171+1028i others(32): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(24): Show |
2 | a0002c0001t0032g0297a0002c0001t0109g0299 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.171+1027_171+1028i others(33): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(25): Show |
2 | a0002c0001t0035g0250a0002c0001t0062g0020 | 2 | HG00544.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.171+1027_171+1028i others(34): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(30): Show |
1 | a0002c0001t0054g0294 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.171+1027_171+1028i others(39): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(31): Show |
1 | a0002c0001t0004g0245 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.171+1027_171+1028i others(40): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(36): Show |
1 | a0002c0001t0072g0248 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.171+1027_171+1028i others(45): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(4): Show |
1 | a0002c0001t0003g0064 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.171+1027_171+1028i others(13): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(7): Show |
12 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(9): Show | 12 | HG00639.hp1 HG01884.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(16): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(17): Show |
1 | a0003c0007t0022g0291 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.171+1027_171+1028i others(26): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(18): Show |
1 | a0003c0007t0022g0290 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.171+1027_171+1028i others(27): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(24): Show |
1 | a0003c0007t0022g0289 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.171+1027_171+1028i others(33): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTGT others(20): Show |
1 | a0001c0017t0055g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.171+1027_171+1028i others(29): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
G | GTTGTTT | 21 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(18): Show | 22 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
GT | G | 20 | a0001c0002t0010g0184a0001c0002t0010g0185a0001c0002t0012g0209others(17): Show | 20 | HG00741.hp1 HG01070.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.171+1057delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673940
|
GTTTTTTT others(5): Show |
G | 1 | a0001c0002t0107g0276 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.171+1046_171+1057d others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673940 | |||||
| chr7:155673941
|
T | TTGTTGTT others(9): Show |
2 | a0001c0004t0021g0151a0001c0004t0042g0082 | 2 | HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.171+1027_171+1028i others(18): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155673941 | |||||
| chr7:155673942
|
T | TG | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02451.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(3): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673942 | ||||||
| chr7:155673942
|
T | TGTTGTTT others(8): Show |
6 | a0001c0004t0005g0137a0001c0004t0005g0139a0001c0004t0005g0152others(3): Show | 6 | HG02451.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.171+1027_171+1028i others(17): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673942 | ||||||
| chr7:155673943
|
T | G | 24 | a0001c0002t0081g0089a0001c0003t0008g0269a0001c0004t0005g0130others(21): Show | 24 | HG00639.hp1 HG00642.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.171+1028T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673943 | ||||||
| chr7:155673944
|
T | G | 35 | a0001c0002t0082g0088a0001c0002t0090g0091a0001c0003t0008g0002others(32): Show | 36 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.171+1029T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673944 | ||||||
| chr7:155673945
|
T | G | 17 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(14): Show | 17 | HG02080.hp2 HG02109.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.171+1030T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673945 | ||||||
| chr7:155673946
|
T | G | 8 | a0001c0002t0081g0089a0001c0003t0005g0256a0001c0003t0099g0084others(5): Show | 8 | HG01175.hp1 HG02717.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+1031T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673946 | ||||||
| chr7:155673947
|
T | G | 14 | a0001c0002t0082g0088a0002c0001t0001g0056a0002c0001t0001g0058others(11): Show | 14 | HG00642.hp2 HG00741.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.171+1032T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673947 | ||||||
| chr7:155673948
|
T | G | 1 | a0002c0001t0002g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.171+1033T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673948 | ||||||
| chr7:155673949
|
T | G | 3 | a0002c0001t0001g0104a0002c0001t0016g0080a0003c0007t0022g0291 | 3 | HG00735.hp1 NA18981.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.171+1034T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673949 | ||||||
| chr7:155673950
|
T | G | 23 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(20): Show | 24 | HG00280.hp1 HG00323.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.171+1035T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673950 | ||||||
| chr7:155673951
|
T | G | 13 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(10): Show | 13 | HG00741.hp1 HG01243.hp1 HG01952.hp2 others(10): Show |
intron_variant | MODIFIER | c.171+1036T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673951 | ||||||
| chr7:155673952
|
T | G | 1 | a0001c0004t0080g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.171+1037T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673952 | ||||||
| chr7:155673953
|
T | G | 1 | a0002c0001t0003g0018 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.171+1038T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673953 | ||||||
| chr7:155673957
|
T | G | 1 | a0002c0001t0003g0018 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.171+1042T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155673957 | ||||||
| chr7:155674048
|
T | C | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.171+1133T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155674048 | ||||||
| chr7:155674054
|
C | T | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.171+1139C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155674054 | ||||||
| chr7:155674266
|
G | A | 7 | a0002c0001t0002g0295a0002c0001t0004g0296a0002c0001t0032g0297others(4): Show | 7 | HG01884.hp2 HG02809.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.171+1351G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155674266 | ||||||
| chr7:155674370
|
A | G | 6 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.171+1455A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155674370 | ||||||
| chr7:155674379
|
C | T | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.171+1464C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155674379 | ||||||
| chr7:155674419
|
G | A | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.171+1504G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155674419 | ||||||
| chr7:155674444
|
T | A | 2 | a0001c0002t0006g0237a0001c0002t0118g0236 | 2 | NA18949.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.171+1529T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155674444 | ||||||
| chr7:155674805
|
T | C | 1 | a0002c0001t0001g0015 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.171+1890T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155674805 | ||||||
| chr7:155675111
|
A | G | 1 | a0001c0002t0006g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.171+2196A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675111 | ||||||
| chr7:155675135
|
C | T | 1 | a0002c0001t0015g0051 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.171+2220C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675135 | ||||||
| chr7:155675163
|
C | T | 2 | a0001c0002t0101g0161a0001c0002t0103g0158 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.171+2248C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675163 | ||||||
| chr7:155675289
|
G | A | 1 | a0001c0004t0005g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.171+2374G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675289 | ||||||
| chr7:155675293
|
C | CA | 27 | a0001c0002t0006g0217a0001c0002t0006g0237a0001c0002t0011g0232others(24): Show | 27 | HG02135.hp1 HG02145.hp2 HG02572.hp2 others(24): Show |
intron_variant | MODIFIER | c.171+2400dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155675293 | |||||
| chr7:155675293
|
CA | C | 25 | a0001c0002t0011g0239a0001c0002t0023g0156a0001c0002t0023g0157others(22): Show | 25 | HG00642.hp1 HG01891.hp1 HG02258.hp2 others(22): Show |
intron_variant | MODIFIER | c.171+2400delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155675293 | |||||
| chr7:155675293
|
CAAAAAAA others(4): Show |
C | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.171+2390_171+2400d others(13): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155675293 | |||||
| chr7:155675319
|
T | C | 3 | a0001c0004t0021g0148a0001c0004t0021g0151a0001c0004t0083g0150 | 3 | HG02559.hp2 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.171+2404T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675319 | ||||||
| chr7:155675384
|
A | T | 1 | a0001c0002t0082g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.171+2469A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675384 | ||||||
| chr7:155675437
|
A | G | 1 | a0002c0001t0003g0037 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.171+2522A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675437 | ||||||
| chr7:155675461
|
T | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+2546T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675461 | ||||||
| chr7:155675555
|
G | A | 5 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.171+2640G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675555 | ||||||
| chr7:155675564
|
C | T | 1 | a0001c0003t0099g0084 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.171+2649C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675564 | ||||||
| chr7:155675582
|
C | T | 4 | a0002c0001t0060g0288a0002c0001t0066g0287a0002c0001t0074g0285others(1): Show | 4 | HG01175.hp2 HG01978.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+2667C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675582 | ||||||
| chr7:155675859
|
G | A | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.172-2749G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675859 | ||||||
| chr7:155675882
|
C | T | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.172-2726C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675882 | ||||||
| chr7:155675999
|
G | A | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.172-2609G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155675999 | ||||||
| chr7:155676195
|
A | G | 1 | a0004c0015t0017g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.172-2413A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676195 | ||||||
| chr7:155676272
|
T | A | 218 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(215): Show | 219 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.172-2336T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676272 | ||||||
| chr7:155676351
|
G | A | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.172-2257G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676351 | ||||||
| chr7:155676375
|
A | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-2233A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676375 | ||||||
| chr7:155676415
|
A | G | 1 | a0002c0001t0003g0016 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.172-2193A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676415 | ||||||
| chr7:155676608
|
G | A | 9 | a0001c0002t0011g0232a0001c0002t0012g0001a0001c0002t0012g0229others(6): Show | 9 | HG02056.hp1 NA18962.hp2 NA18970.hp1 others(6): Show |
intron_variant | MODIFIER | c.172-2000G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676608 | ||||||
| chr7:155676718
|
G | C | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.172-1890G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676718 | ||||||
| chr7:155676741
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.172-1867G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676741 | ||||||
| chr7:155676823
|
C | T | 4 | a0002c0001t0001g0026a0002c0001t0002g0040a0002c0001t0003g0041others(1): Show | 4 | HG01071.hp2 HG01099.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1785C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676823 | ||||||
| chr7:155676878
|
G | C | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.172-1730G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676878 | ||||||
| chr7:155676942
|
C | A | 218 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(215): Show | 219 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.172-1666C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155676942 | ||||||
| chr7:155677090
|
G | C | 2 | a0001c0004t0041g0083a0001c0004t0043g0081 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.172-1518G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677090 | ||||||
| chr7:155677186
|
A | G | 4 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.172-1422A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677186 | ||||||
| chr7:155677221
|
CT | C | 42 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(39): Show | 43 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(40): Show |
intron_variant | MODIFIER | c.172-1372delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155677221 | |||||
| chr7:155677221
|
CTT | C | 157 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(154): Show | 157 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.172-1373_172-1372d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155677221 | |||||
| chr7:155677264
|
G | T | 1 | a0001c0003t0019g0251 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.172-1344G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677264 | ||||||
| chr7:155677382
|
G | A | 1 | a0001c0008t0091g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.172-1226G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677382 | ||||||
| chr7:155677402
|
G | T | 1 | a0001c0002t0081g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.172-1206G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677402 | ||||||
| chr7:155677474
|
T | A | 1 | a0005c0012t0008g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.172-1134T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677474 | ||||||
| chr7:155677478
|
G | T | 1 | a0005c0012t0008g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.172-1130G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677478 | ||||||
| chr7:155677510
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.172-1098A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677510 | ||||||
| chr7:155677703
|
T | A | 1 | a0005c0012t0008g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.172-905T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677703 | ||||||
| chr7:155677704
|
A | T | 1 | a0005c0012t0008g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.172-904A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677704 | ||||||
| chr7:155677821
|
G | T | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.172-787G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677821 | ||||||
| chr7:155677831
|
C | G | 1 | a0002c0005t0014g0170 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.172-777C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677831 | ||||||
| chr7:155677838
|
T | C | 2 | a0001c0004t0021g0151a0001c0004t0083g0150 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.172-770T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155677838 | ||||||
| chr7:155678113
|
A | T | 1 | a0001c0004t0005g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.172-495A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155678113 | ||||||
| chr7:155678127
|
C | T | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.172-481C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155678127 | ||||||
| chr7:155678151
|
CTCATT | C | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.172-453_172-449del others(5): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 155678151 | |||||
| chr7:155678207
|
T | C | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.172-401T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155678207 | ||||||
| chr7:155678373
|
C | G | 1 | a0001c0002t0010g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.172-235C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155678373 | ||||||
| chr7:155678460
|
T | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-148T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 3/17 | chr7 | 155678460 | ||||||
| chr7:155678866
|
A | G | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.248+182A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155678866 | ||||||
| chr7:155678882
|
C | T | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.248+198C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155678882 | ||||||
| chr7:155678956
|
G | C | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.248+272G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155678956 | ||||||
| chr7:155679148
|
G | A | 1 | a0002c0001t0030g0301 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.248+464G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679148 | ||||||
| chr7:155679167
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.248+483G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679167 | ||||||
| chr7:155679178
|
A | AC | 34 | a0001c0003t0005g0256a0001c0003t0007g0213a0001c0003t0008g0002others(31): Show | 35 | HG00280.hp1 HG00323.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.248+494_248+495ins others(1): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679178 | ||||||
| chr7:155679178
|
A | C | 146 | a0001c0004t0005g0138a0001c0004t0005g0139a0001c0004t0005g0140others(143): Show | 146 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.248+494A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679178 | ||||||
| chr7:155679377
|
T | C | 1 | a0002c0001t0002g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.248+693T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679377 | ||||||
| chr7:155679428
|
A | G | 1 | a0001c0008t0086g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.248+744A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679428 | ||||||
| chr7:155679476
|
A | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.248+792A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679476 | ||||||
| chr7:155679486
|
A | G | 5 | a0001c0002t0036g0274a0001c0002t0036g0275a0001c0002t0105g0008others(2): Show | 5 | HG00733.hp1 HG01070.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+802A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679486 | ||||||
| chr7:155679502
|
G | GAT | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.248+819_248+820ins others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 155679502 | |||||
| chr7:155679507
|
A | ACT | 165 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(162): Show | 165 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.248+824_248+825dup others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 155679507 | |||||
| chr7:155679507
|
A | T | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.248+823A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679507 | ||||||
| chr7:155679513
|
A | T | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.248+829A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679513 | ||||||
| chr7:155679674
|
A | T | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.249-916A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679674 | ||||||
| chr7:155679873
|
T | C | 1 | a0001c0002t0036g0274 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.249-717T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679873 | ||||||
| chr7:155679938
|
G | GT | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.249-644dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 155679938 | |||||
| chr7:155679943
|
T | C | 1 | a0001c0002t0104g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.249-647T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155679943 | ||||||
| chr7:155680037
|
T | C | 18 | a0001c0002t0006g0233a0001c0002t0006g0237a0001c0002t0007g0168others(15): Show | 18 | HG00639.hp2 HG00738.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.249-553T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155680037 | ||||||
| chr7:155680158
|
A | G | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.249-432A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155680158 | ||||||
| chr7:155680197
|
TTCTG | T | 3 | a0001c0002t0006g0217a0001c0002t0081g0089a0001c0002t0082g0088 | 3 | HG02976.hp2 HG03209.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.249-389_249-386del others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 155680197 | |||||
| chr7:155680303
|
T | A | 1 | a0002c0001t0003g0016 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.249-287T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155680303 | ||||||
| chr7:155680315
|
C | T | 3 | a0002c0001t0004g0101a0002c0001t0004g0102a0002c0001t0035g0120 | 3 | HG01952.hp2 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.249-275C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155680315 | ||||||
| chr7:155680549
|
C | T | 1 | a0001c0004t0005g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.249-41C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155680549 | ||||||
| chr7:155680569
|
T | G | 4 | a0002c0001t0002g0118a0002c0001t0034g0112a0002c0001t0034g0113others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.249-21T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155680569 | ||||||
| chr7:155680579
|
G | A | 1 | a0001c0002t0081g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.249-11G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155680579 | ||||||
| chr7:155680579
|
G | T | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.249-11G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 4/17 | chr7 | 155680579 | ||||||
| chr7:155681012
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.567+104A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155681012 | ||||||
| chr7:155681019
|
C | T | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.567+111C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155681019 | ||||||
| chr7:155681051
|
G | GA | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+144dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155681051 | |||||
| chr7:155681132
|
G | A | 4 | a0001c0004t0021g0148a0001c0004t0021g0149a0001c0004t0021g0151others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.567+224G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155681132 | ||||||
| chr7:155681253
|
T | G | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.567+345T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155681253 | ||||||
| chr7:155681508
|
C | G | 1 | a0001c0002t0081g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.567+600C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155681508 | ||||||
| chr7:155681629
|
G | C | 1 | a0002c0001t0003g0016 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.567+721G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155681629 | ||||||
| chr7:155681723
|
T | C | 2 | a0001c0009t0010g0240a0001c0009t0028g0242 | 2 | NA18960.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.567+815T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155681723 | ||||||
| chr7:155681882
|
A | G | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.567+974A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155681882 | ||||||
| chr7:155682056
|
G | A | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+1148G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682056 | ||||||
| chr7:155682112
|
G | A | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.567+1204G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682112 | ||||||
| chr7:155682225
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.567+1317A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682225 | ||||||
| chr7:155682403
|
T | C | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.567+1495T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682403 | ||||||
| chr7:155682409
|
T | C | 2 | a0001c0006t0092g0304a0006c0014t0095g0271 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.567+1501T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682409 | ||||||
| chr7:155682531
|
C | G | 9 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(6): Show | 9 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.567+1623C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682531 | ||||||
| chr7:155682567
|
C | G | 2 | a0002c0005t0014g0189a0002c0005t0018g0192 | 2 | HG00639.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.567+1659C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682567 | ||||||
| chr7:155682568
|
G | A | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.567+1660G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682568 | ||||||
| chr7:155682591
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.567+1683A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682591 | ||||||
| chr7:155682811
|
A | G | 2 | a0002c0001t0013g0060a0002c0001t0013g0073 | 2 | NA19004.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.567+1903A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155682811 | ||||||
| chr7:155683007
|
T | TA | 22 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(19): Show | 22 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.567+2111dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155683007 | |||||
| chr7:155683093
|
A | C | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+2185A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155683093 | ||||||
| chr7:155683099
|
T | C | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.567+2191T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155683099 | ||||||
| chr7:155683110
|
A | G | 4 | a0001c0003t0019g0252a0001c0003t0019g0255a0001c0003t0046g0254others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.567+2202A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155683110 | ||||||
| chr7:155683206
|
C | T | 1 | a0002c0001t0001g0011 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.567+2298C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155683206 | ||||||
| chr7:155683272
|
A | G | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+2364A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155683272 | ||||||
| chr7:155683618
|
C | T | 166 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(163): Show | 166 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.567+2710C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155683618 | ||||||
| chr7:155683625
|
C | T | 1 | a0002c0001t0073g0115 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.567+2717C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155683625 | ||||||
| chr7:155683664
|
T | C | 1 | a0002c0001t0001g0066 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.567+2756T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155683664 | ||||||
| chr7:155684043
|
G | A | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.567+3135G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684043 | ||||||
| chr7:155684053
|
G | A | 1 | a0002c0001t0001g0025 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.567+3145G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684053 | ||||||
| chr7:155684142
|
G | T | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.567+3234G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684142 | ||||||
| chr7:155684284
|
C | T | 1 | a0001c0017t0055g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.567+3376C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684284 | ||||||
| chr7:155684295
|
A | G | 6 | a0002c0001t0001g0056a0002c0001t0001g0058a0002c0001t0064g0070others(3): Show | 6 | HG00741.hp1 HG01175.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.567+3387A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684295 | ||||||
| chr7:155684344
|
T | G | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.567+3436T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684344 | ||||||
| chr7:155684356
|
C | T | 2 | a0002c0001t0004g0119a0002c0001t0069g0107 | 2 | HG00323.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.567+3448C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684356 | ||||||
| chr7:155684445
|
G | A | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.567+3537G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684445 | ||||||
| chr7:155684542
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.567+3634C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684542 | ||||||
| chr7:155684673
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.567+3765G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684673 | ||||||
| chr7:155684692
|
T | G | 156 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.567+3784T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684692 | ||||||
| chr7:155684873
|
G | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.567+3965G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684873 | ||||||
| chr7:155684996
|
G | A | 1 | a0001c0002t0090g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.567+4088G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155684996 | ||||||
| chr7:155685209
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.567+4301A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155685209 | ||||||
| chr7:155685339
|
T | C | 166 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(163): Show | 166 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.567+4431T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155685339 | ||||||
| chr7:155685359
|
T | C | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.567+4451T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155685359 | ||||||
| chr7:155685610
|
C | T | 1 | a0002c0001t0033g0021 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.567+4702C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155685610 | ||||||
| chr7:155686027
|
C | G | 2 | a0001c0003t0008g0266a0005c0012t0008g0267 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.567+5119C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686027 | ||||||
| chr7:155686045
|
T | C | 134 | a0002c0001t0001g0009a0002c0001t0001g0010a0002c0001t0001g0011others(131): Show | 134 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.567+5137T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686045 | ||||||
| chr7:155686100
|
T | G | 1 | a0002c0001t0013g0071 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.567+5192T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686100 | ||||||
| chr7:155686464
|
C | T | 2 | a0002c0001t0002g0116a0002c0001t0004g0126 | 2 | HG00735.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.567+5556C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686464 | ||||||
| chr7:155686491
|
A | T | 3 | a0001c0002t0081g0089a0001c0002t0082g0088a0002c0001t0001g0104 | 3 | HG02976.hp2 HG03209.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.567+5583A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686491 | ||||||
| chr7:155686512
|
G | T | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.567+5604G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686512 | ||||||
| chr7:155686587
|
G | T | 18 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(15): Show | 18 | HG00642.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.567+5679G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686587 | ||||||
| chr7:155686606
|
T | C | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.567+5698T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686606 | ||||||
| chr7:155686680
|
C | G | 7 | a0002c0001t0002g0100a0002c0001t0002g0246a0002c0001t0004g0245others(4): Show | 7 | HG00642.hp2 HG00741.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.567+5772C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686680 | ||||||
| chr7:155686867
|
T | G | 1 | a0001c0003t0046g0254 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.567+5959T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686867 | ||||||
| chr7:155686939
|
T | C | 3 | a0001c0004t0021g0148a0001c0004t0021g0151a0001c0004t0083g0150 | 3 | HG02559.hp2 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.567+6031T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155686939 | ||||||
| chr7:155687021
|
T | A | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.567+6113T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687021 | ||||||
| chr7:155687064
|
C | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.567+6156C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687064 | ||||||
| chr7:155687090
|
C | G | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+6182C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687090 | ||||||
| chr7:155687100
|
T | C | 1 | a0001c0002t0023g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.567+6192T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687100 | ||||||
| chr7:155687120
|
T | A | 1 | a0001c0004t0005g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.567+6212T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687120 | ||||||
| chr7:155687135
|
G | C | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.567+6227G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687135 | ||||||
| chr7:155687181
|
G | A | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.567+6273G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687181 | ||||||
| chr7:155687289
|
T | C | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.567+6381T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687289 | ||||||
| chr7:155687475
|
C | G | 1 | a0002c0005t0026g0205 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.567+6567C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687475 | ||||||
| chr7:155687504
|
G | T | 1 | a0001c0004t0042g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.567+6596G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687504 | ||||||
| chr7:155687534
|
G | C | 1 | a0001c0002t0081g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.567+6626G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687534 | ||||||
| chr7:155687558
|
A | G | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.567+6650A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687558 | ||||||
| chr7:155687637
|
T | G | 3 | a0001c0002t0007g0179a0001c0002t0007g0186a0001c0002t0120g0220 | 3 | HG00544.hp1 HG02135.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.567+6729T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687637 | ||||||
| chr7:155687701
|
C | T | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.567+6793C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687701 | ||||||
| chr7:155687808
|
G | A | 156 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.567+6900G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687808 | ||||||
| chr7:155687831
|
C | T | 1 | a0001c0003t0052g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.567+6923C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687831 | ||||||
| chr7:155687832
|
G | T | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.567+6924G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155687832 | ||||||
| chr7:155688002
|
G | A | 5 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.567+7094G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688002 | ||||||
| chr7:155688065
|
A | G | 5 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.567+7157A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688065 | ||||||
| chr7:155688090
|
A | G | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.567+7182A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688090 | ||||||
| chr7:155688179
|
A | G | 1 | a0001c0003t0007g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.567+7271A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688179 | ||||||
| chr7:155688183
|
A | G | 222 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(219): Show | 223 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.567+7275A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688183 | ||||||
| chr7:155688190
|
A | G | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.567+7282A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688190 | ||||||
| chr7:155688234
|
A | G | 1 | a0002c0001t0069g0107 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.567+7326A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688234 | ||||||
| chr7:155688317
|
C | G | 2 | a0001c0002t0089g0093a0001c0002t0090g0091 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.567+7409C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688317 | ||||||
| chr7:155688471
|
T | G | 2 | a0001c0002t0089g0093a0001c0002t0090g0091 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.567+7563T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688471 | ||||||
| chr7:155688621
|
A | G | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+7713A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688621 | ||||||
| chr7:155688687
|
G | A | 1 | a0002c0005t0026g0224 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.567+7779G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688687 | ||||||
| chr7:155688870
|
G | A | 157 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(154): Show | 157 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.567+7962G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688870 | ||||||
| chr7:155688969
|
G | A | 1 | a0001c0017t0055g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.567+8061G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155688969 | ||||||
| chr7:155689032
|
G | A | 134 | a0002c0001t0001g0009a0002c0001t0001g0010a0002c0001t0001g0011others(131): Show | 134 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.567+8124G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689032 | ||||||
| chr7:155689270
|
A | G | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+8362A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689270 | ||||||
| chr7:155689330
|
A | T | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.567+8422A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689330 | ||||||
| chr7:155689387
|
C | T | 1 | a0001c0004t0005g0135 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.567+8479C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689387 | ||||||
| chr7:155689390
|
T | C | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+8482T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689390 | ||||||
| chr7:155689484
|
C | T | 1 | a0002c0001t0063g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.567+8576C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689484 | ||||||
| chr7:155689562
|
A | AATTGTGA others(2): Show |
14 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.567+8654_567+8655i others(11): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689562 | ||||||
| chr7:155689562
|
A | G | 186 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(183): Show | 187 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.567+8654A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689562 | ||||||
| chr7:155689642
|
A | G | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+8734A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689642 | ||||||
| chr7:155689799
|
A | G | 17 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(14): Show | 18 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.567+8891A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689799 | ||||||
| chr7:155689848
|
C | T | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.567+8940C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689848 | ||||||
| chr7:155689882
|
T | A | 5 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.567+8974T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689882 | ||||||
| chr7:155689936
|
T | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.567+9028T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689936 | ||||||
| chr7:155689987
|
C | T | 3 | a0001c0002t0036g0274a0001c0002t0107g0276a0001c0002t0108g0277 | 3 | HG00733.hp1 HG01070.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.567+9079C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689987 | ||||||
| chr7:155689988
|
G | A | 1 | a0001c0003t0052g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.567+9080G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155689988 | ||||||
| chr7:155690280
|
G | A | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.567+9372G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690280 | ||||||
| chr7:155690311
|
G | C | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.567+9403G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690311 | ||||||
| chr7:155690370
|
C | G | 1 | a0001c0002t0027g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.567+9462C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690370 | ||||||
| chr7:155690371
|
G | C | 1 | a0001c0002t0027g0197 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.567+9463G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690371 | ||||||
| chr7:155690374
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.567+9466A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690374 | ||||||
| chr7:155690390
|
T | C | 1 | a0002c0001t0017g0019 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.567+9482T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690390 | ||||||
| chr7:155690535
|
G | A | 3 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090 | 3 | HG02258.hp2 HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.567+9627G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690535 | ||||||
| chr7:155690611
|
G | T | 8 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(5): Show | 8 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.567+9703G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690611 | ||||||
| chr7:155690714
|
C | T | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.567+9806C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690714 | ||||||
| chr7:155690794
|
A | C | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.567+9886A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690794 | ||||||
| chr7:155690911
|
C | T | 1 | a0002c0001t0044g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.568-9862C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690911 | ||||||
| chr7:155690941
|
G | A | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.568-9832G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690941 | ||||||
| chr7:155690954
|
G | T | 1 | a0001c0002t0006g0221 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.568-9819G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155690954 | ||||||
| chr7:155691226
|
A | G | 1 | a0002c0001t0063g0027 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.568-9547A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691226 | ||||||
| chr7:155691343
|
A | G | 5 | a0001c0002t0029g0162a0001c0002t0029g0176a0001c0002t0029g0207others(2): Show | 5 | HG00558.hp2 NA18956.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.568-9430A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691343 | ||||||
| chr7:155691344
|
C | G | 4 | a0001c0003t0008g0257a0001c0003t0008g0269a0001c0003t0009g0261others(1): Show | 4 | NA18983.hp2 NA19010.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-9429C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691344 | ||||||
| chr7:155691387
|
T | G | 1 | a0001c0002t0006g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.568-9386T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691387 | ||||||
| chr7:155691541
|
A | G | 5 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.568-9232A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691541 | ||||||
| chr7:155691607
|
AC | A | 159 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(156): Show | 159 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.568-9165delC | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691607 | ||||||
| chr7:155691657
|
T | G | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.568-9116T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691657 | ||||||
| chr7:155691696
|
C | T | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.568-9077C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691696 | ||||||
| chr7:155691768
|
T | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.568-9005T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691768 | ||||||
| chr7:155691789
|
C | T | 1 | a0001c0002t0116g0188 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.568-8984C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155691789 | ||||||
| chr7:155692051
|
C | CAA | 30 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(27): Show | 31 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.568-8710_568-8709d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155692051 | |||||
| chr7:155692070
|
T | A | 4 | a0001c0004t0021g0148a0001c0004t0021g0149a0001c0004t0021g0151others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-8703T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155692070 | ||||||
| chr7:155692381
|
C | T | 2 | a0001c0002t0037g0201a0001c0002t0037g0243 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.568-8392C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155692381 | ||||||
| chr7:155692443
|
T | G | 1 | a0001c0002t0090g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.568-8330T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155692443 | ||||||
| chr7:155692535
|
C | T | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.568-8238C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155692535 | ||||||
| chr7:155692557
|
C | T | 1 | a0002c0001t0002g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.568-8216C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155692557 | ||||||
| chr7:155692584
|
G | A | 1 | a0002c0001t0004g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.568-8189G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155692584 | ||||||
| chr7:155692641
|
G | C | 200 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(197): Show | 201 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.568-8132G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155692641 | ||||||
| chr7:155692800
|
A | G | 5 | a0001c0004t0005g0138a0001c0004t0005g0139a0001c0004t0005g0140others(2): Show | 5 | HG02647.hp2 NA18906.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.568-7973A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155692800 | ||||||
| chr7:155692902
|
A | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-7871A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155692902 | ||||||
| chr7:155693263
|
C | T | 1 | a0006c0014t0095g0271 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.568-7510C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155693263 | ||||||
| chr7:155693264
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.568-7509G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155693264 | ||||||
| chr7:155693332
|
C | CT | 157 | a0001c0002t0007g0226a0001c0004t0005g0130a0001c0004t0005g0131others(154): Show | 157 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.568-7430dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155693332 | |||||
| chr7:155693554
|
C | T | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.568-7219C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155693554 | ||||||
| chr7:155693634
|
GTTCT | G | 63 | a0002c0001t0001g0009a0002c0001t0001g0010a0002c0001t0001g0011others(60): Show | 63 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.568-7136_568-7133d others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155693634 | |||||
| chr7:155693742
|
C | T | 27 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(24): Show | 28 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(25): Show |
intron_variant | MODIFIER | c.568-7031C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155693742 | ||||||
| chr7:155693989
|
C | T | 1 | a0001c0002t0037g0243 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.568-6784C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155693989 | ||||||
| chr7:155694323
|
C | T | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.568-6450C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694323 | ||||||
| chr7:155694354
|
T | C | 162 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(159): Show | 162 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.568-6419T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694354 | ||||||
| chr7:155694371
|
T | A | 2 | a0002c0001t0001g0015a0002c0001t0001g0017 | 2 | NA18941.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.568-6402T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694371 | ||||||
| chr7:155694377
|
C | G | 220 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(217): Show | 221 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.568-6396C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694377 | ||||||
| chr7:155694437
|
C | T | 203 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(200): Show | 204 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.568-6336C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694437 | ||||||
| chr7:155694448
|
T | G | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.568-6325T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694448 | ||||||
| chr7:155694521
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.568-6252A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694521 | ||||||
| chr7:155694617
|
C | G | 1 | a0001c0002t0039g0167 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.568-6156C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694617 | ||||||
| chr7:155694651
|
T | G | 171 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(168): Show | 171 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.568-6122T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694651 | ||||||
| chr7:155694719
|
C | T | 202 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(199): Show | 203 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.568-6054C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694719 | ||||||
| chr7:155694952
|
T | A | 1 | a0001c0004t0021g0149 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.568-5821T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155694952 | ||||||
| chr7:155695102
|
G | A | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.568-5671G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695102 | ||||||
| chr7:155695166
|
C | G | 4 | a0001c0003t0019g0252a0001c0003t0019g0255a0001c0003t0046g0254others(1): Show | 4 | HG02145.hp2 HG02572.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-5607C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695166 | ||||||
| chr7:155695210
|
A | G | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.568-5563A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695210 | ||||||
| chr7:155695246
|
T | C | 2 | a0001c0003t0096g0078a0001c0003t0100g0077 | 2 | NA18989.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.568-5527T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695246 | ||||||
| chr7:155695247
|
A | C | 2 | a0001c0003t0096g0078a0001c0003t0100g0077 | 2 | NA18989.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.568-5526A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695247 | ||||||
| chr7:155695389
|
C | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.568-5384C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695389 | ||||||
| chr7:155695519
|
G | A | 1 | a0001c0002t0007g0186 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.568-5254G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695519 | ||||||
| chr7:155695539
|
A | G | 1 | a0001c0004t0021g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.568-5234A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695539 | ||||||
| chr7:155695607
|
G | A | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.568-5166G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695607 | ||||||
| chr7:155695892
|
A | G | 1 | a0002c0005t0110g0196 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.568-4881A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695892 | ||||||
| chr7:155695918
|
A | G | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.568-4855A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695918 | ||||||
| chr7:155695932
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.568-4841G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695932 | ||||||
| chr7:155695935
|
C | CGT | 4 | a0001c0003t0008g0268a0001c0003t0009g0259a0001c0003t0009g0270others(1): Show | 4 | HG00280.hp1 HG00323.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.568-4822_568-4821d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155695935 | |||||
| chr7:155695935
|
C | T | 4 | a0001c0004t0005g0138a0001c0004t0005g0139a0001c0004t0005g0140others(1): Show | 4 | HG02647.hp2 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-4838C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695935 | ||||||
| chr7:155695936
|
G | A | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-4837G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155695936 | ||||||
| chr7:155696081
|
G | C | 1 | a0002c0001t0003g0018 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.568-4692G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696081 | ||||||
| chr7:155696255
|
C | T | 1 | a0002c0001t0003g0037 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.568-4518C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696255 | ||||||
| chr7:155696434
|
A | G | 4 | a0002c0001t0001g0026a0002c0001t0001g0105a0002c0001t0003g0041others(1): Show | 4 | HG01071.hp2 HG01099.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.568-4339A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696434 | ||||||
| chr7:155696512
|
T | C | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.568-4261T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696512 | ||||||
| chr7:155696537
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.568-4236C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696537 | ||||||
| chr7:155696606
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.568-4167A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696606 | ||||||
| chr7:155696691
|
A | G | 156 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(153): Show | 156 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.568-4082A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696691 | ||||||
| chr7:155696794
|
G | A | 1 | a0001c0002t0025g0005 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.568-3979G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696794 | ||||||
| chr7:155696816
|
T | C | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.568-3957T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696816 | ||||||
| chr7:155696968
|
C | G | 1 | a0002c0001t0121g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.568-3805C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155696968 | ||||||
| chr7:155697049
|
T | C | 1 | a0002c0005t0038g0193 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.568-3724T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697049 | ||||||
| chr7:155697187
|
T | TGGA | 30 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(27): Show | 31 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.568-3569_568-3567d others(5): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155697187 | |||||
| chr7:155697198
|
G | A | 4 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-3575G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697198 | ||||||
| chr7:155697200
|
G | A | 1 | a0001c0002t0024g0160 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.568-3573G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697200 | ||||||
| chr7:155697220
|
T | A | 1 | a0001c0002t0036g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.568-3553T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697220 | ||||||
| chr7:155697263
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.568-3510C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697263 | ||||||
| chr7:155697404
|
A | G | 162 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(159): Show | 162 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.568-3369A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697404 | ||||||
| chr7:155697410
|
TG | T | 162 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(159): Show | 162 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.568-3362delG | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697410 | ||||||
| chr7:155697566
|
C | A | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.568-3207C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697566 | ||||||
| chr7:155697568
|
C | A | 197 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(194): Show | 198 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.568-3205C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697568 | ||||||
| chr7:155697630
|
T | A | 1 | a0001c0003t0005g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.568-3143T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697630 | ||||||
| chr7:155697711
|
G | A | 6 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-3062G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697711 | ||||||
| chr7:155697779
|
G | A | 1 | a0001c0008t0086g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.568-2994G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155697779 | ||||||
| chr7:155697805
|
G | GT | 4 | a0001c0004t0021g0148a0001c0004t0021g0149a0001c0004t0021g0151others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-2961dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155697805 | |||||
| chr7:155698094
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.568-2679C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698094 | ||||||
| chr7:155698222
|
C | T | 1 | a0002c0001t0003g0067 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.568-2551C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698222 | ||||||
| chr7:155698228
|
G | A | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.568-2545G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698228 | ||||||
| chr7:155698230
|
G | T | 162 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(159): Show | 162 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.568-2543G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698230 | ||||||
| chr7:155698277
|
G | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.568-2496G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698277 | ||||||
| chr7:155698370
|
GA | G | 216 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(213): Show | 217 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.568-2392delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155698370 | |||||
| chr7:155698398
|
C | T | 2 | a0001c0002t0081g0089a0002c0001t0001g0009 | 2 | HG02976.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.568-2375C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698398 | ||||||
| chr7:155698406
|
T | C | 216 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(213): Show | 217 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.568-2367T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698406 | ||||||
| chr7:155698484
|
G | T | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.568-2289G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698484 | ||||||
| chr7:155698514
|
A | G | 157 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(154): Show | 157 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.568-2259A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698514 | ||||||
| chr7:155698545
|
C | T | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.568-2228C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698545 | ||||||
| chr7:155698552
|
G | T | 1 | a0001c0002t0023g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.568-2221G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698552 | ||||||
| chr7:155698682
|
T | G | 1 | a0002c0001t0070g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.568-2091T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698682 | ||||||
| chr7:155698857
|
G | A | 18 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(15): Show | 18 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.568-1916G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155698857 | ||||||
| chr7:155699414
|
C | T | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.568-1359C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155699414 | ||||||
| chr7:155699415
|
G | A | 99 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(96): Show | 99 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.568-1358G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155699415 | ||||||
| chr7:155699548
|
C | T | 1 | a0004c0015t0017g0065 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.568-1225C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155699548 | ||||||
| chr7:155699561
|
A | G | 2 | a0002c0005t0001g0023a0002c0005t0001g0024 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.568-1212A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155699561 | ||||||
| chr7:155699587
|
C | T | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.568-1186C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155699587 | ||||||
| chr7:155699635
|
A | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.568-1138A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155699635 | ||||||
| chr7:155699681
|
G | A | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.568-1092G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155699681 | ||||||
| chr7:155699861
|
A | G | 1 | a0001c0002t0011g0177 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.568-912A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155699861 | ||||||
| chr7:155700067
|
T | G | 1 | a0005c0012t0008g0267 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.568-706T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155700067 | ||||||
| chr7:155700111
|
G | A | 1 | a0002c0001t0002g0127 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.568-662G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | chr7 | 155700111 | ||||||
| chr7:155700546
|
CT | C | 20 | a0001c0004t0043g0081a0002c0001t0001g0012a0002c0001t0002g0096others(17): Show | 20 | HG01255.hp2 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.568-198delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTT | C | 32 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0017t0055g0142others(29): Show | 32 | HG00423.hp1 HG01346.hp1 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.568-199_568-198del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTT | C | 50 | a0002c0001t0001g0010a0002c0001t0001g0015a0002c0001t0001g0017others(47): Show | 50 | HG00544.hp2 HG00621.hp1 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.568-200_568-198del others(3): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTTT | C | 11 | a0001c0006t0092g0304a0002c0001t0001g0009a0002c0001t0001g0056others(8): Show | 11 | HG01243.hp1 HG02486.hp2 HG03831.hp1 others(8): Show |
intron_variant | MODIFIER | c.568-201_568-198del others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTTTTT | C | 8 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(5): Show | 8 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.568-203_568-198del others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTTTTTT others(1): Show |
C | 14 | a0001c0002t0101g0161a0001c0002t0103g0158a0001c0004t0005g0130others(11): Show | 14 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.568-205_568-198del others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTTTTTT others(2): Show |
C | 10 | a0001c0002t0007g0228a0001c0002t0023g0156a0001c0002t0023g0157others(7): Show | 10 | HG00642.hp1 HG01099.hp2 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.568-206_568-198del others(9): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTTTTTT others(3): Show |
C | 81 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(78): Show | 81 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.568-207_568-198del others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTTTTTT others(4): Show |
C | 39 | a0001c0002t0007g0169a0001c0002t0025g0005a0001c0002t0025g0006others(36): Show | 40 | HG00140.hp2 HG00280.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.568-208_568-198del others(11): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0003t0009g0270a0001c0003t0052g0279 | 2 | HG00323.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.568-209_568-198del others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTTTTTT others(6): Show |
C | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.568-210_568-198del others(13): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155700546
|
CTTTTTTT others(12): Show |
C | 4 | a0001c0004t0021g0148a0001c0004t0021g0149a0001c0004t0021g0151others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.568-216_568-198del others(19): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 155700546 | |||||
| chr7:155701042
|
A | G | 5 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.739+98A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701042 | ||||||
| chr7:155701058
|
C | A | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.739+114C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701058 | ||||||
| chr7:155701175
|
T | A | 1 | a0002c0001t0066g0287 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.739+231T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701175 | ||||||
| chr7:155701175
|
T | TA | 146 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(143): Show | 147 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.739+239dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 155701175 | |||||
| chr7:155701176
|
A | T | 1 | a0001c0004t0021g0149 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.739+232A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701176 | ||||||
| chr7:155701217
|
T | C | 1 | a0002c0005t0038g0193 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.739+273T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701217 | ||||||
| chr7:155701230
|
G | T | 1 | a0001c0002t0006g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.739+286G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701230 | ||||||
| chr7:155701333
|
C | T | 1 | a0002c0001t0004g0102 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.739+389C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701333 | ||||||
| chr7:155701334
|
G | A | 1 | a0002c0001t0033g0021 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.739+390G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701334 | ||||||
| chr7:155701523
|
C | G | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.739+579C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701523 | ||||||
| chr7:155701589
|
C | T | 100 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(97): Show | 100 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.739+645C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701589 | ||||||
| chr7:155701590
|
G | A | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.739+646G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701590 | ||||||
| chr7:155701686
|
A | G | 1 | a0002c0019t0003g0014 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.739+742A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701686 | ||||||
| chr7:155701768
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.739+824A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701768 | ||||||
| chr7:155701774
|
G | A | 1 | a0002c0001t0076g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.739+830G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701774 | ||||||
| chr7:155701783
|
GTTCAA | G | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.739+840_739+844del others(5): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701783 | ||||||
| chr7:155701862
|
G | A | 171 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(168): Show | 172 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.739+918G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701862 | ||||||
| chr7:155701894
|
T | A | 1 | a0001c0002t0025g0006 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.739+950T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701894 | ||||||
| chr7:155701932
|
C | T | 6 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.739+988C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701932 | ||||||
| chr7:155701938
|
A | G | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.739+994A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701938 | ||||||
| chr7:155701944
|
C | T | 1 | a0002c0001t0003g0064 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.739+1000C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155701944 | ||||||
| chr7:155702259
|
C | T | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.739+1315C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155702259 | ||||||
| chr7:155702260
|
T | A | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.739+1316T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155702260 | ||||||
| chr7:155702298
|
A | G | 2 | a0001c0003t0005g0256a0001c0003t0099g0084 | 2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.739+1354A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155702298 | ||||||
| chr7:155702375
|
A | G | 1 | a0008c0016t0061g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.739+1431A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155702375 | ||||||
| chr7:155702471
|
A | G | 1 | a0002c0001t0002g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.739+1527A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155702471 | ||||||
| chr7:155702494
|
T | C | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.739+1550T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155702494 | ||||||
| chr7:155702931
|
G | GC | 142 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(139): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.739+1988dupC | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr7 | 155702931 | |||||
| chr7:155702960
|
G | A | 1 | a0001c0003t0008g0257 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.739+2016G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155702960 | ||||||
| chr7:155703059
|
G | C | 1 | a0001c0004t0005g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.739+2115G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155703059 | ||||||
| chr7:155703203
|
T | G | 147 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(144): Show | 148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.739+2259T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155703203 | ||||||
| chr7:155703937
|
A | G | 133 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.740-2923A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155703937 | ||||||
| chr7:155703979
|
G | T | 3 | a0001c0002t0024g0153a0001c0002t0024g0155a0001c0002t0024g0160 | 3 | HG00642.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.740-2881G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155703979 | ||||||
| chr7:155704002
|
G | A | 131 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(128): Show | 131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.740-2858G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704002 | ||||||
| chr7:155704035
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.740-2825A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704035 | ||||||
| chr7:155704057
|
A | G | 1 | a0002c0001t0002g0103 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.740-2803A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704057 | ||||||
| chr7:155704123
|
A | G | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.740-2737A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704123 | ||||||
| chr7:155704272
|
T | G | 8 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(5): Show | 8 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.740-2588T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704272 | ||||||
| chr7:155704277
|
T | C | 1 | a0001c0002t0006g0233 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.740-2583T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704277 | ||||||
| chr7:155704282
|
C | G | 2 | a0001c0002t0101g0161a0001c0002t0103g0158 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.740-2578C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704282 | ||||||
| chr7:155704353
|
C | T | 1 | a0002c0001t0003g0039 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.740-2507C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704353 | ||||||
| chr7:155704503
|
T | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.740-2357T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704503 | ||||||
| chr7:155704729
|
G | A | 132 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.740-2131G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704729 | ||||||
| chr7:155704970
|
A | G | 88 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(85): Show | 88 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.740-1890A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155704970 | ||||||
| chr7:155705641
|
T | C | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.740-1219T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155705641 | ||||||
| chr7:155705678
|
T | A | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.740-1182T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155705678 | ||||||
| chr7:155705734
|
G | A | 1 | a0001c0002t0010g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.740-1126G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155705734 | ||||||
| chr7:155706028
|
G | A | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.740-832G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706028 | ||||||
| chr7:155706035
|
G | A | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.740-825G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706035 | ||||||
| chr7:155706078
|
T | C | 13 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.740-782T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706078 | ||||||
| chr7:155706093
|
A | G | 3 | a0002c0001t0002g0146a0002c0001t0004g0106a0002c0001t0004g0147 | 3 | HG02080.hp2 NA19080.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.740-767A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706093 | ||||||
| chr7:155706093
|
A | T | 1 | a0002c0001t0002g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.740-767A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706093 | ||||||
| chr7:155706263
|
G | A | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.740-597G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706263 | ||||||
| chr7:155706274
|
C | T | 132 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(129): Show | 133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.740-586C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706274 | ||||||
| chr7:155706349
|
C | T | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.740-511C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706349 | ||||||
| chr7:155706451
|
G | A | 5 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.740-409G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706451 | ||||||
| chr7:155706468
|
A | G | 133 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.740-392A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706468 | ||||||
| chr7:155706709
|
C | T | 1 | a0001c0002t0006g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.740-151C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 6/17 | chr7 | 155706709 | ||||||
| chr7:155707105
|
C | T | 133 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.948+37C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155707105 | ||||||
| chr7:155707390
|
A | G | 101 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(98): Show | 101 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.948+322A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155707390 | ||||||
| chr7:155707445
|
A | G | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+377A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155707445 | ||||||
| chr7:155707522
|
A | C | 142 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(139): Show | 143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.948+454A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155707522 | ||||||
| chr7:155707710
|
G | A | 17 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(14): Show | 18 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.948+642G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155707710 | ||||||
| chr7:155707752
|
G | A | 18 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(15): Show | 18 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.948+684G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155707752 | ||||||
| chr7:155707939
|
C | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.948+871C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155707939 | ||||||
| chr7:155707939
|
C | T | 8 | a0001c0002t0010g0184a0001c0002t0010g0185a0001c0002t0010g0187others(5): Show | 8 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.948+871C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155707939 | ||||||
| chr7:155707961
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.948+893A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155707961 | ||||||
| chr7:155708004
|
G | A | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.948+936G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708004 | ||||||
| chr7:155708143
|
T | G | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.948+1075T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708143 | ||||||
| chr7:155708195
|
T | C | 13 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.948+1127T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708195 | ||||||
| chr7:155708200
|
A | G | 2 | a0001c0003t0008g0266a0005c0012t0008g0267 | 2 | NA18979.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.948+1132A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708200 | ||||||
| chr7:155708295
|
A | C | 1 | a0001c0002t0007g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.948+1227A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708295 | ||||||
| chr7:155708487
|
G | A | 7 | a0002c0001t0002g0100a0002c0001t0002g0246a0002c0001t0004g0245others(4): Show | 7 | HG00642.hp2 HG00741.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.948+1419G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708487 | ||||||
| chr7:155708768
|
G | A | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.948+1700G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708768 | ||||||
| chr7:155708781
|
C | T | 1 | a0001c0003t0049g0283 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.948+1713C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708781 | ||||||
| chr7:155708866
|
C | A | 1 | a0001c0004t0021g0149 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.948+1798C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708866 | ||||||
| chr7:155708867
|
C | T | 1 | a0002c0001t0002g0103 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.948+1799C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708867 | ||||||
| chr7:155708954
|
G | T | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.948+1886G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708954 | ||||||
| chr7:155708957
|
C | T | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.948+1889C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708957 | ||||||
| chr7:155708968
|
C | T | 155 | a0001c0003t0048g0280a0001c0004t0005g0130a0001c0004t0005g0131others(152): Show | 155 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.948+1900C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155708968 | ||||||
| chr7:155709050
|
C | CT | 4 | a0002c0001t0001g0031a0002c0001t0015g0028a0002c0001t0015g0045others(1): Show | 4 | HG02165.hp1 HG02165.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.948+1985dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 155709050 | |||||
| chr7:155709139
|
C | T | 8 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(5): Show | 8 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.949-2064C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155709139 | ||||||
| chr7:155709218
|
T | C | 1 | a0002c0001t0003g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.949-1985T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155709218 | ||||||
| chr7:155709394
|
C | T | 1 | a0003c0007t0022g0291 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.949-1809C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155709394 | ||||||
| chr7:155709407
|
C | A | 207 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(204): Show | 208 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.949-1796C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155709407 | ||||||
| chr7:155709510
|
T | C | 1 | a0002c0001t0003g0018 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.949-1693T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155709510 | ||||||
| chr7:155709516
|
C | T | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.949-1687C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155709516 | ||||||
| chr7:155709659
|
C | T | 1 | a0002c0001t0003g0041 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.949-1544C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155709659 | ||||||
| chr7:155709670
|
T | C | 2 | a0001c0003t0005g0256a0001c0003t0099g0084 | 2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.949-1533T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155709670 | ||||||
| chr7:155710077
|
C | T | 2 | a0002c0001t0032g0297a0002c0001t0054g0294 | 2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.949-1126C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710077 | ||||||
| chr7:155710115
|
T | A | 132 | a0002c0001t0001g0009a0002c0001t0001g0010a0002c0001t0001g0011others(129): Show | 132 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.949-1088T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710115 | ||||||
| chr7:155710138
|
T | C | 203 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(200): Show | 204 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.949-1065T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710138 | ||||||
| chr7:155710235
|
A | G | 2 | a0001c0002t0089g0093a0001c0002t0090g0091 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.949-968A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710235 | ||||||
| chr7:155710293
|
C | T | 9 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.949-910C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710293 | ||||||
| chr7:155710405
|
G | A | 154 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(151): Show | 154 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.949-798G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710405 | ||||||
| chr7:155710438
|
ACGGCAGC others(5): Show |
A | 2 | a0001c0002t0101g0161a0001c0002t0103g0158 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.949-763_949-752del others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 155710438 | |||||
| chr7:155710440
|
G | A | 203 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(200): Show | 204 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.949-763G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710440 | ||||||
| chr7:155710544
|
C | A | 6 | a0002c0001t0002g0096a0002c0001t0002g0118a0002c0001t0002g0124others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.949-659C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710544 | ||||||
| chr7:155710569
|
T | A | 2 | a0002c0005t0001g0023a0002c0005t0001g0024 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.949-634T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710569 | ||||||
| chr7:155710756
|
T | C | 169 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(166): Show | 169 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.949-447T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710756 | ||||||
| chr7:155710774
|
G | GC | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.949-428dupC | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 155710774 | |||||
| chr7:155710829
|
A | G | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.949-374A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710829 | ||||||
| chr7:155710908
|
A | AT | 10 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(7): Show | 10 | HG00639.hp2 HG00733.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.949-279dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 155710908 | |||||
| chr7:155710908
|
AT | A | 168 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(165): Show | 168 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.949-279delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 155710908 | |||||
| chr7:155710939
|
G | A | 1 | a0001c0002t0036g0275 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.949-264G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710939 | ||||||
| chr7:155710967
|
G | A | 1 | a0002c0001t0004g0144 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.949-236G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710967 | ||||||
| chr7:155710967
|
G | C | 1 | a0001c0003t0019g0251 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.949-236G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155710967 | ||||||
| chr7:155711073
|
T | C | 1 | a0002c0001t0003g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.949-130T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155711073 | ||||||
| chr7:155711089
|
C | T | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.949-114C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 7/17 | chr7 | 155711089 | ||||||
| chr7:155711544
|
C | CT | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1201+91dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155711544 | |||||
| chr7:155711669
|
G | A | 87 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1201+214G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155711669 | ||||||
| chr7:155711746
|
T | TG | 7 | a0001c0002t0010g0184a0001c0002t0010g0185a0001c0002t0010g0187others(4): Show | 7 | HG02074.hp2 NA18980.hp2 NA18984.hp2 others(4): Show |
intron_variant | MODIFIER | c.1201+292dupG | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155711746 | |||||
| chr7:155711960
|
C | T | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1201+505C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155711960 | ||||||
| chr7:155712156
|
G | T | 1 | a0006c0014t0095g0271 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1201+701G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155712156 | ||||||
| chr7:155712231
|
C | T | 1 | a0001c0004t0005g0131 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1201+776C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155712231 | ||||||
| chr7:155712266
|
C | T | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1201+811C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155712266 | ||||||
| chr7:155712326
|
A | G | 8 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(5): Show | 8 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1201+871A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155712326 | ||||||
| chr7:155712404
|
G | A | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1201+949G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155712404 | ||||||
| chr7:155712803
|
G | A | 129 | a0002c0001t0001g0009a0002c0001t0001g0010a0002c0001t0001g0011others(126): Show | 129 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1201+1348G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155712803 | ||||||
| chr7:155712860
|
G | A | 1 | a0001c0004t0005g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1201+1405G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155712860 | ||||||
| chr7:155712883
|
C | T | 1 | a0002c0001t0001g0025 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1201+1428C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155712883 | ||||||
| chr7:155713177
|
G | T | 1 | a0001c0002t0007g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1201+1722G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155713177 | ||||||
| chr7:155713197
|
G | T | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1201+1742G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155713197 | ||||||
| chr7:155713198
|
G | T | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1201+1743G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155713198 | ||||||
| chr7:155713304
|
G | A | 43 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(40): Show | 44 | HG00280.hp1 HG00323.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.1201+1849G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155713304 | ||||||
| chr7:155713418
|
G | A | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.1201+1963G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155713418 | ||||||
| chr7:155713642
|
G | A | 131 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1201+2187G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155713642 | ||||||
| chr7:155713650
|
T | C | 136 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(133): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1201+2195T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155713650 | ||||||
| chr7:155713672
|
G | A | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1201+2217G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155713672 | ||||||
| chr7:155713891
|
G | A | 133 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(130): Show | 134 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1201+2436G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155713891 | ||||||
| chr7:155714072
|
C | G | 136 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(133): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1201+2617C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714072 | ||||||
| chr7:155714188
|
A | G | 1 | a0002c0001t0002g0123 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1201+2733A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714188 | ||||||
| chr7:155714231
|
A | G | 89 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(86): Show | 89 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.1201+2776A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714231 | ||||||
| chr7:155714247
|
A | G | 1 | a0002c0001t0058g0046 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1201+2792A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714247 | ||||||
| chr7:155714348
|
A | G | 158 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(155): Show | 159 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1201+2893A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714348 | ||||||
| chr7:155714482
|
G | A | 10 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(7): Show | 10 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1201+3027G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714482 | ||||||
| chr7:155714693
|
G | A | 121 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1201+3238G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714693 | ||||||
| chr7:155714700
|
A | G | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1201+3245A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714700 | ||||||
| chr7:155714731
|
G | A | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1201+3276G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714731 | ||||||
| chr7:155714756
|
G | A | 1 | a0001c0002t0006g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1201+3301G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714756 | ||||||
| chr7:155714838
|
C | A | 15 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(12): Show | 15 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1201+3383C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155714838 | ||||||
| chr7:155715038
|
T | G | 2 | a0001c0002t0037g0201a0001c0002t0037g0243 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1202-3347T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715038 | ||||||
| chr7:155715040
|
G | A | 66 | a0001c0002t0006g0173a0001c0002t0006g0175a0001c0002t0006g0180others(63): Show | 66 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1202-3345G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715040 | ||||||
| chr7:155715159
|
C | T | 1 | a0001c0003t0007g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1202-3226C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715159 | ||||||
| chr7:155715188
|
G | A | 3 | a0001c0002t0024g0153a0001c0002t0024g0155a0001c0002t0024g0160 | 3 | HG00642.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1202-3197G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715188 | ||||||
| chr7:155715207
|
G | A | 1 | a0001c0017t0055g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1202-3178G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715207 | ||||||
| chr7:155715309
|
A | T | 1 | a0001c0002t0011g0177 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1202-3076A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715309 | ||||||
| chr7:155715372
|
G | A | 1 | a0006c0014t0095g0271 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1202-3013G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715372 | ||||||
| chr7:155715419
|
T | C | 88 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(85): Show | 88 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.1202-2966T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715419 | ||||||
| chr7:155715425
|
A | G | 1 | a0008c0016t0061g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1202-2960A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715425 | ||||||
| chr7:155715528
|
G | A | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1202-2857G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715528 | ||||||
| chr7:155715554
|
A | G | 1 | a0002c0001t0065g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1202-2831A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715554 | ||||||
| chr7:155715610
|
A | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1202-2775A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715610 | ||||||
| chr7:155715634
|
C | T | 13 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1202-2751C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715634 | ||||||
| chr7:155715863
|
C | T | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202-2522C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155715863 | ||||||
| chr7:155716015
|
TATTATA | T | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1202-2361_1202-235 others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716015 | |||||
| chr7:155716125
|
C | A | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1202-2260C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155716125 | ||||||
| chr7:155716144
|
G | A | 5 | a0002c0001t0002g0040a0002c0001t0078g0117a0003c0007t0022g0289others(2): Show | 5 | HG00735.hp1 HG01517.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1202-2241G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155716144 | ||||||
| chr7:155716184
|
C | T | 1 | a0001c0002t0010g0216 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1202-2201C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155716184 | ||||||
| chr7:155716281
|
C | T | 1 | a0002c0001t0004g0245 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1202-2104C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155716281 | ||||||
| chr7:155716316
|
G | GTTTTTT | 7 | a0001c0002t0023g0159a0001c0002t0024g0153a0001c0002t0024g0155others(4): Show | 7 | HG00642.hp1 HG02630.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202-2058_1202-205 others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT | 9 | a0001c0002t0007g0186a0001c0002t0010g0184a0001c0002t0023g0156others(6): Show | 9 | HG01255.hp1 HG02135.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202-2059_1202-205 others(11): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(1): Show |
31 | a0001c0002t0006g0173a0001c0002t0006g0175a0001c0002t0007g0169others(28): Show | 31 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.1202-2060_1202-205 others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(2): Show |
37 | a0001c0002t0006g0174a0001c0002t0006g0180a0001c0002t0006g0190others(34): Show | 37 | HG00621.hp2 HG00673.hp1 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.1202-2061_1202-205 others(13): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(3): Show |
20 | a0001c0002t0006g0181a0001c0002t0006g0233a0001c0002t0006g0273others(17): Show | 20 | HG00738.hp2 HG02055.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.1202-2062_1202-205 others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(4): Show |
8 | a0001c0003t0005g0256a0001c0003t0009g0270a0001c0003t0052g0279others(5): Show | 8 | HG00323.hp2 HG00735.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1202-2063_1202-205 others(15): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(5): Show |
12 | a0001c0003t0008g0002a0001c0003t0008g0266a0001c0003t0008g0269others(9): Show | 13 | HG00280.hp1 HG01928.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.1202-2064_1202-205 others(16): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(6): Show |
13 | a0001c0002t0031g0092a0001c0002t0053g0090a0001c0002t0089g0093others(10): Show | 13 | HG00639.hp1 HG02258.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1202-2065_1202-205 others(17): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(7): Show |
9 | a0001c0002t0031g0094a0001c0004t0005g0133a0001c0004t0005g0134others(6): Show | 9 | HG02258.hp1 HG02559.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202-2066_1202-205 others(18): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(10): Show |
1 | a0002c0001t0003g0041 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1202-2053_1202-205 others(21): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(11): Show |
16 | a0001c0006t0094g0164a0002c0001t0001g0011a0002c0001t0001g0025others(13): Show | 16 | HG00741.hp1 HG01070.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1202-2053_1202-205 others(22): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(12): Show |
33 | a0001c0006t0093g0166a0001c0017t0055g0142a0002c0001t0001g0009others(30): Show | 33 | HG00423.hp1 HG00621.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.1202-2053_1202-205 others(23): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(13): Show |
17 | a0001c0006t0087g0165a0002c0001t0001g0010a0002c0001t0001g0012others(14): Show | 17 | HG01258.hp2 HG01891.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.1202-2053_1202-205 others(24): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(14): Show |
6 | a0001c0006t0092g0304a0002c0001t0001g0072a0002c0001t0013g0061others(3): Show | 6 | HG00544.hp2 HG01257.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1202-2053_1202-205 others(25): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(15): Show |
3 | a0002c0001t0003g0074a0002c0001t0013g0050a0008c0016t0061g0048 | 3 | HG01346.hp1 HG02135.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1202-2053_1202-205 others(26): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(16): Show |
1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1202-2053_1202-205 others(27): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716316
|
G | GTTTTTTT others(24): Show |
1 | a0001c0004t0021g0149 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1202-2053_1202-205 others(35): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155716316 | |||||
| chr7:155716333
|
A | T | 7 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(4): Show | 7 | HG02055.hp2 HG02486.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1202-2052A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155716333 | ||||||
| chr7:155716375
|
T | A | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1202-2010T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155716375 | ||||||
| chr7:155716612
|
G | A | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1202-1773G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155716612 | ||||||
| chr7:155716716
|
T | C | 1 | a0001c0004t0042g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1202-1669T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155716716 | ||||||
| chr7:155716946
|
T | C | 1 | a0002c0001t0016g0247 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1202-1439T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155716946 | ||||||
| chr7:155717145
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1202-1240C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717145 | ||||||
| chr7:155717193
|
C | T | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1202-1192C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717193 | ||||||
| chr7:155717232
|
A | C | 11 | a0001c0002t0006g0174a0001c0002t0006g0180a0001c0002t0006g0181others(8): Show | 11 | HG01981.hp2 NA18953.hp1 NA18955.hp1 others(8): Show |
intron_variant | MODIFIER | c.1202-1153A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717232 | ||||||
| chr7:155717346
|
C | T | 5 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1202-1039C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717346 | ||||||
| chr7:155717375
|
T | C | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.1202-1010T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717375 | ||||||
| chr7:155717501
|
TG | T | 87 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1202-880delG | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 155717501 | |||||
| chr7:155717613
|
A | C | 87 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1202-772A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717613 | ||||||
| chr7:155717619
|
T | G | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1202-766T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717619 | ||||||
| chr7:155717627
|
T | C | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1202-758T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717627 | ||||||
| chr7:155717721
|
A | G | 1 | a0001c0002t0006g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1202-664A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717721 | ||||||
| chr7:155717768
|
T | G | 1 | a0001c0002t0115g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1202-617T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717768 | ||||||
| chr7:155717770
|
C | T | 131 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1202-615C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717770 | ||||||
| chr7:155717900
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.1202-485A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717900 | ||||||
| chr7:155717910
|
A | G | 1 | a0001c0004t0042g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1202-475A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717910 | ||||||
| chr7:155717914
|
C | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1202-471C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717914 | ||||||
| chr7:155717921
|
G | A | 9 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(6): Show | 9 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202-464G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155717921 | ||||||
| chr7:155718041
|
A | G | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1202-344A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155718041 | ||||||
| chr7:155718060
|
T | C | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1202-325T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155718060 | ||||||
| chr7:155718079
|
C | T | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1202-306C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155718079 | ||||||
| chr7:155718189
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1202-196G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155718189 | ||||||
| chr7:155718223
|
T | C | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1202-162T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 8/17 | chr7 | 155718223 | ||||||
| chr7:155718519
|
A | G | 4 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+76A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155718519 | ||||||
| chr7:155718524
|
G | A | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1260+81G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155718524 | ||||||
| chr7:155718811
|
A | C | 1 | a0002c0001t0004g0147 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1260+368A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155718811 | ||||||
| chr7:155718950
|
T | TTC | 7 | a0002c0001t0001g0053a0002c0001t0001g0055a0002c0001t0001g0066others(4): Show | 7 | HG01070.hp1 HG01071.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1260+524_1260+525d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155718950 | |||||
| chr7:155718966
|
C | T | 31 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(28): Show | 32 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.1260+523C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155718966 | ||||||
| chr7:155718968
|
C | T | 98 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(95): Show | 98 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.1260+525C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155718968 | ||||||
| chr7:155718969
|
A | T | 99 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(96): Show | 99 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.1260+526A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155718969 | ||||||
| chr7:155719177
|
AT | A | 14 | a0001c0002t0105g0008a0001c0003t0005g0256a0001c0003t0019g0251others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1260+745delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155719177 | |||||
| chr7:155719496
|
G | A | 1 | a0001c0004t0005g0131 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1260+1053G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155719496 | ||||||
| chr7:155719587
|
A | G | 130 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(127): Show | 131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1260+1144A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155719587 | ||||||
| chr7:155719645
|
T | A | 1 | a0001c0004t0005g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1260+1202T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155719645 | ||||||
| chr7:155719942
|
T | C | 1 | a0002c0001t0013g0050 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1260+1499T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155719942 | ||||||
| chr7:155720028
|
GA | G | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+1587delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155720028 | |||||
| chr7:155720066
|
T | C | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260+1623T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155720066 | ||||||
| chr7:155720262
|
C | G | 87 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1260+1819C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155720262 | ||||||
| chr7:155720263
|
G | A | 1 | a0002c0001t0002g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1260+1820G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155720263 | ||||||
| chr7:155720457
|
C | T | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1260+2014C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155720457 | ||||||
| chr7:155720475
|
G | A | 1 | a0001c0002t0082g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1260+2032G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155720475 | ||||||
| chr7:155720491
|
T | C | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1260+2048T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155720491 | ||||||
| chr7:155720581
|
A | C | 3 | a0002c0001t0003g0039a0002c0001t0003g0067a0002c0001t0003g0293 | 3 | HG01891.hp2 HG01934.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1260+2138A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155720581 | ||||||
| chr7:155720794
|
A | C | 13 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1260+2351A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155720794 | ||||||
| chr7:155720893
|
A | G | 31 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(28): Show | 32 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.1260+2450A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155720893 | ||||||
| chr7:155721018
|
A | G | 1 | a0001c0002t0102g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1260+2575A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721018 | ||||||
| chr7:155721138
|
CGTA | C | 129 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1260+2701_1260+270 others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155721138 | |||||
| chr7:155721141
|
A | T | 1 | a0001c0002t0006g0180 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1260+2698A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721141 | ||||||
| chr7:155721151
|
A | G | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1260+2708A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721151 | ||||||
| chr7:155721261
|
G | A | 1 | a0002c0001t0044g0292 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1260+2818G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721261 | ||||||
| chr7:155721269
|
A | C | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1260+2826A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721269 | ||||||
| chr7:155721407
|
G | C | 1 | a0002c0001t0004g0101 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1260+2964G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721407 | ||||||
| chr7:155721553
|
C | T | 5 | a0001c0004t0005g0131a0001c0004t0005g0132a0001c0004t0005g0133others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+3110C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721553 | ||||||
| chr7:155721652
|
TATA | T | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1260+3213_1260+321 others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155721652 | |||||
| chr7:155721668
|
T | A | 2 | a0001c0002t0089g0093a0001c0002t0090g0091 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1260+3225T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721668 | ||||||
| chr7:155721761
|
AT | A | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+3320delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155721761 | |||||
| chr7:155721825
|
A | G | 1 | a0001c0002t0006g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1260+3382A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721825 | ||||||
| chr7:155721890
|
A | G | 3 | a0002c0001t0030g0301a0002c0001t0030g0302a0002c0001t0040g0303 | 3 | HG01255.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1260+3447A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721890 | ||||||
| chr7:155721994
|
A | G | 1 | a0002c0001t0064g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1260+3551A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155721994 | ||||||
| chr7:155722134
|
T | C | 2 | a0002c0005t0014g0189a0002c0005t0018g0192 | 2 | HG00639.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1260+3691T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155722134 | ||||||
| chr7:155722424
|
T | C | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1260+3981T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155722424 | ||||||
| chr7:155722448
|
C | T | 1 | a0002c0001t0002g0108 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1260+4005C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155722448 | ||||||
| chr7:155722488
|
T | C | 87 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1260+4045T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155722488 | ||||||
| chr7:155722587
|
G | A | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1260+4144G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155722587 | ||||||
| chr7:155722681
|
A | G | 3 | a0002c0001t0015g0028a0002c0001t0015g0045a0002c0001t0015g0051 | 3 | HG02165.hp1 NA18966.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1260+4238A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155722681 | ||||||
| chr7:155722750
|
G | A | 130 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(127): Show | 131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1260+4307G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155722750 | ||||||
| chr7:155722838
|
T | A | 87 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.1260+4395T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155722838 | ||||||
| chr7:155722843
|
A | G | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1260+4400A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155722843 | ||||||
| chr7:155723097
|
G | A | 1 | a0002c0005t0014g0211 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1260+4654G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723097 | ||||||
| chr7:155723421
|
A | G | 1 | a0002c0001t0001g0009 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1260+4978A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723421 | ||||||
| chr7:155723496
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.1260+5053A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723496 | ||||||
| chr7:155723574
|
G | A | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1260+5131G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723574 | ||||||
| chr7:155723610
|
A | G | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1260+5167A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723610 | ||||||
| chr7:155723715
|
A | G | 31 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(28): Show | 32 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.1260+5272A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723715 | ||||||
| chr7:155723757
|
T | G | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1260+5314T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723757 | ||||||
| chr7:155723826
|
A | C | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260+5383A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723826 | ||||||
| chr7:155723885
|
A | G | 12 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1260+5442A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723885 | ||||||
| chr7:155723986
|
A | G | 10 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(7): Show | 10 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260+5543A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155723986 | ||||||
| chr7:155724210
|
A | G | 13 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.1260+5767A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724210 | ||||||
| chr7:155724258
|
A | G | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1260+5815A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724258 | ||||||
| chr7:155724260
|
T | C | 1 | a0002c0001t0002g0096 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1260+5817T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724260 | ||||||
| chr7:155724332
|
C | T | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1260+5889C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724332 | ||||||
| chr7:155724409
|
A | T | 135 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1260+5966A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724409 | ||||||
| chr7:155724452
|
C | G | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+6009C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724452 | ||||||
| chr7:155724537
|
C | T | 10 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(7): Show | 10 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1260+6094C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724537 | ||||||
| chr7:155724538
|
G | A | 1 | a0002c0001t0001g0145 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1260+6095G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724538 | ||||||
| chr7:155724578
|
A | G | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1260+6135A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724578 | ||||||
| chr7:155724623
|
C | T | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1260+6180C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724623 | ||||||
| chr7:155724638
|
C | T | 135 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1260+6195C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724638 | ||||||
| chr7:155724940
|
A | C | 131 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1260+6497A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724940 | ||||||
| chr7:155724988
|
G | GTT | 36 | a0001c0002t0006g0174a0001c0002t0006g0175a0001c0002t0006g0180others(33): Show | 36 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.1260+6547_1260+654 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724988 | |||||
| chr7:155724990
|
T | G | 4 | a0002c0001t0001g0055a0002c0001t0001g0058a0002c0001t0003g0074others(1): Show | 4 | HG00741.hp1 HG01071.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+6547T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724990 | ||||||
| chr7:155724990
|
T | TG | 4 | a0002c0001t0001g0009a0002c0001t0001g0105a0002c0001t0003g0041others(1): Show | 4 | HG01099.hp1 HG01517.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+6547_1260+654 others(5): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724990 | ||||||
| chr7:155724990
|
T | TTG | 34 | a0002c0001t0001g0012a0002c0001t0001g0015a0002c0001t0001g0017others(31): Show | 34 | HG00280.hp2 HG00423.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1260+6593_1260+659 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
T | TTGTG | 12 | a0002c0001t0001g0056a0002c0001t0002g0114a0002c0001t0002g0146others(9): Show | 12 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.1260+6591_1260+659 others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
T | TTGTGTG | 5 | a0002c0001t0002g0096a0002c0001t0016g0247a0002c0001t0069g0107others(2): Show | 5 | HG00741.hp2 HG01257.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+6589_1260+659 others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
T | TTGTGTGT others(3): Show |
4 | a0002c0001t0001g0053a0002c0001t0001g0072a0002c0001t0002g0118others(1): Show | 4 | HG01257.hp1 HG01258.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+6585_1260+659 others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
T | TTTTG | 18 | a0001c0002t0006g0173a0001c0002t0006g0190a0001c0002t0006g0233others(15): Show | 18 | HG00621.hp2 HG00738.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1260+6548_1260+654 others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
T | TTTTGTG | 6 | a0001c0002t0006g0217a0001c0002t0007g0169a0001c0002t0011g0239others(3): Show | 6 | HG00140.hp2 HG03927.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1260+6548_1260+654 others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
T | TTTTTTTT others(7): Show |
1 | a0001c0002t0023g0157 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1260+6548_1260+654 others(18): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
T | TTTTTTTT others(4): Show |
1 | a0001c0002t0023g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1260+6548_1260+654 others(15): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
T | TTTTTTTT others(5): Show |
2 | a0001c0002t0024g0153a0001c0002t0024g0155 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1260+6548_1260+654 others(16): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTG | T | 33 | a0001c0002t0007g0228a0001c0002t0053g0090a0001c0002t0089g0093others(30): Show | 33 | HG00140.hp1 HG00738.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1260+6593_1260+659 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTGTG | T | 18 | a0001c0002t0031g0092a0001c0004t0042g0082a0001c0006t0087g0165others(15): Show | 18 | HG00621.hp1 HG01517.hp1 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.1260+6591_1260+659 others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTGTGTG | T | 6 | a0001c0002t0111g0182a0001c0004t0021g0149a0001c0004t0021g0151others(3): Show | 6 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1260+6589_1260+659 others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTGTGTGT others(1): Show |
T | 13 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(10): Show | 13 | HG00639.hp1 HG00735.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1260+6587_1260+659 others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTGTGTGT others(3): Show |
T | 7 | a0001c0003t0048g0280a0001c0004t0005g0138a0001c0004t0005g0139others(4): Show | 7 | HG02647.hp2 HG02970.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+6585_1260+659 others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTGTGTGT others(5): Show |
T | 13 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(10): Show | 14 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1260+6583_1260+659 others(16): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTGTGTGT others(7): Show |
T | 6 | a0001c0003t0008g0266a0001c0003t0088g0284a0001c0003t0096g0078others(3): Show | 6 | HG02922.hp2 HG03834.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.1260+6581_1260+659 others(18): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTGTGTGT others(9): Show |
T | 11 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+6579_1260+659 others(20): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTGTGTGT others(13): Show |
T | 3 | a0001c0002t0081g0089a0001c0002t0082g0088a0002c0001t0003g0016 | 3 | HG02976.hp2 HG03209.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1260+6575_1260+659 others(24): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724990
|
TTGTGTGT others(15): Show |
T | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1260+6573_1260+659 others(26): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155724990 | |||||
| chr7:155724992
|
G | T | 15 | a0001c0002t0006g0221a0001c0002t0007g0226a0001c0002t0011g0210others(12): Show | 15 | HG00642.hp1 HG01070.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1260+6549G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724992 | ||||||
| chr7:155724994
|
G | T | 13 | a0001c0002t0007g0228a0001c0002t0023g0159a0001c0002t0025g0005others(10): Show | 13 | HG01070.hp2 HG01099.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1260+6551G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724994 | ||||||
| chr7:155724996
|
G | T | 7 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(4): Show | 7 | HG01891.hp1 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1260+6553G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724996 | ||||||
| chr7:155724998
|
G | T | 5 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+6555G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155724998 | ||||||
| chr7:155725000
|
G | T | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1260+6557G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725000 | ||||||
| chr7:155725004
|
G | T | 13 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(10): Show | 14 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.1260+6561G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725004 | ||||||
| chr7:155725006
|
G | T | 6 | a0001c0003t0008g0266a0001c0003t0088g0284a0001c0003t0096g0078others(3): Show | 6 | HG02922.hp2 HG03834.hp1 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.1260+6563G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725006 | ||||||
| chr7:155725008
|
G | T | 11 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(8): Show | 11 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1260+6565G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725008 | ||||||
| chr7:155725012
|
G | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1260+6569G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725012 | ||||||
| chr7:155725014
|
G | T | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1260+6571G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725014 | ||||||
| chr7:155725052
|
T | G | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1260+6609T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725052 | ||||||
| chr7:155725199
|
AGTT | A | 5 | a0001c0004t0005g0131a0001c0004t0005g0133a0001c0004t0005g0137others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+6760_1260+676 others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155725199 | |||||
| chr7:155725203
|
G | GT | 21 | a0001c0004t0021g0151a0002c0001t0002g0246a0002c0001t0003g0018others(18): Show | 21 | HG00621.hp1 HG00741.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1260+6781dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155725203 | |||||
| chr7:155725203
|
GT | G | 18 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0018t0079g0079others(15): Show | 18 | HG00558.hp1 HG01517.hp1 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1260+6781delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155725203 | |||||
| chr7:155725203
|
GTTTT | G | 9 | a0001c0003t0005g0256a0001c0003t0008g0257a0001c0003t0047g0282others(6): Show | 9 | HG02055.hp2 HG02145.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260+6778_1260+678 others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155725203 | |||||
| chr7:155725203
|
GTTTTT | G | 21 | a0001c0003t0008g0002a0001c0003t0008g0258a0001c0003t0008g0266others(18): Show | 22 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(19): Show |
intron_variant | MODIFIER | c.1260+6777_1260+678 others(9): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155725203 | |||||
| chr7:155725203
|
GTTTTTTT | G | 93 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(90): Show | 93 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.1260+6775_1260+678 others(11): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155725203 | |||||
| chr7:155725256
|
T | G | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1260+6813T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725256 | ||||||
| chr7:155725260
|
G | T | 1 | a0002c0001t0002g0108 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1260+6817G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725260 | ||||||
| chr7:155725266
|
A | C | 1 | a0001c0004t0005g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1260+6823A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725266 | ||||||
| chr7:155725337
|
T | G | 1 | a0002c0001t0002g0129 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1260+6894T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725337 | ||||||
| chr7:155725367
|
T | G | 1 | a0002c0001t0017g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1260+6924T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725367 | ||||||
| chr7:155725393
|
A | G | 3 | a0002c0001t0002g0246a0002c0001t0004g0245a0002c0001t0016g0247 | 3 | HG00741.hp2 HG02602.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1260+6950A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725393 | ||||||
| chr7:155725501
|
T | G | 11 | a0001c0002t0006g0273a0001c0002t0007g0212a0001c0002t0007g0222others(8): Show | 11 | HG00558.hp2 HG00673.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.1260+7058T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725501 | ||||||
| chr7:155725610
|
G | A | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1260+7167G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725610 | ||||||
| chr7:155725665
|
T | C | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1260+7222T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725665 | ||||||
| chr7:155725739
|
G | A | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1260+7296G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725739 | ||||||
| chr7:155725804
|
T | A | 1 | a0002c0001t0071g0122 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1260+7361T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725804 | ||||||
| chr7:155725858
|
A | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1260+7415A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725858 | ||||||
| chr7:155725889
|
T | C | 1 | a0002c0001t0062g0020 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1260+7446T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725889 | ||||||
| chr7:155725906
|
T | C | 3 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0004t0042g0082 | 3 | HG02976.hp2 HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1260+7463T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725906 | ||||||
| chr7:155725996
|
T | C | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+7553T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155725996 | ||||||
| chr7:155726001
|
A | T | 31 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(28): Show | 32 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.1260+7558A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155726001 | ||||||
| chr7:155726025
|
G | A | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1260+7582G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155726025 | ||||||
| chr7:155726265
|
G | A | 1 | a0002c0005t0014g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1260+7822G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155726265 | ||||||
| chr7:155726349
|
A | G | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.1260+7906A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155726349 | ||||||
| chr7:155726361
|
G | GT | 16 | a0001c0002t0007g0215a0001c0002t0010g0185a0001c0002t0031g0092others(13): Show | 16 | HG00423.hp1 HG00735.hp1 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.1260+7929dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155726361 | |||||
| chr7:155726517
|
A | G | 131 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1260+8074A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155726517 | ||||||
| chr7:155726767
|
G | A | 1 | a0002c0001t0002g0146 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1260+8324G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155726767 | ||||||
| chr7:155726819
|
A | G | 1 | a0002c0005t0026g0224 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1260+8376A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155726819 | ||||||
| chr7:155727050
|
C | G | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1260+8607C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727050 | ||||||
| chr7:155727064
|
C | T | 1 | a0002c0005t0014g0223 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1260+8621C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727064 | ||||||
| chr7:155727104
|
A | G | 1 | a0001c0002t0113g0203 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1260+8661A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727104 | ||||||
| chr7:155727152
|
C | T | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.1260+8709C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727152 | ||||||
| chr7:155727167
|
C | G | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1260+8724C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727167 | ||||||
| chr7:155727203
|
C | T | 1 | a0001c0002t0007g0228 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1260+8760C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727203 | ||||||
| chr7:155727363
|
G | A | 130 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(127): Show | 131 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1260+8920G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727363 | ||||||
| chr7:155727609
|
G | C | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1260+9166G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727609 | ||||||
| chr7:155727663
|
T | G | 1 | a0002c0001t0069g0107 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1260+9220T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727663 | ||||||
| chr7:155727774
|
G | A | 1 | a0006c0014t0095g0271 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1260+9331G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727774 | ||||||
| chr7:155727859
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1260+9416G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155727859 | ||||||
| chr7:155727930
|
A | AT | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1260+9496dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155727930 | |||||
| chr7:155728103
|
G | C | 1 | a0002c0001t0002g0278 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1261-9427G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155728103 | ||||||
| chr7:155728166
|
G | C | 2 | a0001c0004t0041g0083a0001c0004t0043g0081 | 2 | HG01884.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1261-9364G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155728166 | ||||||
| chr7:155728211
|
C | G | 136 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(133): Show | 137 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1261-9319C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155728211 | ||||||
| chr7:155728408
|
G | C | 1 | a0002c0001t0040g0303 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1261-9122G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155728408 | ||||||
| chr7:155728530
|
A | G | 1 | a0002c0001t0002g0123 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1261-9000A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155728530 | ||||||
| chr7:155728583
|
C | G | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1261-8947C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155728583 | ||||||
| chr7:155728738
|
A | G | 14 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-8792A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155728738 | ||||||
| chr7:155728961
|
A | G | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1261-8569A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155728961 | ||||||
| chr7:155729044
|
C | T | 10 | a0001c0002t0007g0169a0001c0002t0023g0156a0001c0002t0023g0157others(7): Show | 10 | HG00140.hp2 HG00642.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1261-8486C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729044 | ||||||
| chr7:155729089
|
C | CAGGAGG | 5 | a0001c0002t0006g0173a0001c0002t0006g0217a0001c0002t0007g0215others(2): Show | 5 | HG01255.hp1 HG02683.hp2 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-8440_1261-843 others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155729089 | |||||
| chr7:155729171
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-8359A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729171 | ||||||
| chr7:155729237
|
A | C | 1 | a0001c0002t0106g0202 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1261-8293A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729237 | ||||||
| chr7:155729269
|
G | A | 1 | a0002c0001t0076g0097 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1261-8261G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729269 | ||||||
| chr7:155729432
|
T | C | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1261-8098T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729432 | ||||||
| chr7:155729450
|
C | A | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-8080C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729450 | ||||||
| chr7:155729513
|
G | A | 1 | a0001c0002t0028g0208 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1261-8017G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729513 | ||||||
| chr7:155729697
|
G | A | 2 | a0001c0003t0019g0251a0002c0001t0002g0100 | 2 | HG00642.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1261-7833G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729697 | ||||||
| chr7:155729742
|
CA | C | 28 | a0001c0002t0025g0006a0001c0003t0048g0280a0001c0004t0005g0130others(25): Show | 28 | HG00639.hp1 HG01257.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.1261-7769delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155729742 | |||||
| chr7:155729742
|
CAA | C | 9 | a0001c0002t0007g0212a0001c0002t0007g0222a0001c0002t0007g0244others(6): Show | 9 | HG00673.hp1 HG02809.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-7770_1261-776 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155729742 | |||||
| chr7:155729742
|
CAAA | C | 78 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(75): Show | 78 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.1261-7771_1261-776 others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155729742 | |||||
| chr7:155729742
|
CAAAA | C | 30 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(27): Show | 31 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(28): Show |
intron_variant | MODIFIER | c.1261-7772_1261-776 others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155729742 | |||||
| chr7:155729747
|
A | C | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1261-7783A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729747 | ||||||
| chr7:155729785
|
A | G | 1 | a0002c0001t0002g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1261-7745A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729785 | ||||||
| chr7:155729840
|
G | A | 2 | a0001c0002t0101g0161a0001c0002t0103g0158 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1261-7690G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729840 | ||||||
| chr7:155729846
|
T | C | 4 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-7684T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729846 | ||||||
| chr7:155729941
|
ACTTC | A | 4 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-7580_1261-757 others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155729941 | |||||
| chr7:155729945
|
C | A | 4 | a0001c0003t0047g0282a0001c0003t0049g0283a0001c0003t0051g0281others(1): Show | 4 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-7585C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155729945 | ||||||
| chr7:155730007
|
A | G | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-7523A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730007 | ||||||
| chr7:155730179
|
C | T | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-7351C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730179 | ||||||
| chr7:155730211
|
G | C | 9 | a0002c0001t0002g0040a0002c0001t0002g0049a0002c0001t0002g0103others(6): Show | 9 | HG01517.hp1 HG01981.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-7319G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730211 | ||||||
| chr7:155730542
|
G | A | 3 | a0001c0004t0041g0083a0001c0004t0042g0082a0001c0004t0043g0081 | 3 | HG01884.hp1 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1261-6988G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730542 | ||||||
| chr7:155730568
|
A | G | 1 | a0002c0001t0002g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1261-6962A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730568 | ||||||
| chr7:155730742
|
A | G | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1261-6788A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730742 | ||||||
| chr7:155730767
|
G | A | 1 | a0002c0001t0001g0031 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1261-6763G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730767 | ||||||
| chr7:155730914
|
A | G | 3 | a0002c0001t0002g0109a0002c0001t0002g0110a0002c0001t0002g0111 | 3 | HG00140.hp1 HG00738.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.1261-6616A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730914 | ||||||
| chr7:155730982
|
T | C | 2 | a0002c0005t0001g0023a0002c0005t0001g0024 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1261-6548T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730982 | ||||||
| chr7:155730985
|
G | T | 10 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(7): Show | 10 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-6545G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155730985 | ||||||
| chr7:155731004
|
T | TTTC | 157 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(154): Show | 158 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1261-6521_1261-651 others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155731004 | |||||
| chr7:155731106
|
C | T | 5 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0101g0161others(2): Show | 5 | HG02630.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-6424C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155731106 | ||||||
| chr7:155731222
|
G | A | 4 | a0002c0001t0013g0061a0002c0001t0020g0029a0002c0001t0020g0030others(1): Show | 4 | HG02040.hp1 HG02071.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-6308G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155731222 | ||||||
| chr7:155731228
|
A | G | 131 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1261-6302A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155731228 | ||||||
| chr7:155731250
|
T | C | 121 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1261-6280T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155731250 | ||||||
| chr7:155731297
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-6233C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155731297 | ||||||
| chr7:155731527
|
C | T | 3 | a0002c0001t0004g0101a0002c0001t0004g0102a0002c0001t0035g0120 | 3 | HG01952.hp2 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1261-6003C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155731527 | ||||||
| chr7:155731590
|
A | G | 1 | a0001c0004t0005g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1261-5940A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155731590 | ||||||
| chr7:155731653
|
CAGAA | C | 8 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0024g0153others(5): Show | 8 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1261-5874_1261-587 others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155731653 | |||||
| chr7:155731853
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-5677A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155731853 | ||||||
| chr7:155731914
|
C | T | 1 | a0001c0002t0115g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1261-5616C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155731914 | ||||||
| chr7:155732223
|
T | A | 1 | a0002c0001t0002g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1261-5307T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155732223 | ||||||
| chr7:155732387
|
T | C | 2 | a0002c0001t0001g0053a0002c0001t0001g0072 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1261-5143T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155732387 | ||||||
| chr7:155732420
|
A | G | 2 | a0001c0002t0089g0093a0001c0002t0090g0091 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1261-5110A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155732420 | ||||||
| chr7:155732441
|
C | T | 8 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(5): Show | 8 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.1261-5089C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155732441 | ||||||
| chr7:155732838
|
G | C | 1 | a0003c0007t0022g0291 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1261-4692G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155732838 | ||||||
| chr7:155732853
|
A | G | 131 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1261-4677A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155732853 | ||||||
| chr7:155732882
|
A | G | 1 | a0001c0003t0052g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1261-4648A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155732882 | ||||||
| chr7:155732936
|
G | A | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-4594G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155732936 | ||||||
| chr7:155733013
|
G | A | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.1261-4517G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155733013 | ||||||
| chr7:155733107
|
A | G | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1261-4423A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155733107 | ||||||
| chr7:155733167
|
C | T | 1 | a0002c0001t0002g0096 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1261-4363C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155733167 | ||||||
| chr7:155733168
|
G | A | 1 | a0001c0002t0116g0188 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1261-4362G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155733168 | ||||||
| chr7:155733331
|
A | G | 5 | a0001c0002t0029g0162a0001c0002t0029g0176a0001c0002t0029g0207others(2): Show | 5 | HG00558.hp2 NA18956.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-4199A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155733331 | ||||||
| chr7:155733437
|
A | ATAAAAAT others(74): Show |
1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1261-4044_1261-404 others(85): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155733437 | |||||
| chr7:155733437
|
A | ATAAAAAT others(74): Show |
2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-4036_1261-403 others(85): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155733437 | |||||
| chr7:155733437
|
A | ATAAAAAT others(74): Show |
118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1261-4036_1261-403 others(85): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155733437 | |||||
| chr7:155733443
|
A | T | 1 | a0001c0002t0031g0094 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1261-4087A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155733443 | ||||||
| chr7:155733600
|
A | T | 1 | a0001c0004t0021g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1261-3930A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155733600 | ||||||
| chr7:155733994
|
A | G | 1 | a0002c0001t0035g0120 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1261-3536A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155733994 | ||||||
| chr7:155734113
|
A | C | 5 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-3417A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734113 | ||||||
| chr7:155734239
|
C | T | 3 | a0002c0001t0001g0011a0002c0001t0001g0022a0002c0001t0057g0013 | 3 | NA18961.hp2 NA18970.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1261-3291C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734239 | ||||||
| chr7:155734363
|
C | T | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1261-3167C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734363 | ||||||
| chr7:155734552
|
G | A | 1 | a0002c0001t0017g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1261-2978G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734552 | ||||||
| chr7:155734704
|
C | T | 1 | a0001c0003t0047g0282 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1261-2826C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734704 | ||||||
| chr7:155734766
|
A | G | 2 | a0002c0001t0001g0062a0002c0001t0058g0046 | 2 | HG00423.hp1 NA18940.hp2 |
intron_variant | MODIFIER | c.1261-2764A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734766 | ||||||
| chr7:155734796
|
A | G | 17 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(14): Show | 18 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.1261-2734A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734796 | ||||||
| chr7:155734827
|
C | T | 41 | a0001c0002t0006g0174a0001c0002t0006g0180a0001c0002t0006g0181others(38): Show | 41 | HG00423.hp2 HG00558.hp2 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1261-2703C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734827 | ||||||
| chr7:155734828
|
A | G | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1261-2702A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734828 | ||||||
| chr7:155734891
|
C | T | 2 | a0001c0006t0092g0304a0006c0014t0095g0271 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1261-2639C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155734891 | ||||||
| chr7:155734900
|
A | ATT | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1261-2624_1261-262 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155734900 | |||||
| chr7:155735010
|
C | T | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.1261-2520C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735010 | ||||||
| chr7:155735029
|
T | C | 1 | a0001c0003t0019g0251 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1261-2501T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735029 | ||||||
| chr7:155735058
|
A | G | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-2472A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735058 | ||||||
| chr7:155735069
|
T | C | 42 | a0001c0002t0007g0169a0001c0002t0031g0092a0001c0002t0031g0094others(39): Show | 43 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.1261-2461T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735069 | ||||||
| chr7:155735079
|
G | A | 9 | a0001c0004t0005g0133a0002c0001t0003g0039a0002c0001t0003g0047others(6): Show | 9 | HG01346.hp1 HG01891.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-2451G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735079 | ||||||
| chr7:155735390
|
G | A | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1261-2140G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735390 | ||||||
| chr7:155735418
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1261-2112A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735418 | ||||||
| chr7:155735453
|
C | T | 86 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(83): Show | 86 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1261-2077C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735453 | ||||||
| chr7:155735462
|
T | C | 3 | a0002c0001t0032g0297a0002c0001t0032g0298a0002c0001t0054g0294 | 3 | HG02809.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1261-2068T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735462 | ||||||
| chr7:155735463
|
A | G | 2 | a0002c0001t0004g0119a0002c0001t0069g0107 | 2 | HG00323.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1261-2067A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735463 | ||||||
| chr7:155735497
|
G | A | 4 | a0002c0001t0001g0104a0002c0001t0001g0145a0002c0001t0003g0037others(1): Show | 4 | NA18962.hp1 NA18984.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1261-2033G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735497 | ||||||
| chr7:155735521
|
A | G | 2 | a0001c0003t0005g0256a0001c0003t0099g0084 | 2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1261-2009A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735521 | ||||||
| chr7:155735557
|
A | T | 10 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(7): Show | 10 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-1973A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735557 | ||||||
| chr7:155735567
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1261-1963A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735567 | ||||||
| chr7:155735691
|
GTCTC | G | 288 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(285): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.1261-1815_1261-181 others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155735691 | |||||
| chr7:155735713
|
CTCTCTG | C | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1261-1811_1261-180 others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155735713 | |||||
| chr7:155735718
|
T | C | 69 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(66): Show | 69 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.1261-1812T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735718 | ||||||
| chr7:155735719
|
G | C | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1261-1811G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735719 | ||||||
| chr7:155735721
|
C | G | 15 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(12): Show | 15 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1261-1809C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735721 | ||||||
| chr7:155735724
|
TCTCTCTC others(11): Show |
T | 1 | a0001c0002t0023g0157 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1261-1798_1261-178 others(22): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155735724 | |||||
| chr7:155735726
|
TCTCTCTC others(9): Show |
T | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.1261-1796_1261-178 others(20): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155735726 | |||||
| chr7:155735737
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-1793C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735737 | ||||||
| chr7:155735742
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-1788C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735742 | ||||||
| chr7:155735829
|
GT | G | 10 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(7): Show | 10 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-1700delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155735829 | ||||||
| chr7:155736005
|
G | T | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-1525G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736005 | ||||||
| chr7:155736056
|
A | C | 1 | a0002c0001t0001g0012 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1261-1474A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736056 | ||||||
| chr7:155736129
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-1401G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736129 | ||||||
| chr7:155736146
|
T | C | 14 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-1384T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736146 | ||||||
| chr7:155736175
|
G | A | 1 | a0002c0001t0003g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1261-1355G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736175 | ||||||
| chr7:155736313
|
A | G | 135 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1261-1217A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736313 | ||||||
| chr7:155736462
|
C | T | 135 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1261-1068C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736462 | ||||||
| chr7:155736527
|
T | C | 1 | a0002c0005t0018g0192 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1261-1003T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736527 | ||||||
| chr7:155736541
|
C | A | 1 | a0002c0001t0017g0052 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1261-989C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736541 | ||||||
| chr7:155736726
|
A | G | 1 | a0002c0001t0001g0036 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1261-804A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736726 | ||||||
| chr7:155736751
|
G | A | 18 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(15): Show | 18 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1261-779G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736751 | ||||||
| chr7:155736816
|
A | G | 1 | a0002c0001t0070g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1261-714A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736816 | ||||||
| chr7:155736861
|
A | G | 1 | a0002c0001t0002g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1261-669A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155736861 | ||||||
| chr7:155737003
|
G | A | 18 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(15): Show | 18 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1261-527G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737003 | ||||||
| chr7:155737084
|
T | C | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1261-446T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737084 | ||||||
| chr7:155737151
|
A | G | 120 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.1261-379A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737151 | ||||||
| chr7:155737202
|
C | T | 1 | a0001c0002t0007g0212 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1261-328C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737202 | ||||||
| chr7:155737245
|
C | CAT | 17 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(14): Show | 17 | HG00642.hp1 HG00735.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1261-285_1261-284i others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737245 | ||||||
| chr7:155737245
|
C | CATGT | 67 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(64): Show | 67 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.1261-285_1261-284i others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737245 | ||||||
| chr7:155737245
|
C | CATGTGT | 5 | a0001c0002t0007g0169a0001c0002t0007g0226a0001c0002t0037g0201others(2): Show | 5 | HG00140.hp2 HG02615.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.1261-285_1261-284i others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737245 | ||||||
| chr7:155737245
|
C | CGT | 12 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(9): Show | 12 | HG01243.hp2 HG02145.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.1261-265_1261-264d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737245 | |||||
| chr7:155737245
|
C | CGTGT | 24 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(21): Show | 25 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.1261-267_1261-264d others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737245 | |||||
| chr7:155737245
|
C | CGTGTGT | 8 | a0001c0003t0005g0256a0001c0003t0047g0282a0001c0003t0048g0280others(5): Show | 8 | HG02055.hp2 HG02647.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1261-269_1261-264d others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737245 | |||||
| chr7:155737245
|
C | T | 2 | a0002c0001t0063g0027a0002c0001t0077g0033 | 2 | HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1261-285C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737245 | ||||||
| chr7:155737246
|
G | A | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1261-284G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737246 | ||||||
| chr7:155737247
|
T | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-283T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737247 | ||||||
| chr7:155737249
|
T | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-281T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737249 | ||||||
| chr7:155737251
|
T | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1261-279T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737251 | ||||||
| chr7:155737253
|
T | C | 1 | a0001c0002t0082g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1261-277T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737253 | ||||||
| chr7:155737265
|
T | A | 2 | a0001c0002t0037g0201a0001c0002t0037g0243 | 2 | NA18966.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1261-265T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737265 | ||||||
| chr7:155737291
|
G | T | 4 | a0001c0004t0021g0148a0001c0004t0021g0149a0001c0004t0021g0151others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-239G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737291 | ||||||
| chr7:155737315
|
C | T | 4 | a0001c0004t0021g0148a0001c0004t0021g0149a0001c0004t0021g0151others(1): Show | 4 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-215C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737315 | ||||||
| chr7:155737316
|
G | A | 14 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1261-214G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737316 | ||||||
| chr7:155737328
|
A | G | 2 | a0001c0002t0101g0161a0001c0002t0103g0158 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1261-202A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737328 | ||||||
| chr7:155737331
|
C | T | 4 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-199C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737331 | ||||||
| chr7:155737353
|
C | CTG | 17 | a0001c0002t0023g0156a0002c0001t0001g0012a0002c0001t0001g0015others(14): Show | 17 | HG01891.hp2 HG01934.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.1261-145_1261-144d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
C | CTGTG | 17 | a0001c0002t0011g0177a0001c0003t0007g0213a0001c0003t0008g0002others(14): Show | 18 | HG00323.hp2 HG00621.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.1261-147_1261-144d others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
C | CTGTGTG | 48 | a0001c0002t0006g0173a0001c0002t0006g0175a0001c0002t0006g0217others(45): Show | 48 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.1261-149_1261-144d others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
C | CTGTGTGT others(1): Show |
36 | a0001c0002t0006g0174a0001c0002t0006g0180a0001c0002t0006g0181others(33): Show | 36 | HG00544.hp1 HG00639.hp1 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.1261-151_1261-144d others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
C | CTGTGTGT others(3): Show |
18 | a0001c0002t0006g0233a0001c0002t0007g0222a0001c0002t0007g0226others(15): Show | 18 | HG00673.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1261-153_1261-144d others(12): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
C | CTGTGTGT others(5): Show |
4 | a0001c0002t0024g0160a0001c0003t0048g0280a0001c0004t0041g0083others(1): Show | 4 | HG00642.hp1 HG01884.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-155_1261-144d others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
C | CTGTGTGT others(7): Show |
16 | a0001c0002t0012g0001a0001c0002t0012g0209a0001c0002t0012g0229others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-157_1261-144d others(16): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
C | CTGTGTGT others(9): Show |
9 | a0001c0002t0012g0235a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG02056.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-159_1261-144d others(18): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
C | CTGTGTGT others(11): Show |
2 | a0001c0003t0019g0255a0001c0003t0046g0254 | 2 | HG02572.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1261-161_1261-144d others(20): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
C | CTGTGTGT others(13): Show |
2 | a0001c0002t0102g0154a0001c0004t0005g0139 | 2 | HG02630.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1261-163_1261-144d others(22): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
CTG | C | 3 | a0001c0008t0086g0087a0001c0008t0091g0086a0002c0001t0001g0056 | 3 | HG01243.hp1 HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1261-145_1261-144d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737353
|
CTGTGTG | C | 4 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(1): Show | 4 | HG01891.hp1 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1261-149_1261-144d others(8): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 155737353 | |||||
| chr7:155737375
|
G | A | 1 | a0002c0001t0001g0009 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1261-155G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737375 | ||||||
| chr7:155737459
|
A | G | 1 | a0001c0002t0023g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1261-71A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 9/17 | chr7 | 155737459 | ||||||
| chr7:155737669
|
A | G | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
splice_region_variant&intron_variant | LOW | c.1393+7A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 10/17 | chr7 | 155737669 | ||||||
| chr7:155737803
|
C | A | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1393+141C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 10/17 | chr7 | 155737803 | ||||||
| chr7:155737816
|
G | A | 2 | a0001c0002t0007g0212a0001c0002t0007g0222 | 2 | HG00673.hp1 NA18940.hp1 |
intron_variant | MODIFIER | c.1393+154G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 10/17 | chr7 | 155737816 | ||||||
| chr7:155737849
|
C | T | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1393+187C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 10/17 | chr7 | 155737849 | ||||||
| chr7:155738020
|
C | T | 1 | a0002c0001t0070g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1394-40C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 10/17 | chr7 | 155738020 | ||||||
| chr7:155738035
|
TTAA | T | 3 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0006t0092g0304 | 3 | HG02486.hp2 HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1394-23_1394-21del others(3): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 155738035 | |||||
| chr7:155738531
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.1737+128A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155738531 | ||||||
| chr7:155738656
|
A | G | 4 | a0002c0001t0001g0056a0002c0001t0001g0058a0002c0001t0060g0288others(1): Show | 4 | HG00741.hp1 HG01175.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.1737+253A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155738656 | ||||||
| chr7:155738803
|
A | G | 1 | a0002c0001t0004g0296 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1737+400A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155738803 | ||||||
| chr7:155738816
|
C | G | 5 | a0001c0002t0036g0274a0001c0002t0036g0275a0001c0002t0105g0008others(2): Show | 5 | HG00733.hp1 HG01070.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1737+413C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155738816 | ||||||
| chr7:155738851
|
G | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1737+448G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155738851 | ||||||
| chr7:155739110
|
TG | T | 9 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(6): Show | 9 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1738-604delG | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155739110 | ||||||
| chr7:155739274
|
C | T | 1 | a0002c0001t0070g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1738-441C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155739274 | ||||||
| chr7:155739278
|
T | C | 1 | a0001c0002t0115g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1738-437T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155739278 | ||||||
| chr7:155739400
|
A | G | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1738-315A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155739400 | ||||||
| chr7:155739531
|
G | T | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.1738-184G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155739531 | ||||||
| chr7:155739667
|
G | A | 118 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(115): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1738-48G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 11/17 | chr7 | 155739667 | ||||||
| chr7:155740067
|
G | A | 1 | a0001c0003t0098g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2049+41G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740067 | ||||||
| chr7:155740250
|
C | T | 1 | a0002c0001t0001g0010 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2049+224C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740250 | ||||||
| chr7:155740281
|
G | A | 135 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(132): Show | 136 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.2049+255G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740281 | ||||||
| chr7:155740307
|
A | G | 8 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(5): Show | 8 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2049+281A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740307 | ||||||
| chr7:155740335
|
A | C | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2049+309A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740335 | ||||||
| chr7:155740425
|
A | C | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2049+399A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740425 | ||||||
| chr7:155740451
|
C | T | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2049+425C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740451 | ||||||
| chr7:155740608
|
T | C | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2049+582T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740608 | ||||||
| chr7:155740617
|
T | C | 1 | a0002c0001t0069g0107 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2049+591T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740617 | ||||||
| chr7:155740619
|
G | A | 10 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(7): Show | 10 | HG00735.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.2049+593G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740619 | ||||||
| chr7:155740681
|
C | T | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2049+655C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740681 | ||||||
| chr7:155740699
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2049+673A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740699 | ||||||
| chr7:155740794
|
G | A | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2049+768G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740794 | ||||||
| chr7:155740967
|
C | G | 5 | a0001c0003t0047g0282a0001c0003t0048g0280a0001c0003t0049g0283others(2): Show | 5 | HG02055.hp2 HG02647.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2050-852C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155740967 | ||||||
| chr7:155741112
|
G | T | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2050-707G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155741112 | ||||||
| chr7:155741230
|
C | G | 8 | a0002c0001t0001g0026a0002c0001t0001g0055a0002c0001t0001g0056others(5): Show | 8 | HG00741.hp1 HG01071.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.2050-589C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155741230 | ||||||
| chr7:155741280
|
C | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2050-539C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155741280 | ||||||
| chr7:155741438
|
G | A | 4 | a0001c0004t0005g0138a0001c0004t0005g0139a0001c0004t0005g0140others(1): Show | 4 | HG02647.hp2 NA18906.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2050-381G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155741438 | ||||||
| chr7:155741498
|
T | A | 1 | a0002c0001t0017g0019 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2050-321T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | chr7 | 155741498 | ||||||
| chr7:155741732
|
TTG | T | 3 | a0002c0001t0030g0301a0002c0001t0030g0302a0002c0001t0040g0303 | 3 | HG01255.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2050-83_2050-82del others(2): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 155741732 | |||||
| chr7:155742229
|
C | CTT | 114 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(111): Show | 115 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2337+135_2337+136d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 155742229 | |||||
| chr7:155742229
|
CT | C | 6 | a0002c0001t0001g0015a0002c0001t0020g0030a0002c0001t0121g0069others(3): Show | 6 | HG00621.hp1 HG00735.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2337+136delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 155742229 | |||||
| chr7:155742303
|
G | GTTTA | 231 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(228): Show | 232 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2337+199_2337+202d others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 155742303 | |||||
| chr7:155742412
|
T | C | 1 | a0001c0004t0042g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2337+306T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155742412 | ||||||
| chr7:155742501
|
G | T | 1 | a0002c0001t0002g0278 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2337+395G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155742501 | ||||||
| chr7:155742721
|
C | G | 74 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(71): Show | 74 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.2337+615C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155742721 | ||||||
| chr7:155742857
|
G | A | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2337+751G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155742857 | ||||||
| chr7:155742997
|
C | T | 2 | a0001c0003t0009g0270a0007c0013t0009g0265 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.2337+891C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155742997 | ||||||
| chr7:155743084
|
T | C | 120 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.2337+978T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155743084 | ||||||
| chr7:155743186
|
T | G | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2337+1080T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155743186 | ||||||
| chr7:155743417
|
C | G | 117 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2337+1311C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155743417 | ||||||
| chr7:155743443
|
C | A | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2337+1337C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155743443 | ||||||
| chr7:155743444
|
G | A | 1 | a0001c0006t0092g0304 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2337+1338G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155743444 | ||||||
| chr7:155743506
|
T | C | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2337+1400T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155743506 | ||||||
| chr7:155743824
|
T | G | 114 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(111): Show | 115 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2338-1137T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155743824 | ||||||
| chr7:155743852
|
T | C | 20 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(17): Show | 21 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.2338-1109T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155743852 | ||||||
| chr7:155743901
|
C | T | 17 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(14): Show | 17 | HG00735.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2338-1060C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155743901 | ||||||
| chr7:155744022
|
A | T | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2338-939A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155744022 | ||||||
| chr7:155744040
|
G | A | 14 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2338-921G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155744040 | ||||||
| chr7:155744201
|
A | G | 85 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(82): Show | 85 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2338-760A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155744201 | ||||||
| chr7:155744294
|
T | G | 5 | a0002c0001t0001g0036a0002c0001t0001g0104a0002c0001t0001g0145others(2): Show | 5 | NA18962.hp1 NA18984.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.2338-667T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155744294 | ||||||
| chr7:155744350
|
G | A | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2338-611G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155744350 | ||||||
| chr7:155744394
|
C | T | 1 | a0001c0003t0099g0084 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2338-567C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155744394 | ||||||
| chr7:155744780
|
G | GT | 114 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0180others(111): Show | 115 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.2338-174dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 155744780 | |||||
| chr7:155744780
|
G | GTT | 5 | a0001c0002t0006g0175a0001c0002t0036g0274a0001c0002t0036g0275others(2): Show | 5 | HG00733.hp1 HG01070.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338-175_2338-174d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 155744780 | |||||
| chr7:155744780
|
GT | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2338-174delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr7 | 155744780 | |||||
| chr7:155744831
|
G | T | 1 | a0001c0002t0007g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2338-130G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155744831 | ||||||
| chr7:155744842
|
A | G | 1 | a0001c0002t0027g0199 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.2338-119A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155744842 | ||||||
| chr7:155744857
|
T | C | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2338-104T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 13/17 | chr7 | 155744857 | ||||||
| chr7:155745769
|
A | G | 129 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(126): Show | 130 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.2979+167A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155745769 | ||||||
| chr7:155746106
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2979+504A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746106 | ||||||
| chr7:155746179
|
A | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2979+577A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746179 | ||||||
| chr7:155746191
|
C | T | 44 | a0001c0002t0006g0174a0001c0002t0006g0175a0001c0002t0006g0180others(41): Show | 44 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2979+589C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746191 | ||||||
| chr7:155746208
|
A | G | 8 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(5): Show | 8 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2979+606A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746208 | ||||||
| chr7:155746254
|
G | T | 1 | a0002c0001t0004g0144 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2979+652G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746254 | ||||||
| chr7:155746273
|
T | C | 8 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(5): Show | 8 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2979+671T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746273 | ||||||
| chr7:155746326
|
G | A | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2979+724G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746326 | ||||||
| chr7:155746475
|
C | T | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2979+873C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746475 | ||||||
| chr7:155746616
|
T | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2979+1014T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746616 | ||||||
| chr7:155746650
|
A | G | 117 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2979+1048A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746650 | ||||||
| chr7:155746730
|
A | G | 1 | a0001c0004t0005g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2979+1128A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746730 | ||||||
| chr7:155746798
|
G | A | 1 | a0001c0004t0005g0132 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2979+1196G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746798 | ||||||
| chr7:155746873
|
A | G | 85 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(82): Show | 85 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2979+1271A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155746873 | ||||||
| chr7:155747087
|
A | T | 1 | a0001c0004t0021g0149 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2979+1485A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155747087 | ||||||
| chr7:155747131
|
G | A | 1 | a0001c0002t0102g0154 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2979+1529G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155747131 | ||||||
| chr7:155747404
|
G | A | 2 | a0002c0001t0013g0061a0002c0001t0020g0029 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2979+1802G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155747404 | ||||||
| chr7:155747502
|
T | C | 1 | a0001c0011t0097g0085 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2979+1900T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155747502 | ||||||
| chr7:155747734
|
T | A | 1 | a0002c0001t0002g0124 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2979+2132T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155747734 | ||||||
| chr7:155747867
|
T | G | 1 | a0001c0004t0021g0149 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2979+2265T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155747867 | ||||||
| chr7:155748125
|
C | T | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2979+2523C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748125 | ||||||
| chr7:155748138
|
C | T | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2979+2536C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748138 | ||||||
| chr7:155748233
|
C | G | 1 | a0006c0014t0095g0271 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2979+2631C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748233 | ||||||
| chr7:155748372
|
C | T | 1 | a0002c0001t0001g0009 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2979+2770C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748372 | ||||||
| chr7:155748451
|
A | C | 1 | a0001c0004t0042g0082 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2979+2849A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748451 | ||||||
| chr7:155748481
|
A | G | 13 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2979+2879A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748481 | ||||||
| chr7:155748496
|
T | C | 3 | a0001c0002t0024g0153a0001c0002t0024g0155a0001c0002t0024g0160 | 3 | HG00642.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2979+2894T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748496 | ||||||
| chr7:155748689
|
G | C | 1 | a0001c0006t0093g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2979+3087G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748689 | ||||||
| chr7:155748700
|
T | C | 13 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2979+3098T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748700 | ||||||
| chr7:155748701
|
A | G | 1 | a0002c0001t0001g0035 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.2979+3099A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748701 | ||||||
| chr7:155748781
|
T | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2979+3179T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748781 | ||||||
| chr7:155748827
|
T | C | 1 | a0002c0001t0001g0011 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2979+3225T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748827 | ||||||
| chr7:155748882
|
C | T | 1 | a0001c0003t0046g0254 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2979+3280C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748882 | ||||||
| chr7:155748928
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2979+3326A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155748928 | ||||||
| chr7:155749015
|
C | T | 1 | a0002c0001t0002g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2979+3413C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749015 | ||||||
| chr7:155749029
|
A | G | 1 | a0001c0004t0005g0152 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2979+3427A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749029 | ||||||
| chr7:155749038
|
G | C | 1 | a0002c0001t0003g0074 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2979+3436G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749038 | ||||||
| chr7:155749170
|
G | C | 1 | a0001c0002t0089g0093 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2979+3568G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749170 | ||||||
| chr7:155749228
|
T | C | 1 | a0001c0002t0010g0172 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2979+3626T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749228 | ||||||
| chr7:155749293
|
T | C | 1 | a0001c0002t0081g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2979+3691T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749293 | ||||||
| chr7:155749354
|
T | C | 1 | a0002c0001t0002g0146 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2979+3752T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749354 | ||||||
| chr7:155749385
|
G | T | 1 | a0002c0001t0017g0076 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2979+3783G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749385 | ||||||
| chr7:155749437
|
G | A | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2979+3835G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749437 | ||||||
| chr7:155749443
|
T | A | 1 | a0001c0003t0009g0260 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2979+3841T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749443 | ||||||
| chr7:155749471
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2979+3869C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749471 | ||||||
| chr7:155749558
|
A | G | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2979+3956A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749558 | ||||||
| chr7:155749567
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2979+3965C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749567 | ||||||
| chr7:155749568
|
G | A | 44 | a0001c0002t0006g0174a0001c0002t0006g0175a0001c0002t0006g0180others(41): Show | 44 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2979+3966G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749568 | ||||||
| chr7:155749594
|
GATA | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2979+3995_2979+399 others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155749594 | |||||
| chr7:155749600
|
G | A | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2979+3998G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749600 | ||||||
| chr7:155749714
|
A | T | 138 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(135): Show | 139 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.2979+4112A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749714 | ||||||
| chr7:155749764
|
C | G | 2 | a0002c0001t0004g0106a0002c0005t0018g0225 | 2 | NA18994.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2979+4162C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749764 | ||||||
| chr7:155749773
|
C | T | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2979+4171C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749773 | ||||||
| chr7:155749791
|
T | C | 292 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(289): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2979+4189T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749791 | ||||||
| chr7:155749952
|
G | C | 1 | a0002c0001t0017g0019 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2979+4350G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155749952 | ||||||
| chr7:155750037
|
G | A | 4 | a0002c0001t0013g0050a0002c0001t0015g0028a0002c0001t0015g0045others(1): Show | 4 | HG02135.hp2 HG02165.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.2979+4435G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155750037 | ||||||
| chr7:155750114
|
G | A | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2979+4512G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155750114 | ||||||
| chr7:155750162
|
C | A | 1 | a0001c0003t0099g0084 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2979+4560C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155750162 | ||||||
| chr7:155750327
|
T | C | 1 | a0001c0002t0038g0214 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2979+4725T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155750327 | ||||||
| chr7:155750373
|
A | AC | 151 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(148): Show | 152 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.2979+4771_2979+477 others(5): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155750373 | ||||||
| chr7:155750731
|
G | GT | 52 | a0001c0002t0006g0174a0001c0002t0006g0221a0001c0002t0006g0233others(49): Show | 52 | HG00423.hp2 HG00621.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.2979+5143dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155750731 | |||||
| chr7:155750912
|
C | T | 1 | a0001c0002t0007g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2979+5310C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155750912 | ||||||
| chr7:155751057
|
T | C | 1 | a0001c0002t0029g0176 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2979+5455T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155751057 | ||||||
| chr7:155751099
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2979+5497A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155751099 | ||||||
| chr7:155751324
|
T | A | 13 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.2979+5722T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155751324 | ||||||
| chr7:155751326
|
T | C | 1 | a0002c0001t0070g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2979+5724T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155751326 | ||||||
| chr7:155751471
|
C | G | 117 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2979+5869C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155751471 | ||||||
| chr7:155751559
|
G | A | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2979+5957G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155751559 | ||||||
| chr7:155751792
|
TA | T | 122 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2979+6193delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155751792 | |||||
| chr7:155751970
|
C | G | 2 | a0001c0002t0006g0237a0001c0002t0118g0236 | 2 | NA18949.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2979+6368C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155751970 | ||||||
| chr7:155752046
|
T | G | 122 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2979+6444T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752046 | ||||||
| chr7:155752139
|
C | A | 6 | a0002c0001t0002g0246a0002c0001t0004g0245a0002c0001t0004g0249others(3): Show | 6 | HG00741.hp2 HG01258.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.2979+6537C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752139 | ||||||
| chr7:155752161
|
C | T | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2979+6559C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752161 | ||||||
| chr7:155752187
|
T | C | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2979+6585T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752187 | ||||||
| chr7:155752394
|
G | A | 3 | a0002c0001t0030g0301a0002c0001t0030g0302a0002c0001t0040g0303 | 3 | HG01255.hp2 HG02055.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2979+6792G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752394 | ||||||
| chr7:155752444
|
G | A | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2979+6842G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752444 | ||||||
| chr7:155752562
|
T | TA | 72 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(69): Show | 72 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.2979+6962dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155752562 | |||||
| chr7:155752661
|
C | T | 1 | a0002c0001t0032g0298 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2979+7059C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752661 | ||||||
| chr7:155752663
|
C | T | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2979+7061C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752663 | ||||||
| chr7:155752829
|
G | A | 1 | a0001c0002t0107g0276 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2979+7227G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752829 | ||||||
| chr7:155752853
|
G | A | 2 | a0002c0001t0013g0061a0002c0001t0020g0029 | 2 | HG02040.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2979+7251G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155752853 | ||||||
| chr7:155753078
|
G | A | 117 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2979+7476G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753078 | ||||||
| chr7:155753143
|
G | A | 1 | a0001c0002t0011g0241 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2979+7541G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753143 | ||||||
| chr7:155753414
|
T | A | 85 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(82): Show | 85 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2979+7812T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753414 | ||||||
| chr7:155753481
|
G | T | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2979+7879G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753481 | ||||||
| chr7:155753547
|
G | A | 85 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(82): Show | 85 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2979+7945G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753547 | ||||||
| chr7:155753585
|
C | T | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2979+7983C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753585 | ||||||
| chr7:155753596
|
T | A | 1 | a0001c0017t0055g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2979+7994T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753596 | ||||||
| chr7:155753699
|
A | C | 117 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2979+8097A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753699 | ||||||
| chr7:155753743
|
C | G | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2979+8141C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753743 | ||||||
| chr7:155753776
|
G | A | 117 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2979+8174G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753776 | ||||||
| chr7:155753851
|
G | T | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2979+8249G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753851 | ||||||
| chr7:155753904
|
C | T | 119 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(116): Show | 120 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.2979+8302C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155753904 | ||||||
| chr7:155754085
|
T | C | 2 | a0001c0002t0006g0273a0001c0002t0119g0191 | 2 | NA18983.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2979+8483T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754085 | ||||||
| chr7:155754202
|
G | A | 117 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2979+8600G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754202 | ||||||
| chr7:155754215
|
T | A | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2979+8613T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754215 | ||||||
| chr7:155754386
|
G | C | 7 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.2979+8784G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754386 | ||||||
| chr7:155754433
|
A | G | 122 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.2979+8831A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754433 | ||||||
| chr7:155754609
|
C | G | 1 | a0002c0001t0017g0019 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2979+9007C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754609 | ||||||
| chr7:155754640
|
C | T | 1 | a0001c0004t0084g0141 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2979+9038C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754640 | ||||||
| chr7:155754647
|
C | G | 1 | a0002c0001t0002g0100 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2979+9045C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754647 | ||||||
| chr7:155754683
|
A | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2979+9081A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754683 | ||||||
| chr7:155754821
|
G | A | 2 | a0001c0002t0089g0093a0001c0002t0090g0091 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2980-8991G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754821 | ||||||
| chr7:155754948
|
A | G | 1 | a0001c0004t0083g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2980-8864A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155754948 | ||||||
| chr7:155755042
|
G | GA | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2980-8763dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155755042 | |||||
| chr7:155755058
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2980-8754C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155755058 | ||||||
| chr7:155755164
|
T | G | 92 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(89): Show | 92 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.2980-8648T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155755164 | ||||||
| chr7:155755221
|
G | A | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2980-8591G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155755221 | ||||||
| chr7:155755241
|
T | C | 1 | a0001c0002t0104g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2980-8571T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155755241 | ||||||
| chr7:155755287
|
C | T | 1 | a0002c0001t0002g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2980-8525C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155755287 | ||||||
| chr7:155755421
|
C | T | 1 | a0001c0003t0100g0077 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2980-8391C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155755421 | ||||||
| chr7:155755504
|
T | C | 7 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0006t0087g0165others(4): Show | 7 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2980-8308T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155755504 | ||||||
| chr7:155755672
|
A | G | 1 | a0002c0005t0026g0224 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2980-8140A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155755672 | ||||||
| chr7:155755773
|
C | T | 1 | a0002c0001t0062g0020 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2980-8039C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155755773 | ||||||
| chr7:155755823
|
C | CT | 81 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(78): Show | 81 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.2980-7980dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155755823 | |||||
| chr7:155755823
|
CT | C | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-7980delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155755823 | |||||
| chr7:155755902
|
C | CA | 33 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(30): Show | 34 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(31): Show |
intron_variant | MODIFIER | c.2980-7902dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155755902 | |||||
| chr7:155756034
|
A | T | 2 | a0002c0001t0004g0003a0002c0001t0016g0004 | 2 | NA18956.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2980-7778A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155756034 | ||||||
| chr7:155756115
|
C | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-7697C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155756115 | ||||||
| chr7:155756156
|
A | G | 117 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(114): Show | 118 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.2980-7656A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155756156 | ||||||
| chr7:155756497
|
A | G | 2 | a0001c0002t0116g0188a0001c0011t0097g0085 | 2 | NA19085.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2980-7315A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155756497 | ||||||
| chr7:155756732
|
G | T | 85 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(82): Show | 85 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.2980-7080G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155756732 | ||||||
| chr7:155756824
|
G | GGT | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-6986_2980-698 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155756824 | |||||
| chr7:155756986
|
C | T | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-6826C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155756986 | ||||||
| chr7:155757153
|
A | AGTT | 134 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(131): Show | 135 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.2980-6657_2980-665 others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155757153 | |||||
| chr7:155757204
|
C | T | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2980-6608C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757204 | ||||||
| chr7:155757220
|
C | T | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-6592C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757220 | ||||||
| chr7:155757224
|
C | A | 2 | a0001c0008t0086g0087a0001c0008t0091g0086 | 2 | HG03130.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2980-6588C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757224 | ||||||
| chr7:155757263
|
C | G | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2980-6549C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757263 | ||||||
| chr7:155757270
|
G | A | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-6542G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757270 | ||||||
| chr7:155757305
|
T | C | 1 | a0001c0003t0007g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2980-6507T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757305 | ||||||
| chr7:155757311
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-6501A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757311 | ||||||
| chr7:155757412
|
G | A | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-6400G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757412 | ||||||
| chr7:155757427
|
G | A | 1 | a0008c0016t0061g0048 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2980-6385G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757427 | ||||||
| chr7:155757783
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-6029A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757783 | ||||||
| chr7:155757890
|
G | A | 1 | a0001c0002t0090g0091 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2980-5922G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757890 | ||||||
| chr7:155757902
|
T | C | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-5910T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757902 | ||||||
| chr7:155757988
|
C | T | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2980-5824C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155757988 | ||||||
| chr7:155758059
|
G | T | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2980-5753G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758059 | ||||||
| chr7:155758060
|
G | A | 1 | a0001c0018t0079g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2980-5752G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758060 | ||||||
| chr7:155758130
|
C | A | 126 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.2980-5682C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758130 | ||||||
| chr7:155758327
|
A | T | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2980-5485A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758327 | ||||||
| chr7:155758361
|
G | A | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2980-5451G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758361 | ||||||
| chr7:155758370
|
G | A | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2980-5442G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758370 | ||||||
| chr7:155758401
|
C | T | 67 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(64): Show | 67 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.2980-5411C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758401 | ||||||
| chr7:155758408
|
G | C | 1 | a0001c0004t0005g0140 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2980-5404G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758408 | ||||||
| chr7:155758491
|
T | A | 1 | a0001c0002t0106g0202 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2980-5321T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758491 | ||||||
| chr7:155758606
|
A | G | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-5206A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758606 | ||||||
| chr7:155758659
|
AAGC | A | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-5149_2980-514 others(7): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155758659 | |||||
| chr7:155758861
|
T | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2980-4951T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758861 | ||||||
| chr7:155758959
|
C | T | 1 | a0002c0001t0002g0049 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2980-4853C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155758959 | ||||||
| chr7:155759018
|
T | TGA | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2980-4792_2980-479 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155759018 | |||||
| chr7:155759156
|
A | T | 2 | a0001c0003t0005g0256a0001c0003t0099g0084 | 2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.2980-4656A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759156 | ||||||
| chr7:155759187
|
A | G | 121 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2980-4625A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759187 | ||||||
| chr7:155759244
|
TA | T | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2980-4562delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155759244 | |||||
| chr7:155759258
|
T | C | 32 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(29): Show | 33 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(30): Show |
intron_variant | MODIFIER | c.2980-4554T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759258 | ||||||
| chr7:155759313
|
G | A | 121 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2980-4499G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759313 | ||||||
| chr7:155759329
|
A | G | 34 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(31): Show | 35 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.2980-4483A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759329 | ||||||
| chr7:155759415
|
C | CT | 15 | a0001c0002t0111g0182a0001c0004t0005g0139a0001c0004t0005g0140others(12): Show | 15 | HG02135.hp2 HG02145.hp1 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.2980-4377dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155759415 | |||||
| chr7:155759415
|
C | CTT | 13 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0047g0282others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.2980-4378_2980-437 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155759415 | |||||
| chr7:155759415
|
C | CTTTTTT | 7 | a0001c0002t0081g0089a0001c0003t0008g0002a0001c0003t0008g0257others(4): Show | 8 | HG01928.hp2 HG02273.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2980-4382_2980-437 others(10): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155759415 | |||||
| chr7:155759415
|
C | CTTTTTTT | 10 | a0001c0002t0082g0088a0001c0003t0008g0266a0001c0003t0008g0268others(7): Show | 10 | HG00280.hp1 HG00323.hp2 HG03209.hp2 others(7): Show |
intron_variant | MODIFIER | c.2980-4383_2980-437 others(11): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155759415 | |||||
| chr7:155759415
|
CT | C | 23 | a0001c0002t0006g0181a0001c0002t0007g0222a0001c0002t0012g0231others(20): Show | 23 | HG00639.hp1 HG00639.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.2980-4377delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155759415 | |||||
| chr7:155759415
|
CTT | C | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.2980-4378_2980-437 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 155759415 | |||||
| chr7:155759439
|
A | T | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2980-4373A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759439 | ||||||
| chr7:155759449
|
G | A | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2980-4363G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759449 | ||||||
| chr7:155759457
|
T | G | 34 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(31): Show | 35 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.2980-4355T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759457 | ||||||
| chr7:155759487
|
G | A | 3 | a0002c0001t0015g0028a0002c0001t0015g0045a0002c0001t0015g0051 | 3 | HG02165.hp1 NA18966.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2980-4325G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759487 | ||||||
| chr7:155759542
|
T | A | 1 | a0001c0003t0085g0272 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2980-4270T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759542 | ||||||
| chr7:155759542
|
T | C | 33 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(30): Show | 34 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(31): Show |
intron_variant | MODIFIER | c.2980-4270T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759542 | ||||||
| chr7:155759562
|
C | T | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.2980-4250C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759562 | ||||||
| chr7:155759572
|
C | T | 1 | a0002c0001t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2980-4240C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759572 | ||||||
| chr7:155759574
|
C | T | 1 | a0001c0002t0115g0238 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2980-4238C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759574 | ||||||
| chr7:155759580
|
G | A | 3 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090 | 3 | HG02258.hp2 HG02451.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2980-4232G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759580 | ||||||
| chr7:155759641
|
G | T | 1 | a0002c0001t0001g0145 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2980-4171G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759641 | ||||||
| chr7:155759648
|
T | C | 34 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(31): Show | 35 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.2980-4164T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759648 | ||||||
| chr7:155759665
|
C | T | 1 | a0002c0001t0002g0110 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2980-4147C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759665 | ||||||
| chr7:155759795
|
C | G | 2 | a0001c0006t0092g0304a0006c0014t0095g0271 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2980-4017C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759795 | ||||||
| chr7:155759836
|
A | T | 34 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(31): Show | 35 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.2980-3976A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759836 | ||||||
| chr7:155759880
|
T | C | 121 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2980-3932T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155759880 | ||||||
| chr7:155760070
|
C | T | 5 | a0001c0002t0023g0157a0001c0002t0023g0159a0001c0002t0101g0161others(2): Show | 5 | HG02630.hp2 HG02717.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2980-3742C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760070 | ||||||
| chr7:155760326
|
G | C | 5 | a0001c0002t0024g0153a0001c0002t0024g0155a0001c0002t0024g0160others(2): Show | 5 | HG00642.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2980-3486G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760326 | ||||||
| chr7:155760399
|
GT | G | 10 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(7): Show | 10 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2980-3412delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760399 | ||||||
| chr7:155760402
|
A | T | 10 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(7): Show | 10 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2980-3410A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760402 | ||||||
| chr7:155760590
|
T | C | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2980-3222T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760590 | ||||||
| chr7:155760631
|
T | C | 87 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.2980-3181T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760631 | ||||||
| chr7:155760766
|
A | G | 34 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(31): Show | 35 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.2980-3046A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760766 | ||||||
| chr7:155760773
|
A | T | 6 | a0001c0002t0023g0156a0001c0002t0031g0092a0001c0002t0031g0094others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.2980-3039A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760773 | ||||||
| chr7:155760787
|
C | G | 1 | a0001c0017t0055g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2980-3025C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760787 | ||||||
| chr7:155760795
|
C | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2980-3017C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760795 | ||||||
| chr7:155760833
|
T | G | 4 | a0002c0001t0001g0053a0002c0001t0001g0072a0002c0001t0033g0021others(1): Show | 4 | HG01070.hp1 HG01071.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2980-2979T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760833 | ||||||
| chr7:155760835
|
T | C | 1 | a0002c0005t0018g0206 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2980-2977T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760835 | ||||||
| chr7:155760906
|
G | C | 2 | a0001c0004t0021g0151a0001c0004t0083g0150 | 2 | HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2980-2906G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760906 | ||||||
| chr7:155760971
|
G | A | 33 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(30): Show | 34 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(31): Show |
intron_variant | MODIFIER | c.2980-2841G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760971 | ||||||
| chr7:155760983
|
C | T | 35 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(32): Show | 36 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(33): Show |
intron_variant | MODIFIER | c.2980-2829C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155760983 | ||||||
| chr7:155761010
|
A | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2980-2802A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761010 | ||||||
| chr7:155761049
|
G | A | 2 | a0002c0001t0004g0003a0002c0001t0016g0004 | 2 | NA18956.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.2980-2763G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761049 | ||||||
| chr7:155761114
|
G | A | 36 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(33): Show | 37 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.2980-2698G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761114 | ||||||
| chr7:155761124
|
G | C | 36 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(33): Show | 37 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.2980-2688G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761124 | ||||||
| chr7:155761374
|
G | A | 1 | a0002c0001t0002g0143 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2980-2438G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761374 | ||||||
| chr7:155761537
|
T | G | 36 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(33): Show | 37 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.2980-2275T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761537 | ||||||
| chr7:155761546
|
T | C | 1 | a0001c0002t0011g0163 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2980-2266T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761546 | ||||||
| chr7:155761564
|
C | G | 1 | a0001c0002t0039g0167 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2980-2248C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761564 | ||||||
| chr7:155761696
|
G | A | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2980-2116G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761696 | ||||||
| chr7:155761848
|
C | T | 1 | a0006c0014t0095g0271 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2980-1964C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761848 | ||||||
| chr7:155761880
|
T | C | 36 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(33): Show | 37 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.2980-1932T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761880 | ||||||
| chr7:155761958
|
A | G | 1 | a0001c0002t0012g0235 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2980-1854A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761958 | ||||||
| chr7:155761968
|
T | G | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.2980-1844T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155761968 | ||||||
| chr7:155762237
|
G | A | 2 | a0001c0003t0009g0261a0001c0003t0009g0262 | 2 | NA18983.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.2980-1575G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155762237 | ||||||
| chr7:155762302
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2980-1510C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155762302 | ||||||
| chr7:155762376
|
T | A | 2 | a0001c0003t0009g0270a0007c0013t0009g0265 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.2980-1436T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155762376 | ||||||
| chr7:155762398
|
A | G | 1 | a0001c0003t0052g0279 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2980-1414A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155762398 | ||||||
| chr7:155762604
|
C | A | 1 | a0002c0001t0002g0049 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2980-1208C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155762604 | ||||||
| chr7:155762812
|
T | A | 71 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(68): Show | 71 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.2980-1000T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155762812 | ||||||
| chr7:155762882
|
C | T | 1 | a0001c0003t0088g0284 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2980-930C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155762882 | ||||||
| chr7:155762921
|
T | C | 36 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(33): Show | 37 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.2980-891T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155762921 | ||||||
| chr7:155762965
|
G | C | 304 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(301): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.2980-847G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155762965 | ||||||
| chr7:155763113
|
A | G | 67 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(64): Show | 67 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.2980-699A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763113 | ||||||
| chr7:155763138
|
G | A | 43 | a0001c0002t0006g0174a0001c0002t0006g0175a0001c0002t0006g0180others(40): Show | 43 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.2980-674G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763138 | ||||||
| chr7:155763236
|
T | C | 120 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.2980-576T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763236 | ||||||
| chr7:155763237
|
G | A | 12 | a0001c0002t0006g0174a0001c0002t0006g0180a0001c0002t0006g0181others(9): Show | 12 | HG01981.hp2 NA18953.hp1 NA18955.hp1 others(9): Show |
intron_variant | MODIFIER | c.2980-575G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763237 | ||||||
| chr7:155763320
|
G | A | 120 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.2980-492G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763320 | ||||||
| chr7:155763458
|
A | G | 2 | a0001c0006t0092g0304a0006c0014t0095g0271 | 2 | HG02486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.2980-354A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763458 | ||||||
| chr7:155763529
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2980-283C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763529 | ||||||
| chr7:155763615
|
A | G | 36 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(33): Show | 37 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.2980-197A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763615 | ||||||
| chr7:155763762
|
T | G | 36 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(33): Show | 37 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.2980-50T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763762 | ||||||
| chr7:155763772
|
G | A | 1 | a0001c0002t0010g0172 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2980-40G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 14/17 | chr7 | 155763772 | ||||||
| chr7:155764084
|
G | A | 6 | a0002c0001t0001g0056a0002c0001t0001g0058a0002c0001t0060g0288others(3): Show | 6 | HG00741.hp1 HG01175.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.3186+66G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764084 | ||||||
| chr7:155764282
|
C | T | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3186+264C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764282 | ||||||
| chr7:155764328
|
CG | C | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.3186+311delG | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764328 | ||||||
| chr7:155764497
|
C | T | 14 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(11): Show | 14 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.3186+479C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764497 | ||||||
| chr7:155764612
|
C | T | 36 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0005g0256others(33): Show | 37 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(34): Show |
intron_variant | MODIFIER | c.3186+594C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764612 | ||||||
| chr7:155764736
|
A | G | 1 | a0001c0002t0081g0089 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3186+718A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764736 | ||||||
| chr7:155764780
|
A | G | 286 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(283): Show | 287 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.3186+762A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764780 | ||||||
| chr7:155764796
|
G | A | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.3186+778G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764796 | ||||||
| chr7:155764833
|
G | T | 3 | a0002c0001t0004g0249a0002c0001t0035g0250a0002c0001t0072g0248 | 3 | HG01258.hp1 HG02738.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3186+815G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764833 | ||||||
| chr7:155764871
|
C | T | 6 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(3): Show | 6 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.3186+853C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155764871 | ||||||
| chr7:155765008
|
G | A | 67 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(64): Show | 67 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.3186+990G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765008 | ||||||
| chr7:155765012
|
T | C | 120 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.3186+994T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765012 | ||||||
| chr7:155765105
|
C | G | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3186+1087C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765105 | ||||||
| chr7:155765221
|
G | A | 1 | a0001c0002t0101g0161 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3186+1203G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765221 | ||||||
| chr7:155765226
|
G | A | 17 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(14): Show | 17 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.3186+1208G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765226 | ||||||
| chr7:155765256
|
T | C | 2 | a0001c0003t0085g0272a0001c0004t0084g0141 | 2 | HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3187-1211T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765256 | ||||||
| chr7:155765347
|
C | T | 292 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(289): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.3187-1120C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765347 | ||||||
| chr7:155765429
|
C | T | 1 | a0001c0004t0084g0141 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3187-1038C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765429 | ||||||
| chr7:155765487
|
C | T | 131 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(128): Show | 132 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.3187-980C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765487 | ||||||
| chr7:155765582
|
G | A | 1 | a0001c0002t0006g0175 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3187-885G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765582 | ||||||
| chr7:155765628
|
G | A | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.3187-839G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765628 | ||||||
| chr7:155765639
|
C | G | 1 | a0002c0001t0121g0069 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3187-828C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765639 | ||||||
| chr7:155765686
|
A | G | 1 | a0002c0001t0002g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3187-781A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765686 | ||||||
| chr7:155765812
|
C | T | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.3187-655C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765812 | ||||||
| chr7:155765872
|
T | C | 8 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007others(5): Show | 8 | HG00733.hp1 HG01070.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.3187-595T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765872 | ||||||
| chr7:155765952
|
G | T | 7 | a0001c0002t0111g0182a0002c0001t0002g0049a0002c0001t0002g0103others(4): Show | 7 | HG03834.hp2 HG03942.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.3187-515G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765952 | ||||||
| chr7:155765991
|
G | C | 5 | a0001c0003t0019g0251a0001c0003t0019g0252a0001c0003t0019g0255others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.3187-476G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155765991 | ||||||
| chr7:155766057
|
T | G | 67 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(64): Show | 67 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.3187-410T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155766057 | ||||||
| chr7:155766112
|
G | T | 1 | a0002c0001t0001g0105 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.3187-355G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155766112 | ||||||
| chr7:155766144
|
G | A | 2 | a0001c0004t0043g0081a0002c0001t0109g0299 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3187-323G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155766144 | ||||||
| chr7:155766235
|
C | T | 1 | a0001c0017t0055g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3187-232C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155766235 | ||||||
| chr7:155766238
|
G | C | 1 | a0002c0001t0065g0063 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.3187-229G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155766238 | ||||||
| chr7:155766305
|
C | T | 125 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.3187-162C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155766305 | ||||||
| chr7:155766416
|
C | G | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.3187-51C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 15/17 | chr7 | 155766416 | ||||||
| chr7:155766691
|
G | A | 1 | a0001c0002t0007g0169 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3375+36G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155766691 | ||||||
| chr7:155766709
|
A | G | 120 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(117): Show | 121 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.3375+54A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155766709 | ||||||
| chr7:155766714
|
T | C | 2 | a0001c0004t0043g0081a0002c0001t0109g0299 | 2 | HG01884.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.3375+59T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155766714 | ||||||
| chr7:155766785
|
A | G | 1 | a0002c0001t0003g0041 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3375+130A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155766785 | ||||||
| chr7:155766803
|
C | T | 1 | a0001c0017t0055g0142 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3375+148C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155766803 | ||||||
| chr7:155766822
|
C | T | 16 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3375+167C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155766822 | ||||||
| chr7:155766830
|
G | A | 67 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(64): Show | 67 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.3375+175G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155766830 | ||||||
| chr7:155766883
|
C | T | 1 | a0001c0002t0012g0229 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.3375+228C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155766883 | ||||||
| chr7:155766929
|
G | T | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3375+274G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155766929 | ||||||
| chr7:155767244
|
G | A | 2 | a0002c0001t0004g0098a0002c0001t0068g0099 | 2 | HG02109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3375+589G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155767244 | ||||||
| chr7:155767426
|
A | C | 87 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(84): Show | 87 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.3375+771A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155767426 | ||||||
| chr7:155767427
|
G | A | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3375+772G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155767427 | ||||||
| chr7:155767454
|
A | G | 1 | a0002c0001t0001g0034 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3375+799A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155767454 | ||||||
| chr7:155767562
|
C | G | 1 | a0001c0002t0010g0172 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3375+907C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155767562 | ||||||
| chr7:155767718
|
G | C | 9 | a0001c0002t0023g0156a0001c0002t0023g0157a0001c0002t0023g0159others(6): Show | 9 | HG00642.hp1 HG02630.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.3375+1063G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155767718 | ||||||
| chr7:155767811
|
A | G | 1 | a0001c0002t0106g0202 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3375+1156A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155767811 | ||||||
| chr7:155767858
|
G | A | 155 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(152): Show | 156 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.3375+1203G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155767858 | ||||||
| chr7:155768103
|
G | A | 1 | a0001c0003t0049g0283 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3375+1448G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768103 | ||||||
| chr7:155768129
|
C | T | 1 | a0002c0001t0017g0052 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3375+1474C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768129 | ||||||
| chr7:155768316
|
T | C | 137 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.3375+1661T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768316 | ||||||
| chr7:155768342
|
T | C | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3375+1687T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768342 | ||||||
| chr7:155768357
|
G | A | 17 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(14): Show | 17 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.3375+1702G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768357 | ||||||
| chr7:155768417
|
C | T | 3 | a0001c0006t0087g0165a0001c0006t0093g0166a0001c0006t0094g0164 | 3 | HG02572.hp1 HG02818.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.3375+1762C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768417 | ||||||
| chr7:155768437
|
G | A | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3375+1782G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768437 | ||||||
| chr7:155768640
|
G | C | 34 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(31): Show | 35 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.3375+1985G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768640 | ||||||
| chr7:155768702
|
C | T | 67 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(64): Show | 67 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.3375+2047C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768702 | ||||||
| chr7:155768761
|
C | T | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3375+2106C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768761 | ||||||
| chr7:155768849
|
G | A | 1 | a0002c0001t0003g0016 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3375+2194G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768849 | ||||||
| chr7:155768856
|
G | A | 3 | a0001c0004t0005g0138a0001c0004t0005g0139a0001c0004t0005g0140 | 3 | NA18906.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3375+2201G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768856 | ||||||
| chr7:155768860
|
G | A | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3375+2205G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768860 | ||||||
| chr7:155768870
|
C | T | 67 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(64): Show | 67 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.3375+2215C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768870 | ||||||
| chr7:155768947
|
G | A | 3 | a0001c0004t0005g0130a0001c0004t0005g0134a0001c0004t0005g0135 | 3 | HG00639.hp1 HG03139.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3375+2292G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155768947 | ||||||
| chr7:155769146
|
T | C | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3375+2491T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769146 | ||||||
| chr7:155769160
|
T | C | 1 | a0002c0001t0001g0055 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.3375+2505T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769160 | ||||||
| chr7:155769172
|
T | C | 1 | a0001c0002t0045g0198 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3375+2517T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769172 | ||||||
| chr7:155769228
|
C | T | 16 | a0001c0003t0005g0256a0001c0003t0019g0251a0001c0003t0019g0252others(13): Show | 16 | HG02055.hp2 HG02109.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.3375+2573C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769228 | ||||||
| chr7:155769287
|
A | G | 1 | a0002c0001t0002g0040 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.3375+2632A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769287 | ||||||
| chr7:155769289
|
A | G | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.3375+2634A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769289 | ||||||
| chr7:155769339
|
C | T | 1 | a0002c0001t0001g0022 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3375+2684C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769339 | ||||||
| chr7:155769399
|
C | T | 1 | a0001c0003t0098g0264 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3375+2744C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769399 | ||||||
| chr7:155769445
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3375+2790G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769445 | ||||||
| chr7:155769577
|
C | G | 71 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(68): Show | 71 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.3375+2922C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769577 | ||||||
| chr7:155769623
|
C | T | 2 | a0001c0002t0101g0161a0001c0002t0103g0158 | 2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3375+2968C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769623 | ||||||
| chr7:155769868
|
A | G | 4 | a0002c0001t0002g0146a0002c0001t0004g0106a0002c0001t0004g0147others(1): Show | 4 | HG02080.hp2 NA18994.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.3375+3213A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769868 | ||||||
| chr7:155769951
|
A | T | 1 | a0001c0006t0094g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3375+3296A>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769951 | ||||||
| chr7:155769987
|
A | G | 3 | a0001c0004t0042g0082a0001c0004t0043g0081a0002c0001t0109g0299 | 3 | HG01884.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3375+3332A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155769987 | ||||||
| chr7:155770114
|
G | A | 9 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(6): Show | 9 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3375+3459G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155770114 | ||||||
| chr7:155770116
|
G | A | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3375+3461G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155770116 | ||||||
| chr7:155770240
|
G | A | 1 | a0002c0001t0002g0123 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.3375+3585G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155770240 | ||||||
| chr7:155770321
|
G | A | 34 | a0001c0003t0005g0256a0001c0003t0008g0002a0001c0003t0008g0257others(31): Show | 35 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(32): Show |
intron_variant | MODIFIER | c.3375+3666G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155770321 | ||||||
| chr7:155770451
|
C | A | 1 | a0001c0003t0005g0256 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3375+3796C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155770451 | ||||||
| chr7:155770594
|
C | CT | 16 | a0001c0002t0081g0089a0001c0002t0082g0088a0001c0003t0046g0254others(13): Show | 16 | HG01175.hp1 HG01978.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.3376-3946dupT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155770594 | |||||
| chr7:155770594
|
CT | C | 11 | a0001c0002t0006g0174a0001c0002t0037g0201a0001c0002t0039g0227others(8): Show | 11 | HG00642.hp2 HG02970.hp1 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.3376-3946delT | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155770594 | |||||
| chr7:155770594
|
CTT | C | 80 | a0001c0002t0006g0173a0001c0002t0006g0175a0001c0002t0006g0180others(77): Show | 80 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.3376-3947_3376-394 others(6): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155770594 | |||||
| chr7:155770645
|
G | A | 2 | a0001c0003t0096g0078a0001c0003t0100g0077 | 2 | NA18989.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.3376-3914G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155770645 | ||||||
| chr7:155770680
|
G | T | 2 | a0001c0003t0048g0280a0001c0003t0052g0279 | 2 | HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3376-3879G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155770680 | ||||||
| chr7:155770812
|
T | G | 1 | a0002c0001t0002g0121 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3376-3747T>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155770812 | ||||||
| chr7:155771180
|
G | A | 1 | a0001c0004t0080g0136 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3376-3379G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771180 | ||||||
| chr7:155771196
|
A | G | 5 | a0001c0004t0005g0131a0001c0004t0005g0132a0001c0004t0005g0133others(2): Show | 5 | HG02258.hp1 HG02630.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.3376-3363A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771196 | ||||||
| chr7:155771225
|
T | A | 1 | a0002c0001t0077g0033 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3376-3334T>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771225 | ||||||
| chr7:155771397
|
G | A | 2 | a0001c0003t0009g0270a0007c0013t0009g0265 | 2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.3376-3162G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771397 | ||||||
| chr7:155771398
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3376-3161G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771398 | ||||||
| chr7:155771481
|
C | A | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3376-3078C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771481 | ||||||
| chr7:155771630
|
T | C | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.3376-2929T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771630 | ||||||
| chr7:155771798
|
C | G | 17 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(14): Show | 17 | HG00639.hp1 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.3376-2761C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771798 | ||||||
| chr7:155771856
|
CA | C | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3376-2702delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771856 | ||||||
| chr7:155771959
|
A | G | 5 | a0001c0002t0031g0092a0001c0002t0031g0094a0001c0002t0053g0090others(2): Show | 5 | HG02258.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3376-2600A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155771959 | ||||||
| chr7:155772168
|
TAAACCCC others(11): Show |
T | 4 | a0001c0002t0036g0274a0001c0002t0036g0275a0001c0002t0107g0276others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.3376-2390_3376-237 others(22): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155772168 | ||||||
| chr7:155772187
|
G | C | 4 | a0001c0002t0036g0274a0001c0002t0036g0275a0001c0002t0107g0276others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.3376-2372G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155772187 | ||||||
| chr7:155772243
|
G | T | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3376-2316G>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155772243 | ||||||
| chr7:155772278
|
TTTAGGTT others(4): Show |
T | 2 | a0002c0001t0002g0103a0002c0001t0066g0287 | 2 | HG01978.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.3376-2273_3376-226 others(15): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155772278 | |||||
| chr7:155772281
|
AGGTTCGG others(10): Show |
A | 72 | a0001c0002t0038g0214a0002c0001t0001g0009a0002c0001t0001g0010others(69): Show | 72 | HG00423.hp1 HG00544.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.3376-2273_3376-225 others(21): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155772281 | |||||
| chr7:155772337
|
C | G | 9 | a0001c0004t0005g0130a0001c0004t0005g0131a0001c0004t0005g0132others(6): Show | 9 | HG00639.hp1 HG02258.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.3376-2222C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155772337 | ||||||
| chr7:155772396
|
A | G | 1 | a0001c0004t0041g0083 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3376-2163A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155772396 | ||||||
| chr7:155772506
|
G | A | 3 | a0001c0004t0042g0082a0001c0004t0043g0081a0002c0001t0109g0299 | 3 | HG01884.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3376-2053G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155772506 | ||||||
| chr7:155772620
|
A | G | 2 | a0001c0002t0023g0157a0001c0002t0023g0159 | 2 | HG02717.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.3376-1939A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155772620 | ||||||
| chr7:155772985
|
C | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3376-1574C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155772985 | ||||||
| chr7:155773001
|
A | G | 5 | a0001c0006t0087g0165a0001c0006t0092g0304a0001c0006t0093g0166others(2): Show | 5 | HG02486.hp2 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3376-1558A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155773001 | ||||||
| chr7:155773203
|
T | C | 84 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(81): Show | 84 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.3376-1356T>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155773203 | ||||||
| chr7:155773224
|
G | C | 3 | a0001c0002t0025g0005a0001c0002t0025g0006a0001c0002t0025g0007 | 3 | HG01891.hp1 HG02809.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.3376-1335G>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155773224 | ||||||
| chr7:155773249
|
C | G | 123 | a0001c0002t0006g0173a0001c0002t0006g0174a0001c0002t0006g0175others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.3376-1310C>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155773249 | ||||||
| chr7:155773293
|
C | T | 35 | a0001c0003t0005g0256a0001c0003t0007g0213a0001c0003t0008g0002others(32): Show | 36 | HG00280.hp1 HG00323.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.3376-1266C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155773293 | ||||||
| chr7:155773554
|
C | T | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3376-1005C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155773554 | ||||||
| chr7:155773568
|
C | CA | 64 | a0001c0002t0023g0156a0001c0002t0024g0153a0001c0002t0024g0155others(61): Show | 64 | HG00621.hp1 HG00733.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.3376-964dupA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
C | CAA | 25 | a0001c0002t0024g0160a0001c0004t0021g0149a0001c0004t0083g0150others(22): Show | 25 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.3376-965_3376-964d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
C | CAAA | 8 | a0001c0002t0031g0094a0001c0002t0053g0090a0001c0002t0090g0091others(5): Show | 8 | HG02074.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.3376-966_3376-964d others(5): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
C | CAAAAAAA others(5): Show |
1 | a0001c0006t0087g0165 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3376-975_3376-964d others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
C | CAAAAAAA others(6): Show |
1 | a0001c0006t0093g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3376-976_3376-964d others(15): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
C | CAAAAAAA others(7): Show |
1 | a0001c0006t0094g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3376-977_3376-964d others(16): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
CA | C | 16 | a0001c0002t0006g0175a0001c0002t0007g0215a0001c0002t0010g0183others(13): Show | 16 | HG02040.hp2 HG02080.hp1 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.3376-964delA | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
CAA | C | 54 | a0001c0002t0006g0173a0001c0002t0006g0180a0001c0002t0006g0217others(51): Show | 54 | HG00140.hp2 HG00423.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.3376-965_3376-964d others(4): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
CAAA | C | 11 | a0001c0002t0006g0174a0001c0002t0006g0181a0001c0002t0006g0219others(8): Show | 11 | HG02109.hp1 HG02647.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.3376-966_3376-964d others(5): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
CAAAAAAA | C | 6 | a0001c0002t0036g0274a0001c0002t0082g0088a0002c0001t0002g0108others(3): Show | 6 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.3376-970_3376-964d others(9): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
CAAAAAAA others(4): Show |
C | 2 | a0002c0001t0002g0100a0003c0007t0022g0290 | 2 | HG00642.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.3376-974_3376-964d others(13): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0004t0041g0083a0003c0007t0022g0289a0003c0007t0022g0291 | 3 | HG00735.hp1 HG01884.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3376-975_3376-964d others(14): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0027g0199 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3376-976_3376-964d others(15): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773568
|
CAAAAAAA others(11): Show |
C | 18 | a0001c0003t0008g0002a0001c0003t0008g0257a0001c0003t0008g0258others(15): Show | 19 | HG00280.hp1 HG00323.hp2 HG01928.hp2 others(16): Show |
intron_variant | MODIFIER | c.3376-981_3376-964d others(20): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773568 | |||||
| chr7:155773635
|
C | CTAAGTTG others(20): Show |
2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3376-923_3376-897d others(29): Show |
RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 155773635 | |||||
| chr7:155773807
|
C | T | 1 | a0002c0001t0002g0127 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.3376-752C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155773807 | ||||||
| chr7:155773834
|
C | T | 1 | a0001c0002t0011g0210 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3376-725C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155773834 | ||||||
| chr7:155774066
|
A | G | 4 | a0002c0001t0002g0108a0002c0001t0002g0109a0002c0001t0002g0110others(1): Show | 4 | HG00140.hp1 HG00733.hp2 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.3376-493A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155774066 | ||||||
| chr7:155774144
|
G | A | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3376-415G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155774144 | ||||||
| chr7:155774223
|
A | C | 1 | a0001c0002t0105g0008 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3376-336A>C | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155774223 | ||||||
| chr7:155774360
|
A | G | 1 | a0001c0008t0091g0086 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3376-199A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155774360 | ||||||
| chr7:155774388
|
C | T | 3 | a0003c0007t0022g0289a0003c0007t0022g0290a0003c0007t0022g0291 | 3 | HG00735.hp1 HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.3376-171C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155774388 | ||||||
| chr7:155774415
|
A | G | 2 | a0001c0002t0081g0089a0001c0002t0082g0088 | 2 | HG02976.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.3376-144A>G | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155774415 | ||||||
| chr7:155774471
|
G | A | 1 | a0001c0002t0082g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3376-88G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155774471 | ||||||
| chr7:155774524
|
C | A | 1 | a0001c0002t0010g0172 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3376-35C>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 16/17 | chr7 | 155774524 | ||||||
| chr7:155774805
|
C | T | 1 | a0001c0002t0031g0092 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3464+158C>T | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 17/17 | chr7 | 155774805 | ||||||
| chr7:155774884
|
G | A | 1 | a0001c0002t0007g0226 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3465-109G>A | RBM33 | ENSG00000184863.11 | transcript | ENST00000401878.8 | protein_coding | 17/17 | chr7 | 155774884 |