Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55213 |
| ensemblid | ENSG00000136144.12 |
| hgncid | 18243 |
| symbol | RCBTB1 |
| name | RCC1 and BTB domain containing protein 1 |
| refseq_nuc | NM_018191.4 |
| refseq_prot | NP_060661.3 |
| ensembl_nuc | ENST00000378302.7 |
| ensembl_prot | ENSP00000367552.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 49531946 |
| end | 49585558 |
| strand | - |
| ver | v1.2 |
| region | chr13:49531946-49585558 |
| region5000 | chr13:49526946-49590558 |
| regionname0 | RCBTB1_chr13_49531946_49585558 |
| regionname5000 | RCBTB1_chr13_49526946_49590558 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 531 | 220 | 32 | 48 | 107 | 11 | 21 | 81 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | MVDVG others(526): Show |
chr13 | 49526946 | 49590558 |
| a0002 | 1/0 | 531 | 196 | 63 | 19 | 89 | 5 | 19 | 69 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | MVDVG others(526): Show |
chr13 | 49526946 | 49590558 |
| a0003 | 0/0 | 531 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | MVDVG others(526): Show |
chr13 | 49526946 | 49590558 |
| a0004 | 0/0 | 531 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | MVDVG others(526): Show |
chr13 | 49526946 | 49590558 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1593 | 184 | 26 | 40 | 87 | 10 | 20 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0001c0004 | 0/0 | 1593 | 30 | 5 | 7 | 17 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0001c0009 | 0/0 | 1593 | 3 | 0 | 0 | 3 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0001c0011 | 0/0 | 1593 | 2 | 1 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0001c0014 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0002 | 0/0 | 1593 | 96 | 22 | 7 | 54 | 1 | 12 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0003 | 1/0 | 1593 | 57 | 6 | 10 | 34 | 4 | 2 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0005 | 0/0 | 1593 | 11 | 9 | 2 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0006 | 0/0 | 1593 | 10 | 10 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0007 | 0/0 | 1593 | 9 | 9 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0008 | 0/0 | 1593 | 5 | 5 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0010 | 0/0 | 1593 | 2 | 0 | 0 | 0 | 0 | 2 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0012 | 0/0 | 1593 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0013 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0017 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0018 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0019 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0002c0020 | 0/0 | 1593 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0003c0015 | 0/0 | 1593 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 | ||
| a0004c0016 | 0/0 | 1593 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | ATGGT others(1588): Show |
chr13 | 49526946 | 49590558 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3998 | 133 | 9 | 31 | 69 | 8 | 15 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0002 | 0/0 | 4008 | 3 | 1 | 0 | 2 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0003 | 0/0 | 4008 | 13 | 1 | 5 | 1 | 2 | 4 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0004 | 0/0 | 4008 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0005 | 0/0 | 3993 | 14 | 0 | 0 | 14 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3988): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0007 | 0/0 | 3998 | 10 | 9 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0008 | 0/0 | 3998 | 3 | 2 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0009 | 0/0 | 4008 | 3 | 1 | 2 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0012 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0013 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0014 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0001c0001t0016 | 0/0 | 3992 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3987): Show |
chr13 | 49526946 | 49590558 |
| a0001c0004t0001 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0001c0004t0002 | 0/0 | 4008 | 25 | 1 | 7 | 16 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0004t0003 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0004t0004 | 0/0 | 4008 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0004t0010 | 0/0 | 4008 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0009t0001 | 0/0 | 3998 | 3 | 0 | 0 | 3 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0001c0011t0002 | 0/0 | 4008 | 2 | 1 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0001c0014t0001 | 0/0 | 3998 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0002c0002t0001 | 0/0 | 3998 | 2 | 1 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0002c0002t0002 | 0/0 | 4008 | 43 | 13 | 4 | 19 | 0 | 7 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0002t0003 | 0/0 | 4008 | 5 | 4 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0002t0004 | 0/0 | 4008 | 42 | 0 | 2 | 34 | 1 | 5 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0002t0008 | 0/0 | 3998 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0002c0002t0011 | 0/0 | 4008 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0003t0001 | 0/0 | 3998 | 2 | 1 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0002c0003t0003 | 1/0 | 4008 | 42 | 5 | 9 | 21 | 4 | 2 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0003t0004 | 0/0 | 4008 | 13 | 0 | 1 | 12 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0005t0002 | 0/0 | 4008 | 6 | 5 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0005t0003 | 0/0 | 4008 | 4 | 3 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0005t0015 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0006t0002 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0006t0006 | 0/0 | 4008 | 8 | 8 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0006t0007 | 0/0 | 3998 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0002c0007t0002 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0007t0003 | 0/0 | 4008 | 5 | 5 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0007t0006 | 0/0 | 4008 | 3 | 3 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0008t0008 | 0/0 | 3998 | 5 | 5 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0002c0010t0002 | 0/0 | 4008 | 2 | 0 | 0 | 0 | 0 | 2 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0012t0003 | 0/0 | 4008 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0013t0004 | 0/0 | 4008 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0017t0002 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0018t0002 | 0/0 | 4008 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0019t0003 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0002c0020t0002 | 0/0 | 4008 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| a0003c0015t0001 | 0/0 | 3998 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(3993): Show |
chr13 | 49526946 | 49590558 |
| a0004c0016t0004 | 0/0 | 4008 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | GCTCC others(4003): Show |
chr13 | 49526946 | 49590558 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0308 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0391 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0001g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0002g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0003g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0005g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0007g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0007g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0007g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0007g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0008g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0008g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0008g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0009g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0009g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0009g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0012g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0013g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0014g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0001t0016g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0004g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0004t0010g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0009t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0009t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0009t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0011t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0011t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0001c0014t0001g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0002g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0003g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0004g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0011g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0002t0011g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0001 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0003g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0003t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0005t0015g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0006t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0006t0006g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0006t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0006t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0006t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0006t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0006t0006g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0006t0007g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0007t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0007t0003g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0007t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0007t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0007t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0007t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0007t0006g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0007t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0008t0008g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0008t0008g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0008t0008g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0008t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0008t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0010t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0010t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0012t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0013t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0017t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0018t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0019t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0002c0020t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0003c0015t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| a0004c0016t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0328 | EUR | GBR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0345 | EUR | GBR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0321 | EUR | GBR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00280 | hp1 | a0001 | c0014 | t0001 | g0342 | EUR | FIN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00280 | hp2 | a0002 | c0003 | t0003 | g0001 | EUR | FIN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0346 | EUR | FIN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00544 | hp1 | a0001 | c0004 | t0002 | g0290 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00558 | hp1 | a0002 | c0002 | t0004 | g0210 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00558 | hp2 | a0002 | c0003 | t0004 | g0216 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00597 | hp1 | a0001 | c0004 | t0002 | g0382 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00609 | hp2 | a0002 | c0012 | t0003 | g0235 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0200 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00639 | hp2 | a0002 | c0003 | t0003 | g0225 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00642 | hp1 | a0001 | c0004 | t0002 | g0278 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00642 | hp2 | a0002 | c0003 | t0004 | g0244 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00735 | hp1 | a0002 | c0003 | t0003 | g0273 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0359 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0387 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01069 | hp2 | a0002 | c0003 | t0003 | g0221 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01070 | hp1 | a0001 | c0001 | t0009 | g0330 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01074 | hp1 | a0002 | c0005 | t0002 | g0075 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01074 | hp2 | a0002 | c0003 | t0003 | g0217 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0373 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01099 | hp2 | a0002 | c0003 | t0003 | g0220 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01106 | hp1 | a0001 | c0001 | t0009 | g0375 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0358 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0144 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0399 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01168 | hp2 | a0002 | c0003 | t0003 | g0218 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0378 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01192 | hp1 | a0001 | c0004 | t0002 | g0296 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0361 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01243 | hp1 | a0001 | c0011 | t0002 | g0335 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01243 | hp2 | a0002 | c0005 | t0003 | g0142 | AMR | PUR | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01255 | hp1 | a0001 | c0004 | t0002 | g0275 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01255 | hp2 | a0002 | c0002 | t0004 | g0069 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01256 | hp1 | a0001 | c0004 | t0002 | g0277 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0042 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0365 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0352 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01261 | hp2 | a0002 | c0003 | t0003 | g0227 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0393 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01358 | hp2 | a0002 | c0003 | t0003 | g0224 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01433 | hp1 | a0001 | c0004 | t0002 | g0298 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0372 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01496 | hp1 | a0003 | c0015 | t0001 | g0322 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01496 | hp2 | a0002 | c0002 | t0004 | g0067 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01516 | hp1 | a0002 | c0003 | t0003 | g0219 | EUR | IBS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0343 | EUR | IBS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01517 | hp1 | a0002 | c0003 | t0003 | g0001 | EUR | IBS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0251 | EUR | IBS | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01884 | hp1 | a0002 | c0005 | t0003 | g0140 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01884 | hp2 | a0002 | c0002 | t0011 | g0145 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01891 | hp1 | a0002 | c0006 | t0006 | g0008 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01891 | hp2 | a0002 | c0002 | t0011 | g0191 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0368 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01975 | hp2 | a0001 | c0001 | t0008 | g0319 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0162 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0392 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02015 | hp1 | a0002 | c0002 | t0004 | g0207 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02027 | hp1 | a0002 | c0002 | t0004 | g0181 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0363 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02040 | hp2 | a0002 | c0003 | t0003 | g0233 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0380 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02055 | hp2 | a0002 | c0008 | t0008 | g0076 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02056 | hp1 | a0002 | c0002 | t0004 | g0211 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02056 | hp2 | a0002 | c0003 | t0003 | g0253 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02071 | hp1 | a0001 | c0004 | t0002 | g0303 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02074 | hp1 | a0001 | c0004 | t0002 | g0300 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02080 | hp2 | a0001 | c0004 | t0002 | g0289 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02083 | hp1 | a0002 | c0003 | t0003 | g0230 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02129 | hp1 | a0002 | c0002 | t0004 | g0206 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02129 | hp2 | a0002 | c0002 | t0004 | g0188 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02132 | hp1 | a0002 | c0003 | t0004 | g0242 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0385 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02135 | hp2 | a0001 | c0004 | t0004 | g0384 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02145 | hp2 | a0002 | c0005 | t0003 | g0192 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | CDX | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02155 | hp2 | a0002 | c0002 | t0004 | g0169 | EAS | CDX | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | CDX | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02165 | hp2 | a0002 | c0003 | t0003 | g0234 | EAS | CDX | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02257 | hp1 | a0002 | c0007 | t0006 | g0150 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02258 | hp1 | a0002 | c0005 | t0003 | g0141 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0318 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0329 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0400 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02280 | hp2 | a0002 | c0008 | t0008 | g0105 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02293 | hp1 | a0001 | c0004 | t0002 | g0279 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02300 | hp2 | a0001 | c0004 | t0002 | g0276 | AMR | PEL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02451 | hp1 | a0002 | c0006 | t0006 | g0286 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02451 | hp2 | a0002 | c0002 | t0002 | g0053 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0394 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02523 | hp2 | a0001 | c0004 | t0002 | g0294 | EAS | KHV | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0038 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02615 | hp1 | a0001 | c0004 | t0002 | g0299 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02615 | hp2 | a0002 | c0003 | t0003 | g0223 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02622 | hp1 | a0002 | c0008 | t0008 | g0106 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02622 | hp2 | a0002 | c0003 | t0003 | g0214 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0357 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02647 | hp2 | a0002 | c0006 | t0002 | g0288 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0339 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02698 | hp1 | a0002 | c0018 | t0002 | g0040 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02698 | hp2 | a0002 | c0002 | t0004 | g0158 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02717 | hp1 | a0002 | c0008 | t0008 | g0107 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02717 | hp2 | a0001 | c0004 | t0010 | g0152 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02723 | hp1 | a0002 | c0008 | t0008 | g0154 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0391 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0070 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0310 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02809 | hp2 | a0001 | c0001 | t0007 | g0398 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02818 | hp1 | a0002 | c0007 | t0003 | g0056 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02818 | hp2 | a0002 | c0006 | t0006 | g0009 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02886 | hp2 | a0002 | c0005 | t0002 | g0139 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0061 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02895 | hp2 | a0002 | c0002 | t0003 | g0016 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02896 | hp1 | a0002 | c0007 | t0002 | g0057 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02896 | hp2 | a0002 | c0007 | t0006 | g0146 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02897 | hp1 | a0002 | c0002 | t0003 | g0062 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02897 | hp2 | a0002 | c0007 | t0006 | g0148 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02922 | hp1 | a0001 | c0011 | t0002 | g0351 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02922 | hp2 | a0002 | c0007 | t0003 | g0005 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02965 | hp1 | a0002 | c0006 | t0006 | g0284 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02965 | hp2 | a0002 | c0003 | t0003 | g0222 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02970 | hp1 | a0002 | c0003 | t0003 | g0266 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0401 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0156 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02976 | hp2 | a0002 | c0019 | t0003 | g0143 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03017 | hp1 | a0002 | c0002 | t0004 | g0171 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03017 | hp2 | a0002 | c0003 | t0003 | g0274 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03041 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03041 | hp2 | a0002 | c0005 | t0002 | g0353 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03098 | hp1 | a0002 | c0006 | t0006 | g0287 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03130 | hp2 | a0002 | c0007 | t0003 | g0147 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03139 | hp1 | a0002 | c0006 | t0007 | g0283 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03139 | hp2 | a0001 | c0004 | t0010 | g0149 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0354 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03195 | hp2 | a0002 | c0002 | t0008 | g0054 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0003 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03225 | hp1 | a0002 | c0005 | t0002 | g0313 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0264 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0344 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03453 | hp1 | a0002 | c0007 | t0003 | g0031 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0371 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0030 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03486 | hp2 | a0002 | c0005 | t0002 | g0074 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0068 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03490 | hp2 | a0002 | c0010 | t0002 | g0231 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03491 | hp1 | a0002 | c0003 | t0003 | g0241 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03492 | hp2 | a0002 | c0010 | t0002 | g0255 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0060 | AFR | ESN | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03540 | hp1 | a0002 | c0005 | t0002 | g0153 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03540 | hp2 | a0001 | c0001 | t0013 | g0312 | AFR | GWD | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0327 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03579 | hp2 | a0001 | c0004 | t0001 | g0281 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0119 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0049 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03669 | hp1 | a0002 | c0020 | t0002 | g0071 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03688 | hp2 | a0002 | c0002 | t0004 | g0183 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0370 | SAS | BEB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0376 | SAS | BEB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0041 | SAS | BEB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04115 | hp1 | a0002 | c0013 | t0004 | g0256 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04115 | hp2 | a0002 | c0002 | t0004 | g0178 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0324 | SAS | BEB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0157 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04204 | hp1 | a0002 | c0002 | t0004 | g0175 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0046 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0360 | SAS | STU | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0190 | AFR | YRI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | YRI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18612 | hp1 | a0002 | c0002 | t0004 | g0161 | EAS | CHB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0366 | EAS | CHB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18747 | hp1 | a0001 | c0004 | t0002 | g0302 | EAS | CHB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0035 | AFR | YRI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0367 | AFR | YRI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18939 | hp1 | a0002 | c0002 | t0004 | g0168 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18940 | hp2 | a0002 | c0002 | t0004 | g0209 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18942 | hp2 | a0002 | c0002 | t0004 | g0163 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18943 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18943 | hp2 | a0002 | c0002 | t0004 | g0166 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18944 | hp1 | a0002 | c0002 | t0004 | g0066 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18945 | hp1 | a0002 | c0002 | t0004 | g0349 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18947 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18948 | hp1 | a0002 | c0002 | t0004 | g0164 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0395 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18950 | hp2 | a0002 | c0003 | t0003 | g0364 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18952 | hp1 | a0002 | c0002 | t0004 | g0160 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0386 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18953 | hp2 | a0001 | c0004 | t0002 | g0293 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0239 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18959 | hp2 | a0002 | c0002 | t0004 | g0165 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18961 | hp1 | a0002 | c0003 | t0003 | g0259 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18964 | hp1 | a0002 | c0003 | t0003 | g0258 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0350 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18966 | hp1 | a0001 | c0009 | t0001 | g0101 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18966 | hp2 | a0002 | c0003 | t0003 | g0249 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18969 | hp1 | a0001 | c0004 | t0002 | g0301 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0201 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18971 | hp1 | a0001 | c0004 | t0002 | g0270 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0383 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18973 | hp1 | a0002 | c0003 | t0004 | g0268 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18973 | hp2 | a0001 | c0001 | t0005 | g0118 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18974 | hp2 | a0002 | c0002 | t0004 | g0174 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18977 | hp1 | a0002 | c0002 | t0004 | g0205 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0334 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18980 | hp2 | a0002 | c0003 | t0003 | g0257 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18981 | hp1 | a0002 | c0003 | t0003 | g0237 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0088 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18983 | hp1 | a0002 | c0003 | t0004 | g0267 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18983 | hp2 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18984 | hp2 | a0002 | c0003 | t0003 | g0262 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18985 | hp1 | a0002 | c0002 | t0004 | g0180 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18985 | hp2 | a0001 | c0001 | t0016 | g0080 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18986 | hp1 | a0002 | c0003 | t0003 | g0240 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18994 | hp2 | a0002 | c0003 | t0003 | g0261 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0396 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18998 | hp1 | a0002 | c0003 | t0004 | g0247 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18998 | hp2 | a0001 | c0001 | t0005 | g0374 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0389 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19000 | hp1 | a0002 | c0002 | t0004 | g0172 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19000 | hp2 | a0001 | c0009 | t0001 | g0125 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19003 | hp2 | a0002 | c0003 | t0004 | g0238 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19007 | hp1 | a0002 | c0003 | t0004 | g0271 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19009 | hp2 | a0002 | c0002 | t0004 | g0170 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19010 | hp2 | a0002 | c0003 | t0003 | g0246 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19012 | hp1 | a0002 | c0002 | t0004 | g0208 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19012 | hp2 | a0002 | c0003 | t0004 | g0269 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0052 | AFR | LWK | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0397 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19055 | hp2 | a0002 | c0003 | t0003 | g0229 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0369 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19057 | hp2 | a0002 | c0002 | t0004 | g0028 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19059 | hp1 | a0002 | c0003 | t0003 | g0265 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19060 | hp1 | a0002 | c0002 | t0004 | g0065 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19062 | hp1 | a0002 | c0002 | t0004 | g0064 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19063 | hp1 | a0001 | c0004 | t0002 | g0297 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19064 | hp1 | a0002 | c0003 | t0004 | g0260 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19064 | hp2 | a0001 | c0004 | t0002 | g0292 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19065 | hp2 | a0002 | c0003 | t0003 | g0243 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19066 | hp1 | a0002 | c0002 | t0004 | g0186 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19068 | hp1 | a0002 | c0002 | t0004 | g0182 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19070 | hp2 | a0001 | c0004 | t0002 | g0010 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19075 | hp1 | a0002 | c0002 | t0004 | g0177 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19075 | hp2 | a0002 | c0003 | t0004 | g0215 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19076 | hp1 | a0002 | c0002 | t0004 | g0173 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19076 | hp2 | a0001 | c0004 | t0002 | g0291 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19077 | hp1 | a0001 | c0004 | t0002 | g0304 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19081 | hp1 | a0002 | c0002 | t0004 | g0263 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0159 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19082 | hp1 | a0002 | c0002 | t0004 | g0187 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19082 | hp2 | a0002 | c0002 | t0004 | g0185 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0029 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19085 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19086 | hp1 | a0002 | c0003 | t0003 | g0254 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19086 | hp2 | a0001 | c0009 | t0001 | g0131 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0340 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19088 | hp2 | a0002 | c0003 | t0004 | g0248 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19089 | hp2 | a0002 | c0003 | t0003 | g0245 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0381 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19090 | hp2 | a0002 | c0003 | t0004 | g0272 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0390 | EAS | JPT | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0017 | AFR | YRI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA19240 | hp2 | a0002 | c0006 | t0006 | g0285 | AFR | YRI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20129 | hp1 | a0002 | c0017 | t0002 | g0179 | AFR | ASW | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0151 | AFR | ASW | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0355 | EUR | TSI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20752 | hp2 | a0002 | c0002 | t0004 | g0184 | EUR | TSI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20805 | hp1 | a0002 | c0003 | t0003 | g0001 | EUR | TSI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20905 | hp1 | a0001 | c0004 | t0002 | g0295 | SAS | GIH | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0047 | SAS | GIH | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01123 | hp1 | a0002 | c0003 | t0003 | g0226 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0388 | AMR | CLM | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0032 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02109 | hp2 | a0002 | c0006 | t0006 | g0008 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02486 | hp1 | a0001 | c0001 | t0007 | g0034 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0379 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02559 | hp1 | a0002 | c0003 | t0003 | g0228 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0003 | AFR | ACB | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03471 | hp1 | a0002 | c0005 | t0015 | g0280 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG03471 | hp2 | a0002 | c0007 | t0003 | g0005 | AFR | MSL | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0331 | AFR | USA | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| HG06807 | hp2 | a0001 | c0004 | t0003 | g0282 | AFR | USA | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20300 | hp1 | a0002 | c0002 | t0008 | g0063 | AFR | USA | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA20300 | hp2 | a0002 | c0006 | t0006 | g0009 | AFR | USA | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | LWK | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| NA21309 | hp2 | a0004 | c0016 | t0004 | g0167 | AFR | LWK | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0308 | REF | REF | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| homoSapiens | grch38p0 | a0002 | c0003 | t0003 | g0236 | REF | REF | RCBTB1_chr13_49526946_49590558 | RCBTB1 | chr13 | 49526946 | 49590558 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49551351 | C | T | 1 | a0004 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.829G>A | p.Ala277Thr | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/13 | 1065/4008 | 829/1596 | 277/531 | chr13 | 49551351 | |||
| chr13:49566688 | T | G | 1 | a0003 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.207A>C | p.Glu69Asp | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/13 | 443/4008 | 207/1596 | 69/531 | chr13 | 49566688 | |||
| chr13:49567209 | G | A | 2 | a0001 a0003 |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
missense_variant | MODERATE | c.71C>T | p.Ala24Val | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 3/13 | 307/4008 | 71/1596 | 24/531 | chr13 | 49567209 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49549486 | G | C | 6 | a0001c0001 a0001c0009 a0001c0011 others(3): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
synonymous_variant | LOW | c.1017C>G | p.Pro339Pro | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/13 | 1253/4008 | 1017/1596 | 339/531 | chr13 | 49549486 | |||
| chr13:49549489 | A | G | 1 | a0002c0008 | 5 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
synonymous_variant | LOW | c.1014T>C | p.Thr338Thr | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/13 | 1250/4008 | 1014/1596 | 338/531 | chr13 | 49549489 | |||
| chr13:49549492 | G | A | 1 | a0002c0018 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.1011C>T | p.Ala337Ala | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/13 | 1247/4008 | 1011/1596 | 337/531 | chr13 | 49549492 | |||
| chr13:49549513 | G | A | 8 | a0002c0002 a0002c0006 a0002c0007 others(5): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
synonymous_variant | LOW | c.990C>T | p.Asp330Asp | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/13 | 1226/4008 | 990/1596 | 330/531 | chr13 | 49549513 | |||
| chr13:49549552 | G | A | 1 | a0001c0014 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.951C>T | p.Ser317Ser | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/13 | 1187/4008 | 951/1596 | 317/531 | chr13 | 49549552 | |||
| chr13:49549552 | G | C | 1 | a0001c0009 | 3 | NA18966.hp1 NA19000.hp2 NA19086.hp2 |
synonymous_variant | LOW | c.951C>G | p.Ser317Ser | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/13 | 1187/4008 | 951/1596 | 317/531 | chr13 | 49549552 | |||
| chr13:49549552 | G | T | 9 | a0002c0002 a0002c0006 a0002c0007 others(6): Show |
126 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(123): Show |
synonymous_variant | LOW | c.951C>A | p.Ser317Ser | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/13 | 1187/4008 | 951/1596 | 317/531 | chr13 | 49549552 | |||
| chr13:49549612 | C | T | 1 | a0002c0017 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.891G>A | p.Thr297Thr | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/13 | 1127/4008 | 891/1596 | 297/531 | chr13 | 49549612 | |||
| chr13:49551439 | T | C | 1 | a0002c0007 | 9 | HG02257.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
synonymous_variant | LOW | c.741A>G | p.Ala247Ala | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/13 | 977/4008 | 741/1596 | 247/531 | chr13 | 49551439 | |||
| chr13:49551451 | T | C | 1 | a0002c0006 | 10 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
synonymous_variant | LOW | c.729A>G | p.Ala243Ala | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/13 | 965/4008 | 729/1596 | 243/531 | chr13 | 49551451 | |||
| chr13:49552246 | G | A | 17 | a0001c0001 a0001c0004 a0001c0009 others(14): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
synonymous_variant | LOW | c.643C>T | p.Leu215Leu | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/13 | 879/4008 | 643/1596 | 215/531 | chr13 | 49552246 | |||
| chr13:49559924 | A | G | 1 | a0001c0011 | 2 | HG01243.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.438T>C | p.Asp146Asp | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/13 | 674/4008 | 438/1596 | 146/531 | chr13 | 49559924 | |||
| chr13:49559963 | T | C | 10 | a0002c0002 a0002c0006 a0002c0007 others(7): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
synonymous_variant | LOW | c.399A>G | p.Val133Val | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/13 | 635/4008 | 399/1596 | 133/531 | chr13 | 49559963 | |||
| chr13:49560014 | A | G | 8 | a0002c0002 a0002c0006 a0002c0007 others(5): Show |
124 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(121): Show |
synonymous_variant | LOW | c.348T>C | p.Ile116Ile | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/13 | 584/4008 | 348/1596 | 116/531 | chr13 | 49560014 | |||
| chr13:49567226 | G | A | 9 | a0002c0002 a0002c0006 a0002c0007 others(6): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
synonymous_variant | LOW | c.54C>T | p.Ile18Ile | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 3/13 | 290/4008 | 54/1596 | 18/531 | chr13 | 49567226 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49532196 | A | AATAAAG | 15 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(12): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*1925_*1926insCTTT others(2): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1925 | chr13 | 49532196 | ||||||
| chr13:49532266 | T | C | 1 | a0002c0002t0011 | 2 | HG01884.hp2 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1856A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1856 | chr13 | 49532266 | ||||||
| chr13:49532267 | CTAATA | C | 1 | a0001c0001t0005 | 14 | NA18612.hp2 NA18946.hp1 NA18953.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1850_*1854delTATT others(1): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1850 | chr13 | 49532267 | ||||||
| chr13:49532414 | GA | G | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1707delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1707 | chr13 | 49532414 | ||||||
| chr13:49532425 | T | G | 6 | a0001c0001t0004 a0001c0004t0004 a0002c0002t0004 others(3): Show |
59 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*1697A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1697 | chr13 | 49532425 | ||||||
| chr13:49532448 | G | A | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1674C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1674 | chr13 | 49532448 | ||||||
| chr13:49532819 | A | G | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1303T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1303 | chr13 | 49532819 | ||||||
| chr13:49532840 | T | C | 1 | a0001c0001t0012 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1282A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1282 | chr13 | 49532840 | ||||||
| chr13:49532998 | C | T | 1 | a0001c0001t0009 | 3 | HG01070.hp1 HG01106.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1124G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1124 | chr13 | 49532998 | ||||||
| chr13:49533070 | AAAAGTGA others(8): Show |
A | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1037_*1051delATCA others(11): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1037 | chr13 | 49533070 | ||||||
| chr13:49533095 | C | A | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*1027G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 1027 | chr13 | 49533095 | ||||||
| chr13:49533153 | T | C | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*969A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 969 | chr13 | 49533153 | ||||||
| chr13:49533187 | C | T | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*935G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 935 | chr13 | 49533187 | ||||||
| chr13:49533239 | G | C | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*883C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 883 | chr13 | 49533239 | ||||||
| chr13:49533252 | A | G | 3 | a0001c0001t0007 a0001c0001t0014 a0002c0006t0007 |
12 | HG01106.hp2 HG02486.hp1 HG02559.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*870T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 870 | chr13 | 49533252 | ||||||
| chr13:49533322 | T | A | 1 | a0001c0001t0012 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*800A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 800 | chr13 | 49533322 | ||||||
| chr13:49533534 | C | T | 3 | a0001c0001t0008 a0002c0002t0008 a0002c0008t0008 |
10 | HG01975.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*588G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 588 | chr13 | 49533534 | ||||||
| chr13:49533582 | C | T | 2 | a0002c0006t0006 a0002c0007t0006 |
11 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*540G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 540 | chr13 | 49533582 | ||||||
| chr13:49533768 | G | A | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*354C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 354 | chr13 | 49533768 | ||||||
| chr13:49533782 | T | A | 18 | a0001c0001t0002 a0001c0001t0004 a0001c0004t0002 others(15): Show |
146 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(143): Show |
3_prime_UTR_variant | MODIFIER | c.*340A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 340 | chr13 | 49533782 | ||||||
| chr13:49533837 | G | C | 16 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(13): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*285C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 285 | chr13 | 49533837 | ||||||
| chr13:49533892 | A | G | 1 | a0001c0001t0014 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*230T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 230 | chr13 | 49533892 | ||||||
| chr13:49533979 | A | G | 1 | a0001c0001t0013 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*143T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 143 | chr13 | 49533979 | ||||||
| chr13:49534013 | C | T | 1 | a0001c0004t0010 | 2 | HG02717.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*109G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 109 | chr13 | 49534013 | ||||||
| chr13:49534116 | T | C | 18 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0007 others(15): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*6A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 13/13 | 6 | chr13 | 49534116 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:49534344 | C | G | 11 | a0001c0001t0007g0003 a0001c0001t0007g0030 a0001c0001t0007g0034 others(8): Show |
12 | HG01106.hp2 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.1456-82G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534344 | |||||||
| chr13:49534508 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(173): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.1456-246C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534508 | |||||||
| chr13:49534511 | C | T | 12 | a0001c0004t0010g0149 a0001c0004t0010g0152 a0002c0002t0003g0016 others(9): Show |
14 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1456-249G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534511 | |||||||
| chr13:49534513 | C | T | 1 | a0002c0002t0004g0211 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1456-251G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534513 | |||||||
| chr13:49534514 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1456-252C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534514 | |||||||
| chr13:49534514 | G | GCA | 3 | a0002c0002t0011g0145 a0002c0002t0011g0191 a0002c0003t0003g0261 |
3 | HG01884.hp2 HG01891.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1456-254_1456-253d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534514 | |||||||
| chr13:49534522 | A | T | 1 | a0001c0001t0003g0326 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1456-260T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534522 | |||||||
| chr13:49534529 | C | T | 10 | a0002c0002t0003g0016 a0002c0006t0006g0008 a0002c0006t0006g0009 others(7): Show |
12 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1456-267G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534529 | |||||||
| chr13:49534721 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(183): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.1456-459T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534721 | |||||||
| chr13:49534800 | G | A | 1 | a0001c0004t0002g0304 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1456-538C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534800 | |||||||
| chr13:49534832 | G | A | 1 | a0001c0001t0005g0118 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1456-570C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534832 | |||||||
| chr13:49534863 | G | A | 1 | a0001c0001t0003g0329 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1456-601C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534863 | |||||||
| chr13:49534892 | G | A | 2 | a0002c0002t0011g0145 a0002c0002t0011g0191 |
2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1456-630C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534892 | |||||||
| chr13:49534949 | G | A | 1 | a0002c0008t0008g0105 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1456-687C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49534949 | |||||||
| chr13:49535011 | G | GTGAC | 130 | a0001c0001t0002g0363 a0001c0001t0002g0371 a0001c0001t0002g0385 others(127): Show |
132 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(129): Show |
intron_variant | MODIFIER | c.1456-753_1456-750d others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535011 | |||||||
| chr13:49535149 | A | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(192): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1456-887T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535149 | |||||||
| chr13:49535151 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(192): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.1456-889T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535151 | |||||||
| chr13:49535263 | A | G | 1 | a0002c0005t0003g0192 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1456-1001T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535263 | |||||||
| chr13:49535435 | C | T | 26 | a0001c0004t0004g0384 a0002c0002t0002g0068 a0002c0002t0002g0070 others(23): Show |
26 | HG00558.hp1 HG00621.hp2 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.1456-1173G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535435 | |||||||
| chr13:49535448 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(182): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1456-1186G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535448 | |||||||
| chr13:49535565 | TAGAC | T | 57 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(54): Show |
63 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(60): Show |
intron_variant | MODIFIER | c.1456-1307_1456-130 others(8): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535565 | |||||||
| chr13:49535793 | T | G | 191 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(188): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.1456-1531A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535793 | |||||||
| chr13:49535796 | G | A | 1 | a0002c0007t0006g0150 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1456-1534C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535796 | |||||||
| chr13:49535881 | G | A | 1 | a0002c0005t0002g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1456-1619C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535881 | |||||||
| chr13:49535929 | A | G | 129 | a0001c0001t0004g0119 a0001c0004t0002g0010 a0001c0004t0002g0270 others(126): Show |
131 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.1456-1667T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535929 | |||||||
| chr13:49535954 | C | T | 2 | a0001c0001t0001g0305 a0001c0004t0001g0281 |
2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1456-1692G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535954 | |||||||
| chr13:49535962 | G | T | 3 | a0001c0004t0002g0270 a0001c0004t0002g0292 a0001c0004t0002g0298 |
3 | HG01433.hp1 NA18971.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1456-1700C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535962 | |||||||
| chr13:49535979 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(189): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.1456-1717A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49535979 | |||||||
| chr13:49536023 | C | CA | 30 | a0001c0004t0002g0010 a0001c0004t0002g0270 a0001c0004t0002g0275 others(27): Show |
31 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.1456-1762dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49536023 | |||||||
| chr13:49536196 | A | G | 16 | a0002c0002t0003g0016 a0002c0002t0003g0190 a0002c0006t0002g0288 others(13): Show |
19 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1456-1934T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49536196 | |||||||
| chr13:49536350 | C | G | 320 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(317): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1456-2088G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49536350 | |||||||
| chr13:49536425 | C | T | 2 | a0002c0003t0003g0223 a0002c0003t0003g0228 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1456-2163G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49536425 | |||||||
| chr13:49536506 | A | G | 1 | a0002c0013t0004g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1456-2244T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49536506 | |||||||
| chr13:49536734 | T | C | 2 | a0001c0004t0010g0149 a0001c0004t0010g0152 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1456-2472A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49536734 | |||||||
| chr13:49536999 | T | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(186): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1456-2737A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49536999 | |||||||
| chr13:49537007 | C | A | 1 | a0002c0013t0004g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1456-2745G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537007 | |||||||
| chr13:49537132 | G | T | 1 | a0001c0001t0003g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1456-2870C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537132 | |||||||
| chr13:49537232 | A | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(186): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1456-2970T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537232 | |||||||
| chr13:49537269 | T | C | 1 | a0001c0004t0002g0303 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1456-3007A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537269 | |||||||
| chr13:49537327 | T | A | 1 | a0002c0006t0006g0285 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1456-3065A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537327 | |||||||
| chr13:49537374 | G | A | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(186): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1456-3112C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537374 | |||||||
| chr13:49537486 | C | T | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(186): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1456-3224G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537486 | |||||||
| chr13:49537516 | G | A | 1 | a0001c0001t0001g0309 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.1456-3254C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537516 | |||||||
| chr13:49537522 | C | T | 1 | a0001c0001t0009g0330 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1456-3260G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537522 | |||||||
| chr13:49537626 | G | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(185): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1455+3250C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537626 | |||||||
| chr13:49537775 | G | A | 319 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(316): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1455+3101C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537775 | |||||||
| chr13:49537795 | G | C | 189 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(186): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.1455+3081C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537795 | |||||||
| chr13:49537801 | C | T | 14 | a0001c0001t0007g0003 a0001c0001t0007g0030 a0001c0001t0007g0034 others(11): Show |
15 | HG01106.hp2 HG01975.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1455+3075G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537801 | |||||||
| chr13:49537820 | G | A | 1 | a0002c0002t0002g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1455+3056C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537820 | |||||||
| chr13:49537855 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1455+3021G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537855 | |||||||
| chr13:49537993 | C | G | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(341): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.1455+2883G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49537993 | |||||||
| chr13:49538012 | G | A | 2 | a0001c0004t0010g0149 a0001c0004t0010g0152 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1455+2864C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538012 | |||||||
| chr13:49538019 | C | T | 2 | a0002c0003t0003g0223 a0002c0003t0003g0228 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1455+2857G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538019 | |||||||
| chr13:49538193 | T | G | 1 | a0002c0005t0002g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1455+2683A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538193 | |||||||
| chr13:49538338 | G | A | 3 | a0002c0002t0003g0061 a0002c0002t0003g0062 a0002c0007t0003g0147 |
3 | HG02895.hp1 HG02897.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1455+2538C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538338 | |||||||
| chr13:49538389 | G | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(182): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1455+2487C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538389 | |||||||
| chr13:49538416 | C | T | 314 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(311): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1455+2460G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538416 | |||||||
| chr13:49538549 | A | G | 1 | a0001c0009t0001g0125 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1455+2327T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538549 | |||||||
| chr13:49538594 | G | A | 1 | a0002c0005t0002g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1455+2282C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538594 | |||||||
| chr13:49538707 | C | G | 278 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(275): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1455+2169G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538707 | |||||||
| chr13:49538749 | A | G | 12 | a0002c0002t0003g0016 a0002c0006t0002g0288 a0002c0006t0006g0008 others(9): Show |
14 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1455+2127T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538749 | |||||||
| chr13:49538758 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0005g0340 |
2 | NA18991.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1455+2118A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538758 | |||||||
| chr13:49538758 | T | TAC | 223 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(220): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.1455+2116_1455+211 others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538758 | |||||||
| chr13:49538818 | GTCT | G | 27 | a0002c0002t0002g0070 a0002c0002t0002g0193 a0002c0002t0002g0194 others(24): Show |
27 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1455+2055_1455+205 others(7): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538818 | |||||||
| chr13:49538887 | A | ACT | 6 | a0001c0001t0003g0329 a0001c0001t0003g0343 a0001c0001t0003g0344 others(3): Show |
6 | HG00140.hp1 HG01516.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.1455+1987_1455+198 others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538887 | |||||||
| chr13:49538888 | C | CT | 35 | a0001c0001t0001g0094 a0001c0004t0010g0149 a0001c0004t0010g0152 others(32): Show |
35 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(32): Show |
intron_variant | MODIFIER | c.1455+1987dupA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538888 | |||||||
| chr13:49538889 | T | TC | 183 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(180): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1455+1986_1455+198 others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538889 | |||||||
| chr13:49538942 | G | T | 1 | a0001c0001t0001g0022 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1455+1934C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538942 | |||||||
| chr13:49538956 | C | G | 30 | a0001c0004t0002g0289 a0001c0004t0002g0294 a0002c0002t0002g0070 others(27): Show |
30 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.1455+1920G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538956 | |||||||
| chr13:49538994 | C | T | 8 | a0002c0002t0002g0156 a0002c0002t0002g0194 a0002c0002t0002g0196 others(5): Show |
8 | HG00621.hp2 HG02165.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1455+1882G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538994 | |||||||
| chr13:49538997 | A | G | 105 | a0001c0001t0001g0133 a0001c0001t0001g0323 a0001c0001t0001g0337 others(102): Show |
107 | HG00597.hp1 HG00642.hp1 HG01070.hp1 others(104): Show |
intron_variant | MODIFIER | c.1455+1879T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49538997 | |||||||
| chr13:49539015 | A | G | 90 | a0001c0001t0001g0128 a0001c0001t0001g0133 a0001c0001t0001g0323 others(87): Show |
92 | HG00597.hp1 HG00621.hp2 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.1455+1861T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539015 | |||||||
| chr13:49539016 | C | T | 90 | a0001c0001t0001g0128 a0001c0001t0001g0133 a0001c0001t0001g0323 others(87): Show |
92 | HG00597.hp1 HG00621.hp2 HG01070.hp1 others(89): Show |
intron_variant | MODIFIER | c.1455+1860G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539016 | |||||||
| chr13:49539017 | G | A | 1 | a0001c0001t0003g0011 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1455+1859C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539017 | |||||||
| chr13:49539019 | A | G | 1 | a0002c0002t0002g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1455+1857T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539019 | |||||||
| chr13:49539068 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(170): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.1455+1808G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539068 | |||||||
| chr13:49539079 | A | G | 204 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(201): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.1455+1797T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539079 | |||||||
| chr13:49539082 | C | A | 15 | a0001c0001t0001g0362 a0001c0001t0009g0330 a0001c0001t0009g0331 others(12): Show |
17 | HG00673.hp1 HG01070.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.1455+1794G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539082 | |||||||
| chr13:49539085 | G | T | 1 | a0002c0002t0003g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1455+1791C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539085 | |||||||
| chr13:49539086 | T | C | 28 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0017 others(25): Show |
31 | HG01109.hp2 HG01891.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1455+1790A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539086 | |||||||
| chr13:49539090 | A | G | 2 | a0001c0001t0003g0307 a0002c0002t0002g0400 |
2 | HG02280.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1455+1786T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539090 | |||||||
| chr13:49539100 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(240): Show |
252 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(249): Show |
intron_variant | MODIFIER | c.1455+1776A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539100 | |||||||
| chr13:49539111 | C | T | 2 | a0002c0002t0011g0145 a0002c0002t0011g0191 |
2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.1455+1765G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539111 | |||||||
| chr13:49539122 | T | A | 133 | a0001c0001t0001g0039 a0001c0001t0001g0133 a0001c0001t0001g0337 others(130): Show |
137 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.1455+1754A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539122 | |||||||
| chr13:49539133 | C | T | 1 | a0001c0001t0001g0320 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1455+1743G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539133 | |||||||
| chr13:49539178 | T | A | 2 | a0001c0001t0001g0039 a0001c0001t0003g0326 |
2 | NA18947.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1455+1698A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539178 | |||||||
| chr13:49539178 | T | TA | 203 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(200): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.1455+1697dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539178 | |||||||
| chr13:49539285 | G | T | 2 | a0002c0002t0002g0048 a0002c0002t0002g0051 |
2 | NA18947.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.1455+1591C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539285 | |||||||
| chr13:49539299 | T | C | 5 | a0002c0008t0008g0076 a0002c0008t0008g0105 a0002c0008t0008g0106 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.1455+1577A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539299 | |||||||
| chr13:49539314 | G | A | 208 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(205): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1455+1562C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539314 | |||||||
| chr13:49539328 | T | C | 2 | a0002c0005t0002g0074 a0002c0005t0002g0075 |
2 | HG01074.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1455+1548A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539328 | |||||||
| chr13:49539341 | T | C | 1 | a0001c0001t0002g0385 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1455+1535A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539341 | |||||||
| chr13:49539527 | T | C | 14 | a0001c0001t0007g0003 a0001c0001t0007g0030 a0001c0001t0007g0034 others(11): Show |
15 | HG01106.hp2 HG01975.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1455+1349A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539527 | |||||||
| chr13:49539593 | C | T | 31 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0017 others(28): Show |
32 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1455+1283G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539593 | |||||||
| chr13:49539636 | A | G | 9 | a0002c0003t0003g0007 a0002c0003t0003g0229 a0002c0003t0003g0233 others(6): Show |
10 | HG02040.hp2 NA18943.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.1455+1240T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539636 | |||||||
| chr13:49539644 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0001g0023 |
2 | NA18946.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1455+1232C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49539644 | |||||||
| chr13:49540122 | G | A | 29 | a0002c0002t0002g0068 a0002c0002t0002g0070 a0002c0002t0002g0193 others(26): Show |
29 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.1455+754C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49540122 | |||||||
| chr13:49540355 | T | C | 331 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1455+521A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49540355 | |||||||
| chr13:49540460 | C | T | 1 | a0002c0002t0004g0183 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1455+416G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49540460 | |||||||
| chr13:49540491 | G | C | 1 | a0001c0001t0003g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1455+385C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49540491 | |||||||
| chr13:49540763 | C | A | 1 | a0001c0004t0002g0291 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1455+113G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49540763 | |||||||
| chr13:49540831 | A | G | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1455+45T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49540831 | |||||||
| chr13:49540845 | T | A | 31 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0017 others(28): Show |
32 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1455+31A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49540845 | |||||||
| chr13:49540864 | T | C | 1 | a0002c0002t0003g0016 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1455+12A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 12/12 | chr13 | 49540864 | |||||||
| chr13:49541268 | A | C | 31 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0017 others(28): Show |
32 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1325-262T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 11/12 | chr13 | 49541268 | |||||||
| chr13:49541420 | A | G | 1 | a0002c0002t0004g0164 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1324+256T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 11/12 | chr13 | 49541420 | |||||||
| chr13:49541437 | TA | T | 14 | a0002c0002t0004g0177 a0002c0003t0003g0001 a0002c0003t0003g0217 others(11): Show |
16 | HG00280.hp2 HG00639.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1324+238delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 11/12 | chr13 | 49541437 | |||||||
| chr13:49541533 | C | T | 331 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1324+143G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 11/12 | chr13 | 49541533 | |||||||
| chr13:49541652 | T | C | 1 | a0002c0002t0004g0210 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1324+24A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 11/12 | chr13 | 49541652 | |||||||
| chr13:49541661 | A | G | 31 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0017 others(28): Show |
32 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1324+15T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 11/12 | chr13 | 49541661 | |||||||
| chr13:49542002 | A | G | 332 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1173-175T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542002 | |||||||
| chr13:49542183 | T | G | 5 | a0002c0007t0002g0057 a0002c0007t0003g0005 a0002c0007t0003g0031 others(2): Show |
6 | HG02818.hp1 HG02896.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173-356A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542183 | |||||||
| chr13:49542209 | G | A | 18 | a0001c0001t0001g0336 a0001c0001t0001g0341 a0001c0001t0001g0348 others(15): Show |
20 | HG02132.hp2 HG02523.hp1 NA18612.hp2 others(17): Show |
intron_variant | MODIFIER | c.1173-382C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542209 | |||||||
| chr13:49542213 | C | CAA | 25 | a0001c0004t0002g0010 a0001c0004t0002g0270 a0001c0004t0002g0275 others(22): Show |
26 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.1173-388_1173-387d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542213 | |||||||
| chr13:49542213 | CA | C | 317 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(314): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.1173-387delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542213 | |||||||
| chr13:49542299 | C | T | 31 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0017 others(28): Show |
32 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1173-472G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542299 | |||||||
| chr13:49542307 | A | G | 1 | a0002c0002t0004g0207 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1173-480T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542307 | |||||||
| chr13:49542487 | T | G | 1 | a0001c0009t0001g0101 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1173-660A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542487 | |||||||
| chr13:49542516 | T | G | 26 | a0001c0004t0002g0010 a0001c0004t0002g0270 a0001c0004t0002g0275 others(23): Show |
27 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1173-689A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542516 | |||||||
| chr13:49542658 | C | T | 1 | a0002c0003t0003g0220 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1173-831G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542658 | |||||||
| chr13:49542898 | T | C | 1 | a0002c0002t0002g0200 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1173-1071A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542898 | |||||||
| chr13:49542900 | A | T | 331 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1173-1073T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542900 | |||||||
| chr13:49542954 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1173-1127G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49542954 | |||||||
| chr13:49543004 | T | C | 1 | a0002c0002t0002g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1173-1177A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543004 | |||||||
| chr13:49543093 | T | C | 1 | a0002c0002t0004g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1173-1266A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543093 | |||||||
| chr13:49543123 | C | T | 1 | a0001c0001t0003g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1173-1296G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543123 | |||||||
| chr13:49543124 | G | A | 31 | a0002c0002t0001g0176 a0002c0002t0002g0157 a0002c0002t0003g0162 others(28): Show |
31 | HG01978.hp1 HG02027.hp1 HG02129.hp2 others(28): Show |
intron_variant | MODIFIER | c.1173-1297C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543124 | |||||||
| chr13:49543254 | T | A | 355 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(352): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.1173-1427A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543254 | |||||||
| chr13:49543555 | T | C | 1 | a0002c0003t0003g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1172+1182A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543555 | |||||||
| chr13:49543658 | C | T | 4 | a0001c0004t0002g0300 a0002c0002t0004g0163 a0002c0002t0004g0166 others(1): Show |
4 | HG02074.hp1 NA18942.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1172+1079G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543658 | |||||||
| chr13:49543808 | C | A | 1 | a0002c0002t0002g0400 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1172+929G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543808 | |||||||
| chr13:49543933 | C | T | 1 | a0002c0002t0002g0400 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1172+804G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543933 | |||||||
| chr13:49543970 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1172+767T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543970 | |||||||
| chr13:49543982 | G | C | 343 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(340): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1172+755C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49543982 | |||||||
| chr13:49544249 | C | T | 6 | a0002c0003t0003g0243 a0002c0003t0003g0245 a0002c0003t0003g0246 others(3): Show |
6 | NA18950.hp2 NA19010.hp2 NA19059.hp1 others(3): Show |
intron_variant | MODIFIER | c.1172+488G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49544249 | |||||||
| chr13:49544260 | G | A | 2 | a0002c0003t0003g0223 a0002c0003t0003g0228 |
2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1172+477C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49544260 | |||||||
| chr13:49544285 | C | T | 1 | a0002c0003t0004g0244 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1172+452G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49544285 | |||||||
| chr13:49544337 | C | T | 1 | a0002c0003t0003g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1172+400G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49544337 | |||||||
| chr13:49544377 | G | C | 1 | a0001c0001t0003g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1172+360C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49544377 | |||||||
| chr13:49544400 | C | T | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1172+337G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49544400 | |||||||
| chr13:49544452 | A | G | 2 | a0001c0001t0001g0305 a0001c0001t0012g0327 |
2 | HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1172+285T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49544452 | |||||||
| chr13:49544473 | GAAAC | G | 133 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(130): Show |
137 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(134): Show |
intron_variant | MODIFIER | c.1172+260_1172+263d others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49544473 | |||||||
| chr13:49544473 | GAAACAAA others(1): Show |
G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(207): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1172+256_1172+263d others(10): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 10/12 | chr13 | 49544473 | |||||||
| chr13:49544874 | C | T | 5 | a0002c0005t0002g0139 a0002c0005t0003g0140 a0002c0005t0003g0141 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046-11G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49544874 | |||||||
| chr13:49545171 | C | A | 3 | a0002c0002t0003g0190 a0002c0002t0011g0145 a0002c0002t0011g0191 |
3 | HG01884.hp2 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1046-308G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49545171 | |||||||
| chr13:49545247 | T | G | 1 | a0002c0013t0004g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1046-384A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49545247 | |||||||
| chr13:49545479 | AG | A | 3 | a0002c0002t0003g0190 a0002c0002t0011g0145 a0002c0002t0011g0191 |
3 | HG01884.hp2 HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1046-617delC | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49545479 | |||||||
| chr13:49545787 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1046-924A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49545787 | |||||||
| chr13:49545854 | A | C | 26 | a0001c0004t0002g0010 a0001c0004t0002g0270 a0001c0004t0002g0275 others(23): Show |
27 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1046-991T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49545854 | |||||||
| chr13:49545985 | T | G | 1 | a0002c0002t0011g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1046-1122A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49545985 | |||||||
| chr13:49546130 | T | C | 4 | a0001c0004t0002g0293 a0001c0004t0002g0301 a0001c0004t0002g0302 others(1): Show |
4 | HG02071.hp1 NA18747.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.1046-1267A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546130 | |||||||
| chr13:49546153 | A | C | 1 | a0002c0003t0004g0268 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1046-1290T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546153 | |||||||
| chr13:49546233 | A | G | 9 | a0002c0003t0003g0007 a0002c0003t0003g0229 a0002c0003t0003g0233 others(6): Show |
10 | HG02040.hp2 NA18943.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.1046-1370T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546233 | |||||||
| chr13:49546278 | G | A | 1 | a0002c0002t0002g0400 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1046-1415C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546278 | |||||||
| chr13:49546299 | G | T | 331 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1046-1436C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546299 | |||||||
| chr13:49546301 | C | T | 1 | a0002c0013t0004g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1046-1438G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546301 | |||||||
| chr13:49546318 | TCA | T | 26 | a0001c0004t0002g0010 a0001c0004t0002g0270 a0001c0004t0002g0275 others(23): Show |
27 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1046-1457_1046-145 others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546318 | |||||||
| chr13:49546509 | A | G | 10 | a0002c0003t0003g0243 a0002c0003t0003g0245 a0002c0003t0003g0246 others(7): Show |
10 | HG00735.hp1 HG02056.hp2 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.1046-1646T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546509 | |||||||
| chr13:49546512 | T | C | 1 | a0002c0008t0008g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1046-1649A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546512 | |||||||
| chr13:49546611 | G | A | 13 | a0001c0004t0002g0300 a0002c0002t0003g0016 a0002c0006t0002g0288 others(10): Show |
15 | HG01891.hp1 HG02074.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1046-1748C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546611 | |||||||
| chr13:49546668 | T | G | 1 | a0002c0006t0007g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1046-1805A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546668 | |||||||
| chr13:49546721 | G | A | 4 | a0002c0007t0002g0057 a0002c0007t0003g0005 a0002c0007t0003g0031 others(1): Show |
5 | HG02818.hp1 HG02896.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1046-1858C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546721 | |||||||
| chr13:49546721 | G | C | 2 | a0001c0001t0001g0325 a0001c0001t0001g0361 |
2 | HG01192.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1046-1858C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546721 | |||||||
| chr13:49546743 | G | A | 1 | a0002c0002t0002g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1046-1880C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546743 | |||||||
| chr13:49546849 | A | G | 342 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(339): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1046-1986T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49546849 | |||||||
| chr13:49547075 | G | A | 331 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1046-2212C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547075 | |||||||
| chr13:49547175 | C | CAA | 308 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(305): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1045+2281_1045+228 others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547175 | |||||||
| chr13:49547175 | C | CAAA | 22 | a0001c0001t0001g0336 a0001c0001t0007g0003 a0001c0001t0007g0030 others(19): Show |
23 | HG01106.hp2 HG01109.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1045+2280_1045+228 others(7): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547175 | |||||||
| chr13:49547258 | G | C | 3 | a0001c0001t0009g0330 a0001c0001t0009g0331 a0001c0001t0009g0375 |
3 | HG01070.hp1 HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1045+2200C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547258 | |||||||
| chr13:49547259 | G | T | 3 | a0001c0001t0009g0330 a0001c0001t0009g0331 a0001c0001t0009g0375 |
3 | HG01070.hp1 HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1045+2199C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547259 | |||||||
| chr13:49547260 | C | CTTCCT | 3 | a0001c0001t0009g0330 a0001c0001t0009g0331 a0001c0001t0009g0375 |
3 | HG01070.hp1 HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1045+2197_1045+219 others(9): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547260 | |||||||
| chr13:49547263 | G | GCACCCTT others(2): Show |
3 | a0001c0001t0009g0330 a0001c0001t0009g0331 a0001c0001t0009g0375 |
3 | HG01070.hp1 HG01106.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1045+2194_1045+219 others(13): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547263 | |||||||
| chr13:49547375 | A | G | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(207): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.1045+2083T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547375 | |||||||
| chr13:49547852 | G | C | 6 | a0002c0006t0002g0288 a0002c0006t0006g0009 a0002c0006t0006g0284 others(3): Show |
7 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1045+1606C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547852 | |||||||
| chr13:49547950 | GTTA | G | 331 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1045+1505_1045+150 others(7): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49547950 | |||||||
| chr13:49548056 | G | A | 1 | a0002c0013t0004g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1045+1402C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548056 | |||||||
| chr13:49548061 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1045+1397C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548061 | |||||||
| chr13:49548078 | C | T | 1 | a0001c0001t0001g0328 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1045+1380G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548078 | |||||||
| chr13:49548143 | G | A | 1 | a0001c0001t0001g0378 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1045+1315C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548143 | |||||||
| chr13:49548232 | A | G | 1 | a0002c0002t0003g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1045+1226T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548232 | |||||||
| chr13:49548262 | C | T | 120 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(117): Show |
124 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(121): Show |
intron_variant | MODIFIER | c.1045+1196G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548262 | |||||||
| chr13:49548321 | G | A | 1 | a0002c0013t0004g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1045+1137C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548321 | |||||||
| chr13:49548367 | T | C | 332 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1045+1091A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548367 | |||||||
| chr13:49548388 | C | CA | 26 | a0001c0001t0007g0003 a0001c0001t0007g0030 a0001c0001t0007g0034 others(23): Show |
27 | HG00735.hp1 HG01243.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1045+1069dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548388 | |||||||
| chr13:49548388 | CA | C | 9 | a0001c0001t0001g0085 a0001c0001t0001g0346 a0002c0002t0002g0144 others(6): Show |
9 | HG00323.hp2 HG01069.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1045+1069delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548388 | |||||||
| chr13:49548514 | T | C | 2 | a0002c0002t0003g0061 a0002c0002t0003g0062 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1045+944A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548514 | |||||||
| chr13:49548545 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(179): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1045+913C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548545 | |||||||
| chr13:49548593 | GTA | G | 332 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(329): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1045+863_1045+864d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548593 | |||||||
| chr13:49548652 | T | A | 1 | a0002c0003t0003g0266 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1045+806A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548652 | |||||||
| chr13:49548722 | G | A | 29 | a0001c0004t0001g0281 a0001c0004t0002g0010 a0001c0004t0002g0270 others(26): Show |
30 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1045+736C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548722 | |||||||
| chr13:49548792 | G | T | 319 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(316): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1045+666C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548792 | |||||||
| chr13:49548851 | T | TAAAACAA others(313): Show |
1 | a0002c0013t0004g0256 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1045+606_1045+607i others(322): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548851 | |||||||
| chr13:49548864 | AATT | A | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+591_1045+593d others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548864 | |||||||
| chr13:49548868 | T | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+590A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548868 | |||||||
| chr13:49548870 | A | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+588T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548870 | |||||||
| chr13:49548872 | A | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+586T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548872 | |||||||
| chr13:49548873 | T | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+585A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548873 | |||||||
| chr13:49548874 | A | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+584T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548874 | |||||||
| chr13:49548875 | A | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+583T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548875 | |||||||
| chr13:49548876 | A | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+582T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548876 | |||||||
| chr13:49548877 | G | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+581C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548877 | |||||||
| chr13:49548882 | G | GCTCACGC | 120 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(117): Show |
124 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(121): Show |
intron_variant | MODIFIER | c.1045+575_1045+576i others(9): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548882 | |||||||
| chr13:49548883 | A | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+575T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548883 | |||||||
| chr13:49548888 | G | A | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+570C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548888 | |||||||
| chr13:49548889 | G | T | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+569C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548889 | |||||||
| chr13:49548892 | A | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+566T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548892 | |||||||
| chr13:49548893 | G | A | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+565C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548893 | |||||||
| chr13:49548896 | A | ACTTTGGG others(3): Show |
121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+561_1045+562i others(12): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548896 | |||||||
| chr13:49548898 | A | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+560T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548898 | |||||||
| chr13:49548899 | G | A | 2 | a0001c0004t0002g0289 a0001c0004t0002g0294 |
2 | HG02080.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1045+559C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548899 | |||||||
| chr13:49548900 | T | A | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+558A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548900 | |||||||
| chr13:49548904 | A | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+554T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548904 | |||||||
| chr13:49548907 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+551A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548907 | |||||||
| chr13:49548914 | CCT | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+542_1045+543d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548914 | |||||||
| chr13:49548917 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1045+541C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548917 | |||||||
| chr13:49548923 | A | G | 14 | a0002c0002t0003g0190 a0002c0002t0011g0145 a0002c0002t0011g0191 others(11): Show |
16 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1045+535T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548923 | |||||||
| chr13:49548928 | T | A | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+530A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548928 | |||||||
| chr13:49548930 | C | A | 3 | a0002c0002t0004g0171 a0002c0002t0004g0184 a0004c0016t0004g0167 |
3 | HG03017.hp1 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1045+528G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548930 | |||||||
| chr13:49548935 | A | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+523T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548935 | |||||||
| chr13:49548938 | G | T | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+520C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548938 | |||||||
| chr13:49548945 | C | T | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+513G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548945 | |||||||
| chr13:49548950 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+508A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548950 | |||||||
| chr13:49548962 | A | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+496T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548962 | |||||||
| chr13:49548963 | C | T | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+495G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548963 | |||||||
| chr13:49548971 | A | G | 117 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(114): Show |
120 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(117): Show |
intron_variant | MODIFIER | c.1045+487T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548971 | |||||||
| chr13:49548978 | C | CA | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+479dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548978 | |||||||
| chr13:49548989 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+469A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548989 | |||||||
| chr13:49548993 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+465A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548993 | |||||||
| chr13:49548995 | T | A | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+463A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49548995 | |||||||
| chr13:49549002 | T | G | 123 | a0001c0001t0001g0096 a0001c0004t0002g0300 a0002c0002t0001g0055 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.1045+456A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549002 | |||||||
| chr13:49549005 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+453A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549005 | |||||||
| chr13:49549016 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+442A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549016 | |||||||
| chr13:49549017 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+441A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549017 | |||||||
| chr13:49549018 | A | AG | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+439_1045+440i others(3): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549018 | |||||||
| chr13:49549024 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+434A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549024 | |||||||
| chr13:49549042 | A | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+416T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549042 | |||||||
| chr13:49549046 | C | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+412G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549046 | |||||||
| chr13:49549047 | T | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+411A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549047 | |||||||
| chr13:49549049 | T | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+409A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549049 | |||||||
| chr13:49549053 | A | AC | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+404dupG | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549053 | |||||||
| chr13:49549055 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+403A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549055 | |||||||
| chr13:49549057 | G | A | 122 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(119): Show |
126 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(123): Show |
intron_variant | MODIFIER | c.1045+401C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549057 | |||||||
| chr13:49549060 | A | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+398T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549060 | |||||||
| chr13:49549063 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+395A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549063 | |||||||
| chr13:49549068 | G | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+390C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549068 | |||||||
| chr13:49549069 | T | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.1045+389A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549069 | |||||||
| chr13:49549085 | T | C | 1 | a0001c0004t0002g0279 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1045+373A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549085 | |||||||
| chr13:49549134 | TA | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(179): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1045+323delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549134 | |||||||
| chr13:49549181 | C | T | 188 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(185): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.1045+277G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549181 | |||||||
| chr13:49549189 | A | T | 3 | a0002c0008t0008g0105 a0002c0008t0008g0106 a0002c0008t0008g0154 |
3 | HG02280.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1045+269T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549189 | |||||||
| chr13:49549225 | C | T | 123 | a0001c0001t0001g0397 a0002c0002t0001g0055 a0002c0002t0001g0176 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.1045+233G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549225 | |||||||
| chr13:49549405 | G | C | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1045+53C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 9/12 | chr13 | 49549405 | |||||||
| chr13:49549696 | C | G | 122 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(119): Show |
126 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(123): Show |
intron_variant | MODIFIER | c.855-48G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49549696 | |||||||
| chr13:49549990 | C | CT | 31 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0017 others(28): Show |
32 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.855-343dupA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49549990 | |||||||
| chr13:49550152 | T | C | 1 | a0001c0001t0001g0356 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.855-504A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49550152 | |||||||
| chr13:49550166 | A | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.855-518T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49550166 | |||||||
| chr13:49550412 | A | G | 1 | a0002c0002t0003g0016 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.855-764T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49550412 | |||||||
| chr13:49550485 | G | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(207): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.855-837C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49550485 | |||||||
| chr13:49551029 | C | G | 122 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(119): Show |
126 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(123): Show |
intron_variant | MODIFIER | c.854+297G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49551029 | |||||||
| chr13:49551052 | G | A | 1 | a0002c0002t0002g0026 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.854+274C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49551052 | |||||||
| chr13:49551058 | G | A | 122 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(119): Show |
126 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(123): Show |
intron_variant | MODIFIER | c.854+268C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49551058 | |||||||
| chr13:49551146 | G | A | 6 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0359 others(3): Show |
6 | HG00140.hp2 HG00735.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.854+180C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49551146 | |||||||
| chr13:49551151 | A | G | 6 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0359 others(3): Show |
6 | HG00140.hp2 HG00735.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.854+175T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49551151 | |||||||
| chr13:49551155 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.854+171T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 8/12 | chr13 | 49551155 | |||||||
| chr13:49551486 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.712-18G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551486 | |||||||
| chr13:49551525 | C | G | 5 | a0002c0008t0008g0076 a0002c0008t0008g0105 a0002c0008t0008g0106 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-57G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551525 | |||||||
| chr13:49551542 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.712-74A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551542 | |||||||
| chr13:49551584 | C | T | 1 | a0001c0001t0003g0352 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.712-116G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551584 | |||||||
| chr13:49551654 | G | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.712-186C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551654 | |||||||
| chr13:49551683 | A | G | 1 | a0002c0002t0004g0209 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.712-215T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551683 | |||||||
| chr13:49551774 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.712-306A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551774 | |||||||
| chr13:49551799 | A | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(330): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.712-331T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551799 | |||||||
| chr13:49551832 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.711+346C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551832 | |||||||
| chr13:49551861 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.711+317A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551861 | |||||||
| chr13:49551899 | C | CA | 6 | a0002c0003t0003g0220 a0002c0003t0003g0224 a0002c0003t0003g0253 others(3): Show |
6 | HG00642.hp2 HG01099.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+278dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551899 | |||||||
| chr13:49551899 | CA | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(197): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.711+278delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551899 | |||||||
| chr13:49551899 | CAAA | C | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.711+276_711+278del others(3): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551899 | |||||||
| chr13:49551958 | A | AT | 10 | a0002c0003t0003g0007 a0002c0003t0003g0229 a0002c0003t0003g0233 others(7): Show |
11 | HG02040.hp2 HG02056.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.711+219dupA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551958 | |||||||
| chr13:49551958 | AT | A | 338 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(335): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.711+219delA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551958 | |||||||
| chr13:49551961 | T | G | 1 | a0002c0002t0003g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.711+217A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551961 | |||||||
| chr13:49551962 | T | G | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.711+216A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551962 | |||||||
| chr13:49551963 | T | G | 1 | a0002c0002t0004g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.711+215A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551963 | |||||||
| chr13:49551984 | G | A | 3 | a0002c0003t0001g0239 a0002c0003t0004g0238 a0002c0003t0004g0247 |
3 | NA18957.hp2 NA18998.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.711+194C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 7/12 | chr13 | 49551984 | |||||||
| chr13:49552305 | A | G | 2 | a0001c0004t0002g0382 a0001c0004t0004g0384 |
2 | HG00597.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.604-20T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552305 | |||||||
| chr13:49552345 | CA | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-61delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552345 | |||||||
| chr13:49552354 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-69G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552354 | |||||||
| chr13:49552369 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-84T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552369 | |||||||
| chr13:49552372 | C | G | 1 | a0002c0002t0002g0042 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.604-87G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552372 | |||||||
| chr13:49552488 | A | G | 5 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0153 others(2): Show |
5 | HG01074.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-203T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552488 | |||||||
| chr13:49552531 | T | C | 133 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(130): Show |
137 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(134): Show |
intron_variant | MODIFIER | c.604-246A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552531 | |||||||
| chr13:49552673 | A | G | 2 | a0002c0002t0011g0145 a0002c0002t0011g0191 |
2 | HG01884.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.604-388T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552673 | |||||||
| chr13:49552769 | G | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-484C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552769 | |||||||
| chr13:49552838 | GAAGAT | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-558_604-554del others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552838 | |||||||
| chr13:49552963 | C | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-678G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552963 | |||||||
| chr13:49552966 | C | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-681G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552966 | |||||||
| chr13:49552968 | G | A | 1 | a0002c0002t0002g0042 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.604-683C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49552968 | |||||||
| chr13:49553002 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(71): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.604-717A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553002 | |||||||
| chr13:49553108 | G | C | 5 | a0002c0008t0008g0076 a0002c0008t0008g0105 a0002c0008t0008g0106 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-823C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553108 | |||||||
| chr13:49553144 | C | T | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(207): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.604-859G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553144 | |||||||
| chr13:49553272 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-987A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553272 | |||||||
| chr13:49553384 | T | C | 333 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(330): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.604-1099A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553384 | |||||||
| chr13:49553388 | T | G | 3 | a0002c0008t0008g0105 a0002c0008t0008g0106 a0002c0008t0008g0154 |
3 | HG02280.hp2 HG02622.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.604-1103A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553388 | |||||||
| chr13:49553421 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-1136A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553421 | |||||||
| chr13:49553482 | C | T | 1 | a0002c0003t0004g0272 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.604-1197G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553482 | |||||||
| chr13:49553529 | AGTAACAG others(6): Show |
A | 1 | a0002c0003t0003g0230 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.604-1257_604-1245d others(15): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553529 | |||||||
| chr13:49553583 | T | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(71): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.604-1298A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553583 | |||||||
| chr13:49553656 | A | C | 1 | a0002c0002t0004g0183 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.604-1371T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553656 | |||||||
| chr13:49553669 | T | G | 1 | a0001c0001t0001g0155 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.604-1384A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553669 | |||||||
| chr13:49553774 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.604-1489G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553774 | |||||||
| chr13:49553936 | T | C | 1 | a0001c0004t0003g0282 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.603+1579A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553936 | |||||||
| chr13:49553997 | G | C | 2 | a0001c0001t0001g0328 a0001c0001t0003g0011 |
3 | HG00099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.603+1518C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553997 | |||||||
| chr13:49553999 | A | G | 2 | a0001c0001t0001g0328 a0001c0001t0003g0011 |
3 | HG00099.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.603+1516T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49553999 | |||||||
| chr13:49554061 | C | T | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.603+1454G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554061 | |||||||
| chr13:49554204 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.603+1311T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554204 | |||||||
| chr13:49554251 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+1264T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554251 | |||||||
| chr13:49554299 | T | C | 1 | a0002c0006t0007g0283 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.603+1216A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554299 | |||||||
| chr13:49554349 | A | C | 29 | a0002c0002t0002g0068 a0002c0002t0002g0070 a0002c0002t0002g0193 others(26): Show |
29 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.603+1166T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554349 | |||||||
| chr13:49554378 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+1137A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554378 | |||||||
| chr13:49554500 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+1015T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554500 | |||||||
| chr13:49554530 | C | T | 13 | a0001c0014t0001g0342 a0002c0002t0002g0144 a0002c0002t0002g0151 others(10): Show |
14 | HG00280.hp1 HG01109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.603+985G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554530 | |||||||
| chr13:49554538 | G | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+977C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554538 | |||||||
| chr13:49554589 | A | G | 122 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(119): Show |
126 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(123): Show |
intron_variant | MODIFIER | c.603+926T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554589 | |||||||
| chr13:49554592 | G | A | 10 | a0002c0002t0011g0145 a0002c0002t0011g0191 a0002c0006t0002g0288 others(7): Show |
12 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.603+923C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554592 | |||||||
| chr13:49554609 | T | C | 1 | a0002c0003t0003g0220 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.603+906A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554609 | |||||||
| chr13:49554618 | G | T | 122 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(119): Show |
126 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(123): Show |
intron_variant | MODIFIER | c.603+897C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554618 | |||||||
| chr13:49554647 | A | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+868T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554647 | |||||||
| chr13:49554657 | C | G | 5 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0153 others(2): Show |
5 | HG01074.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.603+858G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554657 | |||||||
| chr13:49554681 | C | G | 4 | a0002c0005t0003g0140 a0002c0005t0003g0141 a0002c0005t0003g0142 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+834G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554681 | |||||||
| chr13:49554708 | G | A | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(341): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.603+807C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554708 | |||||||
| chr13:49554740 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+775T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554740 | |||||||
| chr13:49554758 | T | G | 1 | a0001c0001t0001g0112 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.603+757A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554758 | |||||||
| chr13:49554945 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+570T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554945 | |||||||
| chr13:49554985 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+530G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49554985 | |||||||
| chr13:49555037 | C | G | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(341): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.603+478G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555037 | |||||||
| chr13:49555121 | T | C | 1 | a0001c0001t0001g0399 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.603+394A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555121 | |||||||
| chr13:49555127 | T | G | 3 | a0002c0003t0003g0222 a0002c0003t0003g0223 a0002c0003t0003g0228 |
3 | HG02559.hp1 HG02615.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.603+388A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555127 | |||||||
| chr13:49555145 | C | T | 29 | a0001c0004t0001g0281 a0001c0004t0002g0010 a0001c0004t0002g0270 others(26): Show |
30 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.603+370G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555145 | |||||||
| chr13:49555181 | G | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+334C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555181 | |||||||
| chr13:49555197 | A | C | 1 | a0002c0002t0004g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.603+318T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555197 | |||||||
| chr13:49555297 | T | C | 1 | a0002c0003t0003g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.603+218A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555297 | |||||||
| chr13:49555463 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+52G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555463 | |||||||
| chr13:49555479 | A | G | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(341): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.603+36T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555479 | |||||||
| chr13:49555496 | G | A | 1 | a0002c0003t0003g0273 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.603+19C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 6/12 | chr13 | 49555496 | |||||||
| chr13:49555850 | G | A | 1 | a0002c0002t0004g0206 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.445-177C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49555850 | |||||||
| chr13:49555882 | T | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-209A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49555882 | |||||||
| chr13:49556196 | G | GT | 31 | a0001c0001t0001g0072 a0001c0001t0001g0099 a0001c0001t0001g0128 others(28): Show |
31 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.445-524dupA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556196 | |||||||
| chr13:49556196 | GT | G | 112 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(109): Show |
116 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(113): Show |
intron_variant | MODIFIER | c.445-524delA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556196 | |||||||
| chr13:49556257 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-584A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556257 | |||||||
| chr13:49556283 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG01517.hp2 HG01981.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.445-610C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556283 | |||||||
| chr13:49556300 | C | T | 1 | a0002c0002t0003g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.445-627G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556300 | |||||||
| chr13:49556319 | T | C | 1 | a0001c0001t0001g0325 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.445-646A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556319 | |||||||
| chr13:49556325 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.445-652C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556325 | |||||||
| chr13:49556364 | G | T | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.445-691C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556364 | |||||||
| chr13:49556392 | G | A | 1 | a0002c0002t0002g0400 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.445-719C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556392 | |||||||
| chr13:49556394 | G | A | 6 | a0002c0003t0001g0239 a0002c0003t0004g0215 a0002c0003t0004g0238 others(3): Show |
6 | NA18957.hp2 NA18998.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-721C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556394 | |||||||
| chr13:49556425 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-752G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556425 | |||||||
| chr13:49556442 | G | A | 32 | a0002c0002t0001g0176 a0002c0002t0002g0157 a0002c0002t0003g0162 others(29): Show |
32 | HG01978.hp1 HG02027.hp1 HG02129.hp2 others(29): Show |
intron_variant | MODIFIER | c.445-769C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556442 | |||||||
| chr13:49556453 | G | C | 10 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(7): Show |
10 | HG01346.hp2 HG01928.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.445-780C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556453 | |||||||
| chr13:49556488 | C | G | 3 | a0002c0003t0001g0239 a0002c0003t0004g0238 a0002c0003t0004g0247 |
3 | NA18957.hp2 NA18998.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.445-815G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556488 | |||||||
| chr13:49556583 | G | GA | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-911dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556583 | |||||||
| chr13:49556792 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-1119A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556792 | |||||||
| chr13:49556877 | G | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-1204C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556877 | |||||||
| chr13:49556935 | T | C | 10 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0139 others(7): Show |
10 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.445-1262A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556935 | |||||||
| chr13:49556936 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.445-1263T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556936 | |||||||
| chr13:49556939 | T | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-1266A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49556939 | |||||||
| chr13:49557070 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-1397G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557070 | |||||||
| chr13:49557235 | C | T | 11 | a0002c0002t0003g0190 a0002c0002t0011g0145 a0002c0002t0011g0191 others(8): Show |
13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.445-1562G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557235 | |||||||
| chr13:49557254 | G | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-1581C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557254 | |||||||
| chr13:49557255 | G | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-1582C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557255 | |||||||
| chr13:49557408 | T | C | 8 | a0002c0007t0002g0057 a0002c0007t0003g0005 a0002c0007t0003g0031 others(5): Show |
9 | HG02257.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.445-1735A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557408 | |||||||
| chr13:49557434 | A | G | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.445-1761T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557434 | |||||||
| chr13:49557448 | T | G | 345 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(342): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.445-1775A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557448 | |||||||
| chr13:49557710 | A | G | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.445-2037T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557710 | |||||||
| chr13:49557729 | G | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.445-2056C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557729 | |||||||
| chr13:49557730 | G | A | 6 | a0002c0006t0002g0288 a0002c0006t0006g0009 a0002c0006t0006g0284 others(3): Show |
7 | HG02451.hp1 HG02647.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-2057C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557730 | |||||||
| chr13:49557757 | C | CA | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.445-2085dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557757 | |||||||
| chr13:49557766 | A | T | 1 | a0001c0001t0001g0386 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.445-2093T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557766 | |||||||
| chr13:49557767 | T | A | 3 | a0002c0002t0002g0042 a0002c0002t0004g0163 a0002c0020t0002g0071 |
3 | HG01257.hp1 HG03669.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.445-2094A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557767 | |||||||
| chr13:49557781 | G | C | 1 | a0001c0004t0003g0282 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.445-2108C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49557781 | |||||||
| chr13:49558137 | T | C | 4 | a0002c0002t0002g0144 a0002c0002t0002g0151 a0002c0002t0002g0156 others(1): Show |
4 | HG01109.hp2 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+1781A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558137 | |||||||
| chr13:49558298 | G | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+1620C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558298 | |||||||
| chr13:49558328 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.444+1590G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558328 | |||||||
| chr13:49558330 | C | G | 11 | a0002c0002t0003g0190 a0002c0002t0011g0145 a0002c0002t0011g0191 others(8): Show |
13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.444+1588G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558330 | |||||||
| chr13:49558419 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+1499T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558419 | |||||||
| chr13:49558452 | G | A | 5 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0153 others(2): Show |
5 | HG01074.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+1466C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558452 | |||||||
| chr13:49558458 | G | A | 1 | a0001c0001t0001g0394 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.444+1460C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558458 | |||||||
| chr13:49558462 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.444+1456G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558462 | |||||||
| chr13:49558508 | A | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+1410T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558508 | |||||||
| chr13:49558576 | C | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(207): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.444+1342G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558576 | |||||||
| chr13:49558679 | G | C | 1 | a0002c0003t0003g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.444+1239C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558679 | |||||||
| chr13:49558689 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+1229A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558689 | |||||||
| chr13:49558695 | C | CA | 45 | a0001c0001t0001g0095 a0001c0001t0001g0098 a0001c0001t0001g0100 others(42): Show |
46 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.444+1222dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558695 | |||||||
| chr13:49558695 | C | CAAA | 10 | a0002c0006t0002g0288 a0002c0006t0006g0008 a0002c0006t0006g0009 others(7): Show |
13 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.444+1220_444+1222d others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558695 | |||||||
| chr13:49558695 | C | CAAAA | 77 | a0002c0002t0001g0176 a0002c0002t0002g0004 a0002c0002t0002g0017 others(74): Show |
78 | HG00558.hp1 HG01070.hp2 HG01109.hp1 others(75): Show |
intron_variant | MODIFIER | c.444+1219_444+1222d others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558695 | |||||||
| chr13:49558695 | C | CAAAAA | 31 | a0002c0002t0001g0055 a0002c0002t0002g0026 a0002c0002t0002g0033 others(28): Show |
31 | HG01109.hp2 HG01496.hp2 HG01978.hp1 others(28): Show |
intron_variant | MODIFIER | c.444+1218_444+1222d others(7): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558695 | |||||||
| chr13:49558695 | CA | C | 9 | a0001c0001t0001g0137 a0001c0001t0005g0366 a0001c0009t0001g0131 others(6): Show |
9 | HG01243.hp2 HG01516.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.444+1222delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558695 | |||||||
| chr13:49558718 | T | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+1200A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558718 | |||||||
| chr13:49558773 | C | T | 1 | a0001c0001t0003g0345 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.444+1145G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558773 | |||||||
| chr13:49558802 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+1116G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558802 | |||||||
| chr13:49558833 | G | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+1085C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558833 | |||||||
| chr13:49558842 | G | A | 1 | a0002c0003t0003g0221 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.444+1076C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49558842 | |||||||
| chr13:49559080 | T | C | 1 | a0001c0001t0001g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.444+838A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559080 | |||||||
| chr13:49559162 | T | A | 1 | a0001c0001t0001g0386 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.444+756A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559162 | |||||||
| chr13:49559185 | A | C | 109 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(106): Show |
111 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(108): Show |
intron_variant | MODIFIER | c.444+733T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559185 | |||||||
| chr13:49559336 | A | C | 1 | a0002c0019t0003g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.444+582T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559336 | |||||||
| chr13:49559360 | GAGT | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+555_444+557del others(3): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559360 | |||||||
| chr13:49559378 | T | C | 2 | a0001c0001t0008g0318 a0001c0001t0008g0319 |
2 | HG01975.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.444+540A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559378 | |||||||
| chr13:49559383 | A | G | 5 | a0001c0001t0008g0318 a0001c0001t0008g0319 a0002c0002t0004g0183 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.444+535T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559383 | |||||||
| chr13:49559384 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.444+534G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559384 | |||||||
| chr13:49559389 | G | T | 1 | a0001c0001t0001g0112 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.444+529C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559389 | |||||||
| chr13:49559404 | C | T | 29 | a0002c0002t0002g0068 a0002c0002t0002g0070 a0002c0002t0002g0193 others(26): Show |
29 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.444+514G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559404 | |||||||
| chr13:49559415 | T | G | 8 | a0001c0004t0002g0270 a0001c0004t0002g0275 a0001c0004t0002g0276 others(5): Show |
8 | HG00642.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.444+503A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559415 | |||||||
| chr13:49559428 | G | A | 29 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0017 others(26): Show |
30 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.444+490C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559428 | |||||||
| chr13:49559452 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0003g0352 |
3 | HG00099.hp2 HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.444+466G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559452 | |||||||
| chr13:49559453 | G | A | 105 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(102): Show |
106 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(103): Show |
intron_variant | MODIFIER | c.444+465C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559453 | |||||||
| chr13:49559457 | C | T | 338 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(335): Show |
351 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(348): Show |
intron_variant | MODIFIER | c.444+461G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559457 | |||||||
| chr13:49559458 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0003g0352 |
3 | HG00099.hp2 HG01261.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.444+460G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559458 | |||||||
| chr13:49559467 | T | C | 1 | a0002c0002t0004g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.444+451A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559467 | |||||||
| chr13:49559473 | G | A | 84 | a0001c0001t0001g0305 a0001c0001t0012g0327 a0002c0002t0001g0055 others(81): Show |
88 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(85): Show |
intron_variant | MODIFIER | c.444+445C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559473 | |||||||
| chr13:49559483 | T | C | 7 | a0002c0002t0002g0144 a0002c0002t0002g0151 a0002c0002t0004g0171 others(4): Show |
7 | HG00639.hp2 HG01109.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.444+435A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559483 | |||||||
| chr13:49559519 | G | A | 1 | a0002c0002t0004g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.444+399C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559519 | |||||||
| chr13:49559520 | G | C | 10 | a0002c0002t0011g0145 a0002c0002t0011g0191 a0002c0006t0002g0288 others(7): Show |
12 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.444+398C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559520 | |||||||
| chr13:49559524 | T | C | 1 | a0002c0002t0004g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.444+394A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559524 | |||||||
| chr13:49559528 | T | C | 124 | a0001c0001t0003g0307 a0002c0002t0001g0055 a0002c0002t0001g0176 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.444+390A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559528 | |||||||
| chr13:49559575 | A | G | 7 | a0002c0002t0004g0168 a0002c0002t0004g0169 a0002c0002t0004g0170 others(4): Show |
7 | HG02129.hp2 HG02155.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.444+343T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559575 | |||||||
| chr13:49559580 | C | T | 1 | a0002c0002t0004g0066 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.444+338G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559580 | |||||||
| chr13:49559604 | A | G | 124 | a0001c0001t0001g0336 a0002c0002t0001g0055 a0002c0002t0001g0176 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.444+314T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559604 | |||||||
| chr13:49559620 | T | C | 4 | a0002c0002t0004g0163 a0002c0002t0004g0166 a0002c0002t0004g0173 others(1): Show |
4 | NA18942.hp2 NA18943.hp2 NA19076.hp1 others(1): Show |
intron_variant | MODIFIER | c.444+298A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559620 | |||||||
| chr13:49559655 | C | CA | 175 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(172): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.444+262dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559655 | |||||||
| chr13:49559655 | C | CAAAA | 109 | a0001c0004t0002g0010 a0001c0004t0002g0290 a0001c0004t0002g0291 others(106): Show |
113 | HG00544.hp1 HG00558.hp1 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.444+259_444+262dup others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559655 | |||||||
| chr13:49559655 | C | CAAAAA | 14 | a0002c0002t0002g0041 a0002c0002t0002g0049 a0002c0002t0002g0050 others(11): Show |
15 | HG01070.hp2 HG01109.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.444+258_444+262dup others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559655 | |||||||
| chr13:49559782 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+136T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559782 | |||||||
| chr13:49559837 | G | T | 1 | a0001c0001t0001g0389 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.444+81C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559837 | |||||||
| chr13:49559878 | G | GA | 26 | a0001c0004t0002g0010 a0001c0004t0002g0270 a0001c0004t0002g0275 others(23): Show |
27 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.444+39dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559878 | |||||||
| chr13:49559884 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.444+34T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559884 | |||||||
| chr13:49559911 | T | C | 1 | a0001c0001t0005g0088 | 1 | NA18982.hp2 | splice_region_variant&intron_variant | LOW | c.444+7A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 5/12 | chr13 | 49559911 | |||||||
| chr13:49560222 | T | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(178): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.278-138A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560222 | |||||||
| chr13:49560236 | G | C | 4 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0086 others(1): Show |
4 | HG00544.hp2 NA18960.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-152C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560236 | |||||||
| chr13:49560306 | TAGAA | T | 3 | a0002c0002t0004g0171 a0002c0002t0004g0184 a0004c0016t0004g0167 |
3 | HG03017.hp1 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.278-226_278-223del others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560306 | |||||||
| chr13:49560317 | G | C | 19 | a0002c0002t0002g0194 a0002c0002t0002g0195 a0002c0002t0002g0196 others(16): Show |
19 | HG00558.hp1 HG00621.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.278-233C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560317 | |||||||
| chr13:49560369 | G | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.278-285C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560369 | |||||||
| chr13:49560558 | T | C | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(341): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.278-474A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560558 | |||||||
| chr13:49560612 | A | AT | 78 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(75): Show |
80 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(77): Show |
intron_variant | MODIFIER | c.278-529dupA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560612 | |||||||
| chr13:49560612 | A | ATT | 32 | a0002c0002t0002g0068 a0002c0002t0002g0070 a0002c0002t0002g0193 others(29): Show |
32 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.278-530_278-529dup others(2): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560612 | |||||||
| chr13:49560612 | AT | A | 222 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(219): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.278-529delA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560612 | |||||||
| chr13:49560619 | T | TC | 11 | a0002c0002t0003g0190 a0002c0002t0011g0145 a0002c0002t0011g0191 others(8): Show |
13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.278-536_278-535ins others(1): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560619 | |||||||
| chr13:49560732 | G | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.278-648C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560732 | |||||||
| chr13:49560896 | G | A | 11 | a0002c0002t0003g0190 a0002c0002t0011g0145 a0002c0002t0011g0191 others(8): Show |
13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.278-812C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49560896 | |||||||
| chr13:49561041 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(174): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.278-957T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561041 | |||||||
| chr13:49561068 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.278-984A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561068 | |||||||
| chr13:49561096 | C | T | 94 | a0002c0002t0001g0176 a0002c0002t0002g0068 a0002c0002t0002g0070 others(91): Show |
97 | HG00558.hp1 HG00621.hp2 HG01109.hp2 others(94): Show |
intron_variant | MODIFIER | c.278-1012G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561096 | |||||||
| chr13:49561172 | T | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.278-1088A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561172 | |||||||
| chr13:49561239 | G | T | 1 | a0001c0001t0001g0250 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.278-1155C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561239 | |||||||
| chr13:49561312 | C | T | 5 | a0002c0008t0008g0076 a0002c0008t0008g0105 a0002c0008t0008g0106 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-1228G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561312 | |||||||
| chr13:49561327 | C | A | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.278-1243G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561327 | |||||||
| chr13:49561594 | A | G | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.278-1510T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561594 | |||||||
| chr13:49561729 | A | C | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.278-1645T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561729 | |||||||
| chr13:49561909 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.278-1825G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561909 | |||||||
| chr13:49561929 | T | TA | 12 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(9): Show |
12 | HG02074.hp2 NA18961.hp2 NA18963.hp2 others(9): Show |
intron_variant | MODIFIER | c.278-1846dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561929 | |||||||
| chr13:49561929 | TAA | T | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.278-1847_278-1846d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561929 | |||||||
| chr13:49561958 | C | T | 6 | a0001c0001t0001g0212 a0001c0001t0001g0389 a0001c0001t0001g0390 others(3): Show |
6 | HG02071.hp2 NA18948.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-1874G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561958 | |||||||
| chr13:49561985 | C | T | 29 | a0002c0002t0002g0068 a0002c0002t0002g0070 a0002c0002t0002g0193 others(26): Show |
29 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.278-1901G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49561985 | |||||||
| chr13:49562101 | G | GA | 12 | a0001c0001t0001g0309 a0002c0002t0003g0190 a0002c0002t0011g0145 others(9): Show |
14 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.278-2018dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562101 | |||||||
| chr13:49562101 | GA | G | 10 | a0002c0002t0001g0055 a0002c0002t0002g0026 a0002c0002t0002g0027 others(7): Show |
10 | HG02015.hp2 HG02083.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.278-2018delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562101 | |||||||
| chr13:49562162 | A | T | 1 | a0001c0001t0001g0126 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.278-2078T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562162 | |||||||
| chr13:49562208 | T | C | 5 | a0002c0005t0002g0139 a0002c0005t0003g0140 a0002c0005t0003g0141 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-2124A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562208 | |||||||
| chr13:49562229 | T | C | 1 | a0002c0002t0002g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.278-2145A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562229 | |||||||
| chr13:49562347 | C | T | 1 | a0001c0001t0007g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.278-2263G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562347 | |||||||
| chr13:49562514 | CA | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(197): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.278-2431delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562514 | |||||||
| chr13:49562514 | CAA | C | 66 | a0001c0001t0001g0085 a0001c0001t0005g0334 a0001c0001t0009g0330 others(63): Show |
67 | HG01070.hp1 HG01070.hp2 HG01257.hp1 others(64): Show |
intron_variant | MODIFIER | c.278-2432_278-2431d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562514 | |||||||
| chr13:49562514 | CAAA | C | 55 | a0002c0002t0002g0045 a0002c0002t0002g0068 a0002c0002t0002g0070 others(52): Show |
58 | HG00558.hp1 HG00621.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.278-2433_278-2431d others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562514 | |||||||
| chr13:49562538 | T | A | 357 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(354): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.278-2454A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562538 | |||||||
| chr13:49562673 | C | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.278-2589G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562673 | |||||||
| chr13:49562774 | G | A | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.278-2690C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562774 | |||||||
| chr13:49562776 | CTT | C | 60 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0039 others(57): Show |
60 | HG00597.hp1 HG00621.hp1 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.278-2694_278-2693d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562776 | |||||||
| chr13:49562776 | CTTT | C | 148 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(145): Show |
154 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.278-2695_278-2693d others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562776 | |||||||
| chr13:49562776 | CTTTT | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(87): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(97): Show |
intron_variant | MODIFIER | c.278-2696_278-2693d others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562776 | |||||||
| chr13:49562776 | CTTTTT | C | 84 | a0001c0001t0001g0347 a0001c0001t0001g0395 a0001c0001t0005g0383 others(81): Show |
85 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.278-2697_278-2693d others(7): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562776 | |||||||
| chr13:49562776 | CTTTTTT | C | 8 | a0002c0002t0001g0055 a0002c0002t0002g0017 a0002c0002t0002g0053 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-2698_278-2693d others(8): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562776 | |||||||
| chr13:49562776 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0213 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.278-2702_278-2693d others(12): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562776 | |||||||
| chr13:49562776 | CTTTTTTT others(4): Show |
C | 4 | a0002c0005t0003g0140 a0002c0005t0003g0141 a0002c0005t0003g0142 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-2703_278-2693d others(13): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562776 | |||||||
| chr13:49562780 | T | C | 2 | a0002c0007t0003g0031 a0002c0007t0006g0150 |
2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.278-2696A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562780 | |||||||
| chr13:49562781 | T | C | 33 | a0002c0002t0002g0043 a0002c0002t0002g0051 a0002c0002t0002g0144 others(30): Show |
36 | HG01109.hp2 HG01884.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.278-2697A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562781 | |||||||
| chr13:49562782 | T | C | 81 | a0002c0002t0001g0176 a0002c0002t0002g0004 a0002c0002t0002g0026 others(78): Show |
82 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.278-2698A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562782 | |||||||
| chr13:49562783 | T | C | 8 | a0002c0002t0001g0055 a0002c0002t0002g0017 a0002c0002t0002g0053 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.278-2699A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562783 | |||||||
| chr13:49562806 | T | A | 4 | a0002c0007t0002g0057 a0002c0007t0003g0005 a0002c0007t0003g0031 others(1): Show |
5 | HG02818.hp1 HG02896.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-2722A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562806 | |||||||
| chr13:49562916 | C | T | 1 | a0001c0001t0003g0352 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.278-2832G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49562916 | |||||||
| chr13:49563104 | A | G | 1 | a0002c0002t0002g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.278-3020T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563104 | |||||||
| chr13:49563135 | C | A | 3 | a0001c0009t0001g0101 a0001c0009t0001g0125 a0001c0009t0001g0131 |
3 | NA18966.hp1 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.278-3051G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563135 | |||||||
| chr13:49563153 | A | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.278-3069T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563153 | |||||||
| chr13:49563218 | G | A | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.278-3134C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563218 | |||||||
| chr13:49563227 | T | A | 210 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(207): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.278-3143A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563227 | |||||||
| chr13:49563230 | T | C | 2 | a0002c0003t0003g0217 a0002c0003t0003g0218 |
2 | HG01074.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.278-3146A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563230 | |||||||
| chr13:49563257 | T | C | 110 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(107): Show |
112 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(109): Show |
intron_variant | MODIFIER | c.278-3173A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563257 | |||||||
| chr13:49563259 | G | A | 1 | a0001c0001t0003g0343 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.278-3175C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563259 | |||||||
| chr13:49563333 | CAGAG | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.278-3253_278-3250d others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563333 | |||||||
| chr13:49563347 | C | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.278-3263G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563347 | |||||||
| chr13:49563351 | G | A | 1 | a0002c0003t0003g0274 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.277+3267C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563351 | |||||||
| chr13:49563355 | C | CA | 29 | a0001c0001t0005g0350 a0001c0001t0009g0330 a0001c0001t0009g0331 others(26): Show |
29 | HG00544.hp1 HG01070.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.277+3262dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563355 | |||||||
| chr13:49563355 | C | CAA | 167 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(164): Show |
177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.277+3261_277+3262d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563355 | |||||||
| chr13:49563355 | C | CAAA | 46 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0089 others(43): Show |
46 | HG00597.hp2 HG00741.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.277+3260_277+3262d others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563355 | |||||||
| chr13:49563355 | CA | C | 70 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0026 others(67): Show |
72 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.277+3262delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563355 | |||||||
| chr13:49563398 | T | C | 1 | a0001c0004t0002g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.277+3220A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563398 | |||||||
| chr13:49563400 | T | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+3218A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563400 | |||||||
| chr13:49563514 | T | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+3104A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563514 | |||||||
| chr13:49563527 | G | C | 3 | a0001c0009t0001g0101 a0001c0009t0001g0125 a0001c0009t0001g0131 |
3 | NA18966.hp1 NA19000.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.277+3091C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563527 | |||||||
| chr13:49563552 | C | G | 344 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(341): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.277+3066G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563552 | |||||||
| chr13:49563656 | CA | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+2961delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563656 | |||||||
| chr13:49563661 | G | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+2957C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563661 | |||||||
| chr13:49563709 | C | T | 1 | a0001c0001t0001g0323 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.277+2909G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563709 | |||||||
| chr13:49563775 | A | ATGCTCAG others(10): Show |
1 | a0001c0001t0001g0309 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.277+2826_277+2842d others(19): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563775 | |||||||
| chr13:49563930 | G | A | 7 | a0002c0002t0004g0168 a0002c0002t0004g0169 a0002c0002t0004g0170 others(4): Show |
7 | HG02129.hp2 HG02155.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+2688C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49563930 | |||||||
| chr13:49564107 | C | G | 1 | a0002c0002t0003g0162 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.277+2511G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564107 | |||||||
| chr13:49564173 | C | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+2445G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564173 | |||||||
| chr13:49564286 | A | G | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+2332T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564286 | |||||||
| chr13:49564456 | C | T | 9 | a0002c0002t0002g0156 a0002c0007t0002g0057 a0002c0007t0003g0005 others(6): Show |
10 | HG02257.hp1 HG02818.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+2162G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564456 | |||||||
| chr13:49564543 | C | T | 2 | a0002c0002t0002g0026 a0002c0002t0002g0027 |
2 | HG02015.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.277+2075G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564543 | |||||||
| chr13:49564583 | C | CA | 57 | a0001c0001t0001g0018 a0001c0001t0001g0025 a0001c0001t0001g0039 others(54): Show |
57 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.277+2034dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(3): Show |
24 | a0002c0002t0002g0193 a0002c0002t0002g0194 a0002c0002t0002g0195 others(21): Show |
26 | HG00558.hp1 HG01891.hp1 HG02015.hp1 others(23): Show |
intron_variant | MODIFIER | c.277+2025_277+2034d others(12): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(4): Show |
10 | a0002c0002t0002g0068 a0002c0002t0002g0070 a0002c0002t0002g0198 others(7): Show |
10 | HG00621.hp2 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.277+2024_277+2034d others(13): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(5): Show |
2 | a0002c0002t0002g0058 a0002c0002t0004g0067 |
2 | HG01496.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.277+2023_277+2034d others(14): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(6): Show |
3 | a0002c0002t0002g0004 a0002c0002t0003g0061 a0002c0002t0003g0062 |
4 | HG02895.hp1 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+2022_277+2034d others(15): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(7): Show |
2 | a0002c0002t0002g0032 a0002c0002t0002g0033 |
2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.277+2021_277+2034d others(16): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(10): Show |
1 | a0002c0002t0002g0037 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.277+2018_277+2034d others(19): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(12): Show |
3 | a0002c0007t0003g0147 a0002c0007t0006g0146 a0002c0010t0002g0255 |
3 | HG02896.hp2 HG03130.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.277+2016_277+2034d others(21): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(13): Show |
2 | a0002c0007t0006g0148 a0002c0010t0002g0231 |
2 | HG02897.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.277+2015_277+2034d others(22): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(15): Show |
1 | a0002c0002t0003g0190 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.277+2013_277+2034d others(24): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | C | CAAAAAAA others(25): Show |
2 | a0002c0007t0006g0150 a0002c0013t0004g0256 |
2 | HG02257.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.277+2034_277+2035i others(34): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | CA | C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(66): Show |
76 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.277+2034delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | CAAA | C | 7 | a0002c0002t0001g0055 a0002c0002t0003g0016 a0002c0002t0004g0182 others(4): Show |
8 | HG02257.hp2 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+2032_277+2034d others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | CAAAA | C | 10 | a0002c0002t0002g0017 a0002c0002t0002g0053 a0002c0002t0002g0059 others(7): Show |
10 | HG01109.hp1 HG02027.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.277+2031_277+2034d others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | CAAAAA | C | 26 | a0002c0002t0001g0176 a0002c0002t0002g0157 a0002c0002t0003g0162 others(23): Show |
26 | HG01978.hp1 HG02055.hp2 HG02129.hp2 others(23): Show |
intron_variant | MODIFIER | c.277+2030_277+2034d others(7): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | CAAAAAA | C | 6 | a0002c0002t0004g0161 a0002c0002t0004g0173 a0002c0008t0008g0105 others(3): Show |
6 | HG02280.hp2 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+2029_277+2034d others(8): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564583 | CAAAAAAA others(1): Show |
C | 14 | a0002c0002t0002g0026 a0002c0002t0002g0027 a0002c0002t0002g0029 others(11): Show |
14 | HG01070.hp2 HG01257.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.277+2027_277+2034d others(10): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564583 | |||||||
| chr13:49564619 | C | T | 1 | a0002c0006t0006g0287 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.277+1999G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564619 | |||||||
| chr13:49564620 | G | A | 4 | a0002c0002t0002g0004 a0002c0002t0002g0032 a0002c0002t0002g0033 others(1): Show |
5 | HG02109.hp1 HG02145.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+1998C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564620 | |||||||
| chr13:49564666 | C | T | 78 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(75): Show |
85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.277+1952G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564666 | |||||||
| chr13:49564781 | C | T | 5 | a0002c0005t0002g0139 a0002c0005t0003g0140 a0002c0005t0003g0141 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+1837G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564781 | |||||||
| chr13:49564878 | G | A | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.277+1740C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564878 | |||||||
| chr13:49564884 | C | T | 1 | a0002c0003t0003g0214 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.277+1734G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564884 | |||||||
| chr13:49564890 | CA | C | 127 | a0001c0001t0001g0073 a0001c0001t0001g0085 a0002c0002t0001g0055 others(124): Show |
131 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(128): Show |
intron_variant | MODIFIER | c.277+1727delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564890 | |||||||
| chr13:49564890 | CAAAA | C | 26 | a0001c0004t0002g0010 a0001c0004t0002g0270 a0001c0004t0002g0275 others(23): Show |
27 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.277+1724_277+1727d others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564890 | |||||||
| chr13:49564898 | A | G | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+1720T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564898 | |||||||
| chr13:49564966 | T | C | 9 | a0002c0002t0002g0156 a0002c0007t0002g0057 a0002c0007t0003g0005 others(6): Show |
10 | HG02257.hp1 HG02818.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+1652A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564966 | |||||||
| chr13:49564989 | C | G | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+1629G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564989 | |||||||
| chr13:49564994 | G | GTCCCGCT others(11): Show |
10 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0139 others(7): Show |
10 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+1606_277+1623d others(20): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49564994 | |||||||
| chr13:49565018 | C | T | 1 | a0001c0001t0003g0329 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.277+1600G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565018 | |||||||
| chr13:49565068 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01346.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.277+1550C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565068 | |||||||
| chr13:49565138 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.277+1480G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565138 | |||||||
| chr13:49565139 | C | T | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.277+1479G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565139 | |||||||
| chr13:49565150 | G | C | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.277+1468C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565150 | |||||||
| chr13:49565187 | G | C | 8 | a0002c0006t0002g0288 a0002c0006t0006g0008 a0002c0006t0006g0009 others(5): Show |
10 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+1431C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565187 | |||||||
| chr13:49565240 | C | T | 3 | a0002c0010t0002g0231 a0002c0010t0002g0255 a0002c0013t0004g0256 |
3 | HG03490.hp2 HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.277+1378G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565240 | |||||||
| chr13:49565324 | T | G | 14 | a0001c0001t0007g0003 a0001c0001t0007g0030 a0001c0001t0007g0034 others(11): Show |
15 | HG01106.hp2 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.277+1294A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565324 | |||||||
| chr13:49565378 | C | T | 1 | a0002c0002t0002g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.277+1240G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565378 | |||||||
| chr13:49565383 | T | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+1235A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565383 | |||||||
| chr13:49565435 | A | AC | 4 | a0001c0004t0002g0297 a0002c0002t0002g0059 a0002c0003t0003g0265 others(1): Show |
4 | HG01109.hp1 HG03669.hp1 NA19059.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+1182dupG | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565435 | |||||||
| chr13:49565472 | G | A | 32 | a0002c0002t0001g0176 a0002c0002t0002g0157 a0002c0002t0003g0162 others(29): Show |
32 | HG01978.hp1 HG02027.hp1 HG02129.hp2 others(29): Show |
intron_variant | MODIFIER | c.277+1146C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565472 | |||||||
| chr13:49565478 | G | C | 3 | a0001c0004t0001g0281 a0001c0004t0010g0149 a0001c0004t0010g0152 |
3 | HG02717.hp2 HG03139.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.277+1140C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565478 | |||||||
| chr13:49565506 | C | T | 1 | a0002c0002t0002g0070 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.277+1112G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565506 | |||||||
| chr13:49565524 | AGTGAGGA others(72): Show |
A | 1 | a0001c0001t0001g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.277+1015_277+1093d others(81): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565524 | |||||||
| chr13:49565556 | A | G | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+1062T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565556 | |||||||
| chr13:49565600 | G | A | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+1018C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565600 | |||||||
| chr13:49565607 | A | G | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+1011T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565607 | |||||||
| chr13:49565623 | A | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+995T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565623 | |||||||
| chr13:49565626 | CCCG | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+989_277+991del others(3): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565626 | |||||||
| chr13:49565630 | A | G | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+988T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565630 | |||||||
| chr13:49565643 | G | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+975C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565643 | |||||||
| chr13:49565654 | T | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+964A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565654 | |||||||
| chr13:49565663 | G | A | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+955C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565663 | |||||||
| chr13:49565667 | G | GCAA | 5 | a0002c0008t0008g0076 a0002c0008t0008g0105 a0002c0008t0008g0106 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+950_277+951ins others(3): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565667 | |||||||
| chr13:49565667 | G | GCGA | 118 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(115): Show |
122 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(119): Show |
intron_variant | MODIFIER | c.277+950_277+951ins others(3): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565667 | |||||||
| chr13:49565672 | G | A | 1 | a0002c0005t0003g0142 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.277+946C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565672 | |||||||
| chr13:49565676 | G | GGGAGGTG others(11): Show |
124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+941_277+942ins others(18): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565676 | |||||||
| chr13:49565677 | A | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+941T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565677 | |||||||
| chr13:49565700 | G | A | 5 | a0002c0008t0008g0076 a0002c0008t0008g0105 a0002c0008t0008g0106 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+918C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565700 | |||||||
| chr13:49565711 | C | G | 10 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0139 others(7): Show |
10 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+907G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565711 | |||||||
| chr13:49565743 | C | T | 6 | a0002c0002t0004g0064 a0002c0002t0004g0065 a0002c0002t0004g0066 others(3): Show |
6 | HG01255.hp2 HG01496.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+875G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565743 | |||||||
| chr13:49565747 | A | AC | 5 | a0001c0001t0001g0114 a0001c0001t0001g0126 a0001c0004t0002g0298 others(2): Show |
5 | HG00597.hp2 HG01433.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+870dupG | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565747 | |||||||
| chr13:49565798 | C | T | 123 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(120): Show |
127 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(124): Show |
intron_variant | MODIFIER | c.277+820G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565798 | |||||||
| chr13:49565810 | C | T | 1 | a0002c0002t0002g0157 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.277+808G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565810 | |||||||
| chr13:49565811 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.277+807C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565811 | |||||||
| chr13:49565814 | G | A | 29 | a0002c0002t0001g0055 a0002c0002t0002g0004 a0002c0002t0002g0017 others(26): Show |
30 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.277+804C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565814 | |||||||
| chr13:49565847 | G | A | 3 | a0002c0002t0002g0144 a0002c0002t0002g0151 a0002c0019t0003g0143 |
3 | HG01109.hp2 HG02976.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.277+771C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565847 | |||||||
| chr13:49565855 | A | G | 30 | a0002c0002t0002g0068 a0002c0002t0002g0070 a0002c0002t0002g0193 others(27): Show |
30 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.277+763T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565855 | |||||||
| chr13:49565875 | T | C | 30 | a0002c0002t0002g0068 a0002c0002t0002g0070 a0002c0002t0002g0193 others(27): Show |
30 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.277+743A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565875 | |||||||
| chr13:49565891 | T | C | 34 | a0002c0002t0001g0176 a0002c0002t0002g0157 a0002c0002t0002g0400 others(31): Show |
34 | HG01978.hp1 HG02027.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.277+727A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565891 | |||||||
| chr13:49565900 | C | A | 1 | a0002c0002t0002g0203 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.277+718G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565900 | |||||||
| chr13:49565971 | T | C | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+647A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565971 | |||||||
| chr13:49565972 | G | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+646C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49565972 | |||||||
| chr13:49566054 | T | TGAA | 98 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(95): Show |
99 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(96): Show |
intron_variant | MODIFIER | c.277+561_277+563dup others(3): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566054 | |||||||
| chr13:49566069 | C | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+549G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566069 | |||||||
| chr13:49566124 | A | G | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+494T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566124 | |||||||
| chr13:49566194 | C | T | 3 | a0002c0010t0002g0231 a0002c0010t0002g0255 a0002c0013t0004g0256 |
3 | HG03490.hp2 HG03492.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.277+424G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566194 | |||||||
| chr13:49566257 | TAAAAAAA others(3): Show |
T | 1 | a0002c0002t0002g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.277+351_277+360del others(10): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566257 | |||||||
| chr13:49566257 | TAAAAAAA others(10): Show |
T | 2 | a0002c0002t0002g0193 a0002c0002t0002g0199 |
2 | NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.277+344_277+360del others(17): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566257 | |||||||
| chr13:49566258 | A | T | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.277+360T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566258 | |||||||
| chr13:49566264 | ATAAAAT | A | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.277+348_277+353del others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566264 | |||||||
| chr13:49566268 | A | T | 1 | a0002c0002t0002g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.277+350T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566268 | |||||||
| chr13:49566271 | A | AAAAT | 3 | a0001c0001t0001g0084 a0001c0001t0003g0011 a0002c0003t0004g0248 |
4 | HG01256.hp2 HG01258.hp2 NA19088.hp2 others(1): Show |
intron_variant | MODIFIER | c.277+343_277+346dup others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566271 | |||||||
| chr13:49566271 | A | T | 1 | a0001c0001t0001g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.277+347T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566271 | |||||||
| chr13:49566271 | AAAAT | A | 4 | a0001c0001t0001g0305 a0001c0001t0012g0327 a0001c0004t0010g0149 others(1): Show |
4 | HG03139.hp2 HG03209.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+343_277+346del others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566271 | |||||||
| chr13:49566271 | AAAATAAA others(1): Show |
A | 11 | a0001c0001t0001g0311 a0002c0005t0002g0074 a0002c0005t0002g0075 others(8): Show |
11 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+339_277+346del others(8): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566271 | |||||||
| chr13:49566271 | AAAATAAA others(5): Show |
A | 1 | a0001c0004t0002g0299 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.277+335_277+346del others(12): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566271 | |||||||
| chr13:49566275 | T | A | 1 | a0002c0002t0002g0045 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.277+343A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566275 | |||||||
| chr13:49566276 | AAATAAAT others(4): Show |
A | 121 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(118): Show |
125 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(122): Show |
intron_variant | MODIFIER | c.277+331_277+341del others(11): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566276 | |||||||
| chr13:49566279 | T | A | 2 | a0002c0002t0002g0193 a0002c0002t0002g0199 |
2 | NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.277+339A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566279 | |||||||
| chr13:49566283 | T | A | 2 | a0002c0002t0002g0193 a0002c0002t0002g0199 |
2 | NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.277+335A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566283 | |||||||
| chr13:49566287 | T | A | 2 | a0002c0002t0002g0193 a0002c0002t0002g0199 |
2 | NA18979.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.277+331A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566287 | |||||||
| chr13:49566304 | A | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+314T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566304 | |||||||
| chr13:49566307 | A | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0096 |
2 | HG02300.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.277+311T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566307 | |||||||
| chr13:49566390 | G | A | 1 | a0001c0004t0002g0304 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.277+228C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566390 | |||||||
| chr13:49566393 | G | A | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.277+225C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566393 | |||||||
| chr13:49566434 | T | A | 1 | a0002c0002t0011g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.277+184A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566434 | |||||||
| chr13:49566460 | G | A | 1 | a0001c0001t0003g0326 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.277+158C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 4/12 | chr13 | 49566460 | |||||||
| chr13:49567140 | C | T | 124 | a0002c0002t0001g0055 a0002c0002t0001g0176 a0002c0002t0002g0004 others(121): Show |
128 | HG00558.hp1 HG00621.hp2 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.126+14G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 3/12 | chr13 | 49567140 | |||||||
| chr13:49567465 | C | T | 1 | a0002c0003t0001g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-41-145G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49567465 | |||||||
| chr13:49567503 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | NA18940.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-41-183C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49567503 | |||||||
| chr13:49567571 | T | C | 31 | a0001c0001t0001g0044 a0002c0002t0001g0055 a0002c0002t0002g0004 others(28): Show |
32 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.-41-251A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49567571 | |||||||
| chr13:49567761 | T | C | 101 | a0001c0001t0001g0044 a0001c0001t0001g0381 a0001c0004t0002g0299 others(98): Show |
105 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(102): Show |
intron_variant | MODIFIER | c.-41-441A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49567761 | |||||||
| chr13:49567762 | G | C | 98 | a0001c0001t0001g0044 a0001c0001t0001g0381 a0001c0004t0002g0299 others(95): Show |
102 | HG01070.hp2 HG01109.hp1 HG01109.hp2 others(99): Show |
intron_variant | MODIFIER | c.-41-442C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49567762 | |||||||
| chr13:49567885 | C | T | 7 | a0001c0001t0001g0232 a0001c0001t0001g0320 a0001c0001t0001g0321 others(4): Show |
7 | HG00140.hp2 HG00408.hp2 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41-565G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49567885 | |||||||
| chr13:49567895 | G | A | 1 | a0002c0003t0003g0262 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-41-575C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49567895 | |||||||
| chr13:49567939 | G | C | 30 | a0001c0001t0001g0389 a0001c0001t0001g0390 a0001c0004t0001g0281 others(27): Show |
31 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-41-619C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49567939 | |||||||
| chr13:49568093 | C | T | 92 | a0001c0001t0001g0044 a0001c0001t0001g0305 a0001c0001t0001g0328 others(89): Show |
94 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(91): Show |
intron_variant | MODIFIER | c.-41-773G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568093 | |||||||
| chr13:49568191 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-41-871G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568191 | |||||||
| chr13:49568267 | C | T | 6 | a0001c0004t0010g0149 a0001c0004t0010g0152 a0002c0007t0003g0147 others(3): Show |
6 | HG02257.hp1 HG02717.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.-41-947G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568267 | |||||||
| chr13:49568327 | C | G | 34 | a0001c0001t0001g0039 a0002c0002t0001g0176 a0002c0002t0002g0157 others(31): Show |
34 | HG01978.hp1 HG02027.hp1 HG02129.hp2 others(31): Show |
intron_variant | MODIFIER | c.-41-1007G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568327 | |||||||
| chr13:49568364 | T | C | 205 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(202): Show |
211 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(208): Show |
intron_variant | MODIFIER | c.-41-1044A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568364 | |||||||
| chr13:49568407 | C | T | 5 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0153 others(2): Show |
5 | HG01074.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41-1087G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568407 | |||||||
| chr13:49568423 | G | A | 2 | a0001c0001t0001g0252 a0002c0003t0003g0253 |
2 | HG02056.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-41-1103C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568423 | |||||||
| chr13:49568436 | C | G | 1 | a0001c0004t0001g0281 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-41-1116G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568436 | |||||||
| chr13:49568459 | A | G | 197 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(194): Show |
201 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(198): Show |
intron_variant | MODIFIER | c.-41-1139T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568459 | |||||||
| chr13:49568507 | A | G | 207 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(204): Show |
211 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(208): Show |
intron_variant | MODIFIER | c.-41-1187T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568507 | |||||||
| chr13:49568562 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-41-1242C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568562 | |||||||
| chr13:49568574 | C | T | 163 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(160): Show |
164 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(161): Show |
intron_variant | MODIFIER | c.-41-1254G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568574 | |||||||
| chr13:49568648 | C | CG | 15 | a0001c0001t0001g0018 a0001c0001t0001g0022 a0001c0001t0001g0023 others(12): Show |
15 | HG00544.hp2 HG00621.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-41-1329dupC | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568648 | |||||||
| chr13:49568650 | GGGGA | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(165): Show |
175 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(172): Show |
intron_variant | MODIFIER | c.-41-1334_-41-1331d others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568650 | |||||||
| chr13:49568651 | GGGA | G | 90 | a0001c0001t0001g0044 a0001c0001t0001g0305 a0001c0001t0001g0320 others(87): Show |
96 | HG00140.hp2 HG00544.hp1 HG00642.hp1 others(93): Show |
intron_variant | MODIFIER | c.-41-1334_-41-1332d others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568651 | |||||||
| chr13:49568652 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-41-1332C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568652 | |||||||
| chr13:49568654 | A | G | 76 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(73): Show |
77 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-41-1334T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568654 | |||||||
| chr13:49568659 | G | C | 1 | a0002c0002t0004g0069 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-41-1339C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568659 | |||||||
| chr13:49568659 | G | T | 1 | a0002c0002t0002g0026 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-41-1339C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568659 | |||||||
| chr13:49568669 | A | G | 2 | a0002c0002t0004g0160 a0002c0002t0004g0174 |
2 | NA18952.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.-41-1349T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568669 | |||||||
| chr13:49568734 | T | G | 3 | a0002c0002t0004g0171 a0002c0002t0004g0184 a0004c0016t0004g0167 |
3 | HG03017.hp1 NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-41-1414A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568734 | |||||||
| chr13:49568814 | A | G | 1 | a0002c0002t0002g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-41-1494T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568814 | |||||||
| chr13:49568854 | G | A | 164 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(161): Show |
165 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.-41-1534C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568854 | |||||||
| chr13:49568999 | C | A | 1 | a0001c0001t0001g0092 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-41-1679G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49568999 | |||||||
| chr13:49569107 | G | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-1787C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569107 | |||||||
| chr13:49569159 | G | T | 2 | a0001c0004t0010g0149 a0001c0004t0010g0152 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-41-1839C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569159 | |||||||
| chr13:49569225 | T | C | 77 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-41-1905A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569225 | |||||||
| chr13:49569312 | G | T | 1 | a0002c0005t0002g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-41-1992C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569312 | |||||||
| chr13:49569345 | G | A | 1 | a0001c0004t0004g0384 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-41-2025C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569345 | |||||||
| chr13:49569374 | G | A | 1 | a0002c0002t0002g0029 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-41-2054C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569374 | |||||||
| chr13:49569395 | G | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-2075C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569395 | |||||||
| chr13:49569419 | CA | C | 161 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(158): Show |
162 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.-41-2100delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569419 | |||||||
| chr13:49569428 | A | T | 1 | a0002c0002t0004g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-41-2108T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569428 | |||||||
| chr13:49569429 | A | G | 1 | a0002c0002t0004g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-41-2109T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569429 | |||||||
| chr13:49569429 | A | T | 161 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(158): Show |
162 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.-41-2109T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569429 | |||||||
| chr13:49569431 | G | C | 1 | a0002c0002t0004g0173 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-41-2111C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569431 | |||||||
| chr13:49569434 | A | G | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-2114T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569434 | |||||||
| chr13:49569438 | A | G | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-2118T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569438 | |||||||
| chr13:49569460 | C | A | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-41-2140G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569460 | |||||||
| chr13:49569510 | G | A | 7 | a0002c0002t0004g0168 a0002c0002t0004g0169 a0002c0002t0004g0170 others(4): Show |
7 | HG02129.hp2 HG02155.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41-2190C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569510 | |||||||
| chr13:49569521 | G | A | 161 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(158): Show |
162 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.-41-2201C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569521 | |||||||
| chr13:49569654 | G | T | 336 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-41-2334C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569654 | |||||||
| chr13:49569718 | C | CAA | 159 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(156): Show |
160 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(157): Show |
intron_variant | MODIFIER | c.-41-2400_-41-2399d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569718 | |||||||
| chr13:49569766 | G | T | 7 | a0001c0004t0010g0149 a0001c0004t0010g0152 a0002c0002t0002g0156 others(4): Show |
7 | HG02257.hp1 HG02717.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41-2446C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569766 | |||||||
| chr13:49569829 | C | T | 4 | a0002c0005t0003g0140 a0002c0005t0003g0141 a0002c0005t0003g0142 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-2509G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569829 | |||||||
| chr13:49569843 | G | A | 3 | a0002c0007t0002g0057 a0002c0007t0003g0005 a0002c0007t0003g0056 |
4 | HG02818.hp1 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-2523C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569843 | |||||||
| chr13:49569852 | G | A | 29 | a0001c0001t0001g0212 a0002c0002t0002g0068 a0002c0002t0002g0070 others(26): Show |
29 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.-41-2532C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569852 | |||||||
| chr13:49569879 | A | G | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-2559T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569879 | |||||||
| chr13:49569982 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-41-2662A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49569982 | |||||||
| chr13:49570012 | T | C | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-2692A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49570012 | |||||||
| chr13:49570061 | G | T | 77 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-41-2741C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49570061 | |||||||
| chr13:49570203 | G | A | 1 | a0002c0003t0003g0273 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-41-2883C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49570203 | |||||||
| chr13:49570385 | G | A | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-41-3065C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49570385 | |||||||
| chr13:49570410 | T | C | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-3090A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49570410 | |||||||
| chr13:49570477 | G | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-3157C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49570477 | |||||||
| chr13:49570567 | T | C | 7 | a0002c0002t0004g0168 a0002c0002t0004g0169 a0002c0002t0004g0170 others(4): Show |
7 | HG02129.hp2 HG02155.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.-41-3247A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49570567 | |||||||
| chr13:49570569 | C | T | 1 | a0002c0003t0003g0241 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-41-3249G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49570569 | |||||||
| chr13:49570859 | A | C | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-3539T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49570859 | |||||||
| chr13:49571009 | T | G | 2 | a0001c0004t0010g0149 a0001c0004t0010g0152 |
2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-41-3689A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49571009 | |||||||
| chr13:49571040 | C | T | 5 | a0002c0005t0002g0139 a0002c0005t0003g0140 a0002c0005t0003g0141 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-41-3720G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49571040 | |||||||
| chr13:49571256 | G | T | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-41-3936C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49571256 | |||||||
| chr13:49571258 | A | T | 174 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(171): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-41-3938T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49571258 | |||||||
| chr13:49571313 | C | T | 336 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-41-3993G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49571313 | |||||||
| chr13:49571413 | C | T | 2 | a0001c0001t0001g0355 a0001c0001t0001g0356 |
2 | HG03688.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-41-4093G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49571413 | |||||||
| chr13:49571644 | A | C | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-4324T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49571644 | |||||||
| chr13:49571662 | T | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-4342A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49571662 | |||||||
| chr13:49571977 | C | T | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-41-4657G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49571977 | |||||||
| chr13:49572178 | T | C | 1 | a0001c0001t0003g0011 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-41-4858A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572178 | |||||||
| chr13:49572252 | G | A | 4 | a0002c0002t0002g0144 a0002c0002t0002g0151 a0002c0002t0011g0145 others(1): Show |
4 | HG01109.hp2 HG01884.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-4932C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572252 | |||||||
| chr13:49572276 | G | A | 1 | a0002c0002t0002g0058 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-41-4956C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572276 | |||||||
| chr13:49572292 | A | C | 3 | a0001c0004t0002g0010 a0001c0004t0002g0290 a0001c0004t0002g0297 |
4 | HG00544.hp1 NA18983.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-4972T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572292 | |||||||
| chr13:49572344 | T | G | 1 | a0002c0002t0004g0171 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-41-5024A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572344 | |||||||
| chr13:49572410 | A | C | 9 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(6): Show |
9 | HG01346.hp2 HG01928.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41-5090T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572410 | |||||||
| chr13:49572502 | A | G | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-41-5182T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572502 | |||||||
| chr13:49572611 | T | C | 1 | a0002c0003t0003g0262 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-41-5291A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572611 | |||||||
| chr13:49572660 | C | T | 4 | a0001c0001t0001g0305 a0001c0001t0003g0326 a0001c0001t0012g0327 others(1): Show |
4 | HG03209.hp2 HG03579.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-5340G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572660 | |||||||
| chr13:49572787 | G | T | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-5467C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49572787 | |||||||
| chr13:49573044 | A | G | 25 | a0001c0001t0001g0006 a0001c0001t0001g0077 a0001c0001t0001g0078 others(22): Show |
26 | HG00323.hp1 HG00544.hp2 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.-41-5724T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573044 | |||||||
| chr13:49573052 | C | T | 4 | a0002c0002t0002g0144 a0002c0002t0002g0151 a0002c0002t0011g0145 others(1): Show |
4 | HG01109.hp2 HG01884.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41-5732G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573052 | |||||||
| chr13:49573055 | C | G | 1 | a0001c0001t0001g0082 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-41-5735G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573055 | |||||||
| chr13:49573193 | A | G | 4 | a0001c0001t0001g0362 a0001c0001t0002g0363 a0002c0002t0002g0400 others(1): Show |
4 | HG00673.hp1 HG02027.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.-41-5873T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573193 | |||||||
| chr13:49573258 | T | C | 60 | a0001c0001t0001g0212 a0002c0002t0001g0176 a0002c0002t0002g0068 others(57): Show |
60 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(57): Show |
intron_variant | MODIFIER | c.-41-5938A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573258 | |||||||
| chr13:49573264 | C | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-5944G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573264 | |||||||
| chr13:49573448 | C | CT | 103 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(100): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(108): Show |
intron_variant | MODIFIER | c.-41-6129dupA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573448 | |||||||
| chr13:49573448 | CT | C | 158 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(155): Show |
159 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.-41-6129delA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573448 | |||||||
| chr13:49573464 | T | C | 7 | a0002c0002t0001g0055 a0002c0002t0002g0017 a0002c0002t0002g0053 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-41-6144A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573464 | |||||||
| chr13:49573518 | G | T | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-6198C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573518 | |||||||
| chr13:49573593 | C | T | 1 | a0002c0003t0003g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-41-6273G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573593 | |||||||
| chr13:49573621 | C | T | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-6301G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573621 | |||||||
| chr13:49573655 | T | G | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-6335A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573655 | |||||||
| chr13:49573678 | G | A | 1 | a0002c0002t0002g0070 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-41-6358C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573678 | |||||||
| chr13:49573729 | C | T | 1 | a0002c0002t0002g0042 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-41-6409G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573729 | |||||||
| chr13:49573787 | C | CT | 197 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(194): Show |
201 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(198): Show |
intron_variant | MODIFIER | c.-41-6468dupA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573787 | |||||||
| chr13:49573907 | C | T | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-41-6587G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573907 | |||||||
| chr13:49573996 | C | T | 1 | a0002c0002t0002g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-42+6509G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49573996 | |||||||
| chr13:49574039 | CT | C | 4 | a0002c0002t0002g0144 a0002c0002t0002g0151 a0002c0002t0011g0145 others(1): Show |
4 | HG01109.hp2 HG01884.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+6465delA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574039 | |||||||
| chr13:49574124 | T | G | 1 | a0001c0001t0002g0385 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-42+6381A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574124 | |||||||
| chr13:49574135 | G | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-42+6370C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574135 | |||||||
| chr13:49574150 | A | G | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-42+6355T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574150 | |||||||
| chr13:49574169 | A | T | 1 | a0002c0018t0002g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-42+6336T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574169 | |||||||
| chr13:49574173 | C | T | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+6332G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574173 | |||||||
| chr13:49574206 | C | T | 1 | a0002c0018t0002g0040 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-42+6299G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574206 | |||||||
| chr13:49574253 | A | G | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-42+6252T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574253 | |||||||
| chr13:49574330 | G | A | 7 | a0001c0004t0010g0149 a0001c0004t0010g0152 a0002c0002t0002g0156 others(4): Show |
7 | HG02257.hp1 HG02717.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42+6175C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574330 | |||||||
| chr13:49574664 | A | G | 1 | a0001c0001t0003g0011 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-42+5841T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574664 | |||||||
| chr13:49574684 | T | TA | 15 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(12): Show |
15 | HG00735.hp1 HG02074.hp2 HG03225.hp2 others(12): Show |
intron_variant | MODIFIER | c.-42+5820dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574684 | |||||||
| chr13:49574698 | AAC | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(97): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(104): Show |
intron_variant | MODIFIER | c.-42+5805_-42+5806d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574698 | |||||||
| chr13:49574699 | AC | A | 73 | a0001c0001t0001g0044 a0001c0001t0001g0096 a0001c0001t0001g0367 others(70): Show |
79 | HG00544.hp1 HG00642.hp1 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.-42+5805delG | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574699 | |||||||
| chr13:49574700 | C | A | 158 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(155): Show |
159 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(156): Show |
intron_variant | MODIFIER | c.-42+5805G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574700 | |||||||
| chr13:49574774 | A | C | 8 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0139 others(5): Show |
8 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42+5731T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574774 | |||||||
| chr13:49574787 | C | T | 21 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(18): Show |
21 | HG00140.hp2 HG00735.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.-42+5718G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574787 | |||||||
| chr13:49574890 | T | C | 1 | a0002c0002t0002g0070 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-42+5615A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574890 | |||||||
| chr13:49574928 | TACA | T | 161 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(158): Show |
162 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.-42+5574_-42+5576d others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49574928 | |||||||
| chr13:49575102 | A | C | 4 | a0002c0007t0003g0147 a0002c0007t0006g0146 a0002c0007t0006g0148 others(1): Show |
4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-42+5403T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575102 | |||||||
| chr13:49575179 | A | G | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+5326T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575179 | |||||||
| chr13:49575203 | G | A | 1 | a0002c0005t0002g0153 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-42+5302C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575203 | |||||||
| chr13:49575434 | C | CA | 76 | a0001c0001t0001g0078 a0001c0001t0001g0386 a0001c0001t0016g0080 others(73): Show |
78 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.-42+5070dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575434 | |||||||
| chr13:49575434 | C | CAA | 100 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(97): Show |
101 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.-42+5069_-42+5070d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575434 | |||||||
| chr13:49575434 | CA | C | 40 | a0001c0001t0001g0044 a0001c0001t0007g0003 a0001c0001t0007g0030 others(37): Show |
43 | HG01070.hp2 HG01109.hp1 HG01257.hp1 others(40): Show |
intron_variant | MODIFIER | c.-42+5070delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575434 | |||||||
| chr13:49575513 | C | T | 8 | a0001c0001t0001g0314 a0001c0001t0001g0315 a0001c0001t0001g0316 others(5): Show |
8 | HG01167.hp2 HG01168.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.-42+4992G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575513 | |||||||
| chr13:49575656 | CAT | C | 5 | a0002c0005t0002g0139 a0002c0005t0003g0140 a0002c0005t0003g0141 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-42+4847_-42+4848d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575656 | |||||||
| chr13:49575719 | C | T | 350 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(347): Show |
366 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(363): Show |
intron_variant | MODIFIER | c.-42+4786G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575719 | |||||||
| chr13:49575728 | G | T | 1 | a0001c0001t0001g0399 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-42+4777C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575728 | |||||||
| chr13:49575809 | C | T | 336 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-42+4696G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575809 | |||||||
| chr13:49575850 | C | G | 5 | a0001c0001t0007g0354 a0001c0001t0007g0398 a0001c0001t0013g0312 others(2): Show |
5 | HG02809.hp2 HG03041.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-42+4655G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575850 | |||||||
| chr13:49575853 | A | G | 7 | a0002c0002t0001g0055 a0002c0002t0002g0017 a0002c0002t0002g0053 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-42+4652T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575853 | |||||||
| chr13:49575862 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-42+4643T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575862 | |||||||
| chr13:49575866 | G | A | 1 | a0002c0005t0002g0353 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-42+4639C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575866 | |||||||
| chr13:49575942 | T | C | 1 | a0001c0004t0002g0300 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-42+4563A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49575942 | |||||||
| chr13:49576146 | C | T | 1 | a0001c0001t0001g0399 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-42+4359G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576146 | |||||||
| chr13:49576177 | C | CA | 92 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(89): Show |
94 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.-42+4327dupT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576177 | |||||||
| chr13:49576177 | C | CAA | 42 | a0001c0001t0001g0018 a0001c0001t0001g0024 a0001c0001t0001g0025 others(39): Show |
42 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-42+4326_-42+4327d others(4): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576177 | |||||||
| chr13:49576177 | C | CAAA | 6 | a0001c0001t0001g0134 a0001c0004t0010g0152 a0002c0002t0002g0151 others(3): Show |
6 | HG02257.hp1 HG02717.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-42+4325_-42+4327d others(5): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576177 | |||||||
| chr13:49576177 | CA | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0305 others(101): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.-42+4327delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576177 | |||||||
| chr13:49576309 | T | C | 2 | a0001c0001t0001g0135 a0001c0001t0001g0138 |
2 | NA19062.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-42+4196A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576309 | |||||||
| chr13:49576337 | C | A | 3 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0153 |
3 | HG01074.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-42+4168G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576337 | |||||||
| chr13:49576414 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-42+4091G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576414 | |||||||
| chr13:49576444 | A | G | 8 | a0002c0006t0002g0288 a0002c0006t0006g0008 a0002c0006t0006g0009 others(5): Show |
10 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+4061T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576444 | |||||||
| chr13:49576749 | G | A | 162 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(159): Show |
163 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(160): Show |
intron_variant | MODIFIER | c.-42+3756C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576749 | |||||||
| chr13:49576842 | C | CT | 161 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(158): Show |
162 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.-42+3662dupA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576842 | |||||||
| chr13:49576874 | G | A | 1 | a0002c0005t0002g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-42+3631C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49576874 | |||||||
| chr13:49577307 | A | G | 1 | a0001c0001t0014g0310 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-42+3198T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49577307 | |||||||
| chr13:49577381 | T | C | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+3124A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49577381 | |||||||
| chr13:49577387 | G | T | 1 | a0001c0004t0003g0282 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-42+3118C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49577387 | |||||||
| chr13:49577390 | A | G | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-42+3115T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49577390 | |||||||
| chr13:49577533 | GT | G | 336 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-42+2971delA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49577533 | |||||||
| chr13:49577538 | G | T | 1 | a0002c0003t0003g0229 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-42+2967C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49577538 | |||||||
| chr13:49577728 | C | T | 2 | a0002c0002t0002g0400 a0002c0002t0003g0016 |
2 | HG02280.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-42+2777G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49577728 | |||||||
| chr13:49577790 | C | T | 161 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(158): Show |
162 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(159): Show |
intron_variant | MODIFIER | c.-42+2715G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49577790 | |||||||
| chr13:49577878 | C | G | 10 | a0002c0002t0003g0190 a0002c0002t0011g0191 a0002c0005t0002g0074 others(7): Show |
10 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+2627G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49577878 | |||||||
| chr13:49578073 | T | C | 3 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0153 |
3 | HG01074.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-42+2432A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49578073 | |||||||
| chr13:49578655 | G | A | 3 | a0001c0004t0002g0301 a0001c0004t0002g0302 a0001c0004t0002g0303 |
3 | HG02071.hp1 NA18747.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-42+1850C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49578655 | |||||||
| chr13:49578824 | T | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-42+1681A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49578824 | |||||||
| chr13:49579309 | T | C | 10 | a0002c0002t0003g0190 a0002c0002t0011g0191 a0002c0005t0002g0074 others(7): Show |
10 | HG01074.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-42+1196A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49579309 | |||||||
| chr13:49579390 | G | A | 60 | a0001c0001t0001g0212 a0002c0002t0001g0176 a0002c0002t0002g0068 others(57): Show |
60 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(57): Show |
intron_variant | MODIFIER | c.-42+1115C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49579390 | |||||||
| chr13:49579481 | G | A | 1 | a0002c0020t0002g0071 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-42+1024C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49579481 | |||||||
| chr13:49579517 | T | C | 336 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-42+988A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49579517 | |||||||
| chr13:49579541 | G | A | 32 | a0002c0002t0001g0176 a0002c0002t0002g0157 a0002c0002t0003g0162 others(29): Show |
32 | HG01978.hp1 HG02027.hp1 HG02129.hp2 others(29): Show |
intron_variant | MODIFIER | c.-42+964C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49579541 | |||||||
| chr13:49579573 | G | A | 1 | a0001c0004t0002g0304 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-42+932C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49579573 | |||||||
| chr13:49579611 | G | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-42+894C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49579611 | |||||||
| chr13:49579624 | GA | G | 345 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(342): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-42+880delT | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49579624 | |||||||
| chr13:49579764 | C | T | 1 | a0002c0002t0004g0158 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-42+741G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49579764 | |||||||
| chr13:49580064 | C | A | 1 | a0002c0003t0004g0215 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-42+441G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49580064 | |||||||
| chr13:49580188 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-42+317C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49580188 | |||||||
| chr13:49580417 | T | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(171): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.-42+88A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49580417 | |||||||
| chr13:49580493 | TG | T | 28 | a0001c0001t0001g0212 a0002c0002t0002g0068 a0002c0002t0002g0070 others(25): Show |
28 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.-42+11delC | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 2/12 | chr13 | 49580493 | |||||||
| chr13:49580870 | A | T | 17 | a0001c0001t0001g0044 a0002c0002t0002g0026 a0002c0002t0002g0027 others(14): Show |
17 | HG01070.hp2 HG01257.hp1 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.-121-286T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49580870 | |||||||
| chr13:49580895 | G | T | 1 | a0001c0001t0001g0309 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.-121-311C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49580895 | |||||||
| chr13:49580908 | A | C | 1 | a0002c0002t0002g0157 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-121-324T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49580908 | |||||||
| chr13:49580950 | T | C | 1 | a0002c0005t0003g0142 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-121-366A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49580950 | |||||||
| chr13:49581002 | G | A | 1 | a0001c0001t0001g0393 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-121-418C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581002 | |||||||
| chr13:49581161 | A | C | 1 | a0002c0008t0008g0076 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-121-577T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581161 | |||||||
| chr13:49581234 | T | C | 1 | a0001c0001t0001g0394 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-121-650A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581234 | |||||||
| chr13:49581237 | T | C | 6 | a0001c0004t0002g0270 a0002c0003t0004g0267 a0002c0003t0004g0268 others(3): Show |
6 | NA18971.hp1 NA18973.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-121-653A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581237 | |||||||
| chr13:49581266 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-121-682G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581266 | |||||||
| chr13:49581348 | T | C | 1 | a0002c0003t0003g0273 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-121-764A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581348 | |||||||
| chr13:49581393 | G | A | 3 | a0001c0001t0001g0395 a0001c0001t0001g0396 a0001c0001t0001g0397 |
3 | NA18948.hp2 NA18995.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-121-809C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581393 | |||||||
| chr13:49581458 | G | A | 4 | a0002c0005t0003g0140 a0002c0005t0003g0141 a0002c0005t0003g0142 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-121-874C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581458 | |||||||
| chr13:49581503 | T | C | 336 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-121-919A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581503 | |||||||
| chr13:49581606 | A | G | 348 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(345): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.-121-1022T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581606 | |||||||
| chr13:49581654 | G | A | 1 | a0002c0002t0002g0041 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-121-1070C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581654 | |||||||
| chr13:49581654 | G | C | 19 | a0001c0004t0002g0010 a0001c0004t0002g0275 a0001c0004t0002g0276 others(16): Show |
20 | HG00544.hp1 HG00642.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.-121-1070C>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581654 | |||||||
| chr13:49581737 | A | G | 3 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0153 |
3 | HG01074.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-121-1153T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581737 | |||||||
| chr13:49581806 | G | A | 3 | a0002c0005t0002g0074 a0002c0005t0002g0075 a0002c0005t0002g0153 |
3 | HG01074.hp1 HG03486.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-121-1222C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581806 | |||||||
| chr13:49581906 | T | A | 77 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(74): Show |
78 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-121-1322A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581906 | |||||||
| chr13:49581908 | G | A | 1 | a0001c0001t0007g0038 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-121-1324C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49581908 | |||||||
| chr13:49582029 | A | G | 336 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-121-1445T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582029 | |||||||
| chr13:49582154 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-121-1570C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582154 | |||||||
| chr13:49582186 | A | G | 1 | a0002c0003t0004g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-121-1602T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582186 | |||||||
| chr13:49582206 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-121-1622C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582206 | |||||||
| chr13:49582228 | T | G | 1 | a0002c0002t0008g0063 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-121-1644A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582228 | |||||||
| chr13:49582284 | C | T | 60 | a0001c0001t0001g0212 a0002c0002t0001g0176 a0002c0002t0002g0068 others(57): Show |
60 | HG00558.hp1 HG00621.hp2 HG01255.hp2 others(57): Show |
intron_variant | MODIFIER | c.-121-1700G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582284 | |||||||
| chr13:49582401 | C | G | 1 | a0002c0019t0003g0143 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-121-1817G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582401 | |||||||
| chr13:49582625 | G | A | 1 | a0002c0005t0015g0280 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-121-2041C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582625 | |||||||
| chr13:49582663 | G | A | 1 | a0001c0001t0007g0398 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-121-2079C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582663 | |||||||
| chr13:49582824 | TC | T | 337 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(334): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.-121-2241delG | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49582824 | |||||||
| chr13:49583074 | G | A | 5 | a0002c0005t0002g0139 a0002c0005t0003g0140 a0002c0005t0003g0141 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.-122+2370C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583074 | |||||||
| chr13:49583075 | T | A | 1 | a0002c0002t0004g0188 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-122+2369A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583075 | |||||||
| chr13:49583262 | A | G | 11 | a0001c0001t0007g0003 a0001c0001t0007g0030 a0001c0001t0007g0034 others(8): Show |
13 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-122+2182T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583262 | |||||||
| chr13:49583329 | C | T | 1 | a0001c0001t0003g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-122+2115G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583329 | |||||||
| chr13:49583386 | A | ATG | 5 | a0002c0002t0002g0026 a0002c0002t0002g0027 a0002c0002t0002g0029 others(2): Show |
5 | HG02015.hp2 HG02083.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-122+2056_-122+205 others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583386 | |||||||
| chr13:49583386 | A | ATGTGTGT others(3): Show |
1 | a0001c0001t0001g0305 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-122+2048_-122+205 others(14): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583386 | |||||||
| chr13:49583386 | ATG | A | 160 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0019 others(157): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.-122+2056_-122+205 others(6): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583386 | |||||||
| chr13:49583386 | ATGTG | A | 115 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0022 others(112): Show |
116 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.-122+2054_-122+205 others(8): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583386 | |||||||
| chr13:49583386 | ATGTGTG | A | 13 | a0001c0004t0010g0149 a0001c0004t0010g0152 a0002c0002t0002g0144 others(10): Show |
13 | HG01109.hp2 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-122+2052_-122+205 others(10): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583386 | |||||||
| chr13:49583657 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-122+1787C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583657 | |||||||
| chr13:49583691 | C | T | 202 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(199): Show |
206 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.-122+1753G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583691 | |||||||
| chr13:49583743 | T | C | 1 | a0002c0002t0002g0156 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-122+1701A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49583743 | |||||||
| chr13:49584006 | T | C | 54 | a0001c0004t0002g0010 a0001c0004t0002g0275 a0001c0004t0002g0276 others(51): Show |
55 | HG00544.hp1 HG00642.hp1 HG01192.hp1 others(52): Show |
intron_variant | MODIFIER | c.-122+1438A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584006 | |||||||
| chr13:49584058 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-122+1386C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584058 | |||||||
| chr13:49584099 | T | C | 2 | a0002c0002t0003g0190 a0002c0002t0011g0191 |
2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-122+1345A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584099 | |||||||
| chr13:49584123 | C | A | 8 | a0001c0001t0001g0212 a0002c0002t0004g0205 a0002c0002t0004g0206 others(5): Show |
8 | HG00558.hp1 HG02015.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.-122+1321G>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584123 | |||||||
| chr13:49584268 | A | AT | 336 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-122+1175dupA | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584268 | |||||||
| chr13:49584360 | G | A | 1 | a0001c0001t0001g0399 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-122+1084C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584360 | |||||||
| chr13:49584417 | T | G | 1 | a0002c0005t0003g0192 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-122+1027A>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584417 | |||||||
| chr13:49584664 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0022 others(4): Show |
7 | HG02074.hp2 NA18946.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122+780T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584664 | |||||||
| chr13:49584673 | T | C | 1 | a0002c0003t0003g0274 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-122+771A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584673 | |||||||
| chr13:49584803 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(130): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-122+641T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584803 | |||||||
| chr13:49584835 | C | G | 1 | a0001c0001t0001g0018 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-122+609G>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584835 | |||||||
| chr13:49584909 | T | C | 20 | a0001c0001t0001g0212 a0002c0002t0002g0193 a0002c0002t0002g0194 others(17): Show |
20 | HG00558.hp1 HG00621.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.-122+535A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584909 | |||||||
| chr13:49584937 | A | G | 336 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(333): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.-122+507T>C | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584937 | |||||||
| chr13:49584953 | A | C | 1 | a0002c0002t0002g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-122+491T>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49584953 | |||||||
| chr13:49585029 | G | A | 133 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(130): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.-122+415C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585029 | |||||||
| chr13:49585094 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-122+350G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585094 | |||||||
| chr13:49585117 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(98): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(105): Show |
intron_variant | MODIFIER | c.-122+327C>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585117 | |||||||
| chr13:49585169 | G | T | 202 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(199): Show |
206 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.-122+275C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585169 | |||||||
| chr13:49585170 | A | T | 202 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(199): Show |
206 | HG00323.hp1 HG00408.hp1 HG00544.hp2 others(203): Show |
intron_variant | MODIFIER | c.-122+274T>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585170 | |||||||
| chr13:49585330 | C | T | 2 | a0002c0002t0002g0400 a0002c0002t0003g0016 |
2 | HG02280.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-122+114G>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585330 | |||||||
| chr13:49585331 | G | T | 5 | a0001c0004t0002g0275 a0001c0004t0002g0276 a0001c0004t0002g0277 others(2): Show |
5 | HG00642.hp1 HG01255.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-122+113C>A | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585331 | |||||||
| chr13:49585356 | T | A | 134 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(131): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.-122+88A>T | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585356 | |||||||
| chr13:49585371 | C | CGGGGAAG others(7): Show |
1 | a0002c0002t0002g0400 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-122+59_-122+72dup others(14): Show |
RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585371 | |||||||
| chr13:49585441 | T | C | 1 | a0001c0001t0001g0401 | 1 | HG02970.hp2 | splice_region_variant&intron_variant | LOW | c.-122+3A>G | RCBTB1 | ENSG00000136144.12 | transcript | ENST00000378302.7 | protein_coding | 1/12 | chr13 | 49585441 |