Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1102 |
| ensemblid | ENSG00000136161.13 |
| hgncid | 1914 |
| symbol | RCBTB2 |
| name | RCC1 and BTB domain containing protein 2 |
| refseq_nuc | NM_001268.4 |
| refseq_prot | NP_001259.1 |
| ensembl_nuc | ENST00000344532.8 |
| ensembl_prot | ENSP00000345144.3 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 48488963 |
| end | 48533080 |
| strand | - |
| ver | v1.2 |
| region | chr13:48488963-48533080 |
| region5000 | chr13:48483963-48538080 |
| regionname0 | RCBTB2_chr13_48488963_48533080 |
| regionname5000 | RCBTB2_chr13_48483963_48538080 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 551 | 314 | 89 | 53 | 133 | 7 | 30 | 109 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | MEEEL others(546): Show |
chr13 | 48483963 | 48538080 |
| a0002 | 0/0 | 551 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | MEEEL others(546): Show |
chr13 | 48483963 | 48538080 |
| a0003 | 0/0 | 551 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | MEEEL others(546): Show |
chr13 | 48483963 | 48538080 |
| a0004 | 0/0 | 551 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | MEEEL others(546): Show |
chr13 | 48483963 | 48538080 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1653 | 265 | 70 | 50 | 110 | 6 | 27 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0001c0002 | 0/0 | 1653 | 26 | 0 | 0 | 22 | 1 | 3 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0001c0003 | 0/0 | 1653 | 8 | 6 | 2 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0001c0004 | 0/0 | 1653 | 5 | 5 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0001c0005 | 0/0 | 1653 | 4 | 4 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0001c0007 | 0/0 | 1653 | 3 | 2 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0001c0008 | 0/0 | 1653 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0001c0011 | 0/0 | 1653 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0002c0006 | 0/0 | 1653 | 4 | 3 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0003c0009 | 0/0 | 1653 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 | ||
| a0004c0010 | 0/0 | 1653 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | ATGGA others(1648): Show |
chr13 | 48483963 | 48538080 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3075 | 233 | 50 | 47 | 103 | 6 | 25 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0002 | 0/0 | 3075 | 19 | 17 | 2 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0005 | 0/0 | 3075 | 4 | 0 | 0 | 4 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0006 | 0/0 | 3075 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0007 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0008 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0009 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0010 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0011 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0012 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0001t0015 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0002t0001 | 0/0 | 3075 | 26 | 0 | 0 | 22 | 1 | 3 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0003t0001 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0003t0003 | 0/0 | 3075 | 7 | 5 | 2 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0004t0004 | 0/0 | 3075 | 5 | 5 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0005t0002 | 0/0 | 3075 | 4 | 4 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0007t0001 | 0/0 | 3075 | 3 | 2 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0008t0013 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0008t0014 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0001c0011t0002 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0002c0006t0001 | 0/0 | 3075 | 4 | 3 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0003c0009t0001 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| a0004c0010t0001 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | GCAGT others(3070): Show |
chr13 | 48483963 | 48538080 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 1 | 7 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0003 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0008 | 1/0 | 3 | 0 | 0 | 1 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0010g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0011g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0012g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0001t0015g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0003t0003g0004 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0003t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0003t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0003t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0003t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0004t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0004t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0004t0004g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0004t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0005t0002g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0007t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0007t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0007t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0008t0013g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0008t0014g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0001c0011t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0002c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0002c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0002c0006t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0002c0006t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0003c0009t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| a0004c0010t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0268 | EUR | GBR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | FIN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0231 | EUR | FIN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00558 | hp2 | a0001 | c0007 | t0001 | g0254 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01069 | hp1 | a0001 | c0003 | t0003 | g0004 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01071 | hp2 | a0001 | c0003 | t0003 | g0004 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01109 | hp2 | a0002 | c0006 | t0001 | g0278 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01243 | hp2 | a0001 | c0011 | t0002 | g0246 | AMR | PUR | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01884 | hp1 | a0001 | c0004 | t0004 | g0216 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01975 | hp2 | a0001 | c0001 | t0009 | g0077 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | KHV | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0223 | EAS | CDX | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | CDX | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02630 | hp1 | a0002 | c0006 | t0001 | g0276 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0074 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02723 | hp2 | a0001 | c0003 | t0003 | g0004 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0031 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02965 | hp1 | a0001 | c0004 | t0004 | g0021 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02970 | hp1 | a0001 | c0007 | t0001 | g0260 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02976 | hp1 | a0001 | c0003 | t0001 | g0064 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03017 | hp2 | a0001 | c0001 | t0012 | g0211 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03041 | hp2 | a0001 | c0004 | t0004 | g0021 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03098 | hp1 | a0001 | c0003 | t0003 | g0025 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03098 | hp2 | a0001 | c0007 | t0001 | g0255 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03130 | hp1 | a0001 | c0004 | t0004 | g0218 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03225 | hp2 | a0001 | c0008 | t0014 | g0059 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03453 | hp1 | a0001 | c0005 | t0002 | g0005 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03486 | hp1 | a0001 | c0003 | t0003 | g0026 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0022 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | ESN | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0238 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04228 | hp1 | a0001 | c0001 | t0007 | g0267 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | STU | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18522 | hp1 | a0001 | c0008 | t0013 | g0058 | AFR | YRI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0027 | AFR | YRI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | YRI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0240 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0234 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18950 | hp1 | a0001 | c0001 | t0011 | g0183 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0023 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18975 | hp2 | a0001 | c0002 | t0001 | g0236 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18980 | hp1 | a0001 | c0001 | t0005 | g0096 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18985 | hp1 | a0001 | c0001 | t0010 | g0141 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0241 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19010 | hp1 | a0001 | c0001 | t0015 | g0201 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19010 | hp2 | a0003 | c0009 | t0001 | g0221 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19030 | hp1 | a0001 | c0005 | t0002 | g0005 | AFR | LWK | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19030 | hp2 | a0002 | c0006 | t0001 | g0277 | AFR | LWK | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19043 | hp1 | a0001 | c0005 | t0002 | g0005 | AFR | LWK | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | LWK | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0219 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19074 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | YRI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA19240 | hp2 | a0002 | c0006 | t0001 | g0275 | AFR | YRI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0073 | AFR | ASW | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20752 | hp1 | a0004 | c0010 | t0001 | g0050 | EUR | TSI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0065 | EUR | TSI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | TSI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | GIH | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0028 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03471 | hp1 | a0001 | c0004 | t0004 | g0217 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | USA | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | USA | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | USA | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA20300 | hp2 | a0001 | c0005 | t0002 | g0066 | AFR | USA | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | LWK | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0203 | REF | REF | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | RCBTB2_chr13_48483963_48538080 | RCBTB2 | chr13 | 48483963 | 48538080 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48502727 | C | T | 1 | a0004 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1114G>A | p.Val372Met | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/15 | 1385/3075 | 1114/1656 | 372/551 | chr13 | 48502727 | |||
| chr13:48511831 | T | C | 1 | a0002 | 4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
missense_variant | MODERATE | c.722A>G | p.Asn241Ser | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/15 | 993/3075 | 722/1656 | 241/551 | chr13 | 48511831 | |||
| chr13:48515648 | G | T | 1 | a0003 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.136C>A | p.Arg46Ser | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 5/15 | 407/3075 | 136/1656 | 46/551 | chr13 | 48515648 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48496209 | C | T | 2 | a0001c0002 a0003c0009 |
27 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(24): Show |
synonymous_variant | LOW | c.1497G>A | p.Ala499Ala | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/15 | 1768/3075 | 1497/1656 | 499/551 | chr13 | 48496209 | |||
| chr13:48502767 | G | A | 1 | a0001c0008 | 2 | HG03225.hp2 NA18522.hp1 |
synonymous_variant | LOW | c.1074C>T | p.Ala358Ala | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/15 | 1345/3075 | 1074/1656 | 358/551 | chr13 | 48502767 | |||
| chr13:48502779 | G | A | 1 | a0001c0007 | 3 | HG00558.hp2 HG02970.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1062C>T | p.Asp354Asp | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/15 | 1333/3075 | 1062/1656 | 354/551 | chr13 | 48502779 | |||
| chr13:48502797 | G | A | 1 | a0001c0005 | 4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
synonymous_variant | LOW | c.1044C>T | p.Thr348Thr | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/15 | 1315/3075 | 1044/1656 | 348/551 | chr13 | 48502797 | |||
| chr13:48510748 | T | C | 1 | a0001c0011 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.807A>G | p.Thr269Thr | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/15 | 1078/3075 | 807/1656 | 269/551 | chr13 | 48510748 | |||
| chr13:48511772 | T | G | 1 | a0001c0004 | 5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.781A>C | p.Arg261Arg | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/15 | 1052/3075 | 781/1656 | 261/551 | chr13 | 48511772 | |||
| chr13:48515263 | G | A | 1 | a0001c0003 | 8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
synonymous_variant | LOW | c.291C>T | p.Gly97Gly | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/15 | 562/3075 | 291/1656 | 97/551 | chr13 | 48515263 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48489212 | G | A | 1 | a0001c0004t0004 | 5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*899C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 899 | chr13 | 48489212 | ||||||
| chr13:48489236 | G | A | 1 | a0001c0001t0011 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*875C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 875 | chr13 | 48489236 | ||||||
| chr13:48489304 | T | C | 1 | a0001c0001t0012 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*807A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 807 | chr13 | 48489304 | ||||||
| chr13:48489575 | C | T | 1 | a0001c0001t0006 | 2 | HG02723.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*536G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 536 | chr13 | 48489575 | ||||||
| chr13:48489744 | T | G | 2 | a0001c0008t0013 a0001c0008t0014 |
2 | HG03225.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*367A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 367 | chr13 | 48489744 | ||||||
| chr13:48489785 | T | C | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0005t0002 others(3): Show |
28 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*326A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 326 | chr13 | 48489785 | ||||||
| chr13:48489791 | A | G | 1 | a0001c0001t0010 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*320T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 320 | chr13 | 48489791 | ||||||
| chr13:48489940 | A | C | 1 | a0001c0001t0005 | 4 | NA18980.hp1 NA19063.hp2 NA19074.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*171T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 171 | chr13 | 48489940 | ||||||
| chr13:48489954 | G | A | 1 | a0001c0004t0004 | 5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*157C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 157 | chr13 | 48489954 | ||||||
| chr13:48490085 | G | T | 1 | a0001c0001t0009 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26C>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 26 | chr13 | 48490085 | ||||||
| chr13:48490106 | T | C | 1 | a0001c0008t0014 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 15/15 | 5 | chr13 | 48490106 | ||||||
| chr13:48522348 | C | T | 1 | a0001c0001t0008 | 1 | HG02886.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-64G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 3/15 | chr13 | 48522348 | |||||||
| chr13:48522359 | G | A | 1 | a0001c0001t0015 | 1 | NA19010.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-75C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 3/15 | chr13 | 48522359 | |||||||
| chr13:48524721 | C | T | 1 | a0001c0001t0007 | 1 | HG04228.hp1 | 5_prime_UTR_variant | MODIFIER | c.-182G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/15 | 2782 | chr13 | 48524721 | ||||||
| chr13:48533046 | C | T | 1 | a0001c0003t0003 | 7 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-237G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/15 | 11107 | chr13 | 48533046 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:48490378 | G | C | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516-127C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48490378 | |||||||
| chr13:48490433 | T | C | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516-182A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48490433 | |||||||
| chr13:48490566 | A | G | 2 | a0001c0008t0013g0058 a0001c0008t0014g0059 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1516-315T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48490566 | |||||||
| chr13:48490661 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1516-410A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48490661 | |||||||
| chr13:48490672 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1516-421A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48490672 | |||||||
| chr13:48490710 | A | G | 9 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0007t0001g0254 others(6): Show |
9 | HG00558.hp2 HG01109.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1516-459T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48490710 | |||||||
| chr13:48490764 | C | T | 1 | a0001c0001t0009g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1516-513G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48490764 | |||||||
| chr13:48490821 | A | G | 1 | a0002c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1516-570T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48490821 | |||||||
| chr13:48490830 | A | C | 30 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(27): Show |
30 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1516-579T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48490830 | |||||||
| chr13:48491015 | G | T | 2 | a0001c0003t0003g0004 a0001c0003t0003g0028 |
4 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1516-764C>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491015 | |||||||
| chr13:48491123 | T | C | 19 | a0001c0001t0002g0011 a0001c0001t0002g0056 a0001c0001t0002g0057 others(16): Show |
20 | HG01243.hp2 HG01496.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1516-872A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491123 | |||||||
| chr13:48491153 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0042 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1516-902T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491153 | |||||||
| chr13:48491188 | C | T | 19 | a0001c0001t0002g0011 a0001c0001t0002g0056 a0001c0001t0002g0057 others(16): Show |
20 | HG01243.hp2 HG01496.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1516-937G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491188 | |||||||
| chr13:48491299 | ATTTTC | A | 21 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(18): Show |
21 | HG00738.hp2 HG01168.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.1516-1053_1516-104 others(9): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491299 | |||||||
| chr13:48491386 | C | T | 1 | a0001c0003t0003g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1516-1135G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491386 | |||||||
| chr13:48491400 | G | A | 1 | a0001c0001t0009g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1516-1149C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491400 | |||||||
| chr13:48491429 | A | T | 19 | a0001c0001t0002g0011 a0001c0001t0002g0056 a0001c0001t0002g0057 others(16): Show |
20 | HG01243.hp2 HG01496.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1516-1178T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491429 | |||||||
| chr13:48491476 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1516-1225T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491476 | |||||||
| chr13:48491508 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0213 |
2 | HG01175.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1516-1257T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491508 | |||||||
| chr13:48491604 | A | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1516-1353T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491604 | |||||||
| chr13:48491605 | T | G | 5 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0007t0001g0254 others(2): Show |
5 | HG00558.hp2 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516-1354A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491605 | |||||||
| chr13:48491688 | T | C | 22 | a0001c0001t0002g0011 a0001c0001t0002g0056 a0001c0001t0002g0057 others(19): Show |
23 | HG00558.hp2 HG01243.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.1516-1437A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491688 | |||||||
| chr13:48491770 | A | G | 6 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1516-1519T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48491770 | |||||||
| chr13:48492127 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1516-1876G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492127 | |||||||
| chr13:48492204 | G | A | 5 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
5 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1516-1953C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492204 | |||||||
| chr13:48492220 | C | G | 1 | a0001c0001t0007g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1516-1969G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492220 | |||||||
| chr13:48492414 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1516-2163T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492414 | |||||||
| chr13:48492449 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1516-2198G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492449 | |||||||
| chr13:48492463 | T | G | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00597.hp1 NA19058.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1516-2212A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492463 | |||||||
| chr13:48492538 | C | T | 8 | a0001c0001t0002g0011 a0001c0001t0002g0069 a0001c0001t0002g0072 others(5): Show |
9 | HG01243.hp2 HG01496.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1516-2287G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492538 | |||||||
| chr13:48492646 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0107 others(1): Show |
5 | NA18945.hp1 NA18952.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.1516-2395G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492646 | |||||||
| chr13:48492665 | G | GACTTCTT others(14): Show |
2 | a0001c0004t0004g0021 a0001c0004t0004g0216 |
3 | HG01884.hp1 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1516-2435_1516-241 others(25): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492665 | |||||||
| chr13:48492767 | G | A | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516-2516C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492767 | |||||||
| chr13:48492967 | T | C | 113 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0032 others(110): Show |
123 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.1516-2716A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492967 | |||||||
| chr13:48492984 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1516-2733T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48492984 | |||||||
| chr13:48493102 | G | A | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1516-2851C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493102 | |||||||
| chr13:48493152 | C | T | 6 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1516-2901G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493152 | |||||||
| chr13:48493225 | T | TCA | 29 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0039 others(26): Show |
33 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1515+2964_1515+296 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACA | 3 | a0001c0001t0001g0118 a0001c0001t0001g0162 a0001c0001t0002g0011 |
4 | HG00438.hp1 HG01256.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1515+2962_1515+296 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(1): Show |
4 | a0001c0001t0002g0076 a0001c0001t0006g0073 a0001c0001t0007g0267 others(1): Show |
4 | HG02165.hp2 HG02809.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.1515+2958_1515+296 others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(3): Show |
8 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0072 others(5): Show |
9 | HG02129.hp2 HG02630.hp2 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.1515+2956_1515+296 others(14): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(5): Show |
29 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0002g0057 others(26): Show |
32 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1515+2954_1515+296 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(7): Show |
11 | a0001c0001t0001g0259 a0001c0001t0002g0060 a0001c0001t0002g0061 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1515+2952_1515+296 others(18): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(9): Show |
3 | a0001c0001t0002g0063 a0001c0001t0002g0069 a0001c0002t0001g0223 |
3 | HG02155.hp1 HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1515+2950_1515+296 others(20): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(11): Show |
8 | a0001c0001t0001g0258 a0001c0001t0002g0056 a0001c0004t0004g0021 others(5): Show |
9 | HG01243.hp2 HG01884.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1515+2948_1515+296 others(22): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(13): Show |
2 | a0001c0001t0002g0078 a0001c0008t0014g0059 |
2 | HG02886.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1515+2946_1515+296 others(24): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(15): Show |
2 | a0001c0001t0001g0262 a0001c0001t0002g0075 |
2 | HG01496.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1515+2944_1515+296 others(26): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(17): Show |
1 | a0001c0001t0001g0263 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1515+2942_1515+296 others(28): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(19): Show |
1 | a0001c0001t0001g0265 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1515+2940_1515+296 others(30): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(21): Show |
2 | a0001c0001t0001g0261 a0001c0001t0001g0264 |
2 | HG02145.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1515+2938_1515+296 others(32): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | T | TCACACAC others(23): Show |
1 | a0004c0010t0001g0050 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1515+2936_1515+296 others(34): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | TCA | T | 64 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(61): Show |
68 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1515+2964_1515+296 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | TCACACA | T | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1515+2960_1515+296 others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493225 | TCACACAC others(5): Show |
T | 1 | a0001c0001t0001g0129 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1515+2954_1515+296 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493225 | |||||||
| chr13:48493251 | ACACACAC others(31): Show |
A | 1 | a0002c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1515+2902_1515+293 others(42): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493251 | |||||||
| chr13:48493259 | ACTCTTCT others(6): Show |
A | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1515+2919_1515+293 others(17): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493259 | |||||||
| chr13:48493261 | T | A | 26 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
26 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1515+2930A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493261 | |||||||
| chr13:48493262 | C | CA | 4 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(1): Show |
4 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+2928_1515+292 others(5): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493262 | |||||||
| chr13:48493262 | C | CACACA | 4 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0045 others(1): Show |
4 | HG01109.hp1 HG01884.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+2928_1515+292 others(9): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493262 | |||||||
| chr13:48493262 | C | CACACACA | 5 | a0001c0001t0001g0033 a0001c0001t0001g0043 a0001c0001t0001g0046 others(2): Show |
5 | HG01168.hp1 HG01361.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2928_1515+292 others(11): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493262 | |||||||
| chr13:48493262 | C | CACACACA others(2): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0041 |
3 | HG02257.hp2 HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1515+2928_1515+292 others(13): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493262 | |||||||
| chr13:48493262 | CT | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0048 a0001c0001t0001g0053 |
3 | HG03130.hp2 HG03486.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1515+2928delA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493262 | |||||||
| chr13:48493263 | T | A | 1 | a0001c0001t0001g0039 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1515+2928A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493263 | |||||||
| chr13:48493263 | T | C | 18 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(15): Show |
18 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1515+2928A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493263 | |||||||
| chr13:48493264 | T | A | 21 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(18): Show |
21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+2927A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493264 | |||||||
| chr13:48493264 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0007g0267 |
2 | HG02622.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1515+2927A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493264 | |||||||
| chr13:48493265 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0007g0267 |
2 | HG02622.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1515+2926G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493265 | |||||||
| chr13:48493266 | T | A | 21 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(18): Show |
21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+2925A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493266 | |||||||
| chr13:48493268 | T | A | 21 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(18): Show |
21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+2923A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493268 | |||||||
| chr13:48493270 | T | A | 21 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(18): Show |
21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+2921A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493270 | |||||||
| chr13:48493272 | T | A | 21 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(18): Show |
21 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+2919A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493272 | |||||||
| chr13:48493275 | C | CA | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(7): Show |
10 | HG01168.hp1 HG01361.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1515+2915_1515+291 others(5): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493275 | |||||||
| chr13:48493275 | C | CT | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+2915_1515+291 others(5): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493275 | |||||||
| chr13:48493276 | C | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
6 | HG00738.hp2 HG02258.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1515+2915G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493276 | |||||||
| chr13:48493276 | C | T | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+2915G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493276 | |||||||
| chr13:48493276 | CCT | C | 6 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1515+2913_1515+291 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493276 | |||||||
| chr13:48493277 | C | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(7): Show |
10 | HG01168.hp1 HG01361.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1515+2914G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493277 | |||||||
| chr13:48493278 | T | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
6 | HG00738.hp2 HG02258.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1515+2913A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493278 | |||||||
| chr13:48493280 | T | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0044 a0001c0001t0001g0047 others(3): Show |
6 | HG00738.hp2 HG02258.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1515+2911A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493280 | |||||||
| chr13:48493282 | T | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2909A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493282 | |||||||
| chr13:48493282 | T | TCACC | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+2908_1515+290 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493282 | |||||||
| chr13:48493283 | CTCTCTCC others(5): Show |
C | 1 | a0004c0010t0001g0050 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1515+2896_1515+290 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493283 | |||||||
| chr13:48493284 | T | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2907A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493284 | |||||||
| chr13:48493284 | T | TCACC | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(7): Show |
10 | HG01168.hp1 HG01361.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1515+2906_1515+290 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493284 | |||||||
| chr13:48493285 | CTCTCCA | C | 3 | a0001c0004t0004g0021 a0001c0004t0004g0217 a0001c0004t0004g0218 |
4 | HG02965.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1515+2900_1515+290 others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493285 | |||||||
| chr13:48493286 | T | A | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2905A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493286 | |||||||
| chr13:48493288 | T | C | 7 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0002g0242 others(4): Show |
7 | HG01192.hp1 HG02055.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1515+2903A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493288 | |||||||
| chr13:48493289 | C | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0044 others(5): Show |
8 | HG01192.hp1 HG02055.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1515+2902G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493289 | |||||||
| chr13:48493289 | C | CCACACAC others(5): Show |
2 | a0001c0008t0013g0058 a0001c0008t0014g0059 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1515+2890_1515+290 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493289 | |||||||
| chr13:48493289 | C | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2902G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493289 | |||||||
| chr13:48493290 | C | T | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(7): Show |
10 | HG01168.hp1 HG01361.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1515+2901G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493290 | |||||||
| chr13:48493291 | A | C | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(7): Show |
10 | HG01168.hp1 HG01361.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1515+2900T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493291 | |||||||
| chr13:48493291 | A | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2900T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493291 | |||||||
| chr13:48493293 | A | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2898T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493293 | |||||||
| chr13:48493295 | A | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2896T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493295 | |||||||
| chr13:48493299 | A | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2892T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493299 | |||||||
| chr13:48493301 | A | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2890T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493301 | |||||||
| chr13:48493303 | A | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2888T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493303 | |||||||
| chr13:48493305 | A | T | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2886T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493305 | |||||||
| chr13:48493306 | CA | C | 5 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(2): Show |
5 | HG00738.hp2 HG02258.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2884delT | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493306 | |||||||
| chr13:48493309 | A | ACTCTCTC others(9): Show |
1 | a0001c0001t0001g0138 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1515+2881_1515+288 others(20): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493309 | |||||||
| chr13:48493309 | A | ACTCTCTC others(15): Show |
2 | a0001c0001t0001g0122 a0001c0001t0001g0132 |
2 | NA18989.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1515+2881_1515+288 others(26): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493309 | |||||||
| chr13:48493311 | A | ACT | 4 | a0001c0002t0001g0220 a0001c0002t0001g0223 a0001c0002t0001g0228 others(1): Show |
4 | HG02155.hp1 NA18971.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCT | 3 | a0001c0001t0001g0249 a0001c0001t0001g0269 a0001c0002t0001g0238 |
3 | HG02155.hp2 HG03041.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(1): Show |
6 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0079 others(3): Show |
10 | HG01243.hp1 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(3): Show |
3 | a0001c0001t0001g0112 a0001c0001t0001g0129 a0001c0001t0005g0113 |
3 | NA18955.hp1 NA19063.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(14): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(5): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0087 a0001c0001t0001g0092 others(2): Show |
6 | HG00099.hp1 HG01074.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(7): Show |
7 | a0001c0001t0001g0015 a0001c0001t0001g0084 a0001c0001t0001g0086 others(4): Show |
8 | HG01168.hp2 HG01169.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(18): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(9): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0128 |
2 | HG03491.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(20): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(11): Show |
8 | a0001c0001t0001g0014 a0001c0001t0001g0085 a0001c0001t0001g0088 others(5): Show |
9 | HG00642.hp2 HG03669.hp2 HG04204.hp2 others(6): Show |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(22): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(13): Show |
4 | a0001c0001t0001g0095 a0001c0001t0001g0125 a0001c0001t0005g0096 others(1): Show |
4 | HG01993.hp2 NA18747.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(24): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(15): Show |
3 | a0001c0001t0001g0103 a0001c0001t0001g0133 a0001c0001t0001g0279 |
3 | HG00609.hp2 NA18969.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(26): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(17): Show |
6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0093 others(3): Show |
6 | HG02148.hp2 NA19070.hp1 NA19075.hp1 others(3): Show |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(28): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(19): Show |
7 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0105 others(4): Show |
7 | HG00408.hp1 HG02683.hp1 HG04184.hp1 others(4): Show |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(30): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(21): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0104 a0001c0001t0001g0116 others(2): Show |
6 | NA18950.hp2 NA18951.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+2879_1515+288 others(32): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | ACTCTCTC others(23): Show |
1 | a0001c0001t0001g0115 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1515+2879_1515+288 others(34): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | A | T | 4 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0138 others(1): Show |
4 | HG03942.hp1 NA18989.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.1515+2880T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | ACACACTC others(1): Show |
A | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1515+2872_1515+287 others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493311 | ACACACTC others(9): Show |
A | 10 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(7): Show |
10 | HG01168.hp1 HG01361.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1515+2864_1515+287 others(20): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493311 | |||||||
| chr13:48493313 | A | ACTCTCTC others(1): Show |
5 | a0001c0001t0001g0018 a0001c0001t0001g0155 a0001c0001t0001g0159 others(2): Show |
6 | HG01361.hp1 HG01928.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+2877_1515+287 others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493313 | |||||||
| chr13:48493313 | A | ACTCTCTC others(7): Show |
1 | a0001c0001t0001g0111 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1515+2877_1515+287 others(18): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493313 | |||||||
| chr13:48493313 | A | ACTCTCTC others(9): Show |
1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1515+2877_1515+287 others(20): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493313 | |||||||
| chr13:48493313 | A | ACTCTCTC others(17): Show |
1 | a0001c0001t0001g0126 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1515+2877_1515+287 others(28): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493313 | |||||||
| chr13:48493313 | A | ACTCTCTC others(23): Show |
3 | a0001c0001t0001g0097 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | NA18960.hp1 NA18968.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1515+2877_1515+287 others(34): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493313 | |||||||
| chr13:48493313 | A | ACTCTCTC others(25): Show |
1 | a0001c0001t0001g0013 | 2 | NA18943.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.1515+2877_1515+287 others(36): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493313 | |||||||
| chr13:48493313 | A | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(88): Show |
102 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1515+2878T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493313 | |||||||
| chr13:48493315 | A | ACACACAC others(15): Show |
1 | a0001c0001t0002g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1515+2875_1515+287 others(26): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACACAC others(13): Show |
1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1515+2875_1515+287 others(24): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACACAC others(5): Show |
1 | a0001c0001t0002g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1515+2875_1515+287 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACACAC others(7): Show |
2 | a0001c0001t0002g0072 a0001c0001t0002g0078 |
2 | HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1515+2875_1515+287 others(18): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACACAC others(5): Show |
7 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(4): Show |
8 | HG02572.hp1 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1515+2875_1515+287 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACACAC others(7): Show |
1 | a0001c0001t0002g0076 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1515+2875_1515+287 others(18): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACACAC others(3): Show |
1 | a0001c0001t0002g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1515+2875_1515+287 others(14): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACACTC others(1): Show |
4 | a0001c0001t0002g0067 a0001c0001t0002g0068 a0001c0001t0002g0069 others(1): Show |
4 | HG01243.hp2 HG02647.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+2875_1515+287 others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACACTC others(3): Show |
1 | a0001c0001t0001g0156 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1515+2875_1515+287 others(14): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACACTC others(5): Show |
2 | a0001c0001t0001g0210 a0001c0001t0002g0056 |
2 | HG01257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1515+2875_1515+287 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACT | 3 | a0001c0001t0001g0146 a0001c0001t0001g0185 a0001c0001t0001g0212 |
3 | NA18939.hp1 NA18968.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1515+2875_1515+287 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACACTCTC others(3): Show |
2 | a0001c0001t0001g0198 a0001c0001t0015g0201 |
2 | NA19010.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1515+2875_1515+287 others(14): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACT | 4 | a0001c0001t0001g0135 a0001c0001t0001g0152 a0001c0001t0001g0153 others(1): Show |
4 | HG01256.hp1 HG01952.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1515+2874_1515+287 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACTCT | 6 | a0001c0001t0001g0065 a0001c0001t0001g0143 a0001c0001t0001g0145 others(3): Show |
6 | HG00673.hp1 NA18955.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+2872_1515+287 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACTCTCT | 3 | a0001c0001t0001g0020 a0001c0001t0001g0173 a0001c0001t0001g0206 |
4 | HG00673.hp2 HG00741.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+2870_1515+287 others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACTCTCTC others(9): Show |
1 | a0001c0001t0001g0080 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1515+2875_1515+287 others(20): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACTCTCTC others(13): Show |
1 | a0001c0001t0001g0002 | 4 | HG02559.hp2 HG02615.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+2875_1515+287 others(24): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACTCTCTC others(1): Show |
49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(46): Show |
66 | HG00323.hp1 HG00408.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.1515+2868_1515+287 others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACTCTCTC others(3): Show |
7 | a0001c0001t0001g0029 a0001c0001t0001g0148 a0001c0001t0001g0180 others(4): Show |
7 | HG01074.hp2 HG01175.hp1 HG03942.hp2 others(4): Show |
intron_variant | MODIFIER | c.1515+2866_1515+287 others(14): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | ACTCTCTC others(5): Show |
2 | a0001c0001t0001g0147 a0001c0001t0001g0179 |
2 | HG00438.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.1515+2864_1515+287 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | A | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(110): Show |
126 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.1515+2876T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | ACT | A | 10 | a0001c0001t0001g0136 a0001c0001t0001g0256 a0001c0001t0001g0258 others(7): Show |
10 | HG00558.hp2 HG01928.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1515+2874_1515+287 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | ACTCTCT | A | 7 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1515+2870_1515+287 others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | ACTCTCTC others(5): Show |
A | 1 | a0004c0010t0001g0050 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1515+2864_1515+287 others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493315 | ACTCTCTC others(20): Show |
A | 1 | a0002c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1515+2849_1515+287 others(31): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493315 | |||||||
| chr13:48493316 | C | CT | 5 | a0001c0003t0003g0004 a0001c0003t0003g0025 a0001c0003t0003g0026 others(2): Show |
7 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1515+2874dupA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493316 | |||||||
| chr13:48493316 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1515+2875G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493316 | |||||||
| chr13:48493317 | T | A | 11 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0047 others(8): Show |
11 | HG00738.hp2 HG01192.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1515+2874A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493317 | |||||||
| chr13:48493317 | TC | T | 3 | a0001c0001t0001g0036 a0001c0001t0001g0044 a0001c0001t0007g0267 |
3 | HG03225.hp1 HG03540.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1515+2873delG | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493317 | |||||||
| chr13:48493318 | C | CACT | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG01192.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+2872_1515+287 others(7): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493318 | |||||||
| chr13:48493319 | T | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0042 a0001c0001t0001g0047 others(4): Show |
7 | HG00738.hp2 HG02258.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1515+2872A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493319 | |||||||
| chr13:48493321 | T | A | 6 | a0001c0001t0001g0030 a0001c0001t0001g0047 a0001c0001t0001g0049 others(3): Show |
6 | HG00738.hp2 HG01975.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1515+2870A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493321 | |||||||
| chr13:48493323 | T | A | 12 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0035 others(9): Show |
12 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1515+2868A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493323 | |||||||
| chr13:48493323 | T | TCACC | 5 | a0001c0003t0003g0004 a0001c0003t0003g0025 a0001c0003t0003g0026 others(2): Show |
7 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1515+2867_1515+286 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493323 | |||||||
| chr13:48493323 | T | TCACCCTC others(28): Show |
1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1515+2867_1515+286 others(39): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493323 | |||||||
| chr13:48493325 | T | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0035 others(10): Show |
13 | HG00099.hp2 HG00738.hp2 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1515+2866A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493325 | |||||||
| chr13:48493325 | T | TCACCCTC others(22): Show |
1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1515+2865_1515+286 others(33): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493325 | |||||||
| chr13:48493325 | T | TCACCCTC others(28): Show |
1 | a0001c0001t0007g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1515+2865_1515+286 others(39): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493325 | |||||||
| chr13:48493325 | T | TCACCCTC others(34): Show |
3 | a0001c0001t0001g0036 a0001c0001t0002g0243 a0001c0001t0002g0244 |
3 | HG02055.hp1 HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1515+2865_1515+286 others(45): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493325 | |||||||
| chr13:48493325 | T | TCACCCTC others(36): Show |
2 | a0001c0001t0002g0242 a0001c0001t0002g0245 |
2 | HG01192.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1515+2865_1515+286 others(47): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493325 | |||||||
| chr13:48493327 | T | A | 14 | a0001c0001t0001g0030 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
14 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1515+2864A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493327 | |||||||
| chr13:48493327 | T | TCACCCTC others(36): Show |
1 | a0001c0001t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1515+2863_1515+286 others(47): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493327 | |||||||
| chr13:48493327 | T | TCCACACA others(22): Show |
1 | a0001c0003t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1515+2863_1515+286 others(33): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493327 | |||||||
| chr13:48493329 | T | TCCACACA others(22): Show |
2 | a0001c0003t0003g0025 a0001c0003t0003g0026 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1515+2861_1515+286 others(33): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493329 | |||||||
| chr13:48493329 | T | TCCACACA others(24): Show |
3 | a0001c0003t0003g0004 a0001c0003t0003g0027 a0001c0003t0003g0028 |
5 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+2861_1515+286 others(35): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493329 | |||||||
| chr13:48493354 | C | G | 25 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0219 others(22): Show |
27 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.1515+2837G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493354 | |||||||
| chr13:48493684 | G | C | 3 | a0001c0004t0004g0218 a0001c0008t0013g0058 a0001c0008t0014g0059 |
3 | HG03130.hp1 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1515+2507C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493684 | |||||||
| chr13:48493906 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1515+2285A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48493906 | |||||||
| chr13:48494178 | A | T | 1 | a0001c0001t0001g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1515+2013T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48494178 | |||||||
| chr13:48494283 | T | C | 73 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(70): Show |
82 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1515+1908A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48494283 | |||||||
| chr13:48494303 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1515+1888A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48494303 | |||||||
| chr13:48494324 | C | T | 3 | a0001c0001t0001g0178 a0001c0005t0002g0005 a0001c0005t0002g0066 |
5 | HG01069.hp2 HG03453.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1515+1867G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48494324 | |||||||
| chr13:48494392 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1515+1799C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48494392 | |||||||
| chr13:48494597 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1515+1594G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48494597 | |||||||
| chr13:48494659 | A | AT | 11 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(8): Show |
11 | HG00558.hp2 HG01109.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1515+1531dupA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48494659 | |||||||
| chr13:48494684 | T | C | 11 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(8): Show |
11 | HG00558.hp2 HG01109.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1515+1507A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48494684 | |||||||
| chr13:48495076 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0174 a0001c0001t0001g0177 |
4 | HG01361.hp1 HG01928.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+1115G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495076 | |||||||
| chr13:48495222 | T | C | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1515+969A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495222 | |||||||
| chr13:48495279 | C | T | 180 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(177): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1515+912G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495279 | |||||||
| chr13:48495287 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1515+904G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495287 | |||||||
| chr13:48495337 | T | C | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+854A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495337 | |||||||
| chr13:48495395 | A | G | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1515+796T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495395 | |||||||
| chr13:48495402 | A | AAC | 82 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(79): Show |
88 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.1515+788_1515+789i others(4): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495402 | |||||||
| chr13:48495623 | T | C | 16 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(13): Show |
16 | HG00558.hp2 HG01109.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1515+568A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495623 | |||||||
| chr13:48495795 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1515+396A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495795 | |||||||
| chr13:48495796 | A | C | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1515+395T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495796 | |||||||
| chr13:48495802 | C | T | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1515+389G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495802 | |||||||
| chr13:48495804 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1515+387T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495804 | |||||||
| chr13:48495805 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1515+386A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495805 | |||||||
| chr13:48495806 | T | G | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1515+385A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495806 | |||||||
| chr13:48495987 | A | ATCCTT | 82 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(79): Show |
88 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.1515+199_1515+203d others(7): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48495987 | |||||||
| chr13:48496038 | T | C | 180 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(177): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1515+153A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48496038 | |||||||
| chr13:48496164 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+27G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 14/14 | chr13 | 48496164 | |||||||
| chr13:48496327 | G | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG00738.hp2 HG01168.hp1 |
splice_region_variant&intron_variant | LOW | c.1385-6C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496327 | |||||||
| chr13:48496329 | A | T | 1 | a0001c0003t0001g0064 | 1 | HG02976.hp1 | splice_region_variant&intron_variant | LOW | c.1385-8T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496329 | |||||||
| chr13:48496376 | G | C | 82 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(79): Show |
88 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(85): Show |
intron_variant | MODIFIER | c.1385-55C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496376 | |||||||
| chr13:48496597 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1385-276A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496597 | |||||||
| chr13:48496601 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1385-280G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496601 | |||||||
| chr13:48496668 | C | T | 22 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(19): Show |
23 | HG01243.hp2 HG01496.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.1385-347G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496668 | |||||||
| chr13:48496746 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1385-425T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496746 | |||||||
| chr13:48496781 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1385-460C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496781 | |||||||
| chr13:48496786 | G | A | 26 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(23): Show |
27 | HG01192.hp1 HG01243.hp2 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.1385-465C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496786 | |||||||
| chr13:48496790 | A | AGAGGGGA others(8): Show |
14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0053 others(11): Show |
17 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1385-484_1385-470d others(17): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496790 | |||||||
| chr13:48496790 | A | AGAGGGGA others(23): Show |
3 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 |
3 | HG02630.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1385-470_1385-469i others(32): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496790 | |||||||
| chr13:48496790 | A | AGAGGGGA others(23): Show |
4 | a0001c0001t0001g0032 a0001c0001t0001g0036 a0001c0001t0001g0042 others(1): Show |
4 | HG01884.hp2 HG02818.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1385-499_1385-470d others(32): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496790 | |||||||
| chr13:48496790 | A | AGAGGGGA others(38): Show |
14 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0043 others(11): Show |
14 | HG00738.hp2 HG01168.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.1385-514_1385-470d others(47): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496790 | |||||||
| chr13:48496790 | AGAGGGGA others(8): Show |
A | 2 | a0001c0001t0002g0057 a0001c0001t0002g0060 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1385-484_1385-470d others(17): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496790 | |||||||
| chr13:48496801 | G | GAGAGGAG others(8): Show |
1 | a0002c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1385-481_1385-480i others(17): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496801 | |||||||
| chr13:48496806 | G | A | 1 | a0001c0001t0007g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1385-485C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496806 | |||||||
| chr13:48496810 | GGAGGGGA others(23): Show |
G | 3 | a0001c0002t0001g0230 a0001c0005t0002g0005 a0001c0005t0002g0066 |
5 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.1385-519_1385-490d others(32): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496810 | |||||||
| chr13:48496814 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1385-493C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496814 | |||||||
| chr13:48496840 | A | G | 28 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(25): Show |
28 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1385-519T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496840 | |||||||
| chr13:48496843 | G | GGGGAGAG others(22): Show |
5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1385-523_1385-522i others(31): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496843 | |||||||
| chr13:48496892 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1385-571A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48496892 | |||||||
| chr13:48497226 | T | C | 3 | a0001c0002t0001g0233 a0001c0002t0001g0234 a0003c0009t0001g0221 |
3 | HG02165.hp2 NA18944.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1385-905A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48497226 | |||||||
| chr13:48497885 | G | A | 5 | a0001c0003t0003g0004 a0001c0003t0003g0025 a0001c0003t0003g0026 others(2): Show |
7 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1385-1564C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48497885 | |||||||
| chr13:48497927 | A | G | 180 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(177): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.1385-1606T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48497927 | |||||||
| chr13:48497933 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1385-1612C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48497933 | |||||||
| chr13:48498075 | G | A | 6 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1384+1546C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48498075 | |||||||
| chr13:48498222 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1384+1399T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48498222 | |||||||
| chr13:48498429 | G | A | 26 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
26 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.1384+1192C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48498429 | |||||||
| chr13:48498458 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1384+1163G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48498458 | |||||||
| chr13:48498520 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.1384+1101G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48498520 | |||||||
| chr13:48498609 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1384+1012T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48498609 | |||||||
| chr13:48498718 | G | C | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1384+903C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48498718 | |||||||
| chr13:48498730 | C | CA | 39 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(36): Show |
39 | HG00558.hp2 HG00738.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1384+890dupT | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48498730 | |||||||
| chr13:48498730 | CA | C | 6 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(3): Show |
7 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1384+890delT | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48498730 | |||||||
| chr13:48499009 | T | A | 1 | a0001c0001t0001g0188 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1384+612A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499009 | |||||||
| chr13:48499110 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1384+511G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499110 | |||||||
| chr13:48499111 | A | AAC | 42 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(39): Show |
48 | HG00099.hp1 HG00735.hp2 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.1384+508_1384+509d others(4): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACAC | 14 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0084 others(11): Show |
14 | HG00438.hp2 HG00597.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1384+506_1384+509d others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACACAC | 3 | a0001c0002t0001g0225 a0001c0003t0001g0064 a0001c0003t0003g0027 |
3 | HG02976.hp1 NA18522.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1384+504_1384+509d others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACACACA others(1): Show |
5 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
7 | HG01069.hp1 HG01071.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1384+502_1384+509d others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACACACA others(3): Show |
9 | a0001c0001t0001g0030 a0001c0001t0001g0033 a0001c0001t0001g0042 others(6): Show |
9 | HG01109.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1384+500_1384+509d others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACACACA others(5): Show |
4 | a0001c0001t0001g0263 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
4 | HG01192.hp1 NA18906.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384+498_1384+509d others(14): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACACACA others(7): Show |
4 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG01361.hp2 HG01884.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1384+496_1384+509d others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACACACA others(9): Show |
8 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0001c0001t0001g0258 others(5): Show |
8 | HG01109.hp1 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384+494_1384+509d others(18): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACACACA others(11): Show |
6 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0256 others(3): Show |
6 | HG02970.hp1 HG03098.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.1384+492_1384+509d others(20): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACACACA others(13): Show |
8 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0043 others(5): Show |
8 | HG00558.hp2 HG00738.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1384+490_1384+509d others(22): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | A | AACACACA others(15): Show |
1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1384+488_1384+509d others(24): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499111 | AAC | A | 3 | a0001c0001t0001g0195 a0001c0005t0002g0005 a0001c0005t0002g0066 |
5 | HG03453.hp1 NA18987.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384+508_1384+509d others(4): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499111 | |||||||
| chr13:48499140 | A | T | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1384+481T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499140 | |||||||
| chr13:48499142 | A | ACACACAC others(19): Show |
1 | a0001c0001t0001g0037 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1384+478_1384+479i others(28): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACACACAC others(17): Show |
2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1384+478_1384+479i others(26): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACACACAC others(13): Show |
1 | a0001c0001t0001g0038 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1384+478_1384+479i others(22): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACACACAC others(9): Show |
2 | a0001c0001t0001g0039 a0001c0001t0001g0257 |
2 | HG02622.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1384+478_1384+479i others(18): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACACACAC others(1): Show |
3 | a0001c0002t0001g0228 a0001c0002t0001g0229 a0001c0002t0001g0236 |
3 | NA18971.hp2 NA18975.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1384+478_1384+479i others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACACACT | 18 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0219 others(15): Show |
20 | HG00323.hp2 HG02155.hp1 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.1384+478_1384+479i others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACACACTC others(1): Show |
4 | a0001c0002t0001g0222 a0001c0002t0001g0235 a0001c0008t0013g0058 others(1): Show |
4 | HG02129.hp2 HG03225.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384+478_1384+479i others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACACACTC others(3): Show |
2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1384+478_1384+479i others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACT | 10 | a0001c0001t0001g0013 a0001c0001t0001g0097 a0001c0001t0001g0102 others(7): Show |
11 | HG02109.hp2 HG02647.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1384+477_1384+478d others(4): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACTCT | 4 | a0001c0001t0001g0101 a0001c0001t0001g0194 a0001c0001t0001g0268 others(1): Show |
4 | HG00099.hp2 HG01243.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1384+475_1384+478d others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | ACTCTCT | 6 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(3): Show |
7 | HG01496.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1384+473_1384+478d others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | A | T | 3 | a0001c0001t0002g0056 a0001c0001t0006g0073 a0001c0001t0006g0074 |
3 | HG02723.hp1 HG02922.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1384+479T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499142 | ACT | A | 23 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0080 others(20): Show |
25 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.1384+477_1384+478d others(4): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499142 | |||||||
| chr13:48499144 | T | A | 33 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0033 others(30): Show |
37 | HG01069.hp1 HG01071.hp2 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.1384+477A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499144 | |||||||
| chr13:48499146 | T | A | 33 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0033 others(30): Show |
36 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1384+475A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499146 | |||||||
| chr13:48499148 | T | A | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384+473A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499148 | |||||||
| chr13:48499164 | T | A | 5 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(2): Show |
5 | HG01192.hp1 HG02055.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1384+457A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499164 | |||||||
| chr13:48499166 | T | A | 14 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(11): Show |
16 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1384+455A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499166 | |||||||
| chr13:48499168 | T | A | 27 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(24): Show |
29 | HG00642.hp1 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1384+453A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499168 | |||||||
| chr13:48499508 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1384+113T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 13/14 | chr13 | 48499508 | |||||||
| chr13:48499975 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1245-215C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48499975 | |||||||
| chr13:48500182 | A | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245-422T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500182 | |||||||
| chr13:48500233 | C | A | 37 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(34): Show |
37 | HG00558.hp2 HG00738.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.1245-473G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500233 | |||||||
| chr13:48500295 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1245-535G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500295 | |||||||
| chr13:48500330 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1245-570G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500330 | |||||||
| chr13:48500375 | T | C | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245-615A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500375 | |||||||
| chr13:48500383 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1245-623G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500383 | |||||||
| chr13:48500421 | G | A | 30 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(27): Show |
30 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.1245-661C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500421 | |||||||
| chr13:48500422 | G | A | 1 | a0001c0001t0007g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1245-662C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500422 | |||||||
| chr13:48500506 | C | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1245-746G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500506 | |||||||
| chr13:48500785 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1244+957C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500785 | |||||||
| chr13:48500836 | C | G | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1244+906G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500836 | |||||||
| chr13:48500956 | G | A | 1 | a0001c0002t0001g0241 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1244+786C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500956 | |||||||
| chr13:48500977 | A | G | 3 | a0001c0001t0002g0069 a0001c0001t0002g0075 a0001c0011t0002g0246 |
3 | HG01243.hp2 HG01496.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1244+765T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48500977 | |||||||
| chr13:48501027 | A | T | 1 | a0001c0007t0001g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1244+715T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48501027 | |||||||
| chr13:48501298 | T | C | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1244+444A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48501298 | |||||||
| chr13:48501359 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1244+383C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48501359 | |||||||
| chr13:48501449 | A | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1244+293T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48501449 | |||||||
| chr13:48501483 | G | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0247 a0001c0001t0001g0248 others(5): Show |
10 | HG01074.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1244+259C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48501483 | |||||||
| chr13:48501592 | A | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1244+150T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48501592 | |||||||
| chr13:48501702 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1244+40G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 12/14 | chr13 | 48501702 | |||||||
| chr13:48501877 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1118-9T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48501877 | |||||||
| chr13:48502009 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1118-141G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48502009 | |||||||
| chr13:48502132 | T | G | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1118-264A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48502132 | |||||||
| chr13:48502169 | A | AAC | 65 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(62): Show |
68 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(65): Show |
intron_variant | MODIFIER | c.1118-303_1118-302d others(4): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48502169 | |||||||
| chr13:48502197 | C | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1118-329G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48502197 | |||||||
| chr13:48502407 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1117+317G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48502407 | |||||||
| chr13:48502474 | C | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+250G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48502474 | |||||||
| chr13:48502546 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1117+178A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48502546 | |||||||
| chr13:48502656 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1117+68G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48502656 | |||||||
| chr13:48502694 | C | G | 1 | a0001c0003t0003g0025 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1117+30G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 11/14 | chr13 | 48502694 | |||||||
| chr13:48502932 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.927-18G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48502932 | |||||||
| chr13:48502952 | C | CA | 187 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(184): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.927-39_927-38insT | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48502952 | |||||||
| chr13:48503467 | G | GC | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.927-554dupG | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503467 | |||||||
| chr13:48503468 | C | T | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.927-554G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503468 | |||||||
| chr13:48503470 | GT | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.927-557delA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503470 | |||||||
| chr13:48503506 | C | A | 1 | a0001c0003t0003g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.927-592G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503506 | |||||||
| chr13:48503532 | A | G | 11 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(8): Show |
12 | HG01884.hp1 HG02145.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.927-618T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503532 | |||||||
| chr13:48503544 | A | AT | 74 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(71): Show |
83 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.927-631dupA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503544 | |||||||
| chr13:48503544 | A | ATT | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.927-632_927-631dup others(2): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503544 | |||||||
| chr13:48503544 | AT | A | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.927-631delA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503544 | |||||||
| chr13:48503605 | A | G | 107 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(104): Show |
115 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.927-691T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503605 | |||||||
| chr13:48503663 | C | A | 2 | a0001c0008t0013g0058 a0001c0008t0014g0059 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.927-749G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503663 | |||||||
| chr13:48503792 | G | A | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.927-878C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48503792 | |||||||
| chr13:48504149 | G | A | 1 | a0001c0001t0001g0194 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.927-1235C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504149 | |||||||
| chr13:48504339 | T | C | 1 | a0001c0003t0003g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.927-1425A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504339 | |||||||
| chr13:48504344 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
2 | HG02896.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.927-1430G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504344 | |||||||
| chr13:48504387 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.927-1473G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504387 | |||||||
| chr13:48504419 | A | C | 11 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(8): Show |
12 | HG01884.hp1 HG02145.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.927-1505T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504419 | |||||||
| chr13:48504482 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.927-1568G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504482 | |||||||
| chr13:48504500 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.927-1586C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504500 | |||||||
| chr13:48504535 | C | T | 25 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(22): Show |
25 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.927-1621G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504535 | |||||||
| chr13:48504589 | T | G | 2 | a0001c0008t0013g0058 a0001c0008t0014g0059 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.927-1675A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504589 | |||||||
| chr13:48504599 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.927-1685C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504599 | |||||||
| chr13:48504777 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0065 |
5 | HG00738.hp1 HG01346.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.927-1863G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504777 | |||||||
| chr13:48504801 | C | T | 1 | a0001c0001t0001g0256 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.927-1887G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504801 | |||||||
| chr13:48504856 | T | C | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.927-1942A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48504856 | |||||||
| chr13:48505042 | ATTTC | A | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.927-2132_927-2129d others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505042 | |||||||
| chr13:48505046 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.927-2132G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505046 | |||||||
| chr13:48505119 | CCACTAGG others(12): Show |
C | 5 | a0001c0001t0001g0029 a0001c0001t0001g0166 a0001c0001t0001g0167 others(2): Show |
5 | HG00597.hp1 NA18979.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.927-2224_927-2206d others(21): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505119 | |||||||
| chr13:48505149 | C | A | 1 | a0001c0001t0001g0029 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.927-2235G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505149 | |||||||
| chr13:48505173 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.927-2259G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505173 | |||||||
| chr13:48505292 | C | A | 1 | a0001c0001t0001g0043 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.927-2378G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505292 | |||||||
| chr13:48505367 | T | C | 30 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(27): Show |
30 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.927-2453A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505367 | |||||||
| chr13:48505476 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.927-2562C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505476 | |||||||
| chr13:48505515 | T | C | 66 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(63): Show |
71 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.927-2601A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505515 | |||||||
| chr13:48505648 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0089 a0001c0001t0001g0094 |
5 | HG01243.hp1 HG02572.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.927-2734T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505648 | |||||||
| chr13:48505762 | G | GA | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.927-2849dupT | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505762 | |||||||
| chr13:48505771 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.927-2857T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505771 | |||||||
| chr13:48505781 | G | A | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.927-2867C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505781 | |||||||
| chr13:48505802 | C | A | 1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.927-2888G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505802 | |||||||
| chr13:48505981 | A | C | 1 | a0001c0001t0002g0072 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.927-3067T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48505981 | |||||||
| chr13:48506183 | C | T | 3 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 |
3 | HG00597.hp1 NA19058.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.927-3269G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48506183 | |||||||
| chr13:48506198 | G | C | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.927-3284C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48506198 | |||||||
| chr13:48506228 | G | A | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.927-3314C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48506228 | |||||||
| chr13:48506240 | C | T | 16 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(13): Show |
16 | HG00738.hp2 HG01168.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.927-3326G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48506240 | |||||||
| chr13:48506434 | G | A | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.927-3520C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48506434 | |||||||
| chr13:48506805 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.926+3824G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48506805 | |||||||
| chr13:48506816 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+3813G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48506816 | |||||||
| chr13:48506833 | T | C | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+3796A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48506833 | |||||||
| chr13:48506928 | C | G | 14 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(11): Show |
16 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.926+3701G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48506928 | |||||||
| chr13:48507062 | C | A | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.926+3567G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48507062 | |||||||
| chr13:48507118 | T | A | 1 | a0001c0001t0001g0154 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.926+3511A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48507118 | |||||||
| chr13:48507255 | A | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+3374T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48507255 | |||||||
| chr13:48507270 | C | T | 4 | a0001c0001t0002g0069 a0001c0001t0002g0075 a0001c0001t0009g0077 others(1): Show |
4 | HG01243.hp2 HG01496.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.926+3359G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48507270 | |||||||
| chr13:48507363 | G | A | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.926+3266C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48507363 | |||||||
| chr13:48507402 | A | G | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+3227T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48507402 | |||||||
| chr13:48507753 | A | G | 11 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(8): Show |
12 | HG01884.hp1 HG02145.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.926+2876T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48507753 | |||||||
| chr13:48507865 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.926+2764C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48507865 | |||||||
| chr13:48508007 | T | G | 7 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(4): Show |
8 | HG02572.hp1 HG02630.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.926+2622A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508007 | |||||||
| chr13:48508029 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.926+2600C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508029 | |||||||
| chr13:48508283 | A | T | 1 | a0001c0003t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.926+2346T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508283 | |||||||
| chr13:48508311 | T | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+2318A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508311 | |||||||
| chr13:48508412 | G | GTTTTTTT others(3): Show |
3 | a0001c0004t0004g0021 a0001c0004t0004g0217 a0001c0004t0004g0218 |
4 | HG02965.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.926+2207_926+2216d others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508412 | |||||||
| chr13:48508412 | G | GTTTTTTT others(4): Show |
1 | a0001c0004t0004g0216 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.926+2206_926+2216d others(13): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508412 | |||||||
| chr13:48508412 | GT | G | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+2216delA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508412 | |||||||
| chr13:48508464 | A | G | 1 | a0001c0003t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.926+2165T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508464 | |||||||
| chr13:48508647 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.926+1982C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508647 | |||||||
| chr13:48508649 | C | T | 4 | a0001c0003t0003g0004 a0001c0003t0003g0025 a0001c0003t0003g0026 others(1): Show |
6 | HG01069.hp1 HG01071.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.926+1980G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508649 | |||||||
| chr13:48508693 | T | C | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+1936A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508693 | |||||||
| chr13:48508862 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.926+1767G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48508862 | |||||||
| chr13:48509042 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.926+1587A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509042 | |||||||
| chr13:48509108 | A | T | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.926+1521T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509108 | |||||||
| chr13:48509123 | G | A | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.926+1506C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509123 | |||||||
| chr13:48509139 | C | T | 5 | a0001c0003t0003g0004 a0001c0003t0003g0025 a0001c0003t0003g0026 others(2): Show |
7 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.926+1490G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509139 | |||||||
| chr13:48509145 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.926+1484C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509145 | |||||||
| chr13:48509337 | T | C | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG01192.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.926+1292A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509337 | |||||||
| chr13:48509456 | T | A | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+1173A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509456 | |||||||
| chr13:48509560 | T | C | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+1069A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509560 | |||||||
| chr13:48509569 | G | A | 3 | a0001c0002t0001g0023 a0001c0002t0001g0235 a0001c0002t0001g0239 |
4 | HG02129.hp2 NA18956.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.926+1060C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509569 | |||||||
| chr13:48509967 | T | C | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+662A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509967 | |||||||
| chr13:48509979 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0094 |
2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.926+650T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509979 | |||||||
| chr13:48509990 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0149 a0001c0001t0001g0197 |
5 | NA18953.hp1 NA18970.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+639C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509990 | |||||||
| chr13:48509995 | T | C | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+634A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48509995 | |||||||
| chr13:48510131 | T | C | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.926+498A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48510131 | |||||||
| chr13:48510190 | C | T | 106 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(103): Show |
114 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.926+439G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48510190 | |||||||
| chr13:48510209 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.926+420A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48510209 | |||||||
| chr13:48510222 | C | G | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.926+407G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48510222 | |||||||
| chr13:48510270 | C | T | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG01192.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.926+359G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48510270 | |||||||
| chr13:48510559 | A | G | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.926+70T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48510559 | |||||||
| chr13:48510584 | A | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.926+45T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 10/14 | chr13 | 48510584 | |||||||
| chr13:48510808 | A | G | 6 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-37T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48510808 | |||||||
| chr13:48510883 | G | A | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-112C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48510883 | |||||||
| chr13:48511020 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.784-249C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48511020 | |||||||
| chr13:48511092 | A | G | 6 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-321T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48511092 | |||||||
| chr13:48511147 | T | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-376A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48511147 | |||||||
| chr13:48511279 | G | A | 60 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(57): Show |
63 | HG00099.hp2 HG00558.hp2 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.783+491C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48511279 | |||||||
| chr13:48511307 | A | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG04115.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.783+463T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48511307 | |||||||
| chr13:48511385 | AT | A | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+384delA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48511385 | |||||||
| chr13:48511412 | T | TTATATG | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+352_783+357dup others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48511412 | |||||||
| chr13:48511651 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.783+119A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48511651 | |||||||
| chr13:48511713 | A | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.783+57T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 9/14 | chr13 | 48511713 | |||||||
| chr13:48511880 | G | C | 1 | a0001c0001t0001g0134 | 1 | NA19004.hp2 | splice_region_variant&intron_variant | LOW | c.676-3C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 8/14 | chr13 | 48511880 | |||||||
| chr13:48511981 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+35G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 8/14 | chr13 | 48511981 | |||||||
| chr13:48512206 | G | C | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-32C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 7/14 | chr13 | 48512206 | |||||||
| chr13:48512462 | G | A | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+267C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 7/14 | chr13 | 48512462 | |||||||
| chr13:48512462 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.516+267C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 7/14 | chr13 | 48512462 | |||||||
| chr13:48512463 | G | A | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+266C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 7/14 | chr13 | 48512463 | |||||||
| chr13:48512505 | G | A | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+224C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 7/14 | chr13 | 48512505 | |||||||
| chr13:48512631 | G | A | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.516+98C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 7/14 | chr13 | 48512631 | |||||||
| chr13:48512932 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.350-37G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48512932 | |||||||
| chr13:48512949 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.350-54C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48512949 | |||||||
| chr13:48513145 | A | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-250T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48513145 | |||||||
| chr13:48513173 | T | C | 1 | a0001c0001t0002g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.350-278A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48513173 | |||||||
| chr13:48513223 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.350-328G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48513223 | |||||||
| chr13:48513402 | A | G | 26 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
26 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.350-507T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48513402 | |||||||
| chr13:48513408 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-513G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48513408 | |||||||
| chr13:48513735 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-840G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48513735 | |||||||
| chr13:48513780 | T | C | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.350-885A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48513780 | |||||||
| chr13:48513875 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.350-980G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48513875 | |||||||
| chr13:48514079 | G | C | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.349+1126C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514079 | |||||||
| chr13:48514153 | T | C | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+1052A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514153 | |||||||
| chr13:48514191 | G | A | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+1014C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514191 | |||||||
| chr13:48514206 | A | G | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.349+999T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514206 | |||||||
| chr13:48514287 | A | C | 38 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(35): Show |
38 | HG00558.hp2 HG00738.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.349+918T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514287 | |||||||
| chr13:48514288 | T | C | 21 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(18): Show |
24 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.349+917A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514288 | |||||||
| chr13:48514318 | C | G | 180 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(177): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.349+887G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514318 | |||||||
| chr13:48514462 | C | A | 30 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(27): Show |
30 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.349+743G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514462 | |||||||
| chr13:48514510 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0065 |
5 | HG00738.hp1 HG01346.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+695C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514510 | |||||||
| chr13:48514567 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.349+638C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514567 | |||||||
| chr13:48514669 | G | A | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+536C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514669 | |||||||
| chr13:48514850 | T | TA | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+354dupT | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514850 | |||||||
| chr13:48514938 | G | A | 10 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(7): Show |
12 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+267C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514938 | |||||||
| chr13:48514972 | C | T | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+233G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514972 | |||||||
| chr13:48514974 | T | C | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+231A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48514974 | |||||||
| chr13:48515013 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.349+192G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48515013 | |||||||
| chr13:48515024 | A | G | 1 | a0002c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.349+181T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48515024 | |||||||
| chr13:48515053 | C | T | 49 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(46): Show |
53 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.349+152G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48515053 | |||||||
| chr13:48515087 | T | C | 74 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(71): Show |
83 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.349+118A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48515087 | |||||||
| chr13:48515105 | C | A | 1 | a0001c0002t0001g0236 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.349+100G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 6/14 | chr13 | 48515105 | |||||||
| chr13:48515484 | CT | C | 94 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(91): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.198+101delA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 5/14 | chr13 | 48515484 | |||||||
| chr13:48515498 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.198+88G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 5/14 | chr13 | 48515498 | |||||||
| chr13:48515905 | T | C | 1 | a0001c0001t0001g0249 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.43-164A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48515905 | |||||||
| chr13:48515910 | C | T | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-169G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48515910 | |||||||
| chr13:48515931 | C | T | 9 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0002g0057 others(6): Show |
9 | HG01192.hp2 HG01981.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.43-190G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48515931 | |||||||
| chr13:48515939 | C | T | 1 | a0001c0001t0005g0096 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.43-198G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48515939 | |||||||
| chr13:48515958 | C | T | 6 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-217G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48515958 | |||||||
| chr13:48516096 | CAGAG | C | 179 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(176): Show |
196 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.43-359_43-356delCT others(2): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516096 | |||||||
| chr13:48516200 | C | T | 1 | a0001c0003t0003g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.43-459G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516200 | |||||||
| chr13:48516216 | G | A | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-475C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516216 | |||||||
| chr13:48516264 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.43-523T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516264 | |||||||
| chr13:48516497 | T | C | 1 | a0001c0001t0002g0078 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43-756A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516497 | |||||||
| chr13:48516516 | T | C | 15 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(12): Show |
16 | HG01243.hp2 HG01496.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.43-775A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516516 | |||||||
| chr13:48516550 | T | A | 3 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 |
3 | HG02630.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.43-809A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516550 | |||||||
| chr13:48516770 | G | A | 17 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(14): Show |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.43-1029C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516770 | |||||||
| chr13:48516780 | T | C | 17 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(14): Show |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.43-1039A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516780 | |||||||
| chr13:48516789 | T | C | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-1048A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516789 | |||||||
| chr13:48516894 | T | G | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-1153A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48516894 | |||||||
| chr13:48517011 | C | T | 21 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(18): Show |
24 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.43-1270G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517011 | |||||||
| chr13:48517152 | C | G | 2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.43-1411G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517152 | |||||||
| chr13:48517155 | C | T | 1 | a0001c0003t0003g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.43-1414G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517155 | |||||||
| chr13:48517248 | T | C | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG01192.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-1507A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517248 | |||||||
| chr13:48517312 | G | A | 2 | a0001c0002t0001g0226 a0001c0002t0001g0227 |
2 | NA19060.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.43-1571C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517312 | |||||||
| chr13:48517394 | A | G | 5 | a0001c0003t0003g0004 a0001c0003t0003g0025 a0001c0003t0003g0026 others(2): Show |
7 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-1653T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517394 | |||||||
| chr13:48517399 | G | A | 10 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(7): Show |
12 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.43-1658C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517399 | |||||||
| chr13:48517503 | T | C | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-1762A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517503 | |||||||
| chr13:48517696 | T | C | 13 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(10): Show |
14 | HG01243.hp2 HG01496.hp2 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.43-1955A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517696 | |||||||
| chr13:48517728 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.43-1987T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517728 | |||||||
| chr13:48517783 | C | A | 16 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0043 others(13): Show |
16 | HG00738.hp2 HG01168.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.43-2042G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517783 | |||||||
| chr13:48517806 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.43-2065G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517806 | |||||||
| chr13:48517929 | C | G | 180 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(177): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.43-2188G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517929 | |||||||
| chr13:48517978 | C | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(14): Show |
17 | HG00738.hp2 HG01168.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.43-2237G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517978 | |||||||
| chr13:48517982 | A | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0010 others(199): Show |
222 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.43-2241T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48517982 | |||||||
| chr13:48518173 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.43-2432C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518173 | |||||||
| chr13:48518209 | G | A | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2468C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518209 | |||||||
| chr13:48518349 | A | G | 17 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(14): Show |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.43-2608T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518349 | |||||||
| chr13:48518404 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.43-2663G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518404 | |||||||
| chr13:48518458 | C | CA | 22 | a0001c0001t0001g0002 a0001c0001t0001g0080 a0001c0001t0001g0152 others(19): Show |
27 | HG00323.hp2 HG02129.hp2 HG02148.hp1 others(24): Show |
intron_variant | MODIFIER | c.43-2718dupT | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518458 | |||||||
| chr13:48518458 | CA | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0070 a0001c0001t0001g0071 others(15): Show |
20 | HG00597.hp2 HG00642.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.43-2718delT | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518458 | |||||||
| chr13:48518458 | CAA | C | 8 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0084 others(5): Show |
9 | HG00099.hp1 HG01993.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.43-2719_43-2718del others(2): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518458 | |||||||
| chr13:48518471 | AAAT | A | 6 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0003t0003g0025 others(3): Show |
6 | HG02818.hp1 HG03098.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-2733_43-2731del others(3): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518471 | |||||||
| chr13:48518472 | A | AAAAAAAA others(4): Show |
2 | a0001c0004t0004g0217 a0001c0004t0004g0218 |
2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.43-2732_43-2731ins others(11): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518472 | A | AAAAAAAA others(5): Show |
2 | a0001c0004t0004g0021 a0001c0004t0004g0216 |
3 | HG01884.hp1 HG02965.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.43-2732_43-2731ins others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518472 | A | AAAATATA others(3): Show |
2 | a0001c0001t0001g0055 a0001c0001t0008g0031 |
2 | HG01361.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.43-2732_43-2731ins others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518472 | A | AAATAT | 6 | a0001c0001t0001g0037 a0001c0001t0001g0040 a0001c0001t0001g0041 others(3): Show |
6 | HG00738.hp2 HG01168.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.43-2732_43-2731ins others(5): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518472 | A | AAT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0042 a0001c0001t0001g0190 others(8): Show |
11 | HG02818.hp2 HG02886.hp2 HG03688.hp2 others(8): Show |
intron_variant | MODIFIER | c.43-2733_43-2732dup others(2): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518472 | A | AATAT | 9 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0044 others(6): Show |
10 | HG00609.hp1 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.43-2735_43-2732dup others(4): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518472 | A | AT | 3 | a0001c0001t0001g0007 a0001c0001t0006g0073 a0001c0001t0006g0074 |
3 | HG02723.hp1 NA19090.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.43-2732_43-2731ins others(1): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518472 | A | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0020 others(14): Show |
19 | HG00673.hp2 HG00741.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.43-2731T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518472 | AAT | A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0013 others(53): Show |
64 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.43-2733_43-2732del others(2): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518472 | AATAT | A | 7 | a0001c0001t0001g0105 a0001c0001t0001g0261 a0001c0001t0001g0262 others(4): Show |
8 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-2735_43-2732del others(4): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518472 | |||||||
| chr13:48518473 | AT | A | 9 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
9 | HG00597.hp1 HG01261.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.43-2733delA | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518473 | |||||||
| chr13:48518473 | ATAT | A | 3 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG02145.hp1 HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.43-2735_43-2733del others(3): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518473 | |||||||
| chr13:48518474 | T | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0065 a0001c0001t0001g0135 others(12): Show |
16 | HG00673.hp1 HG00738.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.43-2733A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518474 | |||||||
| chr13:48518476 | T | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0125 a0001c0001t0001g0134 |
3 | HG02572.hp2 NA18747.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.43-2735A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518476 | |||||||
| chr13:48518480 | T | A | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-2739A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518480 | |||||||
| chr13:48518536 | C | T | 38 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(35): Show |
38 | HG00558.hp2 HG00738.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.43-2795G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518536 | |||||||
| chr13:48518698 | G | T | 25 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(22): Show |
25 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.43-2957C>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518698 | |||||||
| chr13:48518972 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0015g0201 |
2 | NA19010.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.42+2926A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48518972 | |||||||
| chr13:48519082 | A | C | 17 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(14): Show |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.42+2816T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48519082 | |||||||
| chr13:48519097 | A | G | 2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.42+2801T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48519097 | |||||||
| chr13:48519289 | C | G | 17 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(14): Show |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.42+2609G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48519289 | |||||||
| chr13:48519328 | C | T | 8 | a0001c0001t0001g0126 a0001c0001t0002g0057 a0001c0001t0002g0060 others(5): Show |
8 | HG02074.hp1 HG02145.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+2570G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48519328 | |||||||
| chr13:48519447 | C | T | 30 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(27): Show |
30 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.42+2451G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48519447 | |||||||
| chr13:48519549 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.42+2349C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48519549 | |||||||
| chr13:48519675 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.42+2223T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48519675 | |||||||
| chr13:48519825 | T | C | 25 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0219 others(22): Show |
27 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.42+2073A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48519825 | |||||||
| chr13:48520238 | A | G | 17 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(14): Show |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.42+1660T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520238 | |||||||
| chr13:48520303 | T | C | 10 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(7): Show |
12 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+1595A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520303 | |||||||
| chr13:48520462 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.42+1436G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520462 | |||||||
| chr13:48520554 | C | T | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG01192.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+1344G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520554 | |||||||
| chr13:48520639 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.42+1259G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520639 | |||||||
| chr13:48520681 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.42+1217C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520681 | |||||||
| chr13:48520701 | T | C | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.42+1197A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520701 | |||||||
| chr13:48520734 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.42+1164T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520734 | |||||||
| chr13:48520790 | A | G | 74 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(71): Show |
83 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.42+1108T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520790 | |||||||
| chr13:48520821 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.42+1077G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520821 | |||||||
| chr13:48520821 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | HG00323.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.42+1077G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520821 | |||||||
| chr13:48520837 | C | CAAAAAAG others(319): Show |
1 | a0001c0001t0007g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.42+1060_42+1061ins others(326): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520837 | |||||||
| chr13:48520837 | C | CAAAAAAG others(340): Show |
1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.42+1060_42+1061ins others(347): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520837 | |||||||
| chr13:48520906 | ATATATTC others(2): Show |
A | 17 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(14): Show |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.42+983_42+991delAT others(7): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520906 | |||||||
| chr13:48520976 | C | T | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+922G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48520976 | |||||||
| chr13:48521060 | A | T | 17 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(14): Show |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.42+838T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48521060 | |||||||
| chr13:48521494 | A | G | 1 | a0001c0001t0007g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.42+404T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48521494 | |||||||
| chr13:48521646 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.42+252C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48521646 | |||||||
| chr13:48521656 | TC | T | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+241delG | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48521656 | |||||||
| chr13:48521790 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.42+108C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48521790 | |||||||
| chr13:48521836 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.42+62A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48521836 | |||||||
| chr13:48521880 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.42+18C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48521880 | |||||||
| chr13:48521886 | T | C | 25 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0219 others(22): Show |
27 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.42+12A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48521886 | |||||||
| chr13:48521887 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.42+11A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 4/14 | chr13 | 48521887 | |||||||
| chr13:48522000 | T | C | 2 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
2 | HG04115.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-23-38A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 3/14 | chr13 | 48522000 | |||||||
| chr13:48522016 | G | C | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-23-54C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 3/14 | chr13 | 48522016 | |||||||
| chr13:48522106 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-144G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 3/14 | chr13 | 48522106 | |||||||
| chr13:48522427 | A | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-119-24T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48522427 | |||||||
| chr13:48522460 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-119-57C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48522460 | |||||||
| chr13:48522818 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-119-415A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48522818 | |||||||
| chr13:48522978 | C | T | 27 | a0001c0001t0001g0149 a0001c0002t0001g0022 a0001c0002t0001g0023 others(24): Show |
29 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(26): Show |
intron_variant | MODIFIER | c.-119-575G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48522978 | |||||||
| chr13:48523062 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-119-659G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523062 | |||||||
| chr13:48523109 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-119-706G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523109 | |||||||
| chr13:48523451 | A | G | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-119-1048T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523451 | |||||||
| chr13:48523582 | T | C | 1 | a0001c0001t0009g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-120+1077A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523582 | |||||||
| chr13:48523617 | A | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-120+1042T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523617 | |||||||
| chr13:48523651 | G | C | 25 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0219 others(22): Show |
27 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.-120+1008C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523651 | |||||||
| chr13:48523659 | G | A | 5 | a0001c0003t0003g0004 a0001c0003t0003g0025 a0001c0003t0003g0026 others(2): Show |
7 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-120+1000C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523659 | |||||||
| chr13:48523751 | C | G | 106 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(103): Show |
114 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.-120+908G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523751 | |||||||
| chr13:48523777 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-120+882G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523777 | |||||||
| chr13:48523915 | T | C | 1 | a0001c0001t0007g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-120+744A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523915 | |||||||
| chr13:48523918 | G | A | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-120+741C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523918 | |||||||
| chr13:48523968 | T | C | 5 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(2): Show |
5 | HG02145.hp1 HG02818.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-120+691A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48523968 | |||||||
| chr13:48524077 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-120+582C>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48524077 | |||||||
| chr13:48524111 | GCTTT | G | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-120+544_-120+547d others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48524111 | |||||||
| chr13:48524200 | G | A | 47 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0256 others(44): Show |
50 | HG00323.hp2 HG00558.hp2 HG01243.hp2 others(47): Show |
intron_variant | MODIFIER | c.-120+459C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48524200 | |||||||
| chr13:48524260 | T | C | 5 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG02257.hp2 HG02622.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-120+399A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48524260 | |||||||
| chr13:48524431 | G | A | 2 | a0001c0001t0002g0069 a0001c0011t0002g0246 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-120+228C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48524431 | |||||||
| chr13:48524442 | G | C | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-120+217C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48524442 | |||||||
| chr13:48524494 | T | C | 25 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0219 others(22): Show |
27 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.-120+165A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48524494 | |||||||
| chr13:48524506 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-120+153G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 2/14 | chr13 | 48524506 | |||||||
| chr13:48524935 | A | G | 10 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(7): Show |
12 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-218-178T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48524935 | |||||||
| chr13:48525092 | T | TA | 6 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-218-336dupT | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525092 | |||||||
| chr13:48525264 | G | A | 17 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(14): Show |
19 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.-218-507C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525264 | |||||||
| chr13:48525359 | A | G | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-602T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525359 | |||||||
| chr13:48525372 | TGATATAT others(3): Show |
T | 1 | a0001c0001t0002g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-218-625_-218-616d others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525372 | |||||||
| chr13:48525372 | TGATATAT others(5): Show |
T | 1 | a0001c0001t0002g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-218-627_-218-616d others(14): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525372 | |||||||
| chr13:48525372 | TGATATAT others(7): Show |
T | 1 | a0001c0001t0002g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-218-629_-218-616d others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525372 | |||||||
| chr13:48525373 | G | GATATATA others(3): Show |
1 | a0001c0005t0002g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-218-626_-218-617d others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GAT | G | 36 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(33): Show |
40 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.-218-618_-218-617d others(4): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATAT | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(55): Show |
63 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-218-620_-218-617d others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATATAT | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(35): Show |
40 | HG00741.hp1 HG01109.hp1 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.-218-622_-218-617d others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATATATA others(1): Show |
G | 42 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0013 others(39): Show |
44 | HG00323.hp2 HG00597.hp1 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-218-624_-218-617d others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATATATA others(3): Show |
G | 32 | a0001c0001t0001g0024 a0001c0001t0001g0034 a0001c0001t0001g0037 others(29): Show |
32 | HG00099.hp1 HG00558.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.-218-626_-218-617d others(12): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATATATA others(5): Show |
G | 23 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0036 others(20): Show |
26 | HG00673.hp2 HG01071.hp1 HG01257.hp2 others(23): Show |
intron_variant | MODIFIER | c.-218-628_-218-617d others(14): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATATATA others(7): Show |
G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0080 others(13): Show |
21 | HG01071.hp2 HG01074.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-218-630_-218-617d others(16): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATATATA others(9): Show |
G | 5 | a0001c0001t0001g0256 a0001c0001t0001g0265 a0001c0003t0003g0004 others(2): Show |
6 | HG01069.hp1 HG01884.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-632_-218-617d others(18): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATATATA others(11): Show |
G | 6 | a0001c0001t0001g0252 a0001c0001t0001g0261 a0001c0001t0001g0262 others(3): Show |
6 | HG00099.hp2 HG02145.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-634_-218-617d others(20): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATATATA others(13): Show |
G | 3 | a0001c0001t0001g0253 a0001c0001t0002g0056 a0001c0003t0001g0064 |
3 | HG02922.hp2 HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-218-636_-218-617d others(22): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525373 | GATATATA others(15): Show |
G | 5 | a0001c0001t0009g0077 a0002c0006t0001g0275 a0002c0006t0001g0276 others(2): Show |
5 | HG01109.hp2 HG01975.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-638_-218-617d others(24): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525373 | |||||||
| chr13:48525383 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-218-626A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525383 | |||||||
| chr13:48525579 | C | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG00673.hp1 NA18953.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-822G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525579 | |||||||
| chr13:48525646 | A | G | 1 | a0001c0002t0001g0240 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-218-889T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525646 | |||||||
| chr13:48525970 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-218-1213C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48525970 | |||||||
| chr13:48526175 | T | C | 10 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(7): Show |
12 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-218-1418A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526175 | |||||||
| chr13:48526190 | C | T | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-1433G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526190 | |||||||
| chr13:48526428 | T | C | 180 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0012 others(177): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.-218-1671A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526428 | |||||||
| chr13:48526494 | C | A | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-1737G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526494 | |||||||
| chr13:48526589 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
3 | HG02257.hp2 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-218-1832G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526589 | |||||||
| chr13:48526643 | G | A | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-1886C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526643 | |||||||
| chr13:48526727 | C | CCAACA | 40 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(37): Show |
43 | HG00323.hp2 HG01243.hp2 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.-218-1975_-218-197 others(9): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526727 | |||||||
| chr13:48526765 | A | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0042 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-218-2008T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526765 | |||||||
| chr13:48526939 | T | G | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-218-2182A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526939 | |||||||
| chr13:48526996 | T | C | 1 | a0001c0002t0001g0237 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-218-2239A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526996 | |||||||
| chr13:48526999 | C | G | 2 | a0001c0001t0001g0142 a0001c0001t0010g0141 |
2 | NA18985.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-218-2242G>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48526999 | |||||||
| chr13:48527307 | A | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG01109.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.-218-2550T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527307 | |||||||
| chr13:48527318 | C | CTCATATA others(27): Show |
1 | a0001c0001t0002g0060 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-218-2562_-218-256 others(38): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527318 | |||||||
| chr13:48527320 | C | CAT | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00738.hp2 HG01168.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.-218-2565_-218-256 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527320 | |||||||
| chr13:48527320 | C | CATAT | 8 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-218-2567_-218-256 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527320 | |||||||
| chr13:48527320 | C | CATATAT | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0008g0031 |
3 | HG01884.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-218-2569_-218-256 others(10): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527320 | |||||||
| chr13:48527320 | C | CATATATA others(8): Show |
1 | a0001c0001t0002g0244 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-218-2564_-218-256 others(19): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527320 | |||||||
| chr13:48527320 | C | CATATATA others(63): Show |
1 | a0001c0001t0002g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-218-2564_-218-256 others(74): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527320 | |||||||
| chr13:48527322 | T | TATATATA others(4): Show |
7 | a0001c0003t0003g0004 a0001c0003t0003g0025 a0001c0003t0003g0026 others(4): Show |
9 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-218-2566_-218-256 others(15): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527322 | |||||||
| chr13:48527324 | T | TATATATA others(4): Show |
1 | a0001c0005t0002g0005 | 3 | HG03453.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-218-2568_-218-256 others(15): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527324 | |||||||
| chr13:48527324 | T | TATATATA others(40): Show |
2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02717.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-218-2568_-218-256 others(51): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527324 | |||||||
| chr13:48527326 | T | TATATATA others(201): Show |
1 | a0001c0001t0007g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-218-2570_-218-256 others(212): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527326 | |||||||
| chr13:48527326 | T | TATATATA others(807): Show |
1 | a0001c0005t0002g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-218-2570_-218-256 others(818): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527326 | |||||||
| chr13:48527329 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0134 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-218-2573_-218-257 others(38): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527329 | |||||||
| chr13:48527329 | A | ATATATAT others(59): Show |
1 | a0001c0001t0001g0079 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-218-2573_-218-257 others(70): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527329 | |||||||
| chr13:48527329 | A | ATATATAT others(25): Show |
6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG00642.hp2 HG01928.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-2604_-218-257 others(36): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527329 | |||||||
| chr13:48527336 | T | TATGA | 3 | a0001c0004t0004g0021 a0001c0004t0004g0217 a0001c0004t0004g0218 |
4 | HG02965.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-2580_-218-257 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527336 | |||||||
| chr13:48527337 | G | A | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0007t0001g0254 others(1): Show |
4 | HG00558.hp2 HG03098.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-2580C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527337 | |||||||
| chr13:48527337 | G | C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
3 | NA19006.hp1 NA19066.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-218-2580C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527337 | |||||||
| chr13:48527337 | G | GAT | 3 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0245 |
3 | HG01192.hp1 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-218-2582_-218-258 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527337 | |||||||
| chr13:48527337 | G | GATAT | 13 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(10): Show |
14 | HG01496.hp2 HG01975.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.-218-2584_-218-258 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527337 | |||||||
| chr13:48527337 | G | T | 5 | a0001c0001t0001g0269 a0001c0004t0004g0021 a0001c0004t0004g0216 others(2): Show |
6 | HG01884.hp1 HG02155.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-2580C>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527337 | |||||||
| chr13:48527338 | A | T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0007t0001g0254 others(1): Show |
4 | HG00558.hp2 HG03098.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-2581T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527338 | |||||||
| chr13:48527339 | T | G | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0007t0001g0254 others(1): Show |
4 | HG00558.hp2 HG03098.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-2582A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527339 | |||||||
| chr13:48527350 | A | G | 1 | a0001c0005t0002g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-218-2593T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527350 | |||||||
| chr13:48527351 | T | A | 1 | a0001c0005t0002g0066 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-218-2594A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527351 | |||||||
| chr13:48527351 | T | TATCATAT others(26): Show |
2 | a0001c0001t0001g0258 a0001c0001t0001g0259 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-218-2595_-218-259 others(37): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527351 | |||||||
| chr13:48527351 | T | TATCATAT others(31): Show |
1 | a0001c0007t0001g0260 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-218-2595_-218-259 others(42): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527351 | |||||||
| chr13:48527351 | TG | T | 8 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0268 others(5): Show |
8 | HG00099.hp2 HG00558.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-218-2595delC | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527351 | |||||||
| chr13:48527352 | G | C | 61 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(58): Show |
64 | HG00323.hp2 HG00738.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.-218-2595C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527352 | |||||||
| chr13:48527352 | G | T | 4 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0005t0002g0066 others(1): Show |
4 | HG02109.hp1 HG02559.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-2595C>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527352 | |||||||
| chr13:48527354 | T | TATATATA others(60): Show |
1 | a0001c0002t0001g0238 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-218-2598_-218-259 others(71): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527354 | |||||||
| chr13:48527354 | T | TATATATA others(32): Show |
1 | a0001c0002t0001g0219 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-218-2598_-218-259 others(43): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527354 | |||||||
| chr13:48527354 | T | TATATATA others(30): Show |
19 | a0001c0002t0001g0023 a0001c0002t0001g0220 a0001c0002t0001g0222 others(16): Show |
20 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.-218-2598_-218-259 others(41): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527354 | |||||||
| chr13:48527354 | T | TATATATA others(58): Show |
1 | a0001c0002t0001g0022 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-218-2598_-218-259 others(69): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527354 | |||||||
| chr13:48527356 | T | TATATATA others(17): Show |
6 | a0001c0001t0002g0056 a0001c0001t0002g0067 a0001c0001t0002g0068 others(3): Show |
6 | HG01192.hp1 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-2600_-218-259 others(28): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(62): Show |
1 | a0001c0001t0002g0072 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(73): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(86): Show |
2 | a0001c0001t0001g0070 a0001c0001t0001g0071 |
2 | HG02630.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-218-2600_-218-259 others(97): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(60): Show |
1 | a0001c0001t0002g0076 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(71): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(4): Show |
2 | a0001c0001t0002g0057 a0001c0001t0002g0060 |
2 | HG02818.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-218-2600_-218-259 others(15): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(94): Show |
1 | a0001c0001t0006g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(105): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(60): Show |
1 | a0001c0001t0006g0073 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(71): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(58): Show |
2 | a0001c0008t0013g0058 a0001c0008t0014g0059 |
2 | HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-218-2600_-218-259 others(69): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(56): Show |
1 | a0001c0001t0009g0077 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(67): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(2): Show |
10 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(7): Show |
11 | HG01884.hp1 HG02055.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-218-2600_-218-259 others(13): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(28): Show |
2 | a0001c0002t0001g0240 a0001c0002t0001g0241 |
2 | NA18939.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-218-2600_-218-259 others(39): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(842): Show |
1 | a0001c0005t0002g0005 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(853): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(803): Show |
1 | a0001c0005t0002g0005 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(814): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(788): Show |
1 | a0001c0005t0002g0005 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(799): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATA others(87): Show |
1 | a0002c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(98): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATG others(154): Show |
1 | a0001c0003t0003g0026 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(165): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATG others(152): Show |
1 | a0001c0003t0003g0025 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(163): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATATG others(89): Show |
3 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 |
3 | HG02630.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-218-2600_-218-259 others(100): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TATATGAT others(13): Show |
3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 |
3 | HG02257.hp2 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-218-2600_-218-259 others(24): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TC | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00099.hp2 HG00558.hp2 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-2600_-218-259 others(5): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527356 | T | TCATATAT others(43): Show |
1 | a0001c0001t0002g0061 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-218-2600_-218-259 others(54): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527356 | |||||||
| chr13:48527357 | ATATT | A | 22 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0036 others(19): Show |
22 | HG00738.hp2 HG01168.hp1 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.-218-2604_-218-260 others(8): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527357 | |||||||
| chr13:48527358 | T | TATATATA others(60): Show |
1 | a0001c0001t0002g0011 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-218-2602_-218-260 others(71): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527358 | |||||||
| chr13:48527358 | T | TATATATA others(58): Show |
1 | a0001c0001t0002g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-218-2602_-218-260 others(69): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527358 | |||||||
| chr13:48527358 | T | TATATATA others(58): Show |
1 | a0001c0001t0002g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-218-2602_-218-260 others(69): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527358 | |||||||
| chr13:48527358 | T | TGATATAT others(65): Show |
1 | a0001c0001t0002g0069 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-218-2602_-218-260 others(76): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527358 | |||||||
| chr13:48527358 | T | TGATATAT others(63): Show |
1 | a0001c0011t0002g0246 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-218-2602_-218-260 others(74): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527358 | |||||||
| chr13:48527359 | ATT | A | 2 | a0001c0001t0007g0267 a0001c0003t0003g0004 |
4 | HG01069.hp1 HG01071.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-2604_-218-260 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527359 | |||||||
| chr13:48527361 | T | A | 80 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(77): Show |
86 | HG00099.hp2 HG00323.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.-218-2604A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527361 | |||||||
| chr13:48527369 | G | A | 2 | a0001c0002t0001g0240 a0001c0002t0001g0241 |
2 | NA18939.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-218-2612C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527369 | G | C | 22 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0219 others(19): Show |
24 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(21): Show |
intron_variant | MODIFIER | c.-218-2612C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527369 | G | GAT | 5 | a0001c0001t0001g0016 a0001c0001t0001g0079 a0001c0001t0002g0242 others(2): Show |
6 | HG02055.hp1 HG02074.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-218-2614_-218-261 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527369 | G | GATATATA others(62): Show |
1 | a0001c0002t0001g0239 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-218-2613_-218-261 others(73): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527369 | G | GATATATA others(27): Show |
40 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0015 others(37): Show |
43 | HG00408.hp1 HG00438.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.-218-2613_-218-261 others(38): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527369 | G | GATATATA others(59): Show |
9 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0088 others(6): Show |
11 | HG00099.hp1 HG01243.hp1 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.-218-2613_-218-261 others(70): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527369 | G | GATATATA others(91): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0083 a0001c0001t0001g0084 others(2): Show |
6 | HG01256.hp2 HG01258.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-218-2613_-218-261 others(102): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527369 | G | GATATATA others(89): Show |
1 | a0001c0001t0001g0130 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-218-2613_-218-261 others(100): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527369 | G | GATATATA others(25): Show |
12 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0030 others(9): Show |
15 | HG01074.hp1 HG02109.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-218-2613_-218-261 others(36): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527369 | G | GATATATA others(23): Show |
1 | a0001c0001t0001g0250 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-218-2613_-218-261 others(34): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527369 | |||||||
| chr13:48527370 | A | T | 2 | a0001c0002t0001g0240 a0001c0002t0001g0241 |
2 | NA18939.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-218-2613T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527370 | |||||||
| chr13:48527371 | T | C | 2 | a0001c0002t0001g0240 a0001c0002t0001g0241 |
2 | NA18939.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-218-2614A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527371 | |||||||
| chr13:48527371 | T | TATATATA others(82): Show |
1 | a0001c0001t0001g0268 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-218-2615_-218-261 others(93): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527371 | |||||||
| chr13:48527371 | T | TATATATA others(49): Show |
1 | a0001c0001t0002g0078 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-218-2615_-218-261 others(60): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527371 | |||||||
| chr13:48527371 | T | TATATATA others(143): Show |
1 | a0001c0003t0003g0028 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-218-2615_-218-261 others(154): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527371 | |||||||
| chr13:48527371 | T | TATATATA others(180): Show |
1 | a0001c0003t0003g0027 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-218-2615_-218-261 others(191): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527371 | |||||||
| chr13:48527371 | T | TATATATA others(4): Show |
1 | a0001c0001t0007g0267 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-218-2625_-218-261 others(15): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527371 | |||||||
| chr13:48527371 | T | TATATATA others(137): Show |
1 | a0001c0003t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-218-2615_-218-261 others(148): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527371 | |||||||
| chr13:48527371 | T | TATATATA others(169): Show |
1 | a0001c0003t0003g0004 | 3 | HG01069.hp1 HG01071.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-218-2615_-218-261 others(180): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527371 | |||||||
| chr13:48527371 | T | TATC | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-218-2615_-218-261 others(7): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527371 | |||||||
| chr13:48527380 | A | G | 1 | a0001c0001t0001g0029 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-218-2623T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527380 | |||||||
| chr13:48527381 | T | A | 1 | a0001c0001t0001g0029 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-218-2624A>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527381 | |||||||
| chr13:48527426 | TCTC | T | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-2672_-218-267 others(7): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527426 | |||||||
| chr13:48527548 | G | A | 1 | a0002c0006t0001g0278 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-218-2791C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527548 | |||||||
| chr13:48527688 | A | G | 4 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0008t0013g0058 others(1): Show |
4 | HG02818.hp1 HG03225.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-218-2931T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527688 | |||||||
| chr13:48527947 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-218-3190A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48527947 | |||||||
| chr13:48528131 | G | C | 10 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(7): Show |
12 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-218-3374C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48528131 | |||||||
| chr13:48528376 | C | T | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-218-3619G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48528376 | |||||||
| chr13:48528402 | T | G | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-218-3645A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48528402 | |||||||
| chr13:48528448 | C | A | 8 | a0001c0001t0001g0020 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
9 | HG00741.hp1 HG01192.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-218-3691G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48528448 | |||||||
| chr13:48528575 | A | G | 7 | a0001c0001t0002g0057 a0001c0001t0002g0060 a0001c0001t0002g0061 others(4): Show |
7 | HG02145.hp1 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-3818T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48528575 | |||||||
| chr13:48528798 | A | G | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-218-4041T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48528798 | |||||||
| chr13:48529019 | C | T | 2 | a0001c0001t0002g0067 a0001c0001t0002g0068 |
2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-219+4009G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529019 | |||||||
| chr13:48529100 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-219+3928C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529100 | |||||||
| chr13:48529270 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0080 |
5 | HG02559.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-219+3758G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529270 | |||||||
| chr13:48529391 | A | C | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-219+3637T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529391 | |||||||
| chr13:48529516 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | NA18973.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-219+3512T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529516 | |||||||
| chr13:48529557 | G | A | 10 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(7): Show |
12 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-219+3471C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529557 | |||||||
| chr13:48529800 | CTT | C | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-219+3226_-219+322 others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529800 | |||||||
| chr13:48529938 | T | C | 6 | a0001c0003t0001g0064 a0001c0003t0003g0004 a0001c0003t0003g0025 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-219+3090A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529938 | |||||||
| chr13:48529950 | G | A | 40 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(37): Show |
43 | HG00323.hp2 HG01243.hp2 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.-219+3078C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529950 | |||||||
| chr13:48529978 | C | T | 25 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(22): Show |
25 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.-219+3050G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48529978 | |||||||
| chr13:48530052 | G | A | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-219+2976C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530052 | |||||||
| chr13:48530068 | G | C | 1 | a0001c0001t0001g0213 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-219+2960C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530068 | |||||||
| chr13:48530108 | C | T | 4 | a0001c0004t0004g0021 a0001c0004t0004g0216 a0001c0004t0004g0217 others(1): Show |
5 | HG01884.hp1 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.-219+2920G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530108 | |||||||
| chr13:48530192 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-219+2836C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530192 | |||||||
| chr13:48530236 | A | G | 5 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 others(2): Show |
5 | HG02145.hp2 HG02922.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.-219+2792T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530236 | |||||||
| chr13:48530279 | G | A | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-219+2749C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530279 | |||||||
| chr13:48530333 | A | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0080 |
5 | HG02559.hp2 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-219+2695T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530333 | |||||||
| chr13:48530427 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-219+2601G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530427 | |||||||
| chr13:48530685 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-219+2343A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530685 | |||||||
| chr13:48530733 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-219+2295G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530733 | |||||||
| chr13:48530936 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-219+2092C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48530936 | |||||||
| chr13:48531006 | C | T | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-219+2022G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531006 | |||||||
| chr13:48531220 | T | C | 1 | a0001c0001t0001g0215 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-219+1808A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531220 | |||||||
| chr13:48531412 | G | A | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-219+1616C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531412 | |||||||
| chr13:48531443 | C | T | 40 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0002g0011 others(37): Show |
43 | HG00323.hp2 HG01243.hp2 HG01496.hp2 others(40): Show |
intron_variant | MODIFIER | c.-219+1585G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531443 | |||||||
| chr13:48531468 | C | T | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG01192.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-219+1560G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531468 | |||||||
| chr13:48531503 | A | G | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG01192.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-219+1525T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531503 | |||||||
| chr13:48531630 | G | A | 6 | a0001c0001t0001g0268 a0001c0001t0007g0267 a0001c0004t0004g0021 others(3): Show |
7 | HG00099.hp2 HG01884.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-219+1398C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531630 | |||||||
| chr13:48531700 | T | G | 25 | a0001c0002t0001g0022 a0001c0002t0001g0023 a0001c0002t0001g0219 others(22): Show |
27 | HG00323.hp2 HG02129.hp2 HG02155.hp1 others(24): Show |
intron_variant | MODIFIER | c.-219+1328A>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531700 | |||||||
| chr13:48531707 | T | C | 4 | a0001c0001t0002g0242 a0001c0001t0002g0243 a0001c0001t0002g0244 others(1): Show |
4 | HG01192.hp1 HG02055.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-219+1321A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531707 | |||||||
| chr13:48531709 | T | C | 1 | a0001c0001t0001g0265 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-219+1319A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531709 | |||||||
| chr13:48531792 | T | C | 3 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0253 |
3 | HG02109.hp2 HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-219+1236A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48531792 | |||||||
| chr13:48532101 | A | T | 2 | a0001c0005t0002g0005 a0001c0005t0002g0066 |
4 | HG03453.hp1 NA19030.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-219+927T>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532101 | |||||||
| chr13:48532144 | A | G | 7 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(4): Show |
7 | HG00558.hp2 HG02109.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-219+884T>C | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532144 | |||||||
| chr13:48532259 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-219+769T>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532259 | |||||||
| chr13:48532429 | G | A | 1 | a0001c0011t0002g0246 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-219+599C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532429 | |||||||
| chr13:48532569 | G | GC | 9 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0247 others(6): Show |
11 | HG01074.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-219+458dupG | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532569 | |||||||
| chr13:48532569 | GC | G | 50 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(47): Show |
52 | HG00558.hp2 HG00738.hp2 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.-219+458delG | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532569 | |||||||
| chr13:48532571 | C | A | 37 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(34): Show |
37 | HG00558.hp2 HG00738.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.-219+457G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532571 | |||||||
| chr13:48532613 | C | A | 1 | a0001c0001t0001g0266 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-219+415G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532613 | |||||||
| chr13:48532704 | G | GGGCA | 6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG00738.hp2 HG01168.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.-219+320_-219+323d others(6): Show |
RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532704 | |||||||
| chr13:48532741 | G | C | 2 | a0001c0001t0001g0268 a0001c0001t0007g0267 |
2 | HG00099.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.-219+287C>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532741 | |||||||
| chr13:48532794 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0269 a0001c0001t0001g0270 others(4): Show |
8 | HG00597.hp2 HG02129.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.-219+234A>G | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532794 | |||||||
| chr13:48532795 | G | A | 4 | a0002c0006t0001g0275 a0002c0006t0001g0276 a0002c0006t0001g0277 others(1): Show |
4 | HG01109.hp2 HG02630.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-219+233C>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532795 | |||||||
| chr13:48532799 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-219+229G>T | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532799 | |||||||
| chr13:48532814 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-219+214G>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532814 | |||||||
| chr13:48532925 | G | T | 26 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0001c0001t0001g0033 others(23): Show |
26 | HG00738.hp2 HG01109.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.-219+103C>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532925 | |||||||
| chr13:48532954 | G | T | 1 | a0001c0001t0001g0029 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-219+74C>A | RCBTB2 | ENSG00000136161.13 | transcript | ENST00000344532.8 | protein_coding | 1/14 | chr13 | 48532954 |