Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5934 |
| ensemblid | ENSG00000103479.17 |
| hgncid | 9894 |
| symbol | RBL2 |
| name | RB transcriptional corepressor like 2 |
| refseq_nuc | NM_005611.4 |
| refseq_prot | NP_005602.3 |
| ensembl_nuc | ENST00000262133.11 |
| ensembl_prot | ENSP00000262133.6 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 53434471 |
| end | 53491648 |
| strand | + |
| ver | v1.2 |
| region | chr16:53434471-53491648 |
| region5000 | chr16:53429471-53496648 |
| regionname0 | RBL2_chr16_53434471_53491648 |
| regionname5000 | RBL2_chr16_53429471_53496648 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 1139 | 244 | 90 | 38 | 74 | 5 | 36 | 56 | RBL2_chr16_53429471_53496648 | RBL2 | MPSGG others(1134): Show |
chr16 | 53429471 | 53496648 |
| a0002 | 0/1 | 1139 | 25 | 1 | 15 | 0 | 4 | 4 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | MPSGG others(1134): Show |
chr16 | 53429471 | 53496648 |
| a0003 | 0/0 | 1139 | 3 | 0 | 0 | 3 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | MPSGG others(1134): Show |
chr16 | 53429471 | 53496648 |
| a0004 | 0/0 | 1139 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | MPSGG others(1134): Show |
chr16 | 53429471 | 53496648 |
| a0005 | 0/0 | 1148 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | MPSGG others(1143): Show |
chr16 | 53429471 | 53496648 |
| a0006 | 0/0 | 1139 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | MPSGG others(1134): Show |
chr16 | 53429471 | 53496648 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 3417 | 102 | 9 | 28 | 43 | 2 | 19 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0001c0002 | 0/0 | 3417 | 76 | 38 | 8 | 17 | 3 | 10 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0001c0003 | 0/0 | 3417 | 57 | 36 | 2 | 12 | 0 | 7 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0001c0005 | 0/0 | 3417 | 3 | 3 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0001c0007 | 0/0 | 3417 | 3 | 3 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0001c0010 | 0/0 | 3417 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0001c0011 | 0/0 | 3417 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0001c0013 | 0/0 | 3417 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0002c0004 | 0/1 | 3417 | 25 | 1 | 15 | 0 | 4 | 4 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0003c0006 | 0/0 | 3417 | 3 | 0 | 0 | 3 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0004c0008 | 0/0 | 3417 | 2 | 0 | 1 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 | ||
| a0005c0009 | 0/0 | 3444 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3439): Show |
chr16 | 53429471 | 53496648 | ||
| a0006c0012 | 0/0 | 3417 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | ATGCC others(3412): Show |
chr16 | 53429471 | 53496648 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4854 | 97 | 8 | 28 | 39 | 2 | 19 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0001c0001t0003 | 0/0 | 4855 | 2 | 0 | 0 | 2 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4850): Show |
chr16 | 53429471 | 53496648 |
| a0001c0001t0005 | 0/0 | 4854 | 2 | 0 | 0 | 2 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0001c0001t0007 | 0/0 | 4854 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0001c0002t0001 | 0/0 | 4854 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0001c0002t0002 | 0/0 | 4854 | 59 | 22 | 8 | 17 | 3 | 9 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0001c0002t0003 | 0/0 | 4855 | 2 | 1 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4850): Show |
chr16 | 53429471 | 53496648 |
| a0001c0002t0004 | 0/0 | 4855 | 11 | 11 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4850): Show |
chr16 | 53429471 | 53496648 |
| a0001c0002t0006 | 0/0 | 4854 | 2 | 2 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0001c0002t0008 | 0/0 | 4855 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4850): Show |
chr16 | 53429471 | 53496648 |
| a0001c0003t0002 | 0/0 | 4854 | 12 | 9 | 1 | 0 | 0 | 2 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0001c0003t0003 | 0/0 | 4855 | 44 | 26 | 1 | 12 | 0 | 5 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4850): Show |
chr16 | 53429471 | 53496648 |
| a0001c0003t0004 | 0/0 | 4855 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4850): Show |
chr16 | 53429471 | 53496648 |
| a0001c0005t0001 | 0/0 | 4854 | 3 | 3 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0001c0007t0004 | 0/0 | 4855 | 3 | 3 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4850): Show |
chr16 | 53429471 | 53496648 |
| a0001c0010t0004 | 0/0 | 4855 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4850): Show |
chr16 | 53429471 | 53496648 |
| a0001c0011t0001 | 0/0 | 4854 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0001c0013t0001 | 0/0 | 4854 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0002c0004t0003 | 0/1 | 4855 | 25 | 1 | 15 | 0 | 4 | 4 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4850): Show |
chr16 | 53429471 | 53496648 |
| a0003c0006t0001 | 0/0 | 4854 | 3 | 0 | 0 | 3 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0004c0008t0002 | 0/0 | 4854 | 2 | 0 | 1 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| a0005c0009t0001 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4876): Show |
chr16 | 53429471 | 53496648 |
| a0006c0012t0001 | 0/0 | 4854 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | GGCGG others(4849): Show |
chr16 | 53429471 | 53496648 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0052 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0005g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0002t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0003t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0005t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0005t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0007t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0007t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0007t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0010t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0011t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0001c0013t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0002c0004t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0003c0006t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0003c0006t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0003c0006t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0004c0008t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0004c0008t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0005c0009t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| a0006c0012t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0255 | EUR | GBR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0159 | EUR | GBR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00280 | hp1 | a0002 | c0004 | t0003 | g0185 | EUR | FIN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00323 | hp1 | a0004 | c0008 | t0002 | g0212 | EUR | FIN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00323 | hp2 | a0002 | c0004 | t0003 | g0193 | EUR | FIN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | CHS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00408 | hp2 | a0003 | c0006 | t0001 | g0003 | EAS | CHS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | CHS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00639 | hp1 | a0002 | c0004 | t0003 | g0004 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00642 | hp2 | a0002 | c0004 | t0003 | g0190 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00733 | hp1 | a0002 | c0004 | t0003 | g0004 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0254 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00738 | hp1 | a0002 | c0004 | t0003 | g0180 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0238 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00741 | hp1 | a0002 | c0004 | t0003 | g0181 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01069 | hp1 | a0002 | c0004 | t0003 | g0196 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01070 | hp1 | a0002 | c0004 | t0003 | g0187 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0211 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0157 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01074 | hp1 | a0002 | c0004 | t0003 | g0195 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01106 | hp1 | a0002 | c0004 | t0003 | g0189 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01106 | hp2 | a0001 | c0003 | t0003 | g0167 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01109 | hp1 | a0002 | c0004 | t0003 | g0182 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0149 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01192 | hp1 | a0002 | c0004 | t0003 | g0146 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01255 | hp1 | a0004 | c0008 | t0002 | g0154 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01255 | hp2 | a0002 | c0004 | t0003 | g0203 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0220 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0156 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0155 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01361 | hp2 | a0002 | c0004 | t0003 | g0004 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01496 | hp1 | a0002 | c0004 | t0003 | g0188 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0221 | EUR | IBS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01515 | hp2 | a0002 | c0004 | t0003 | g0186 | EUR | IBS | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0176 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0084 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01891 | hp1 | a0001 | c0003 | t0003 | g0179 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0206 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02056 | hp1 | a0001 | c0003 | t0003 | g0170 | EAS | KHV | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0197 | EAS | KHV | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | KHV | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | KHV | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0144 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0092 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02155 | hp1 | a0001 | c0003 | t0003 | g0011 | EAS | CDX | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0093 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02257 | hp2 | a0001 | c0007 | t0004 | g0090 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0256 | AMR | PEL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02451 | hp1 | a0001 | c0002 | t0008 | g0098 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0216 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02523 | hp1 | a0003 | c0006 | t0001 | g0107 | EAS | KHV | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02572 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0251 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0257 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02622 | hp1 | a0005 | c0009 | t0001 | g0043 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0085 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0246 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02630 | hp2 | a0001 | c0003 | t0002 | g0148 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0207 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0258 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02717 | hp2 | a0001 | c0003 | t0003 | g0174 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0160 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0094 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0199 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02818 | hp2 | a0001 | c0002 | t0004 | g0243 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0135 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02895 | hp1 | a0001 | c0003 | t0003 | g0136 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02895 | hp2 | a0001 | c0002 | t0002 | g0017 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0129 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0236 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02897 | hp2 | a0001 | c0003 | t0003 | g0132 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0230 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02922 | hp2 | a0001 | c0003 | t0003 | g0201 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02965 | hp1 | a0001 | c0003 | t0003 | g0175 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02965 | hp2 | a0001 | c0002 | t0004 | g0245 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02970 | hp1 | a0001 | c0003 | t0002 | g0205 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0244 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02976 | hp2 | a0001 | c0002 | t0004 | g0250 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0241 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03041 | hp1 | a0001 | c0003 | t0003 | g0139 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0086 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0150 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03098 | hp2 | a0001 | c0003 | t0002 | g0237 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03130 | hp2 | a0001 | c0010 | t0004 | g0252 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0128 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0151 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03195 | hp1 | a0001 | c0003 | t0004 | g0169 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0249 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0177 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03225 | hp1 | a0001 | c0002 | t0003 | g0019 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03225 | hp2 | a0001 | c0002 | t0004 | g0248 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03239 | hp1 | a0001 | c0003 | t0002 | g0158 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03453 | hp2 | a0001 | c0002 | t0002 | g0232 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03490 | hp1 | a0002 | c0004 | t0003 | g0204 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03491 | hp1 | a0002 | c0004 | t0003 | g0184 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03516 | hp1 | a0001 | c0003 | t0003 | g0133 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03516 | hp2 | a0001 | c0003 | t0003 | g0141 | AFR | ESN | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0083 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03540 | hp2 | a0001 | c0003 | t0003 | g0140 | AFR | GWD | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0138 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03654 | hp1 | a0001 | c0003 | t0003 | g0171 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03654 | hp2 | a0001 | c0002 | t0003 | g0253 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03688 | hp2 | a0001 | c0003 | t0003 | g0239 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03710 | hp1 | a0002 | c0004 | t0003 | g0192 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0259 | SAS | PJL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03831 | hp1 | a0001 | c0003 | t0003 | g0142 | SAS | BEB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | BEB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0219 | SAS | BEB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04115 | hp1 | a0001 | c0003 | t0003 | g0172 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0161 | SAS | BEB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | BEB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0143 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04228 | hp1 | a0001 | c0002 | t0002 | g0012 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG04228 | hp2 | a0002 | c0004 | t0003 | g0183 | SAS | STU | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0152 | AFR | YRI | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0178 | AFR | YRI | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18906 | hp1 | a0001 | c0003 | t0003 | g0168 | AFR | YRI | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18906 | hp2 | a0001 | c0002 | t0004 | g0247 | AFR | YRI | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18944 | hp2 | a0001 | c0003 | t0003 | g0215 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18949 | hp2 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18962 | hp1 | a0001 | c0003 | t0003 | g0163 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18967 | hp1 | a0001 | c0003 | t0003 | g0166 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18967 | hp2 | a0001 | c0013 | t0001 | g0099 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18986 | hp1 | a0001 | c0003 | t0003 | g0202 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18988 | hp1 | a0001 | c0003 | t0003 | g0164 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18993 | hp2 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0229 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19000 | hp2 | a0001 | c0001 | t0005 | g0082 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19007 | hp2 | a0001 | c0003 | t0003 | g0165 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19010 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19030 | hp1 | a0001 | c0003 | t0003 | g0200 | AFR | LWK | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19030 | hp2 | a0001 | c0003 | t0002 | g0209 | AFR | LWK | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0233 | AFR | LWK | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19043 | hp2 | a0001 | c0007 | t0004 | g0013 | AFR | LWK | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19065 | hp1 | a0003 | c0006 | t0001 | g0009 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19066 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19070 | hp2 | a0001 | c0003 | t0003 | g0011 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19090 | hp1 | a0001 | c0003 | t0003 | g0214 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19240 | hp1 | a0001 | c0002 | t0006 | g0235 | AFR | YRI | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0210 | AFR | YRI | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ASW | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA20129 | hp2 | a0001 | c0003 | t0003 | g0137 | AFR | ASW | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA20752 | hp2 | a0002 | c0004 | t0003 | g0147 | EUR | TSI | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA20905 | hp2 | a0001 | c0003 | t0003 | g0162 | SAS | GIH | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG01123 | hp2 | a0002 | c0004 | t0003 | g0145 | AMR | CLM | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02109 | hp1 | a0001 | c0002 | t0004 | g0088 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02109 | hp2 | a0001 | c0003 | t0003 | g0130 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02486 | hp1 | a0001 | c0003 | t0003 | g0134 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0234 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0153 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG02559 | hp2 | a0001 | c0003 | t0003 | g0173 | AFR | ACB | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0127 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0231 | AFR | MSL | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG06807 | hp1 | a0002 | c0004 | t0003 | g0191 | AFR | USA | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| HG06807 | hp2 | a0001 | c0007 | t0004 | g0091 | AFR | USA | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18955 | hp1 | a0006 | c0012 | t0001 | g0002 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA18955 | hp2 | a0001 | c0011 | t0001 | g0071 | EAS | JPT | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA20300 | hp1 | a0001 | c0003 | t0002 | g0208 | AFR | USA | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA20300 | hp2 | a0001 | c0003 | t0003 | g0131 | AFR | USA | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA21309 | hp1 | a0001 | c0002 | t0004 | g0087 | AFR | LWK | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | LWK | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| homoSapiens | chm13v2 | a0002 | c0004 | t0003 | g0194 | REF | REF | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0052 | REF | REF | RBL2_chr16_53429471_53496648 | RBL2 | chr16 | 53429471 | 53496648 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:53434650 | G | GAAGACGC others(20): Show |
1 | a0005 | 1 | HG02622.hp1 | disruptive_inframe_insertion | MODERATE | c.95_121dupAAGACGCCG others(18): Show |
p.Ser40_Pro41insGlnA others(23): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/22 | 208/4854 | 122/3420 | 41/1139 | INFO_REALIGN_3_PRIME | chr16 | 53434650 | ||
| chr16:53447098 | A | G | 1 | a0002 | 24 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(21): Show |
missense_variant | MODERATE | c.629A>G | p.Tyr210Cys | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/22 | 715/4854 | 629/3420 | 210/1139 | chr16 | 53447098 | |||
| chr16:53464311 | A | T | 1 | a0003 | 3 | HG00408.hp2 HG02523.hp1 NA19065.hp1 |
missense_variant | MODERATE | c.1646A>T | p.Asn549Ile | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/22 | 1732/4854 | 1646/3420 | 549/1139 | chr16 | 53464311 | |||
| chr16:53465462 | G | C | 1 | a0004 | 2 | HG00323.hp1 HG01255.hp1 |
missense_variant | MODERATE | c.1723G>C | p.Glu575Gln | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/22 | 1809/4854 | 1723/3420 | 575/1139 | chr16 | 53465462 | |||
| chr16:53469966 | A | G | 1 | a0006 | 1 | NA18955.hp1 | missense_variant | MODERATE | c.2026A>G | p.Ser676Gly | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 15/22 | 2112/4854 | 2026/3420 | 676/1139 | chr16 | 53469966 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:53434718 | C | T | 1 | a0001c0007 | 3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.162C>T | p.Ser54Ser | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/22 | 248/4854 | 162/3420 | 54/1139 | chr16 | 53434718 | |||
| chr16:53439024 | T | C | 1 | a0001c0010 | 1 | HG03130.hp2 | synonymous_variant | LOW | c.249T>C | p.Asp83Asp | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/22 | 335/4854 | 249/3420 | 83/1139 | chr16 | 53439024 | |||
| chr16:53442709 | A | G | 1 | a0003c0006 | 3 | HG00408.hp2 HG02523.hp1 NA19065.hp1 |
synonymous_variant | LOW | c.423A>G | p.Leu141Leu | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/22 | 509/4854 | 423/3420 | 141/1139 | chr16 | 53442709 | |||
| chr16:53453501 | C | T | 1 | a0001c0013 | 1 | NA18967.hp2 | synonymous_variant | LOW | c.816C>T | p.Pro272Pro | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 6/22 | 902/4854 | 816/3420 | 272/1139 | chr16 | 53453501 | |||
| chr16:53470022 | G | A | 7 | a0001c0002 a0001c0003 a0001c0005 others(4): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
synonymous_variant | LOW | c.2082G>A | p.Thr694Thr | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 15/22 | 2168/4854 | 2082/3420 | 694/1139 | chr16 | 53470022 | |||
| chr16:53470031 | C | G | 2 | a0001c0003 a0002c0004 |
81 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(78): Show |
synonymous_variant | LOW | c.2091C>G | p.Arg697Arg | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 15/22 | 2177/4854 | 2091/3420 | 697/1139 | chr16 | 53470031 | |||
| chr16:53470809 | T | C | 6 | a0001c0002 a0001c0003 a0001c0007 others(3): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
synonymous_variant | LOW | c.2590T>C | p.Leu864Leu | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/22 | 2676/4854 | 2590/3420 | 864/1139 | chr16 | 53470809 | |||
| chr16:53480718 | C | T | 1 | a0001c0011 | 1 | NA18955.hp2 | synonymous_variant | LOW | c.3033C>T | p.Asn1011Asn | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/22 | 3119/4854 | 3033/3420 | 1011/1139 | chr16 | 53480718 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:53434487 | C | G | 1 | a0001c0002t0006 | 2 | HG02486.hp2 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-70C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/22 | 70 | chr16 | 53434487 | ||||||
| chr16:53490396 | G | C | 12 | a0001c0001t0003 a0001c0002t0002 a0001c0002t0003 others(9): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*96G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 22/22 | 96 | chr16 | 53490396 | ||||||
| chr16:53490598 | T | C | 1 | a0001c0001t0007 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*298T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 22/22 | 298 | chr16 | 53490598 | ||||||
| chr16:53490758 | A | AT | 9 | a0001c0001t0003 a0001c0002t0003 a0001c0002t0004 others(6): Show |
89 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*464dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 22/22 | 465 | INFO_REALIGN_3_PRIME | chr16 | 53490758 | |||||
| chr16:53490919 | C | T | 4 | a0001c0002t0004 a0001c0003t0004 a0001c0007t0004 others(1): Show |
16 | HG02109.hp1 HG02257.hp2 HG02572.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*619C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 22/22 | 619 | chr16 | 53490919 | ||||||
| chr16:53490949 | A | G | 1 | a0001c0001t0005 | 2 | NA19000.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*649A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 22/22 | 649 | chr16 | 53490949 | ||||||
| chr16:53491079 | T | A | 1 | a0001c0002t0008 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*779T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 22/22 | 779 | chr16 | 53491079 | ||||||
| chr16:53491554 | T | A | 5 | a0001c0002t0004 a0001c0002t0008 a0001c0003t0004 others(2): Show |
17 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1254T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 22/22 | 1254 | chr16 | 53491554 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:53434843 | C | T | 8 | a0001c0002t0002g0012 a0001c0002t0002g0254 a0001c0002t0002g0255 others(5): Show |
9 | HG00140.hp1 HG00735.hp2 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.240+47C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53434843 | |||||||
| chr16:53434895 | G | C | 1 | a0001c0007t0004g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.240+99G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53434895 | |||||||
| chr16:53434913 | G | C | 5 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+117G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53434913 | |||||||
| chr16:53434933 | G | T | 10 | a0001c0002t0004g0243 a0001c0002t0004g0244 a0001c0002t0004g0245 others(7): Show |
10 | HG02572.hp2 HG02630.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+137G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53434933 | |||||||
| chr16:53435017 | G | C | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.240+221G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53435017 | |||||||
| chr16:53435050 | C | T | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.240+254C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53435050 | |||||||
| chr16:53435070 | A | C | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.240+274A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53435070 | |||||||
| chr16:53435075 | T | C | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.240+279T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53435075 | |||||||
| chr16:53435292 | G | C | 9 | a0001c0003t0003g0127 a0001c0003t0003g0128 a0001c0003t0003g0129 others(6): Show |
9 | HG02109.hp2 HG02486.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.240+496G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53435292 | |||||||
| chr16:53435551 | A | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(32): Show |
38 | HG00408.hp2 HG00621.hp2 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.240+755A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53435551 | |||||||
| chr16:53436022 | C | T | 1 | a0001c0002t0008g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.240+1226C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53436022 | |||||||
| chr16:53436178 | G | GT | 6 | a0001c0001t0001g0126 a0001c0002t0002g0240 a0001c0002t0002g0241 others(3): Show |
6 | HG02135.hp1 HG02886.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+1391dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53436178 | ||||||
| chr16:53436218 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02717.hp1 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.240+1422C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53436218 | |||||||
| chr16:53436228 | A | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.240+1432A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53436228 | |||||||
| chr16:53436540 | C | A | 2 | a0001c0002t0004g0243 a0001c0002t0004g0244 |
2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.240+1744C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53436540 | |||||||
| chr16:53436553 | G | A | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.240+1757G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53436553 | |||||||
| chr16:53436789 | G | A | 6 | a0001c0003t0003g0136 a0001c0003t0003g0137 a0001c0003t0003g0138 others(3): Show |
6 | HG02895.hp1 HG03041.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+1993G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53436789 | |||||||
| chr16:53436866 | T | C | 6 | a0001c0003t0003g0136 a0001c0003t0003g0137 a0001c0003t0003g0138 others(3): Show |
6 | HG02895.hp1 HG03041.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.240+2070T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53436866 | |||||||
| chr16:53436876 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.240+2080G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53436876 | |||||||
| chr16:53437052 | C | CT | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.241-1953dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53437052 | ||||||
| chr16:53437137 | T | G | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.241-1879T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53437137 | |||||||
| chr16:53437166 | C | T | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.241-1850C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53437166 | |||||||
| chr16:53437282 | A | T | 1 | a0001c0003t0002g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.241-1734A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53437282 | |||||||
| chr16:53437308 | G | GT | 24 | a0001c0001t0001g0124 a0001c0001t0005g0082 a0001c0001t0005g0125 others(21): Show |
25 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.241-1694dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53437308 | ||||||
| chr16:53437445 | T | G | 154 | a0001c0002t0001g0089 a0001c0002t0002g0001 a0001c0002t0002g0006 others(151): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.241-1571T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53437445 | |||||||
| chr16:53437476 | C | T | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.241-1540C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53437476 | |||||||
| chr16:53437611 | A | G | 3 | a0001c0007t0004g0013 a0001c0007t0004g0090 a0001c0007t0004g0091 |
3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.241-1405A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53437611 | |||||||
| chr16:53437753 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.241-1263C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53437753 | |||||||
| chr16:53437828 | C | T | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-1188C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53437828 | |||||||
| chr16:53438363 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.241-653A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53438363 | |||||||
| chr16:53438473 | G | A | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.241-543G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53438473 | |||||||
| chr16:53438614 | C | T | 1 | a0001c0010t0004g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.241-402C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53438614 | |||||||
| chr16:53438800 | C | T | 1 | a0001c0003t0002g0237 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.241-216C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53438800 | |||||||
| chr16:53438843 | C | CA | 20 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0022 others(17): Show |
21 | HG00621.hp1 HG00741.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.241-144dupA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53438843 | ||||||
| chr16:53438843 | CA | C | 85 | a0001c0001t0001g0009 a0001c0001t0001g0075 a0001c0001t0001g0076 others(82): Show |
89 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.241-144delA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53438843 | ||||||
| chr16:53438843 | CAA | C | 16 | a0001c0002t0001g0089 a0001c0002t0002g0017 a0001c0002t0002g0018 others(13): Show |
16 | HG00323.hp1 HG01070.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.241-145_241-144del others(2): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53438843 | ||||||
| chr16:53438843 | CAAA | C | 40 | a0001c0002t0002g0001 a0001c0002t0002g0012 a0001c0002t0002g0217 others(37): Show |
44 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.241-146_241-144del others(3): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53438843 | ||||||
| chr16:53438843 | CAAAAA | C | 6 | a0001c0002t0002g0006 a0001c0002t0002g0093 a0001c0002t0002g0094 others(3): Show |
7 | HG02257.hp1 HG02257.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.241-148_241-144del others(5): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53438843 | ||||||
| chr16:53438843 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0078 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.241-156_241-144del others(13): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53438843 | ||||||
| chr16:53438843 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0003g0079 a0001c0001t0003g0080 |
2 | HG00408.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.241-159_241-144del others(16): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53438843 | ||||||
| chr16:53438843 | CAAAAAAA others(10): Show |
C | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.241-160_241-144del others(17): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr16 | 53438843 | ||||||
| chr16:53438875 | G | A | 1 | a0001c0002t0003g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.241-141G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 1/21 | chr16 | 53438875 | |||||||
| chr16:53439239 | G | A | 1 | a0002c0004t0003g0147 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.371+93G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53439239 | |||||||
| chr16:53439615 | G | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0033 others(3): Show |
6 | HG00741.hp2 HG01074.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.371+469G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53439615 | |||||||
| chr16:53439637 | G | C | 1 | a0001c0003t0003g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.371+491G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53439637 | |||||||
| chr16:53439792 | A | T | 17 | a0001c0002t0001g0089 a0001c0002t0004g0087 a0001c0002t0004g0088 others(14): Show |
17 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.371+646A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53439792 | |||||||
| chr16:53439954 | C | CA | 13 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0023 others(10): Show |
14 | HG00621.hp2 HG00642.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.371+832dupA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53439954 | ||||||
| chr16:53439954 | C | CAA | 7 | a0001c0002t0003g0019 a0001c0003t0002g0148 a0001c0003t0002g0205 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.371+831_371+832dup others(2): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53439954 | ||||||
| chr16:53439954 | C | CAAAAA | 9 | a0001c0002t0002g0006 a0001c0002t0002g0093 a0001c0002t0002g0094 others(6): Show |
10 | HG02257.hp1 HG02258.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.371+828_371+832dup others(5): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53439954 | ||||||
| chr16:53439954 | C | CAAAAAAA others(5): Show |
1 | a0001c0010t0004g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.371+821_371+832dup others(12): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53439954 | ||||||
| chr16:53439954 | C | CAAAAAAA others(8): Show |
1 | a0001c0002t0004g0245 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.371+818_371+832dup others(15): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53439954 | ||||||
| chr16:53439954 | CAAAAA | C | 21 | a0001c0002t0002g0001 a0001c0002t0002g0143 a0001c0002t0002g0210 others(18): Show |
24 | HG00438.hp1 HG00544.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.371+828_371+832del others(5): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53439954 | ||||||
| chr16:53439954 | CAAAAAA | C | 112 | a0001c0002t0002g0010 a0001c0002t0002g0012 a0001c0002t0002g0014 others(109): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.371+827_371+832del others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53439954 | ||||||
| chr16:53439954 | CAAAAAAA others(5): Show |
C | 1 | a0001c0002t0001g0089 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.371+821_371+832del others(12): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53439954 | ||||||
| chr16:53440064 | G | A | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.371+918G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440064 | |||||||
| chr16:53440141 | C | A | 2 | a0001c0001t0001g0124 a0001c0001t0005g0125 |
2 | NA19010.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.371+995C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440141 | |||||||
| chr16:53440196 | C | T | 129 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(126): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.371+1050C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440196 | |||||||
| chr16:53440248 | T | C | 55 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(52): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.371+1102T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440248 | |||||||
| chr16:53440338 | G | A | 66 | a0001c0003t0003g0011 a0001c0003t0003g0127 a0001c0003t0003g0128 others(63): Show |
69 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.371+1192G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440338 | |||||||
| chr16:53440553 | A | G | 1 | a0002c0004t0003g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.371+1407A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440553 | |||||||
| chr16:53440611 | G | A | 1 | a0001c0003t0003g0162 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.371+1465G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440611 | |||||||
| chr16:53440656 | C | T | 75 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(72): Show |
78 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.371+1510C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440656 | |||||||
| chr16:53440665 | C | T | 8 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0120 others(5): Show |
8 | HG00621.hp2 HG01934.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.371+1519C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440665 | |||||||
| chr16:53440697 | AT | A | 3 | a0001c0003t0003g0163 a0001c0003t0003g0164 a0001c0003t0003g0165 |
3 | NA18962.hp1 NA18988.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.371+1552delT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440697 | |||||||
| chr16:53440711 | A | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.371+1565A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440711 | |||||||
| chr16:53440713 | C | T | 1 | a0001c0002t0004g0088 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.371+1567C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440713 | |||||||
| chr16:53440781 | C | T | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.371+1635C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440781 | |||||||
| chr16:53440858 | T | G | 25 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(22): Show |
25 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.371+1712T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440858 | |||||||
| chr16:53440860 | T | G | 1 | a0001c0002t0002g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.371+1714T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53440860 | |||||||
| chr16:53440953 | C | CT | 63 | a0001c0001t0001g0021 a0001c0001t0001g0024 a0001c0001t0001g0025 others(60): Show |
69 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.372-1681dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53440953 | ||||||
| chr16:53440953 | C | CTT | 60 | a0001c0001t0001g0074 a0001c0002t0002g0144 a0001c0002t0002g0227 others(57): Show |
62 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.372-1682_372-1681d others(4): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53440953 | ||||||
| chr16:53440953 | C | CTTT | 22 | a0001c0003t0002g0148 a0001c0003t0002g0206 a0001c0003t0002g0207 others(19): Show |
23 | HG01192.hp1 HG01255.hp2 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.372-1683_372-1681d others(5): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr16 | 53440953 | ||||||
| chr16:53441007 | T | G | 1 | a0001c0003t0003g0167 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.372-1651T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53441007 | |||||||
| chr16:53441484 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.372-1174G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53441484 | |||||||
| chr16:53441738 | A | G | 158 | a0001c0001t0007g0083 a0001c0002t0001g0089 a0001c0002t0002g0001 others(155): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.372-920A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53441738 | |||||||
| chr16:53441856 | T | C | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.372-802T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53441856 | |||||||
| chr16:53441969 | C | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.372-689C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53441969 | |||||||
| chr16:53442130 | C | T | 22 | a0002c0004t0003g0004 a0002c0004t0003g0145 a0002c0004t0003g0146 others(19): Show |
24 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.372-528C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53442130 | |||||||
| chr16:53442247 | A | G | 3 | a0001c0007t0004g0013 a0001c0007t0004g0090 a0001c0007t0004g0091 |
3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.372-411A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53442247 | |||||||
| chr16:53442309 | C | G | 1 | a0001c0002t0002g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.372-349C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53442309 | |||||||
| chr16:53442446 | T | C | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.372-212T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 2/21 | chr16 | 53442446 | |||||||
| chr16:53442892 | G | A | 129 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(126): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.572+34G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53442892 | |||||||
| chr16:53443107 | TTTATTA | T | 31 | a0001c0002t0002g0001 a0001c0002t0002g0012 a0001c0002t0002g0159 others(28): Show |
35 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.572+255_572+260del others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 53443107 | ||||||
| chr16:53443249 | G | T | 17 | a0001c0002t0001g0089 a0001c0002t0004g0087 a0001c0002t0004g0088 others(14): Show |
17 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.572+391G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53443249 | |||||||
| chr16:53443293 | A | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02717.hp1 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.572+435A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53443293 | |||||||
| chr16:53443590 | A | T | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.572+732A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53443590 | |||||||
| chr16:53443709 | G | A | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.572+851G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53443709 | |||||||
| chr16:53443820 | TGGG | T | 68 | a0001c0003t0002g0236 a0001c0003t0002g0237 a0001c0003t0003g0011 others(65): Show |
71 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.572+965_572+967del others(3): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 53443820 | ||||||
| chr16:53443974 | C | T | 4 | a0001c0003t0003g0176 a0001c0003t0003g0177 a0001c0003t0003g0178 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.572+1116C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53443974 | |||||||
| chr16:53444055 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.572+1197C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444055 | |||||||
| chr16:53444110 | G | A | 154 | a0001c0002t0001g0089 a0001c0002t0002g0001 a0001c0002t0002g0006 others(151): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.572+1252G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444110 | |||||||
| chr16:53444121 | T | C | 3 | a0001c0007t0004g0013 a0001c0007t0004g0090 a0001c0007t0004g0091 |
3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.572+1263T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444121 | |||||||
| chr16:53444231 | A | G | 1 | a0001c0011t0001g0071 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.572+1373A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444231 | |||||||
| chr16:53444343 | G | A | 1 | a0001c0003t0002g0237 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.572+1485G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444343 | |||||||
| chr16:53444450 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.572+1592G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444450 | |||||||
| chr16:53444501 | C | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+1643C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444501 | |||||||
| chr16:53444540 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.572+1682G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444540 | |||||||
| chr16:53444552 | T | TAATA | 11 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(8): Show |
11 | HG00741.hp2 HG01074.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.572+1721_572+1724d others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 53444552 | ||||||
| chr16:53444552 | T | TAATAAAT others(1): Show |
7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.572+1717_572+1724d others(10): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 53444552 | ||||||
| chr16:53444552 | T | TAATAAAT others(5): Show |
5 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(2): Show |
6 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.572+1713_572+1724d others(14): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 53444552 | ||||||
| chr16:53444562 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.572+1704A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444562 | |||||||
| chr16:53444587 | CAT | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+1732_572+1733d others(4): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 53444587 | ||||||
| chr16:53444614 | G | A | 1 | a0001c0003t0003g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.572+1756G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444614 | |||||||
| chr16:53444673 | C | A | 5 | a0001c0002t0002g0010 a0001c0002t0002g0150 a0001c0002t0002g0151 others(2): Show |
6 | HG02258.hp1 HG02559.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+1815C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444673 | |||||||
| chr16:53444799 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.572+1941G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444799 | |||||||
| chr16:53444947 | C | T | 2 | a0001c0002t0001g0089 a0001c0002t0008g0098 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.572+2089C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53444947 | |||||||
| chr16:53445025 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.573-2017C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445025 | |||||||
| chr16:53445143 | A | G | 1 | a0001c0002t0004g0245 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.573-1899A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445143 | |||||||
| chr16:53445172 | G | C | 157 | a0001c0002t0001g0089 a0001c0002t0002g0001 a0001c0002t0002g0006 others(154): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.573-1870G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445172 | |||||||
| chr16:53445195 | C | T | 1 | a0004c0008t0002g0212 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.573-1847C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445195 | |||||||
| chr16:53445196 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.573-1846G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445196 | |||||||
| chr16:53445233 | G | C | 2 | a0001c0003t0002g0236 a0001c0003t0002g0237 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.573-1809G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445233 | |||||||
| chr16:53445326 | CA | C | 133 | a0001c0001t0001g0070 a0001c0002t0001g0089 a0001c0002t0002g0001 others(130): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.573-1698delA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 53445326 | ||||||
| chr16:53445326 | CAA | C | 8 | a0001c0002t0002g0258 a0001c0002t0004g0250 a0001c0003t0002g0208 others(5): Show |
8 | HG01069.hp1 HG02683.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.573-1699_573-1698d others(4): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 53445326 | ||||||
| chr16:53445528 | A | G | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.573-1514A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445528 | |||||||
| chr16:53445592 | G | A | 7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.573-1450G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445592 | |||||||
| chr16:53445606 | T | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0041 others(1): Show |
4 | HG02683.hp2 HG02735.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.573-1436T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445606 | |||||||
| chr16:53445619 | C | T | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.573-1423C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445619 | |||||||
| chr16:53445694 | T | C | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.573-1348T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445694 | |||||||
| chr16:53445707 | C | T | 2 | a0001c0003t0003g0200 a0001c0003t0003g0201 |
2 | HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.573-1335C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445707 | |||||||
| chr16:53445740 | G | A | 66 | a0001c0003t0003g0011 a0001c0003t0003g0127 a0001c0003t0003g0128 others(63): Show |
69 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.573-1302G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445740 | |||||||
| chr16:53445923 | C | G | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.573-1119C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445923 | |||||||
| chr16:53445943 | G | A | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.573-1099G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53445943 | |||||||
| chr16:53446142 | C | G | 1 | a0001c0007t0004g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.573-900C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446142 | |||||||
| chr16:53446200 | C | T | 55 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(52): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.573-842C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446200 | |||||||
| chr16:53446296 | G | A | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.573-746G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446296 | |||||||
| chr16:53446297 | T | C | 7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.573-745T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446297 | |||||||
| chr16:53446338 | A | AGT | 161 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(158): Show |
170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.573-703_573-702dup others(2): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr16 | 53446338 | ||||||
| chr16:53446382 | C | G | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.573-660C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446382 | |||||||
| chr16:53446399 | G | A | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.573-643G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446399 | |||||||
| chr16:53446453 | T | G | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.573-589T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446453 | |||||||
| chr16:53446618 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.573-424G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446618 | |||||||
| chr16:53446648 | G | T | 1 | a0001c0003t0002g0158 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.573-394G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446648 | |||||||
| chr16:53446711 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.573-331A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446711 | |||||||
| chr16:53446797 | C | T | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.573-245C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446797 | |||||||
| chr16:53446880 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.573-162A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 3/21 | chr16 | 53446880 | |||||||
| chr16:53447167 | T | C | 1 | a0001c0002t0004g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.637+61T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447167 | |||||||
| chr16:53447170 | T | G | 1 | a0001c0003t0003g0142 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.637+64T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447170 | |||||||
| chr16:53447230 | A | G | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.637+124A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447230 | |||||||
| chr16:53447297 | A | G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+191A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447297 | |||||||
| chr16:53447300 | C | CTTCTCTT others(1): Show |
54 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(51): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.637+197_637+204dup others(8): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 53447300 | ||||||
| chr16:53447500 | A | G | 22 | a0002c0004t0003g0004 a0002c0004t0003g0145 a0002c0004t0003g0146 others(19): Show |
24 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.637+394A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447500 | |||||||
| chr16:53447510 | G | C | 136 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(133): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.637+404G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447510 | |||||||
| chr16:53447650 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.637+544T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447650 | |||||||
| chr16:53447713 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.637+607C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447713 | |||||||
| chr16:53447751 | TCTC | T | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.637+648_637+650del others(3): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 53447751 | ||||||
| chr16:53447755 | C | T | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.637+649C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447755 | |||||||
| chr16:53447972 | T | C | 1 | a0001c0002t0002g0150 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.637+866T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447972 | |||||||
| chr16:53447996 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.637+890C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53447996 | |||||||
| chr16:53448023 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0070 |
3 | HG02735.hp2 HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.637+917T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53448023 | |||||||
| chr16:53448160 | ATTTTAT | A | 66 | a0001c0003t0003g0011 a0001c0003t0003g0127 a0001c0003t0003g0128 others(63): Show |
69 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.637+1059_637+1064d others(8): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 53448160 | ||||||
| chr16:53448165 | AT | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(171): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.637+1069delT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 53448165 | ||||||
| chr16:53448261 | A | G | 1 | a0002c0004t0003g0195 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.637+1155A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53448261 | |||||||
| chr16:53448405 | C | T | 1 | a0001c0007t0004g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.637+1299C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53448405 | |||||||
| chr16:53448452 | C | T | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.637+1346C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53448452 | |||||||
| chr16:53448453 | G | A | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.637+1347G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53448453 | |||||||
| chr16:53448543 | G | A | 1 | a0001c0003t0004g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.637+1437G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53448543 | |||||||
| chr16:53448676 | G | A | 1 | a0001c0002t0002g0219 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.637+1570G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53448676 | |||||||
| chr16:53448780 | G | A | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.637+1674G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53448780 | |||||||
| chr16:53448982 | G | A | 7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.637+1876G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53448982 | |||||||
| chr16:53449136 | G | A | 8 | a0001c0002t0004g0243 a0001c0002t0004g0244 a0001c0002t0004g0246 others(5): Show |
8 | HG02572.hp2 HG02630.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.637+2030G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449136 | |||||||
| chr16:53449203 | G | A | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+2097G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449203 | |||||||
| chr16:53449214 | C | T | 1 | a0001c0003t0003g0175 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.637+2108C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449214 | |||||||
| chr16:53449226 | A | G | 65 | a0001c0003t0003g0011 a0001c0003t0003g0127 a0001c0003t0003g0128 others(62): Show |
68 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.637+2120A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449226 | |||||||
| chr16:53449227 | T | G | 1 | a0002c0004t0003g0196 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.637+2121T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449227 | |||||||
| chr16:53449319 | A | G | 2 | a0001c0002t0004g0087 a0001c0002t0004g0088 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.637+2213A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449319 | |||||||
| chr16:53449450 | T | C | 1 | a0004c0008t0002g0154 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.638-2253T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449450 | |||||||
| chr16:53449464 | A | G | 154 | a0001c0002t0001g0089 a0001c0002t0002g0001 a0001c0002t0002g0006 others(151): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.638-2239A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449464 | |||||||
| chr16:53449505 | G | T | 66 | a0001c0003t0003g0011 a0001c0003t0003g0127 a0001c0003t0003g0128 others(63): Show |
69 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.638-2198G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449505 | |||||||
| chr16:53449586 | G | GA | 16 | a0001c0001t0005g0082 a0001c0002t0002g0144 a0001c0002t0002g0254 others(13): Show |
16 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.638-2097dupA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 53449586 | ||||||
| chr16:53449586 | GA | G | 28 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0002t0001g0089 others(25): Show |
29 | HG00323.hp2 HG02109.hp1 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.638-2097delA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 53449586 | ||||||
| chr16:53449680 | A | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-2023A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449680 | |||||||
| chr16:53449769 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.638-1934T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449769 | |||||||
| chr16:53449789 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.638-1914G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449789 | |||||||
| chr16:53449831 | G | A | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.638-1872G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449831 | |||||||
| chr16:53449882 | A | G | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.638-1821A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449882 | |||||||
| chr16:53449958 | C | CT | 72 | a0001c0001t0001g0066 a0001c0001t0001g0068 a0001c0001t0001g0121 others(69): Show |
75 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.638-1726dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 53449958 | ||||||
| chr16:53449991 | A | G | 3 | a0001c0001t0001g0074 a0001c0002t0006g0234 a0001c0002t0006g0235 |
3 | HG01361.hp1 HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.638-1712A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53449991 | |||||||
| chr16:53450068 | C | A | 131 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(128): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.638-1635C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53450068 | |||||||
| chr16:53450283 | G | T | 1 | a0001c0003t0003g0127 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.638-1420G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53450283 | |||||||
| chr16:53450485 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.638-1218C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53450485 | |||||||
| chr16:53450491 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.638-1212T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53450491 | |||||||
| chr16:53450871 | A | G | 2 | a0001c0003t0003g0167 a0001c0003t0003g0174 |
2 | HG01106.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.638-832A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53450871 | |||||||
| chr16:53451042 | A | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0114 a0001c0001t0001g0118 |
3 | HG01261.hp1 HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.638-661A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53451042 | |||||||
| chr16:53451148 | CACTT | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.638-553_638-550del others(4): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | INFO_REALIGN_3_PRIME | chr16 | 53451148 | ||||||
| chr16:53451183 | T | C | 1 | a0001c0003t0004g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.638-520T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53451183 | |||||||
| chr16:53451289 | T | G | 5 | a0002c0004t0003g0146 a0002c0004t0003g0180 a0002c0004t0003g0184 others(2): Show |
5 | HG00280.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.638-414T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53451289 | |||||||
| chr16:53451398 | C | A | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.638-305C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53451398 | |||||||
| chr16:53451469 | G | A | 2 | a0001c0003t0002g0236 a0001c0003t0002g0237 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.638-234G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53451469 | |||||||
| chr16:53451521 | T | G | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.638-182T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 4/21 | chr16 | 53451521 | |||||||
| chr16:53451848 | A | G | 1 | a0001c0002t0002g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.766+17A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53451848 | |||||||
| chr16:53451995 | TG | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0075 |
3 | HG00280.hp2 HG01169.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.766+166delG | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 53451995 | ||||||
| chr16:53452035 | A | C | 7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.766+204A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53452035 | |||||||
| chr16:53452104 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.766+273G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53452104 | |||||||
| chr16:53452125 | G | A | 136 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(133): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.766+294G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53452125 | |||||||
| chr16:53452145 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.766+314A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53452145 | |||||||
| chr16:53452266 | AAACT | A | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.766+439_766+442del others(4): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr16 | 53452266 | ||||||
| chr16:53452279 | T | C | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.766+448T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53452279 | |||||||
| chr16:53452820 | C | T | 5 | a0002c0004t0003g0146 a0002c0004t0003g0180 a0002c0004t0003g0184 others(2): Show |
5 | HG00280.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-632C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53452820 | |||||||
| chr16:53452927 | C | T | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.767-525C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53452927 | |||||||
| chr16:53452930 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.767-522A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53452930 | |||||||
| chr16:53453256 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.767-196G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53453256 | |||||||
| chr16:53453306 | C | T | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.767-146C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53453306 | |||||||
| chr16:53453345 | G | A | 1 | a0001c0002t0002g0220 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.767-107G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 5/21 | chr16 | 53453345 | |||||||
| chr16:53453636 | C | T | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.927+24C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 6/21 | chr16 | 53453636 | |||||||
| chr16:53453677 | G | A | 5 | a0002c0004t0003g0146 a0002c0004t0003g0180 a0002c0004t0003g0184 others(2): Show |
5 | HG00280.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.928-28G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 6/21 | chr16 | 53453677 | |||||||
| chr16:53453785 | TAA | T | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.992+19_992+20delAA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr16 | 53453785 | ||||||
| chr16:53453819 | G | A | 1 | a0001c0003t0003g0134 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.992+50G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 7/21 | chr16 | 53453819 | |||||||
| chr16:53453865 | A | C | 1 | a0002c0004t0003g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.992+96A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 7/21 | chr16 | 53453865 | |||||||
| chr16:53454005 | C | T | 17 | a0001c0002t0002g0010 a0001c0002t0002g0144 a0001c0002t0002g0150 others(14): Show |
18 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.992+236C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 7/21 | chr16 | 53454005 | |||||||
| chr16:53454520 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.993-136T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 7/21 | chr16 | 53454520 | |||||||
| chr16:53455044 | T | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+202T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455044 | |||||||
| chr16:53455278 | A | T | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1179+436A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455278 | |||||||
| chr16:53455404 | A | T | 4 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0232 others(1): Show |
4 | HG02922.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1179+562A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455404 | |||||||
| chr16:53455426 | G | A | 2 | a0001c0001t0001g0069 a0005c0009t0001g0043 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1179+584G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455426 | |||||||
| chr16:53455430 | G | C | 1 | a0001c0003t0003g0136 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1179+588G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455430 | |||||||
| chr16:53455479 | G | C | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1179+637G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455479 | |||||||
| chr16:53455529 | A | G | 1 | a0002c0004t0003g0191 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1179+687A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455529 | |||||||
| chr16:53455793 | G | A | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1179+951G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455793 | |||||||
| chr16:53455920 | A | G | 1 | a0001c0001t0001g0038 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1179+1078A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455920 | |||||||
| chr16:53455984 | C | G | 15 | a0001c0002t0004g0087 a0001c0002t0004g0088 a0001c0002t0004g0243 others(12): Show |
15 | HG02109.hp1 HG02257.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1179+1142C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53455984 | |||||||
| chr16:53456114 | T | A | 1 | a0001c0002t0008g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1179+1272T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53456114 | |||||||
| chr16:53456126 | T | C | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1179+1284T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53456126 | |||||||
| chr16:53456186 | G | GAAA | 157 | a0001c0002t0001g0089 a0001c0002t0002g0001 a0001c0002t0002g0006 others(154): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.1179+1346_1179+134 others(7): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53456186 | ||||||
| chr16:53456284 | C | G | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1179+1442C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53456284 | |||||||
| chr16:53456534 | T | C | 1 | a0001c0001t0001g0117 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1179+1692T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53456534 | |||||||
| chr16:53456595 | G | A | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1179+1753G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53456595 | |||||||
| chr16:53456764 | C | T | 136 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(133): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1179+1922C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53456764 | |||||||
| chr16:53456815 | A | G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1179+1973A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53456815 | |||||||
| chr16:53456837 | C | A | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1179+1995C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53456837 | |||||||
| chr16:53456964 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1179+2122A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53456964 | |||||||
| chr16:53457011 | G | A | 1 | a0003c0006t0001g0107 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1179+2169G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457011 | |||||||
| chr16:53457183 | C | A | 66 | a0001c0003t0003g0011 a0001c0003t0003g0127 a0001c0003t0003g0128 others(63): Show |
69 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1180-2268C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457183 | |||||||
| chr16:53457258 | C | CCTTT | 5 | a0002c0004t0003g0004 a0002c0004t0003g0181 a0002c0004t0003g0182 others(2): Show |
7 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(8): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(2): Show |
4 | a0001c0003t0003g0011 a0001c0003t0003g0166 a0001c0003t0003g0197 others(1): Show |
5 | HG02071.hp1 HG02155.hp1 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(13): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(3): Show |
1 | a0001c0003t0003g0214 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1180-2193_1180-219 others(14): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(5): Show |
3 | a0001c0003t0003g0170 a0001c0003t0003g0198 a0001c0003t0003g0202 |
3 | HG02056.hp1 NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(16): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(6): Show |
1 | a0001c0003t0003g0137 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1180-2193_1180-219 others(17): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(9): Show |
1 | a0001c0003t0003g0138 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1180-2193_1180-219 others(20): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(15): Show |
3 | a0001c0003t0003g0163 a0001c0003t0003g0164 a0001c0003t0003g0165 |
3 | NA18962.hp1 NA18988.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(26): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(16): Show |
3 | a0001c0003t0003g0142 a0001c0003t0003g0171 a0001c0003t0003g0172 |
3 | HG03654.hp1 HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(27): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(17): Show |
1 | a0002c0004t0003g0187 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1180-2193_1180-219 others(28): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(18): Show |
7 | a0001c0003t0003g0128 a0001c0003t0003g0129 a0001c0003t0003g0132 others(4): Show |
7 | HG01074.hp1 HG01496.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(29): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(19): Show |
9 | a0001c0003t0003g0127 a0001c0003t0003g0130 a0001c0003t0003g0131 others(6): Show |
9 | HG01106.hp1 HG01106.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(30): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(20): Show |
4 | a0001c0003t0003g0173 a0001c0003t0003g0176 a0001c0003t0003g0200 others(1): Show |
4 | HG01069.hp1 HG01884.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(31): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(21): Show |
2 | a0001c0003t0003g0177 a0002c0004t0003g0190 |
2 | HG00642.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(32): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(22): Show |
3 | a0001c0003t0003g0178 a0002c0004t0003g0145 a0002c0004t0003g0183 |
3 | HG01123.hp2 HG04228.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(33): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(23): Show |
4 | a0001c0003t0003g0162 a0001c0003t0003g0179 a0002c0004t0003g0146 others(1): Show |
4 | HG00280.hp1 HG01192.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(34): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(24): Show |
3 | a0001c0003t0003g0134 a0001c0003t0003g0175 a0002c0004t0003g0180 |
3 | HG00738.hp1 HG02486.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(35): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(26): Show |
1 | a0001c0003t0003g0133 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1180-2193_1180-219 others(37): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(27): Show |
2 | a0001c0003t0003g0141 a0002c0004t0003g0192 |
2 | HG03516.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(38): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(29): Show |
2 | a0001c0003t0003g0139 a0001c0003t0004g0169 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(40): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(30): Show |
1 | a0001c0003t0003g0136 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1180-2193_1180-219 others(41): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(31): Show |
1 | a0001c0003t0003g0174 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1180-2193_1180-219 others(42): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CCTTTTTT others(40): Show |
2 | a0001c0003t0003g0140 a0001c0003t0003g0239 |
2 | HG03540.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1180-2193_1180-219 others(51): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457258 | |||||||
| chr16:53457258 | C | CTTTTT | 14 | a0001c0002t0004g0087 a0001c0002t0004g0088 a0001c0002t0004g0243 others(11): Show |
14 | HG02109.hp1 HG02572.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180-2178_1180-217 others(9): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT | 6 | a0001c0003t0002g0205 a0001c0003t0002g0206 a0001c0003t0002g0209 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1180-2180_1180-217 others(11): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT others(5): Show |
1 | a0001c0002t0002g0006 | 2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1180-2185_1180-217 others(16): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT others(6): Show |
3 | a0001c0002t0002g0092 a0001c0002t0002g0093 a0001c0002t0002g0094 |
3 | HG02145.hp2 HG02257.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1180-2186_1180-217 others(17): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT others(7): Show |
4 | a0001c0002t0002g0144 a0001c0002t0002g0210 a0001c0002t0002g0221 others(1): Show |
4 | HG01515.hp1 HG02145.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-2187_1180-217 others(18): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT others(8): Show |
26 | a0001c0002t0002g0001 a0001c0002t0002g0012 a0001c0002t0002g0014 others(23): Show |
30 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.1180-2188_1180-217 others(19): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT others(9): Show |
17 | a0001c0002t0002g0016 a0001c0002t0002g0156 a0001c0002t0002g0159 others(14): Show |
17 | HG00140.hp2 HG00438.hp1 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.1180-2189_1180-217 others(20): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT others(10): Show |
4 | a0001c0002t0002g0152 a0001c0002t0002g0157 a0001c0002t0002g0218 others(1): Show |
4 | HG01071.hp2 HG02135.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-2190_1180-217 others(21): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT others(11): Show |
4 | a0001c0002t0002g0010 a0001c0002t0002g0143 a0001c0002t0002g0153 others(1): Show |
5 | HG01255.hp1 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1180-2191_1180-217 others(22): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT others(14): Show |
2 | a0001c0001t0007g0083 a0001c0005t0001g0084 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1180-2174_1180-217 others(25): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457258 | C | CTTTTTTT others(15): Show |
2 | a0001c0005t0001g0085 a0001c0005t0001g0086 |
2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1180-2174_1180-217 others(26): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53457258 | ||||||
| chr16:53457277 | T | G | 4 | a0002c0004t0003g0145 a0002c0004t0003g0190 a0002c0004t0003g0192 others(1): Show |
4 | HG00642.hp2 HG01069.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180-2174T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457277 | |||||||
| chr16:53457370 | C | G | 1 | a0001c0002t0004g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1180-2081C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457370 | |||||||
| chr16:53457411 | C | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0117 |
2 | NA19063.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1180-2040C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457411 | |||||||
| chr16:53457548 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1180-1903C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457548 | |||||||
| chr16:53457550 | T | A | 1 | a0002c0004t0003g0181 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1180-1901T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457550 | |||||||
| chr16:53457711 | C | T | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1180-1740C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457711 | |||||||
| chr16:53457952 | G | T | 1 | a0002c0004t0003g0193 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1180-1499G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53457952 | |||||||
| chr16:53458748 | A | G | 1 | a0001c0003t0004g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1180-703A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53458748 | |||||||
| chr16:53458946 | A | G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180-505A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53458946 | |||||||
| chr16:53459024 | A | G | 2 | a0002c0004t0003g0190 a0002c0004t0003g0196 |
2 | HG00642.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.1180-427A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53459024 | |||||||
| chr16:53459272 | C | T | 2 | a0001c0001t0001g0069 a0005c0009t0001g0043 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1180-179C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | chr16 | 53459272 | |||||||
| chr16:53459434 | AT | A | 66 | a0001c0003t0003g0011 a0001c0003t0003g0127 a0001c0003t0003g0128 others(63): Show |
69 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
splice_region_variant&intron_variant | LOW | c.1180-7delT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr16 | 53459434 | ||||||
| chr16:53459670 | A | G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1346+53A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53459670 | |||||||
| chr16:53459865 | CA | C | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1346+252delA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr16 | 53459865 | ||||||
| chr16:53459926 | G | C | 2 | a0001c0001t0001g0120 a0001c0011t0001g0071 |
2 | NA18955.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.1346+309G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53459926 | |||||||
| chr16:53459973 | G | T | 1 | a0001c0001t0001g0065 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1346+356G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53459973 | |||||||
| chr16:53460024 | T | G | 1 | a0001c0010t0004g0252 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1346+407T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53460024 | |||||||
| chr16:53460165 | T | G | 1 | a0001c0003t0002g0205 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1346+548T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53460165 | |||||||
| chr16:53460206 | A | G | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1346+589A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53460206 | |||||||
| chr16:53460698 | A | G | 1 | a0001c0005t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1347-1043A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53460698 | |||||||
| chr16:53460705 | T | C | 130 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(127): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1347-1036T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53460705 | |||||||
| chr16:53460911 | G | C | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1347-830G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53460911 | |||||||
| chr16:53461210 | C | T | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1347-531C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53461210 | |||||||
| chr16:53461397 | C | T | 2 | a0001c0002t0004g0087 a0001c0002t0004g0088 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1347-344C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53461397 | |||||||
| chr16:53461439 | C | T | 1 | a0001c0002t0002g0228 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1347-302C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53461439 | |||||||
| chr16:53461498 | A | T | 41 | a0001c0001t0001g0036 a0001c0001t0001g0064 a0001c0002t0001g0089 others(38): Show |
43 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1347-243A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53461498 | |||||||
| chr16:53461500 | T | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0104 a0002c0004t0003g0204 |
3 | HG03490.hp1 HG04184.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.1347-241T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53461500 | |||||||
| chr16:53461541 | G | GT | 7 | a0001c0001t0001g0025 a0001c0001t0001g0063 a0001c0003t0002g0148 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1347-187dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr16 | 53461541 | ||||||
| chr16:53461541 | GT | G | 56 | a0001c0001t0001g0073 a0001c0002t0002g0001 a0001c0002t0002g0010 others(53): Show |
61 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.1347-187delT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr16 | 53461541 | ||||||
| chr16:53461660 | T | A | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1347-81T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 9/21 | chr16 | 53461660 | |||||||
| chr16:53461979 | A | G | 2 | a0001c0002t0002g0223 a0001c0002t0002g0229 |
2 | NA18948.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1456+129A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53461979 | |||||||
| chr16:53462001 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1456+151T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462001 | |||||||
| chr16:53462138 | A | G | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1456+288A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462138 | |||||||
| chr16:53462161 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1456+311G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462161 | |||||||
| chr16:53462161 | G | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1456+311G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462161 | |||||||
| chr16:53462261 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1457-291G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462261 | |||||||
| chr16:53462269 | C | A | 55 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(52): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.1457-283C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462269 | |||||||
| chr16:53462277 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1457-275T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462277 | |||||||
| chr16:53462298 | A | C | 1 | a0001c0002t0001g0089 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1457-254A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462298 | |||||||
| chr16:53462375 | A | G | 4 | a0001c0002t0002g0230 a0001c0002t0002g0231 a0001c0002t0002g0232 others(1): Show |
4 | HG02922.hp1 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1457-177A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462375 | |||||||
| chr16:53462422 | A | G | 1 | a0001c0002t0008g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1457-130A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462422 | |||||||
| chr16:53462527 | G | GT | 17 | a0001c0002t0001g0089 a0001c0002t0004g0087 a0001c0002t0004g0088 others(14): Show |
17 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1457-14dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr16 | 53462527 | ||||||
| chr16:53462527 | GT | G | 54 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(51): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.1457-14delT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr16 | 53462527 | ||||||
| chr16:53462528 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1457-24T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 10/21 | chr16 | 53462528 | |||||||
| chr16:53462686 | G | A | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1560+31G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53462686 | |||||||
| chr16:53462723 | G | C | 1 | a0001c0013t0001g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1560+68G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53462723 | |||||||
| chr16:53462825 | T | TTATG | 7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1560+190_1560+193d others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr16 | 53462825 | ||||||
| chr16:53462889 | G | A | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1560+234G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53462889 | |||||||
| chr16:53462904 | G | T | 7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1560+249G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53462904 | |||||||
| chr16:53462981 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1560+326T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53462981 | |||||||
| chr16:53463051 | G | A | 1 | a0001c0002t0008g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1560+396G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463051 | |||||||
| chr16:53463071 | C | T | 2 | a0001c0003t0003g0133 a0001c0003t0003g0134 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1560+416C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463071 | |||||||
| chr16:53463131 | G | A | 1 | a0002c0004t0003g0195 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1560+476G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463131 | |||||||
| chr16:53463133 | A | G | 158 | a0001c0001t0007g0083 a0001c0002t0001g0089 a0001c0002t0002g0001 others(155): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1560+478A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463133 | |||||||
| chr16:53463339 | G | A | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1560+684G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463339 | |||||||
| chr16:53463505 | G | T | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1561-721G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463505 | |||||||
| chr16:53463511 | G | T | 2 | a0001c0002t0001g0089 a0001c0002t0008g0098 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1561-715G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463511 | |||||||
| chr16:53463561 | C | CT | 42 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0032 others(39): Show |
42 | HG00438.hp2 HG00735.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1561-641dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr16 | 53463561 | ||||||
| chr16:53463561 | C | CTTT | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1561-643_1561-641d others(5): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr16 | 53463561 | ||||||
| chr16:53463599 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1561-627G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463599 | |||||||
| chr16:53463634 | C | T | 1 | a0001c0005t0001g0084 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1561-592C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463634 | |||||||
| chr16:53463862 | C | T | 66 | a0001c0003t0003g0011 a0001c0003t0003g0127 a0001c0003t0003g0128 others(63): Show |
69 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1561-364C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463862 | |||||||
| chr16:53463869 | C | G | 1 | a0001c0005t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1561-357C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53463869 | |||||||
| chr16:53464098 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1561-128A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 11/21 | chr16 | 53464098 | |||||||
| chr16:53464379 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1698+16T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53464379 | |||||||
| chr16:53464490 | T | C | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1698+127T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53464490 | |||||||
| chr16:53464635 | G | C | 1 | a0001c0002t0004g0246 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1698+272G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53464635 | |||||||
| chr16:53464743 | C | G | 75 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(72): Show |
78 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.1698+380C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53464743 | |||||||
| chr16:53464796 | G | T | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1698+433G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53464796 | |||||||
| chr16:53464832 | C | T | 3 | a0002c0004t0003g0145 a0002c0004t0003g0190 a0002c0004t0003g0196 |
3 | HG00642.hp2 HG01069.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1698+469C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53464832 | |||||||
| chr16:53464954 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1699-484C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53464954 | |||||||
| chr16:53465139 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0075 |
3 | HG00280.hp2 HG01169.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1699-299C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53465139 | |||||||
| chr16:53465299 | T | C | 2 | a0001c0003t0002g0236 a0001c0003t0002g0237 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1699-139T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53465299 | |||||||
| chr16:53465378 | G | T | 1 | a0001c0003t0003g0168 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1699-60G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 12/21 | chr16 | 53465378 | |||||||
| chr16:53465687 | A | G | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1863+85A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/21 | chr16 | 53465687 | |||||||
| chr16:53465699 | A | C | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1863+97A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/21 | chr16 | 53465699 | |||||||
| chr16:53465711 | C | G | 1 | a0001c0001t0001g0035 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1863+109C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/21 | chr16 | 53465711 | |||||||
| chr16:53465813 | T | C | 158 | a0001c0001t0007g0083 a0001c0002t0001g0089 a0001c0002t0002g0001 others(155): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1863+211T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/21 | chr16 | 53465813 | |||||||
| chr16:53466028 | ATCT | A | 10 | a0001c0002t0004g0243 a0001c0002t0004g0244 a0001c0002t0004g0245 others(7): Show |
10 | HG02572.hp2 HG02630.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1863+430_1863+432d others(5): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr16 | 53466028 | ||||||
| chr16:53466092 | C | A | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1863+490C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/21 | chr16 | 53466092 | |||||||
| chr16:53466115 | T | C | 2 | a0001c0002t0001g0089 a0001c0002t0008g0098 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1863+513T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/21 | chr16 | 53466115 | |||||||
| chr16:53466584 | C | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1864-474C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/21 | chr16 | 53466584 | |||||||
| chr16:53466901 | G | GT | 7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1864-147dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr16 | 53466901 | ||||||
| chr16:53467289 | G | A | 1 | a0001c0003t0003g0140 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1975+120G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53467289 | |||||||
| chr16:53467519 | C | T | 1 | a0001c0003t0003g0174 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1975+350C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53467519 | |||||||
| chr16:53467630 | C | T | 1 | a0001c0007t0004g0090 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1975+461C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53467630 | |||||||
| chr16:53467631 | G | A | 1 | a0001c0003t0004g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1975+462G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53467631 | |||||||
| chr16:53467797 | T | C | 7 | a0001c0003t0003g0142 a0001c0003t0003g0162 a0001c0003t0003g0163 others(4): Show |
7 | HG03654.hp1 HG03831.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.1975+628T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53467797 | |||||||
| chr16:53467844 | A | G | 7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1975+675A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53467844 | |||||||
| chr16:53467886 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1975+717C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53467886 | |||||||
| chr16:53467971 | A | C | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1975+802A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53467971 | |||||||
| chr16:53467982 | A | G | 4 | a0001c0002t0002g0143 a0001c0002t0002g0149 a0001c0002t0004g0087 others(1): Show |
4 | HG01169.hp2 HG02109.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1975+813A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53467982 | |||||||
| chr16:53468034 | G | A | 134 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(131): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1975+865G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53468034 | |||||||
| chr16:53468256 | A | T | 20 | a0001c0002t0001g0089 a0001c0002t0002g0143 a0001c0002t0002g0149 others(17): Show |
20 | HG01169.hp2 HG02109.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.1975+1087A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53468256 | |||||||
| chr16:53468383 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1975+1214C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53468383 | |||||||
| chr16:53468445 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02717.hp1 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1975+1276C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53468445 | |||||||
| chr16:53468615 | A | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0040 a0001c0001t0001g0070 |
3 | HG02735.hp2 HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1976-1301A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53468615 | |||||||
| chr16:53468936 | G | GTT | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1976-979_1976-978d others(4): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr16 | 53468936 | ||||||
| chr16:53469170 | T | C | 1 | a0002c0004t0003g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1976-746T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53469170 | |||||||
| chr16:53469198 | C | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0033 others(3): Show |
6 | HG00741.hp2 HG01074.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1976-718C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53469198 | |||||||
| chr16:53469412 | AAGAC | A | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.1976-500_1976-497d others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr16 | 53469412 | ||||||
| chr16:53469528 | G | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1976-388G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 14/21 | chr16 | 53469528 | |||||||
| chr16:53471051 | T | C | 1 | a0002c0004t0003g0204 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2703+129T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471051 | |||||||
| chr16:53471254 | G | T | 2 | a0002c0004t0003g0190 a0002c0004t0003g0196 |
2 | HG00642.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.2703+332G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471254 | |||||||
| chr16:53471324 | T | G | 1 | a0001c0002t0002g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2703+402T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471324 | |||||||
| chr16:53471381 | G | A | 1 | a0001c0002t0004g0247 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2703+459G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471381 | |||||||
| chr16:53471399 | T | A | 1 | a0001c0003t0002g0238 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2703+477T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471399 | |||||||
| chr16:53471465 | T | C | 30 | a0001c0002t0002g0001 a0001c0002t0002g0012 a0001c0002t0002g0213 others(27): Show |
34 | HG00140.hp1 HG00438.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.2703+543T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471465 | |||||||
| chr16:53471546 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2703+624G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471546 | |||||||
| chr16:53471593 | C | G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2703+671C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471593 | |||||||
| chr16:53471594 | G | A | 3 | a0001c0007t0004g0013 a0001c0007t0004g0090 a0001c0007t0004g0091 |
3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2703+672G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471594 | |||||||
| chr16:53471677 | C | T | 1 | a0002c0004t0003g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2703+755C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471677 | |||||||
| chr16:53471721 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2703+799G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471721 | |||||||
| chr16:53471819 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2703+897G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53471819 | |||||||
| chr16:53472658 | G | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2703+1736G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53472658 | |||||||
| chr16:53472698 | C | T | 10 | a0001c0002t0004g0243 a0001c0002t0004g0244 a0001c0002t0004g0245 others(7): Show |
10 | HG02572.hp2 HG02630.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2703+1776C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53472698 | |||||||
| chr16:53473052 | T | C | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02717.hp1 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2703+2130T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53473052 | |||||||
| chr16:53473062 | G | C | 1 | a0001c0001t0001g0049 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2703+2140G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53473062 | |||||||
| chr16:53473353 | G | GT | 12 | a0002c0004t0003g0004 a0002c0004t0003g0147 a0002c0004t0003g0181 others(9): Show |
14 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.2703+2440dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53473353 | ||||||
| chr16:53473433 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2703+2511G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53473433 | |||||||
| chr16:53473465 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0068 |
3 | HG02280.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2703+2543G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53473465 | |||||||
| chr16:53473751 | T | C | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2703+2829T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53473751 | |||||||
| chr16:53473771 | G | A | 1 | a0002c0004t0003g0203 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2703+2849G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53473771 | |||||||
| chr16:53474202 | G | A | 1 | a0002c0004t0003g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2703+3280G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53474202 | |||||||
| chr16:53474258 | T | C | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01169.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2703+3336T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53474258 | |||||||
| chr16:53474301 | T | TTTTA | 5 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0008g0098 others(2): Show |
5 | HG02257.hp2 HG02451.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2703+3407_2703+341 others(8): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53474301 | ||||||
| chr16:53474301 | T | TTTTATTT others(1): Show |
7 | a0001c0002t0004g0243 a0001c0002t0004g0244 a0001c0002t0004g0245 others(4): Show |
7 | HG02630.hp1 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2703+3403_2703+341 others(12): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53474301 | ||||||
| chr16:53474301 | T | TTTTATTT others(5): Show |
3 | a0001c0002t0004g0247 a0001c0002t0004g0251 a0001c0010t0004g0252 |
3 | HG02572.hp2 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2703+3399_2703+341 others(16): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53474301 | ||||||
| chr16:53474301 | TTTTA | T | 81 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(78): Show |
85 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2703+3407_2703+341 others(8): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53474301 | ||||||
| chr16:53474301 | TTTTATTT others(1): Show |
T | 55 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(52): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.2703+3403_2703+341 others(12): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53474301 | ||||||
| chr16:53474510 | T | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2703+3588T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53474510 | |||||||
| chr16:53474595 | C | T | 134 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(131): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2703+3673C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53474595 | |||||||
| chr16:53474728 | G | A | 8 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(5): Show |
8 | HG01169.hp2 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2703+3806G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53474728 | |||||||
| chr16:53474881 | C | CT | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2703+3968dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53474881 | ||||||
| chr16:53474890 | T | A | 23 | a0001c0001t0001g0035 a0002c0004t0003g0004 a0002c0004t0003g0145 others(20): Show |
25 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.2703+3968T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53474890 | |||||||
| chr16:53475171 | C | A | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2704-3983C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53475171 | |||||||
| chr16:53475219 | G | A | 77 | a0001c0002t0004g0087 a0001c0002t0004g0088 a0001c0003t0002g0148 others(74): Show |
80 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.2704-3935G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53475219 | |||||||
| chr16:53475339 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | HG02717.hp1 HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2704-3815C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53475339 | |||||||
| chr16:53475408 | A | G | 7 | a0001c0003t0003g0142 a0001c0003t0003g0162 a0001c0003t0003g0163 others(4): Show |
7 | HG03654.hp1 HG03831.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.2704-3746A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53475408 | |||||||
| chr16:53475835 | C | CT | 30 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0044 others(27): Show |
31 | HG02109.hp1 HG02135.hp2 HG02257.hp2 others(28): Show |
intron_variant | MODIFIER | c.2704-3291dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53475835 | ||||||
| chr16:53475835 | C | CTT | 8 | a0001c0001t0001g0022 a0001c0001t0001g0095 a0001c0002t0002g0016 others(5): Show |
8 | HG00741.hp2 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2704-3292_2704-329 others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53475835 | ||||||
| chr16:53475835 | CT | C | 10 | a0001c0001t0001g0037 a0001c0001t0001g0058 a0001c0002t0001g0089 others(7): Show |
10 | HG00544.hp1 HG00642.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2704-3291delT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53475835 | ||||||
| chr16:53475835 | CTT | C | 67 | a0001c0002t0006g0234 a0001c0002t0006g0235 a0001c0003t0002g0148 others(64): Show |
70 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.2704-3292_2704-329 others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53475835 | ||||||
| chr16:53475907 | C | T | 13 | a0001c0002t0004g0243 a0001c0002t0004g0244 a0001c0002t0004g0245 others(10): Show |
13 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2704-3247C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53475907 | |||||||
| chr16:53476024 | G | A | 154 | a0001c0002t0001g0089 a0001c0002t0002g0001 a0001c0002t0002g0006 others(151): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2704-3130G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53476024 | |||||||
| chr16:53476297 | G | T | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2704-2857G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53476297 | |||||||
| chr16:53476557 | A | T | 18 | a0001c0002t0001g0089 a0001c0002t0003g0019 a0001c0002t0004g0087 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.2704-2597A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53476557 | |||||||
| chr16:53476592 | A | G | 256 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.2704-2562A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53476592 | |||||||
| chr16:53476769 | T | C | 1 | a0001c0002t0002g0241 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2704-2385T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53476769 | |||||||
| chr16:53476775 | G | A | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.2704-2379G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53476775 | |||||||
| chr16:53476794 | C | T | 10 | a0001c0002t0004g0243 a0001c0002t0004g0244 a0001c0002t0004g0245 others(7): Show |
10 | HG02572.hp2 HG02630.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.2704-2360C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53476794 | |||||||
| chr16:53476819 | T | C | 55 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(52): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.2704-2335T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53476819 | |||||||
| chr16:53476987 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2704-2167G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53476987 | |||||||
| chr16:53477036 | C | T | 2 | a0001c0002t0004g0087 a0001c0002t0004g0088 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2704-2118C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53477036 | |||||||
| chr16:53477057 | T | TTG | 74 | a0001c0002t0006g0234 a0001c0002t0006g0235 a0001c0003t0002g0148 others(71): Show |
77 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.2704-2073_2704-207 others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53477057 | ||||||
| chr16:53477057 | T | TTGTG | 39 | a0001c0002t0002g0010 a0001c0002t0002g0012 a0001c0002t0002g0014 others(36): Show |
41 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.2704-2075_2704-207 others(8): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53477057 | ||||||
| chr16:53477057 | T | TTGTGTG | 17 | a0001c0002t0002g0001 a0001c0002t0002g0213 a0001c0002t0002g0217 others(14): Show |
20 | HG00438.hp1 HG00544.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.2704-2077_2704-207 others(10): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53477057 | ||||||
| chr16:53477057 | TTG | T | 114 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(111): Show |
119 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2704-2073_2704-207 others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53477057 | ||||||
| chr16:53477057 | TTGTG | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2704-2075_2704-207 others(8): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53477057 | ||||||
| chr16:53477084 | G | A | 1 | a0001c0003t0003g0202 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2704-2070G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53477084 | |||||||
| chr16:53477180 | C | T | 2 | a0001c0002t0004g0087 a0001c0002t0004g0088 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2704-1974C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53477180 | |||||||
| chr16:53477285 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2704-1869G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53477285 | |||||||
| chr16:53477377 | G | A | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2704-1777G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53477377 | |||||||
| chr16:53477662 | T | C | 3 | a0001c0002t0002g0156 a0001c0002t0002g0157 a0001c0002t0002g0211 |
3 | HG01070.hp2 HG01071.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.2704-1492T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53477662 | |||||||
| chr16:53477787 | T | TTA | 2 | a0001c0001t0001g0069 a0005c0009t0001g0043 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2704-1355_2704-135 others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53477787 | ||||||
| chr16:53478014 | G | A | 136 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(133): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.2704-1140G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53478014 | |||||||
| chr16:53478170 | C | T | 1 | a0001c0002t0002g0092 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2704-984C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53478170 | |||||||
| chr16:53478393 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2704-761A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53478393 | |||||||
| chr16:53478436 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2704-718C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53478436 | |||||||
| chr16:53478491 | C | T | 13 | a0001c0002t0004g0243 a0001c0002t0004g0244 a0001c0002t0004g0245 others(10): Show |
13 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.2704-663C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53478491 | |||||||
| chr16:53478545 | C | CT | 177 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
186 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.2704-593dupT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53478545 | ||||||
| chr16:53478545 | C | CTT | 22 | a0001c0001t0001g0024 a0001c0001t0001g0039 a0001c0001t0001g0055 others(19): Show |
22 | HG01884.hp2 HG02056.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.2704-594_2704-593d others(4): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53478545 | ||||||
| chr16:53478545 | C | CTTT | 48 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(45): Show |
53 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.2704-595_2704-593d others(5): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr16 | 53478545 | ||||||
| chr16:53478576 | G | A | 138 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(135): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2704-578G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53478576 | |||||||
| chr16:53478892 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2704-262G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53478892 | |||||||
| chr16:53479121 | C | T | 138 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(135): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2704-33C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53479121 | |||||||
| chr16:53479143 | T | C | 134 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(131): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2704-11T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 17/21 | chr16 | 53479143 | |||||||
| chr16:53479272 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2775+47T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 18/21 | chr16 | 53479272 | |||||||
| chr16:53479540 | C | G | 158 | a0001c0001t0007g0083 a0001c0002t0001g0089 a0001c0002t0002g0001 others(155): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2775+315C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 18/21 | chr16 | 53479540 | |||||||
| chr16:53479607 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.2776-279G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 18/21 | chr16 | 53479607 | |||||||
| chr16:53480006 | T | C | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2881+15T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 19/21 | chr16 | 53480006 | |||||||
| chr16:53480240 | A | C | 1 | a0001c0003t0004g0169 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2881+249A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 19/21 | chr16 | 53480240 | |||||||
| chr16:53480530 | G | A | 2 | a0001c0003t0003g0133 a0001c0003t0003g0134 |
2 | HG02486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2882-37G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 19/21 | chr16 | 53480530 | |||||||
| chr16:53480869 | C | A | 3 | a0001c0002t0002g0010 a0001c0002t0002g0152 a0001c0002t0002g0153 |
4 | HG02258.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3084+100C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53480869 | |||||||
| chr16:53480884 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0076 a0001c0001t0001g0109 |
3 | HG00642.hp1 HG01256.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.3084+115T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53480884 | |||||||
| chr16:53480908 | C | T | 75 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(72): Show |
78 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.3084+139C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53480908 | |||||||
| chr16:53480938 | C | A | 55 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(52): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.3084+169C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53480938 | |||||||
| chr16:53481090 | C | T | 1 | a0003c0006t0001g0107 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.3084+321C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53481090 | |||||||
| chr16:53481175 | T | C | 1 | a0001c0003t0002g0158 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3084+406T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53481175 | |||||||
| chr16:53481181 | T | C | 75 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(72): Show |
78 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.3084+412T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53481181 | |||||||
| chr16:53481206 | G | A | 75 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(72): Show |
78 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.3084+437G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53481206 | |||||||
| chr16:53481391 | C | T | 3 | a0001c0007t0004g0013 a0001c0007t0004g0090 a0001c0007t0004g0091 |
3 | HG02257.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3085-280C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53481391 | |||||||
| chr16:53481514 | A | G | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3085-157A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | chr16 | 53481514 | |||||||
| chr16:53481652 | AT | A | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG01169.hp2 HG02717.hp1 HG02809.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.3085-7delT | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr16 | 53481652 | ||||||
| chr16:53482015 | G | C | 1 | a0001c0001t0001g0041 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.3249+180G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482015 | |||||||
| chr16:53482047 | T | C | 132 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.3249+212T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482047 | |||||||
| chr16:53482081 | A | T | 7 | a0001c0003t0003g0142 a0001c0003t0003g0162 a0001c0003t0003g0163 others(4): Show |
7 | HG03654.hp1 HG03831.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.3249+246A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482081 | |||||||
| chr16:53482225 | G | A | 5 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(2): Show |
5 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+390G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482225 | |||||||
| chr16:53482358 | G | A | 1 | a0001c0003t0003g0174 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3249+523G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482358 | |||||||
| chr16:53482535 | C | T | 3 | a0001c0005t0001g0084 a0001c0005t0001g0085 a0001c0005t0001g0086 |
3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3249+700C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482535 | |||||||
| chr16:53482536 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3249+701G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482536 | |||||||
| chr16:53482605 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3249+770T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482605 | |||||||
| chr16:53482627 | G | A | 7 | a0001c0003t0002g0148 a0001c0003t0002g0205 a0001c0003t0002g0206 others(4): Show |
7 | HG01891.hp2 HG02451.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.3249+792G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482627 | |||||||
| chr16:53482627 | G | C | 145 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(142): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.3249+792G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482627 | |||||||
| chr16:53482668 | G | C | 7 | a0001c0001t0001g0027 a0001c0001t0001g0057 a0001c0001t0001g0100 others(4): Show |
7 | HG00621.hp1 HG01934.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.3249+833G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482668 | |||||||
| chr16:53482764 | C | T | 134 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(131): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.3249+929C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482764 | |||||||
| chr16:53482812 | C | CA | 15 | a0001c0001t0001g0042 a0001c0001t0001g0049 a0001c0001t0001g0059 others(12): Show |
15 | HG00438.hp2 HG01109.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.3249+994dupA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53482812 | ||||||
| chr16:53482812 | CA | C | 103 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(100): Show |
109 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.3249+994delA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53482812 | ||||||
| chr16:53482912 | A | G | 68 | a0001c0002t0003g0253 a0001c0003t0003g0011 a0001c0003t0003g0127 others(65): Show |
71 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.3249+1077A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53482912 | |||||||
| chr16:53483038 | A | T | 140 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(137): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.3249+1203A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483038 | |||||||
| chr16:53483283 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.3249+1448G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483283 | |||||||
| chr16:53483330 | G | A | 76 | a0001c0002t0003g0253 a0001c0003t0002g0148 a0001c0003t0002g0205 others(73): Show |
79 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(76): Show |
intron_variant | MODIFIER | c.3249+1495G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483330 | |||||||
| chr16:53483478 | C | T | 5 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+1643C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483478 | |||||||
| chr16:53483518 | A | T | 1 | a0001c0003t0003g0172 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3249+1683A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483518 | |||||||
| chr16:53483520 | A | C | 1 | a0001c0002t0003g0019 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3249+1685A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483520 | |||||||
| chr16:53483768 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3249+1933C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483768 | |||||||
| chr16:53483799 | T | A | 1 | a0001c0002t0004g0088 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3249+1964T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483799 | |||||||
| chr16:53483856 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3249+2021G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483856 | |||||||
| chr16:53483866 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3249+2031A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483866 | |||||||
| chr16:53483922 | A | G | 1 | a0001c0002t0002g0213 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3249+2087A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483922 | |||||||
| chr16:53483926 | T | TA | 26 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(23): Show |
27 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.3249+2108dupA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53483926 | ||||||
| chr16:53483926 | TA | T | 120 | a0001c0001t0001g0032 a0001c0001t0001g0121 a0001c0002t0002g0001 others(117): Show |
129 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.3249+2108delA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53483926 | ||||||
| chr16:53483943 | A | AG | 16 | a0001c0002t0001g0089 a0001c0002t0004g0087 a0001c0002t0004g0088 others(13): Show |
16 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.3249+2110dupG | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53483943 | ||||||
| chr16:53483943 | A | G | 1 | a0001c0007t0004g0013 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3249+2108A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483943 | |||||||
| chr16:53483979 | TAA | T | 158 | a0001c0001t0007g0083 a0001c0002t0001g0089 a0001c0002t0002g0001 others(155): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3249+2147_3249+214 others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53483979 | ||||||
| chr16:53483995 | T | A | 2 | a0001c0002t0002g0218 a0001c0002t0002g0227 |
2 | HG02135.hp2 NA18949.hp2 |
intron_variant | MODIFIER | c.3249+2160T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53483995 | |||||||
| chr16:53484206 | C | G | 2 | a0001c0002t0002g0157 a0001c0002t0002g0211 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.3249+2371C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53484206 | |||||||
| chr16:53484293 | T | C | 5 | a0002c0004t0003g0146 a0002c0004t0003g0180 a0002c0004t0003g0184 others(2): Show |
5 | HG00280.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.3249+2458T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53484293 | |||||||
| chr16:53484316 | T | C | 157 | a0001c0002t0001g0089 a0001c0002t0002g0001 a0001c0002t0002g0006 others(154): Show |
166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.3249+2481T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53484316 | |||||||
| chr16:53484443 | T | C | 1 | a0001c0002t0002g0242 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3249+2608T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53484443 | |||||||
| chr16:53484458 | C | G | 135 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(132): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3249+2623C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53484458 | |||||||
| chr16:53484627 | G | A | 1 | a0001c0002t0002g0217 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.3249+2792G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53484627 | |||||||
| chr16:53484758 | GCTCTGGG others(2): Show |
G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+2934_3249+294 others(13): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53484758 | ||||||
| chr16:53484768 | C | T | 2 | a0001c0005t0001g0084 a0001c0005t0001g0086 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3249+2933C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53484768 | |||||||
| chr16:53484774 | G | T | 133 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(130): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.3249+2939G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53484774 | |||||||
| chr16:53484828 | T | A | 2 | a0001c0002t0004g0087 a0001c0002t0004g0088 |
2 | HG02109.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3249+2993T>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53484828 | |||||||
| chr16:53485004 | T | TA | 69 | a0001c0002t0003g0019 a0001c0002t0003g0253 a0001c0003t0003g0011 others(66): Show |
72 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.3249+3181dupA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53485004 | ||||||
| chr16:53485004 | TA | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(17): Show |
21 | HG00280.hp2 HG00438.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.3249+3181delA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53485004 | ||||||
| chr16:53485103 | T | C | 2 | a0001c0001t0003g0079 a0001c0001t0003g0080 |
2 | HG00408.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.3249+3268T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53485103 | |||||||
| chr16:53485123 | T | C | 135 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(132): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3249+3288T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53485123 | |||||||
| chr16:53485148 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3249+3313C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53485148 | |||||||
| chr16:53485326 | C | A | 3 | a0001c0002t0002g0006 a0001c0002t0002g0093 a0001c0002t0002g0094 |
4 | HG02257.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3249+3491C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53485326 | |||||||
| chr16:53485652 | C | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3249+3817C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53485652 | |||||||
| chr16:53485750 | G | A | 54 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(51): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3249+3915G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53485750 | |||||||
| chr16:53485852 | TAAAAAA | T | 10 | a0001c0002t0002g0155 a0001c0002t0002g0156 a0001c0002t0002g0157 others(7): Show |
10 | HG00323.hp1 HG00738.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.3249+4021_3249+402 others(10): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53485852 | ||||||
| chr16:53485856 | A | AAAAAAAC | 13 | a0001c0002t0004g0243 a0001c0002t0004g0244 a0001c0002t0004g0245 others(10): Show |
13 | HG02257.hp2 HG02572.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.3249+4026_3249+402 others(11): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53485856 | ||||||
| chr16:53485856 | A | AAAAAAC | 9 | a0001c0002t0001g0089 a0001c0002t0002g0006 a0001c0002t0002g0092 others(6): Show |
10 | HG01884.hp2 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.3249+4039_3249+404 others(10): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53485856 | ||||||
| chr16:53485856 | A | C | 45 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(42): Show |
50 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.3249+4021A>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53485856 | |||||||
| chr16:53485961 | C | G | 15 | a0001c0002t0001g0089 a0001c0002t0004g0243 a0001c0002t0004g0244 others(12): Show |
15 | HG02257.hp2 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.3249+4126C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53485961 | |||||||
| chr16:53485966 | A | G | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3249+4131A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53485966 | |||||||
| chr16:53486001 | G | A | 1 | a0001c0003t0002g0236 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.3250-4129G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486001 | |||||||
| chr16:53486124 | T | TGAAA | 3 | a0001c0002t0002g0006 a0001c0002t0002g0093 a0001c0002t0002g0094 |
4 | HG02257.hp1 HG02258.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3250-4005_3250-400 others(8): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53486124 | ||||||
| chr16:53486125 | G | GA | 12 | a0001c0001t0001g0066 a0001c0001t0001g0073 a0001c0003t0003g0128 others(9): Show |
12 | HG00438.hp2 HG01109.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.3250-3985dupA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53486125 | ||||||
| chr16:53486125 | G | GAA | 11 | a0001c0002t0001g0089 a0001c0002t0004g0243 a0001c0002t0004g0244 others(8): Show |
11 | HG02451.hp1 HG02572.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.3250-3986_3250-398 others(6): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53486125 | ||||||
| chr16:53486125 | GA | G | 120 | a0001c0001t0001g0056 a0001c0001t0005g0125 a0001c0002t0002g0001 others(117): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.3250-3985delA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53486125 | ||||||
| chr16:53486161 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3250-3969G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486161 | |||||||
| chr16:53486228 | G | A | 3 | a0001c0002t0002g0010 a0001c0002t0002g0152 a0001c0002t0002g0153 |
4 | HG02258.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.3250-3902G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486228 | |||||||
| chr16:53486342 | G | A | 2 | a0001c0002t0006g0234 a0001c0002t0006g0235 |
2 | HG02486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3250-3788G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486342 | |||||||
| chr16:53486473 | T | C | 1 | a0001c0005t0001g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3250-3657T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486473 | |||||||
| chr16:53486680 | T | C | 2 | a0001c0003t0003g0200 a0001c0005t0001g0085 |
2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3250-3450T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486680 | |||||||
| chr16:53486701 | G | A | 84 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(81): Show |
88 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.3250-3429G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486701 | |||||||
| chr16:53486748 | A | G | 2 | a0001c0003t0002g0236 a0001c0003t0002g0237 |
2 | HG02896.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.3250-3382A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486748 | |||||||
| chr16:53486877 | A | G | 4 | a0002c0004t0003g0145 a0002c0004t0003g0190 a0002c0004t0003g0192 others(1): Show |
4 | HG00642.hp2 HG01069.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.3250-3253A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486877 | |||||||
| chr16:53486892 | A | G | 79 | a0001c0002t0003g0253 a0001c0002t0004g0087 a0001c0002t0004g0088 others(76): Show |
82 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.3250-3238A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486892 | |||||||
| chr16:53486903 | A | T | 15 | a0001c0002t0001g0089 a0001c0002t0004g0243 a0001c0002t0004g0244 others(12): Show |
15 | HG02257.hp2 HG02451.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.3250-3227A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53486903 | |||||||
| chr16:53487075 | T | C | 1 | a0001c0005t0001g0085 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3250-3055T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53487075 | |||||||
| chr16:53487086 | T | C | 158 | a0001c0001t0007g0083 a0001c0002t0001g0089 a0001c0002t0002g0001 others(155): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.3250-3044T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53487086 | |||||||
| chr16:53487268 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.3250-2862C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53487268 | |||||||
| chr16:53487485 | C | T | 2 | a0001c0005t0001g0084 a0001c0005t0001g0086 |
2 | HG01884.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3250-2645C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53487485 | |||||||
| chr16:53487551 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.3250-2579C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53487551 | |||||||
| chr16:53487589 | TAGAAGAC others(3): Show |
T | 1 | a0001c0002t0002g0144 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3250-2536_3250-252 others(14): Show |
RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53487589 | ||||||
| chr16:53487681 | G | A | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3250-2449G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53487681 | |||||||
| chr16:53487737 | A | T | 1 | a0001c0001t0001g0115 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3250-2393A>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53487737 | |||||||
| chr16:53487829 | G | A | 1 | a0001c0001t0007g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3250-2301G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53487829 | |||||||
| chr16:53487928 | G | T | 2 | a0001c0002t0001g0089 a0001c0002t0008g0098 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3250-2202G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53487928 | |||||||
| chr16:53488095 | C | T | 2 | a0001c0001t0003g0079 a0001c0001t0003g0080 |
2 | HG00408.hp1 HG02071.hp2 |
intron_variant | MODIFIER | c.3250-2035C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488095 | |||||||
| chr16:53488170 | T | G | 1 | a0002c0004t0003g0146 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3250-1960T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488170 | |||||||
| chr16:53488260 | T | C | 54 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(51): Show |
59 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3250-1870T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488260 | |||||||
| chr16:53488312 | G | T | 2 | a0001c0003t0003g0198 a0001c0003t0003g0202 |
2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.3250-1818G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488312 | |||||||
| chr16:53488324 | G | T | 3 | a0001c0002t0006g0234 a0001c0002t0006g0235 a0001c0007t0004g0091 |
3 | HG02486.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3250-1806G>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488324 | |||||||
| chr16:53488357 | A | G | 2 | a0004c0008t0002g0154 a0004c0008t0002g0212 |
2 | HG00323.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.3250-1773A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488357 | |||||||
| chr16:53488430 | G | A | 1 | a0002c0004t0003g0191 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3250-1700G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488430 | |||||||
| chr16:53488550 | G | A | 2 | a0001c0002t0002g0014 a0001c0002t0004g0087 |
2 | HG02647.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3250-1580G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488550 | |||||||
| chr16:53488627 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.3250-1503C>T | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488627 | |||||||
| chr16:53488837 | T | C | 137 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0002t0002g0001 others(134): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.3250-1293T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488837 | |||||||
| chr16:53488995 | G | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3250-1135G>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53488995 | |||||||
| chr16:53489002 | C | G | 4 | a0001c0002t0002g0006 a0001c0002t0002g0092 a0001c0002t0002g0093 others(1): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.3250-1128C>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53489002 | |||||||
| chr16:53489059 | TA | T | 150 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0002t0002g0001 others(147): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.3250-1055delA | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53489059 | ||||||
| chr16:53489460 | G | A | 1 | a0001c0003t0003g0170 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3250-670G>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53489460 | |||||||
| chr16:53489499 | G | GC | 55 | a0001c0002t0002g0001 a0001c0002t0002g0010 a0001c0002t0002g0012 others(52): Show |
60 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.3250-627dupC | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53489499 | ||||||
| chr16:53489624 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3250-506T>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53489624 | |||||||
| chr16:53489653 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3250-477C>A | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53489653 | |||||||
| chr16:53489682 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0124 |
2 | NA19010.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.3250-448T>C | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53489682 | |||||||
| chr16:53489891 | A | G | 1 | a0002c0004t0003g0182 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3250-239A>G | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | chr16 | 53489891 | |||||||
| chr16:53490035 | AG | A | 134 | a0001c0002t0002g0001 a0001c0002t0002g0006 a0001c0002t0002g0010 others(131): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.3250-92delG | RBL2 | ENSG00000103479.17 | transcript | ENST00000262133.11 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr16 | 53490035 |