Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23786 |
| ensemblid | ENSG00000099968.18 |
| hgncid | 17164 |
| symbol | BCL2L13 |
| name | BCL2 like 13 |
| refseq_nuc | NM_015367.4 |
| refseq_prot | NP_056182.2 |
| ensembl_nuc | ENST00000317582.10 |
| ensembl_prot | ENSP00000318883.5 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 17638757 |
| end | 17730855 |
| strand | + |
| ver | v1.2 |
| region | chr22:17638757-17730855 |
| region5000 | chr22:17633757-17735855 |
| regionname0 | BCL2L13_chr22_17638757_17730855 |
| regionname5000 | BCL2L13_chr22_17633757_17735855 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 485 | 264 | 80 | 44 | 92 | 13 | 33 | 71 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | MASSS others(480): Show |
chr22 | 17633757 | 17735855 |
| a0002 | 0/0 | 485 | 19 | 4 | 11 | 0 | 3 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | MASSS others(480): Show |
chr22 | 17633757 | 17735855 |
| a0003 | 0/0 | 485 | 13 | 2 | 8 | 1 | 0 | 2 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | MASSS others(480): Show |
chr22 | 17633757 | 17735855 |
| a0004 | 0/0 | 485 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | MASSS others(480): Show |
chr22 | 17633757 | 17735855 |
| a0005 | 0/0 | 485 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | MASSS others(480): Show |
chr22 | 17633757 | 17735855 |
| a0006 | 0/0 | 485 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | MASSS others(480): Show |
chr22 | 17633757 | 17735855 |
| a0007 | 0/0 | 485 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | MASSS others(480): Show |
chr22 | 17633757 | 17735855 |
| a0008 | 0/0 | 485 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | MASSS others(480): Show |
chr22 | 17633757 | 17735855 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1455 | 200 | 60 | 34 | 79 | 7 | 19 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0001c0002 | 1/0 | 1455 | 57 | 17 | 7 | 12 | 6 | 14 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0001c0007 | 0/0 | 1455 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0001c0009 | 0/0 | 1455 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0001c0012 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0001c0014 | 0/0 | 1455 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0002c0003 | 0/0 | 1455 | 19 | 4 | 11 | 0 | 3 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0003c0004 | 0/0 | 1455 | 8 | 2 | 5 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0003c0005 | 0/0 | 1455 | 5 | 0 | 3 | 1 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0004c0006 | 0/0 | 1455 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0005c0008 | 0/0 | 1455 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0006c0010 | 0/0 | 1455 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0007c0013 | 0/0 | 1455 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 | ||
| a0008c0011 | 0/0 | 1455 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ATGGC others(1450): Show |
chr22 | 17633757 | 17735855 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/1 | 4958 | 42 | 2 | 15 | 13 | 3 | 8 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0003 | 0/0 | 4960 | 34 | 12 | 0 | 21 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0004 | 0/0 | 4959 | 19 | 1 | 1 | 11 | 2 | 4 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0005 | 0/0 | 4959 | 20 | 8 | 2 | 8 | 0 | 2 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0006 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0007 | 0/0 | 4960 | 11 | 11 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0008 | 0/0 | 4960 | 8 | 4 | 1 | 2 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0009 | 0/0 | 4965 | 4 | 0 | 4 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4960): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0010 | 0/0 | 4961 | 5 | 0 | 1 | 4 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4956): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0011 | 0/0 | 4960 | 5 | 0 | 1 | 4 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0013 | 0/0 | 4959 | 4 | 0 | 0 | 4 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0017 | 0/0 | 4960 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0018 | 0/0 | 4958 | 3 | 0 | 1 | 2 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0020 | 0/0 | 4965 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4960): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0021 | 0/0 | 4960 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0022 | 0/0 | 4960 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0023 | 0/0 | 4960 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0024 | 0/0 | 4960 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0028 | 0/0 | 4960 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0029 | 0/0 | 4959 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0032 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0033 | 0/0 | 4958 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0034 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0036 | 0/0 | 4961 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4956): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0038 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0039 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0040 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0041 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0043 | 0/0 | 4960 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0046 | 0/0 | 4961 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4956): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0047 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0048 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0050 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0051 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0053 | 0/0 | 4958 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0054 | 0/0 | 4958 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0055 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0056 | 0/0 | 4958 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0059 | 0/0 | 4964 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4959): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0060 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0061 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0063 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0064 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0065 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0066 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0001t0067 | 0/0 | 4960 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0001 | 1/0 | 4959 | 26 | 0 | 5 | 9 | 1 | 10 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0006 | 0/0 | 4959 | 11 | 3 | 1 | 1 | 3 | 3 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0012 | 0/0 | 4960 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0014 | 0/0 | 4959 | 4 | 4 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0025 | 0/0 | 4959 | 2 | 0 | 0 | 0 | 2 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0026 | 0/0 | 4960 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0027 | 0/0 | 4959 | 2 | 1 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0035 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0037 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0042 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0045 | 0/0 | 4958 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0052 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0002t0068 | 0/0 | 4959 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0007t0009 | 0/0 | 4965 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4960): Show |
chr22 | 17633757 | 17735855 |
| a0001c0007t0044 | 0/0 | 4965 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4960): Show |
chr22 | 17633757 | 17735855 |
| a0001c0009t0004 | 0/0 | 4959 | 2 | 0 | 2 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0001c0012t0002 | 0/0 | 4958 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4953): Show |
chr22 | 17633757 | 17735855 |
| a0001c0014t0007 | 0/0 | 4960 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0002c0003t0001 | 0/0 | 4959 | 17 | 4 | 11 | 0 | 1 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0002c0003t0057 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0002c0003t0058 | 0/0 | 4959 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0003c0004t0015 | 0/0 | 4959 | 3 | 0 | 3 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0003c0004t0016 | 0/0 | 4959 | 3 | 1 | 1 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0003c0004t0030 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0003c0004t0031 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0003c0005t0006 | 0/0 | 4959 | 5 | 0 | 3 | 1 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0004c0006t0001 | 0/0 | 4959 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0004c0006t0049 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0004c0006t0062 | 0/0 | 4959 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0005c0008t0019 | 0/0 | 4960 | 3 | 3 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0006c0010t0001 | 0/0 | 4959 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4954): Show |
chr22 | 17633757 | 17735855 |
| a0007c0013t0003 | 0/0 | 4960 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| a0008c0011t0023 | 0/0 | 4960 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | ACCCT others(4955): Show |
chr22 | 17633757 | 17735855 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0219 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0009g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0009g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0009g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0010g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0011g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0013g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0013g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0013g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0013g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0017g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0017g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0017g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0018g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0018g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0018g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0020g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0020g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0020g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0021g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0021g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0021g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0022g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0022g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0023g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0024g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0024g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0028g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0028g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0029g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0029g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0032g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0033g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0034g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0036g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0038g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0039g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0040g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0041g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0043g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0046g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0047g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0048g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0050g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0051g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0053g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0054g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0055g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0056g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0059g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0060g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0061g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0063g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0064g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0065g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0066g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0001t0067g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0002 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0006g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0012g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0012g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0012g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0014g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0014g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0014g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0014g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0025g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0025g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0026g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0026g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0027g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0027g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0035g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0037g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0042g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0045g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0052g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0002t0068g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0007t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0007t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0007t0044g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0009t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0009t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0012t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0001c0014t0007g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0057g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0002c0003t0058g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0015g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0015g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0015g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0016g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0016g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0016g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0030g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0004t0031g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0003c0005t0006g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0004c0006t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0004c0006t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0004c0006t0049g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0004c0006t0062g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0005c0008t0019g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0005c0008t0019g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0005c0008t0019g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0006c0010t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0007c0013t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| a0008c0011t0023g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0193 | EUR | GBR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00099 | hp2 | a0001 | c0002 | t0006 | g0105 | EUR | GBR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00140 | hp1 | a0002 | c0003 | t0057 | g0272 | EUR | GBR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00140 | hp2 | a0001 | c0001 | t0043 | g0006 | EUR | GBR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0202 | EUR | FIN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0270 | EUR | FIN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00323 | hp1 | a0001 | c0001 | t0047 | g0129 | EUR | FIN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0200 | EUR | FIN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0242 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00408 | hp2 | a0001 | c0002 | t0068 | g0292 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00423 | hp1 | a0003 | c0005 | t0006 | g0087 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00423 | hp2 | a0001 | c0001 | t0051 | g0206 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00438 | hp2 | a0001 | c0001 | t0018 | g0214 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00544 | hp1 | a0001 | c0001 | t0018 | g0215 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0162 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00609 | hp2 | a0001 | c0001 | t0029 | g0168 | EAS | CHS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0259 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00733 | hp1 | a0001 | c0001 | t0009 | g0041 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0261 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00735 | hp1 | a0001 | c0001 | t0033 | g0127 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00735 | hp2 | a0002 | c0003 | t0001 | g0274 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00738 | hp1 | a0001 | c0002 | t0006 | g0073 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0241 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0283 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0267 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01069 | hp2 | a0002 | c0003 | t0001 | g0291 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0290 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01074 | hp2 | a0003 | c0005 | t0006 | g0088 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01081 | hp1 | a0003 | c0005 | t0006 | g0089 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01081 | hp2 | a0001 | c0001 | t0053 | g0125 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0138 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01109 | hp2 | a0003 | c0004 | t0015 | g0252 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01167 | hp1 | a0001 | c0001 | t0022 | g0238 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01167 | hp2 | a0001 | c0001 | t0018 | g0195 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0264 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01168 | hp2 | a0001 | c0001 | t0009 | g0039 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01169 | hp1 | a0002 | c0003 | t0001 | g0263 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01169 | hp2 | a0001 | c0001 | t0022 | g0237 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01175 | hp2 | a0003 | c0004 | t0030 | g0104 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01192 | hp1 | a0001 | c0014 | t0007 | g0015 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01243 | hp1 | a0001 | c0001 | t0046 | g0046 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01243 | hp2 | a0001 | c0001 | t0048 | g0126 | AMR | PUR | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01255 | hp1 | a0002 | c0003 | t0001 | g0271 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01255 | hp2 | a0001 | c0001 | t0064 | g0106 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01256 | hp1 | a0001 | c0009 | t0004 | g0156 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01258 | hp1 | a0001 | c0009 | t0004 | g0155 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01258 | hp2 | a0002 | c0003 | t0001 | g0273 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0117 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01261 | hp2 | a0001 | c0002 | t0027 | g0011 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0279 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01361 | hp1 | a0003 | c0005 | t0006 | g0085 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01361 | hp2 | a0001 | c0001 | t0011 | g0158 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0234 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01496 | hp2 | a0001 | c0001 | t0009 | g0037 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0177 | EUR | IBS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01516 | hp2 | a0001 | c0002 | t0025 | g0069 | EUR | IBS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01517 | hp1 | a0002 | c0003 | t0058 | g0005 | EUR | IBS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01517 | hp2 | a0001 | c0002 | t0025 | g0070 | EUR | IBS | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01884 | hp1 | a0001 | c0002 | t0012 | g0009 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01884 | hp2 | a0003 | c0004 | t0031 | g0253 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01934 | hp2 | a0003 | c0004 | t0016 | g0090 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01978 | hp2 | a0001 | c0001 | t0010 | g0239 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01981 | hp1 | a0001 | c0001 | t0009 | g0036 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0269 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0277 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0118 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02040 | hp2 | a0001 | c0002 | t0052 | g0281 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02055 | hp1 | a0003 | c0004 | t0016 | g0092 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02055 | hp2 | a0001 | c0002 | t0012 | g0300 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02071 | hp1 | a0001 | c0002 | t0006 | g0080 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0181 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0132 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | KHV | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0077 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02145 | hp2 | a0001 | c0002 | t0027 | g0075 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02148 | hp2 | a0003 | c0004 | t0015 | g0083 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0148 | EAS | CDX | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | CDX | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02257 | hp1 | a0001 | c0001 | t0020 | g0233 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0063 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02258 | hp1 | a0001 | c0002 | t0035 | g0296 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02258 | hp2 | a0001 | c0001 | t0007 | g0099 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02280 | hp1 | a0001 | c0002 | t0012 | g0301 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02280 | hp2 | a0004 | c0006 | t0062 | g0095 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02300 | hp1 | a0001 | c0001 | t0054 | g0173 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02300 | hp2 | a0003 | c0004 | t0015 | g0084 | AMR | PEL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0145 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02451 | hp2 | a0001 | c0001 | t0050 | g0249 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02572 | hp1 | a0001 | c0001 | t0028 | g0298 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02602 | hp1 | a0001 | c0001 | t0056 | g0204 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02602 | hp2 | a0001 | c0002 | t0006 | g0071 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02615 | hp1 | a0001 | c0001 | t0021 | g0024 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0003 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02622 | hp1 | a0001 | c0002 | t0026 | g0293 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0018 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02647 | hp1 | a0001 | c0001 | t0028 | g0297 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02683 | hp1 | a0001 | c0001 | t0040 | g0197 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0288 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0199 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02698 | hp2 | a0001 | c0001 | t0008 | g0228 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02717 | hp1 | a0001 | c0002 | t0014 | g0068 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0247 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02723 | hp1 | a0001 | c0001 | t0041 | g0240 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0185 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0203 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02809 | hp2 | a0001 | c0002 | t0006 | g0078 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02818 | hp2 | a0001 | c0001 | t0020 | g0225 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02886 | hp1 | a0004 | c0006 | t0049 | g0094 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02886 | hp2 | a0002 | c0003 | t0001 | g0003 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02895 | hp1 | a0001 | c0001 | t0021 | g0022 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02895 | hp2 | a0001 | c0001 | t0024 | g0244 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02896 | hp1 | a0001 | c0001 | t0061 | g0113 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02896 | hp2 | a0001 | c0002 | t0014 | g0065 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02897 | hp1 | a0001 | c0001 | t0024 | g0243 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02897 | hp2 | a0001 | c0002 | t0014 | g0067 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02922 | hp1 | a0007 | c0013 | t0003 | g0028 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02922 | hp2 | a0001 | c0002 | t0006 | g0081 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02965 | hp2 | a0005 | c0008 | t0019 | g0254 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0220 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03017 | hp1 | a0001 | c0001 | t0005 | g0170 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0285 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0223 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03041 | hp2 | a0001 | c0001 | t0017 | g0019 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0025 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03130 | hp2 | a0001 | c0007 | t0009 | g0040 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0112 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0227 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03225 | hp1 | a0004 | c0006 | t0001 | g0093 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03225 | hp2 | a0001 | c0007 | t0009 | g0059 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0122 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03453 | hp2 | a0001 | c0002 | t0026 | g0294 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03486 | hp1 | a0001 | c0002 | t0012 | g0008 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0062 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03490 | hp1 | a0002 | c0003 | t0001 | g0265 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03492 | hp2 | a0003 | c0005 | t0006 | g0086 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03516 | hp1 | a0004 | c0006 | t0001 | g0096 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | ESN | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03540 | hp1 | a0005 | c0008 | t0019 | g0295 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | GWD | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03579 | hp1 | a0001 | c0002 | t0006 | g0076 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03654 | hp1 | a0003 | c0004 | t0016 | g0091 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03654 | hp2 | a0001 | c0002 | t0006 | g0072 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03710 | hp1 | a0001 | c0001 | t0005 | g0141 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03710 | hp2 | a0001 | c0002 | t0006 | g0079 | SAS | PJL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0186 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0289 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0152 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0284 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0201 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0175 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0098 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04184 | hp1 | a0001 | c0002 | t0001 | g0260 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0124 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0278 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | STU | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0111 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18522 | hp2 | a0001 | c0001 | t0017 | g0020 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | CHB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0119 | EAS | CHB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18906 | hp1 | a0005 | c0008 | t0019 | g0255 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18942 | hp1 | a0001 | c0001 | t0039 | g0194 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0257 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18943 | hp2 | a0001 | c0001 | t0013 | g0180 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18946 | hp1 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18946 | hp2 | a0001 | c0001 | t0036 | g0097 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18952 | hp2 | a0001 | c0001 | t0010 | g0226 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18953 | hp2 | a0001 | c0001 | t0010 | g0235 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18956 | hp2 | a0001 | c0001 | t0008 | g0230 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18957 | hp1 | a0001 | c0001 | t0011 | g0116 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18963 | hp1 | a0001 | c0001 | t0066 | g0189 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18964 | hp2 | a0001 | c0001 | t0055 | g0211 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0187 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18968 | hp2 | a0008 | c0011 | t0023 | g0109 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18979 | hp1 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18979 | hp2 | a0001 | c0001 | t0013 | g0236 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18989 | hp1 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18998 | hp1 | a0001 | c0001 | t0011 | g0142 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19003 | hp2 | a0001 | c0001 | t0011 | g0166 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19007 | hp2 | a0001 | c0001 | t0013 | g0192 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19009 | hp1 | a0001 | c0001 | t0023 | g0108 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0280 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19030 | hp1 | a0001 | c0002 | t0037 | g0064 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0248 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19043 | hp1 | a0001 | c0001 | t0008 | g0232 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19056 | hp2 | a0001 | c0012 | t0002 | g0171 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19065 | hp2 | a0001 | c0001 | t0067 | g0154 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0102 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19078 | hp2 | a0001 | c0001 | t0010 | g0221 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19079 | hp1 | a0001 | c0001 | t0013 | g0179 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19079 | hp2 | a0001 | c0001 | t0008 | g0224 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19085 | hp1 | a0001 | c0001 | t0011 | g0157 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19089 | hp1 | a0001 | c0001 | t0059 | g0149 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19089 | hp2 | a0001 | c0001 | t0010 | g0135 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19090 | hp2 | a0001 | c0001 | t0029 | g0184 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19240 | hp1 | a0001 | c0002 | t0014 | g0066 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA19240 | hp2 | a0001 | c0007 | t0044 | g0033 | AFR | YRI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20129 | hp1 | a0001 | c0001 | t0038 | g0229 | AFR | ASW | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20129 | hp2 | a0001 | c0002 | t0042 | g0010 | AFR | ASW | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20752 | hp1 | a0001 | c0002 | t0006 | g0082 | EUR | TSI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0128 | EUR | TSI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20805 | hp1 | a0001 | c0002 | t0006 | g0074 | EUR | TSI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0191 | EUR | TSI | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20905 | hp1 | a0001 | c0002 | t0045 | g0002 | SAS | GIH | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20905 | hp2 | a0001 | c0001 | t0032 | g0146 | SAS | GIH | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01123 | hp1 | a0006 | c0010 | t0001 | g0262 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG01123 | hp2 | a0002 | c0003 | t0001 | g0282 | AMR | CLM | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02109 | hp1 | a0001 | c0001 | t0063 | g0299 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02109 | hp2 | a0001 | c0001 | t0065 | g0016 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0287 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0222 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02559 | hp1 | a0001 | c0001 | t0021 | g0023 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | ACB | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03471 | hp1 | a0001 | c0001 | t0060 | g0021 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0121 | AFR | MSL | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0035 | AFR | USA | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | USA | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | USA | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | USA | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0231 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| NA21309 | hp2 | a0001 | c0001 | t0034 | g0167 | AFR | LWK | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0219 | REF | REF | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0002 | REF | REF | BCL2L13_chr22_17633757_17735855 | BCL2L13 | chr22 | 17633757 | 17735855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:17683229 | T | G | 1 | a0003 | 13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
missense_variant | MODERATE | c.137T>G | p.Ile46Arg | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/7 | 317/4959 | 137/1458 | 46/485 | chr22 | 17683229 | |||
| chr22:17683255 | A | G | 1 | a0004 | 4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
missense_variant | MODERATE | c.163A>G | p.Ile55Val | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/7 | 343/4959 | 163/1458 | 55/485 | chr22 | 17683255 | |||
| chr22:17689010 | G | A | 1 | a0006 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.254G>A | p.Arg85His | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/7 | 434/4959 | 254/1458 | 85/485 | chr22 | 17689010 | |||
| chr22:17702357 | G | T | 1 | a0005 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.571G>T | p.Ala191Ser | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/7 | 751/4959 | 571/1458 | 191/485 | chr22 | 17702357 | |||
| chr22:17727154 | C | T | 1 | a0002 | 19 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(16): Show |
missense_variant | MODERATE | c.1078C>T | p.Pro360Ser | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1258/4959 | 1078/1458 | 360/485 | chr22 | 17727154 | |||
| chr22:17727286 | C | A | 1 | a0008 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.1210C>A | p.Pro404Thr | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1390/4959 | 1210/1458 | 404/485 | chr22 | 17727286 | |||
| chr22:17727361 | A | G | 1 | a0007 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1285A>G | p.Ser429Gly | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1465/4959 | 1285/1458 | 429/485 | chr22 | 17727361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:17702272 | A | G | 1 | a0001c0009 | 2 | HG01256.hp1 HG01258.hp1 |
synonymous_variant | LOW | c.486A>G | p.Gln162Gln | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/7 | 666/4959 | 486/1458 | 162/485 | chr22 | 17702272 | |||
| chr22:17726730 | A | G | 1 | a0001c0007 | 3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.654A>G | p.Ala218Ala | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 834/4959 | 654/1458 | 218/485 | chr22 | 17726730 | |||
| chr22:17726847 | A | G | 7 | a0001c0001 a0001c0007 a0001c0009 others(4): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
synonymous_variant | LOW | c.771A>G | p.Ser257Ser | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 951/4959 | 771/1458 | 257/485 | chr22 | 17726847 | |||
| chr22:17726952 | C | T | 1 | a0003c0004 | 8 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(5): Show |
synonymous_variant | LOW | c.876C>T | p.Asn292Asn | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1056/4959 | 876/1458 | 292/485 | chr22 | 17726952 | |||
| chr22:17727003 | C | T | 1 | a0001c0014 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.927C>T | p.His309His | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1107/4959 | 927/1458 | 309/485 | chr22 | 17727003 | |||
| chr22:17727411 | C | T | 1 | a0001c0012 | 1 | NA19056.hp2 | synonymous_variant | LOW | c.1335C>T | p.Pro445Pro | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1515/4959 | 1335/1458 | 445/485 | chr22 | 17727411 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:17638807 | C | T | 1 | a0001c0002t0068 | 1 | HG00408.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/7 | 16905 | chr22 | 17638807 | ||||||
| chr22:17655675 | A | G | 1 | a0001c0001t0067 | 1 | NA19065.hp2 | 5_prime_UTR_variant | MODIFIER | c.-37A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/7 | 37 | chr22 | 17655675 | ||||||
| chr22:17727643 | T | G | 1 | a0003c0004t0030 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*109T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 109 | chr22 | 17727643 | ||||||
| chr22:17727706 | C | T | 1 | a0001c0001t0066 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*172C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 172 | chr22 | 17727706 | ||||||
| chr22:17727739 | C | T | 1 | a0001c0001t0065 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 205 | chr22 | 17727739 | ||||||
| chr22:17727788 | C | T | 2 | a0001c0001t0063 a0001c0001t0064 |
2 | HG01255.hp2 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*254C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 254 | chr22 | 17727788 | ||||||
| chr22:17727794 | T | G | 6 | a0001c0001t0032 a0001c0001t0033 a0003c0004t0015 others(3): Show |
10 | HG00735.hp1 HG01109.hp2 HG01175.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*260T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 260 | chr22 | 17727794 | ||||||
| chr22:17727852 | G | A | 3 | a0003c0004t0015 a0003c0004t0030 a0003c0004t0031 |
5 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*318G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 318 | chr22 | 17727852 | ||||||
| chr22:17727900 | G | A | 1 | a0001c0001t0034 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*366G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 366 | chr22 | 17727900 | ||||||
| chr22:17727938 | G | C | 36 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0008 others(33): Show |
121 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(118): Show |
3_prime_UTR_variant | MODIFIER | c.*404G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 404 | chr22 | 17727938 | ||||||
| chr22:17728034 | TG | T | 5 | a0001c0002t0045 a0003c0004t0015 a0003c0004t0016 others(2): Show |
9 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*503delG | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 503 | INFO_REALIGN_3_PRIME | chr22 | 17728034 | |||||
| chr22:17728056 | C | G | 14 | a0001c0001t0009 a0001c0001t0020 a0001c0001t0021 others(11): Show |
26 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*522C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 522 | chr22 | 17728056 | ||||||
| chr22:17728099 | A | AGGCTG | 5 | a0001c0001t0009 a0001c0001t0020 a0001c0001t0059 others(2): Show |
11 | HG00733.hp1 HG01168.hp2 HG01496.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*569_*570insGGGCT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 570 | INFO_REALIGN_3_PRIME | chr22 | 17728099 | |||||
| chr22:17728130 | G | C | 2 | a0001c0002t0035 a0003c0004t0031 |
2 | HG01884.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*596G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 596 | chr22 | 17728130 | ||||||
| chr22:17728130 | G | GC | 8 | a0001c0001t0010 a0001c0001t0022 a0001c0001t0028 others(5): Show |
15 | HG00323.hp1 HG01167.hp1 HG01169.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*599dupC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 600 | INFO_REALIGN_3_PRIME | chr22 | 17728130 | |||||
| chr22:17728211 | G | C | 2 | a0001c0001t0023 a0008c0011t0023 |
2 | NA18968.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*677G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 677 | chr22 | 17728211 | ||||||
| chr22:17728212 | T | C | 1 | a0001c0002t0037 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*678T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 678 | chr22 | 17728212 | ||||||
| chr22:17728254 | G | GA | 34 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(31): Show |
112 | HG00140.hp2 HG00733.hp1 HG01109.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*720_*721insA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 721 | chr22 | 17728254 | ||||||
| chr22:17728255 | T | C | 34 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(31): Show |
112 | HG00140.hp2 HG00733.hp1 HG01109.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*721T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 721 | chr22 | 17728255 | ||||||
| chr22:17728266 | C | T | 1 | a0002c0003t0058 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*732C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 732 | chr22 | 17728266 | ||||||
| chr22:17728269 | G | A | 1 | a0001c0001t0022 | 2 | HG01167.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*735G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 735 | chr22 | 17728269 | ||||||
| chr22:17728419 | G | C | 6 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0020 others(3): Show |
20 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*885G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 885 | chr22 | 17728419 | ||||||
| chr22:17728439 | T | C | 35 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(32): Show |
138 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*905T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 905 | chr22 | 17728439 | ||||||
| chr22:17728526 | A | G | 1 | a0005c0008t0019 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*992A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 992 | chr22 | 17728526 | ||||||
| chr22:17728567 | A | G | 1 | a0001c0001t0040 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1033A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1033 | chr22 | 17728567 | ||||||
| chr22:17728601 | A | G | 1 | a0001c0001t0039 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1067A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1067 | chr22 | 17728601 | ||||||
| chr22:17728752 | A | C | 1 | a0001c0001t0056 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1218A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1218 | chr22 | 17728752 | ||||||
| chr22:17728875 | C | G | 1 | a0002c0003t0057 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1341 | chr22 | 17728875 | ||||||
| chr22:17728999 | G | A | 1 | a0001c0001t0050 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1465G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1465 | chr22 | 17728999 | ||||||
| chr22:17729191 | A | G | 1 | a0001c0001t0055 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1657A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1657 | chr22 | 17729191 | ||||||
| chr22:17729217 | T | C | 7 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0032 others(4): Show |
30 | HG00423.hp2 HG00438.hp1 HG01256.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1683T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 1683 | chr22 | 17729217 | ||||||
| chr22:17729569 | C | T | 1 | a0005c0008t0019 | 3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2035C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2035 | chr22 | 17729569 | ||||||
| chr22:17729764 | C | T | 14 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 others(11): Show |
65 | HG00140.hp2 HG00733.hp1 HG01167.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2230C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2230 | chr22 | 17729764 | ||||||
| chr22:17729765 | G | A | 6 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0014 others(3): Show |
24 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2231G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2231 | chr22 | 17729765 | ||||||
| chr22:17729865 | G | A | 1 | a0001c0002t0052 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2331G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2331 | chr22 | 17729865 | ||||||
| chr22:17729986 | G | T | 1 | a0001c0001t0005 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2452G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2452 | chr22 | 17729986 | ||||||
| chr22:17730010 | GC | G | 12 | a0001c0001t0002 a0001c0001t0018 a0001c0001t0033 others(9): Show |
54 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2478delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2478 | INFO_REALIGN_3_PRIME | chr22 | 17730010 | |||||
| chr22:17730029 | A | G | 1 | a0001c0007t0044 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2495A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2495 | chr22 | 17730029 | ||||||
| chr22:17730089 | G | A | 1 | a0001c0001t0053 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2555G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2555 | chr22 | 17730089 | ||||||
| chr22:17730157 | A | G | 4 | a0003c0004t0015 a0003c0004t0016 a0003c0004t0030 others(1): Show |
8 | HG01109.hp2 HG01175.hp2 HG01884.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2623A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2623 | chr22 | 17730157 | ||||||
| chr22:17730291 | G | A | 33 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(30): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2757G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2757 | chr22 | 17730291 | ||||||
| chr22:17730427 | C | T | 1 | a0001c0001t0051 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2893C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 2893 | chr22 | 17730427 | ||||||
| chr22:17730544 | G | A | 1 | a0001c0001t0054 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3010G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 3010 | chr22 | 17730544 | ||||||
| chr22:17730797 | C | T | 3 | a0001c0001t0028 a0001c0001t0029 a0001c0001t0046 |
5 | HG00609.hp2 HG01243.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3263C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 7/7 | 3263 | chr22 | 17730797 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:17638965 | C | T | 2 | a0001c0002t0012g0300 a0001c0002t0012g0301 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-51+79C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17638965 | |||||||
| chr22:17638971 | G | C | 1 | a0001c0001t0043g0006 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-51+85G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17638971 | |||||||
| chr22:17638979 | G | A | 1 | a0001c0001t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-51+93G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17638979 | |||||||
| chr22:17639069 | C | T | 1 | a0001c0001t0063g0299 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-51+183C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639069 | |||||||
| chr22:17639092 | G | C | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+206G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639092 | |||||||
| chr22:17639116 | G | A | 1 | a0001c0002t0027g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-51+230G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639116 | |||||||
| chr22:17639244 | ACTT | A | 46 | a0001c0001t0002g0004 a0001c0001t0028g0297 a0001c0001t0028g0298 others(43): Show |
47 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.-51+362_-51+364del others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17639244 | ||||||
| chr22:17639332 | G | A | 3 | a0001c0002t0001g0256 a0001c0002t0001g0257 a0001c0002t0001g0258 |
3 | HG00544.hp2 NA18942.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.-51+446G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639332 | |||||||
| chr22:17639341 | A | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+455A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639341 | |||||||
| chr22:17639414 | C | T | 2 | a0003c0004t0015g0252 a0003c0004t0031g0253 |
2 | HG01109.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.-51+528C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639414 | |||||||
| chr22:17639434 | C | T | 2 | a0001c0001t0003g0250 a0001c0001t0003g0251 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-51+548C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639434 | |||||||
| chr22:17639474 | A | G | 3 | a0001c0001t0007g0247 a0001c0001t0007g0248 a0001c0001t0050g0249 |
3 | HG02451.hp2 HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-51+588A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639474 | |||||||
| chr22:17639611 | C | T | 1 | a0001c0002t0001g0199 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-51+725C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639611 | |||||||
| chr22:17639646 | C | G | 1 | a0001c0001t0004g0246 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-51+760C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639646 | |||||||
| chr22:17639684 | G | C | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+798G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639684 | |||||||
| chr22:17639687 | C | G | 1 | a0001c0001t0002g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-51+801C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639687 | |||||||
| chr22:17639690 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-51+804C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639690 | |||||||
| chr22:17639718 | T | C | 14 | a0001c0001t0005g0012 a0001c0001t0007g0013 a0001c0001t0007g0014 others(11): Show |
14 | HG01192.hp1 HG02109.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-51+832T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639718 | |||||||
| chr22:17639720 | G | A | 148 | a0001c0001t0002g0004 a0001c0001t0003g0001 a0001c0001t0003g0007 others(145): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.-51+834G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17639720 | |||||||
| chr22:17639856 | C | CT | 52 | a0001c0001t0002g0004 a0001c0001t0005g0241 a0001c0001t0005g0242 others(49): Show |
53 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.-51+985dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17639856 | ||||||
| chr22:17639856 | C | CTT | 6 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0001c0002t0026g0293 others(3): Show |
6 | HG02258.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+984_-51+985dup others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17639856 | ||||||
| chr22:17639856 | CT | C | 47 | a0001c0001t0002g0100 a0001c0001t0002g0103 a0001c0001t0003g0001 others(44): Show |
48 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(45): Show |
intron_variant | MODIFIER | c.-51+985delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17639856 | ||||||
| chr22:17640043 | G | A | 25 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(22): Show |
25 | HG00738.hp1 HG01261.hp2 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51+1157G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640043 | |||||||
| chr22:17640171 | AC | A | 25 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(22): Show |
25 | HG00738.hp1 HG01261.hp2 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.-51+1290delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640171 | ||||||
| chr22:17640192 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+1306G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640192 | |||||||
| chr22:17640228 | G | A | 12 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(9): Show |
12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+1342G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640228 | |||||||
| chr22:17640229 | T | G | 12 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(9): Show |
12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+1343T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640229 | |||||||
| chr22:17640270 | A | G | 23 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(20): Show |
24 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.-51+1384A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640270 | |||||||
| chr22:17640339 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-51+1453G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640339 | |||||||
| chr22:17640391 | C | G | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1505C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640391 | |||||||
| chr22:17640458 | A | G | 1 | a0001c0001t0043g0006 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-51+1572A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640458 | |||||||
| chr22:17640592 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+1706G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640592 | |||||||
| chr22:17640701 | T | TA | 45 | a0001c0001t0006g0077 a0001c0001t0024g0243 a0001c0001t0024g0244 others(42): Show |
45 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.-51+1829dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640701 | ||||||
| chr22:17640702 | A | T | 21 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(18): Show |
21 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.-51+1816A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640702 | |||||||
| chr22:17640769 | G | T | 1 | a0001c0001t0005g0220 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-51+1883G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640769 | |||||||
| chr22:17640775 | G | A | 1 | a0001c0001t0064g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-51+1889G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640775 | |||||||
| chr22:17640860 | T | C | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-51+1974T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640860 | |||||||
| chr22:17640882 | T | A | 1 | a0001c0001t0003g0026 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-51+1996T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640882 | |||||||
| chr22:17640882 | T | TTA | 5 | a0001c0001t0002g0117 a0001c0001t0004g0118 a0001c0001t0004g0119 others(2): Show |
5 | HG01123.hp1 HG01261.hp1 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+2012_-51+2013d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640882 | ||||||
| chr22:17640894 | AT | A | 89 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(86): Show |
90 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.-51+2009delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640894 | |||||||
| chr22:17640896 | A | AT | 9 | a0001c0001t0002g0103 a0001c0001t0002g0216 a0001c0001t0002g0217 others(6): Show |
9 | HG01192.hp1 HG02723.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+2011dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640896 | ||||||
| chr22:17640896 | A | C | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+2010A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640896 | |||||||
| chr22:17640898 | A | AT | 115 | a0001c0001t0002g0004 a0001c0001t0002g0123 a0001c0001t0002g0128 others(112): Show |
116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.-51+2022dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17640898 | ||||||
| chr22:17640898 | A | T | 100 | a0001c0001t0002g0100 a0001c0001t0002g0103 a0001c0001t0002g0207 others(97): Show |
101 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-51+2012A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640898 | |||||||
| chr22:17640899 | T | TA | 28 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0003g0060 others(25): Show |
28 | HG01070.hp1 HG01071.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.-51+2013_-51+2014i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640899 | |||||||
| chr22:17640900 | T | A | 1 | a0002c0003t0001g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-51+2014T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640900 | |||||||
| chr22:17640912 | G | A | 19 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(16): Show |
19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+2026G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640912 | |||||||
| chr22:17640921 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+2035C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17640921 | |||||||
| chr22:17641040 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+2154G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641040 | |||||||
| chr22:17641127 | C | T | 1 | a0001c0002t0006g0082 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-51+2241C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641127 | |||||||
| chr22:17641362 | G | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51+2476G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641362 | |||||||
| chr22:17641387 | A | AT | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51+2510dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17641387 | ||||||
| chr22:17641406 | C | T | 1 | a0001c0001t0008g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-51+2520C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641406 | |||||||
| chr22:17641566 | G | A | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-51+2680G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641566 | |||||||
| chr22:17641596 | G | A | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-51+2710G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641596 | |||||||
| chr22:17641740 | TC | T | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+2855delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641740 | |||||||
| chr22:17641798 | G | GT | 19 | a0001c0001t0002g0103 a0001c0001t0002g0205 a0001c0001t0002g0207 others(16): Show |
19 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(16): Show |
intron_variant | MODIFIER | c.-51+2931dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17641798 | ||||||
| chr22:17641798 | GT | G | 49 | a0001c0001t0002g0123 a0001c0001t0005g0012 a0001c0001t0007g0013 others(46): Show |
49 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(46): Show |
intron_variant | MODIFIER | c.-51+2931delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17641798 | ||||||
| chr22:17641800 | T | TG | 4 | a0001c0001t0003g0110 a0001c0002t0006g0080 a0001c0002t0006g0081 others(1): Show |
4 | HG02071.hp1 HG02922.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-51+2914_-51+2915i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641800 | |||||||
| chr22:17641801 | T | G | 59 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(56): Show |
60 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.-51+2915T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641801 | |||||||
| chr22:17641802 | T | G | 23 | a0001c0001t0065g0016 a0001c0002t0012g0008 a0001c0002t0012g0009 others(20): Show |
23 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-51+2916T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641802 | |||||||
| chr22:17641803 | T | G | 5 | a0004c0006t0001g0096 a0004c0006t0049g0094 a0004c0006t0062g0095 others(2): Show |
5 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+2917T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641803 | |||||||
| chr22:17641834 | C | T | 2 | a0001c0001t0008g0232 a0001c0001t0020g0231 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-51+2948C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641834 | |||||||
| chr22:17641884 | C | T | 1 | a0001c0001t0056g0204 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-51+2998C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641884 | |||||||
| chr22:17641893 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+3007G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641893 | |||||||
| chr22:17641901 | G | A | 1 | a0001c0001t0003g0250 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-51+3015G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17641901 | |||||||
| chr22:17641989 | CGGGGTTT others(1807): Show |
C | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-51+3114_-51+4927d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17641989 | ||||||
| chr22:17642129 | CT | C | 195 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(192): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.-51+3264delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17642129 | ||||||
| chr22:17642129 | CTTT | C | 43 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(40): Show |
44 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.-51+3262_-51+3264d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17642129 | ||||||
| chr22:17642156 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-51+3270G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642156 | |||||||
| chr22:17642189 | G | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-51+3303G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642189 | |||||||
| chr22:17642210 | G | A | 14 | a0001c0002t0001g0199 a0003c0004t0015g0083 a0003c0004t0015g0084 others(11): Show |
14 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.-51+3324G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642210 | |||||||
| chr22:17642216 | C | G | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-51+3330C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642216 | |||||||
| chr22:17642334 | T | C | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-51+3448T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642334 | |||||||
| chr22:17642597 | A | AT | 28 | a0001c0001t0002g0205 a0001c0001t0004g0196 a0001c0001t0004g0246 others(25): Show |
28 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.-51+3724dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17642597 | ||||||
| chr22:17642697 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+3811G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17642697 | |||||||
| chr22:17643031 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-51+4145C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643031 | |||||||
| chr22:17643254 | T | C | 155 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(152): Show |
156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.-51+4368T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643254 | |||||||
| chr22:17643276 | A | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+4390A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643276 | |||||||
| chr22:17643396 | G | A | 71 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(68): Show |
72 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.-51+4510G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643396 | |||||||
| chr22:17643422 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-51+4536G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643422 | |||||||
| chr22:17643466 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+4580G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643466 | |||||||
| chr22:17643507 | T | C | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+4621T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643507 | |||||||
| chr22:17643536 | C | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+4650C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643536 | |||||||
| chr22:17643684 | G | C | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+4798G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643684 | |||||||
| chr22:17643749 | G | T | 3 | a0001c0007t0009g0040 a0001c0007t0009g0059 a0001c0007t0044g0033 |
3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-51+4863G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643749 | |||||||
| chr22:17643763 | G | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+4877G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643763 | |||||||
| chr22:17643787 | G | A | 1 | a0001c0002t0026g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-51+4901G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643787 | |||||||
| chr22:17643801 | G | A | 1 | a0001c0001t0004g0102 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-51+4915G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643801 | |||||||
| chr22:17643860 | T | A | 2 | a0001c0001t0007g0013 a0001c0001t0007g0014 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-51+4974T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643860 | |||||||
| chr22:17643888 | C | T | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5002C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643888 | |||||||
| chr22:17643897 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5011G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643897 | |||||||
| chr22:17643902 | G | C | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5016G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643902 | |||||||
| chr22:17643903 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5017G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643903 | |||||||
| chr22:17643909 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-51+5023G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643909 | |||||||
| chr22:17643913 | A | T | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5027A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643913 | |||||||
| chr22:17643915 | CTTTTTTA others(1985): Show |
C | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+5030_-51+7021d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643915 | |||||||
| chr22:17643977 | C | T | 19 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(16): Show |
19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+5091C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17643977 | |||||||
| chr22:17644062 | C | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51+5176C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644062 | |||||||
| chr22:17644112 | T | C | 1 | a0001c0002t0006g0082 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-51+5226T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644112 | |||||||
| chr22:17644130 | C | T | 3 | a0003c0004t0016g0090 a0003c0004t0016g0091 a0003c0004t0016g0092 |
3 | HG01934.hp2 HG02055.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-51+5244C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644130 | |||||||
| chr22:17644169 | C | A | 1 | a0001c0001t0002g0212 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-51+5283C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644169 | |||||||
| chr22:17644306 | C | G | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-51+5420C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644306 | |||||||
| chr22:17644310 | G | A | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51+5424G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644310 | |||||||
| chr22:17644334 | C | CT | 24 | a0001c0001t0004g0101 a0001c0001t0004g0152 a0001c0001t0004g0185 others(21): Show |
24 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.-51+5463dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17644334 | ||||||
| chr22:17644334 | CT | C | 8 | a0001c0001t0002g0103 a0001c0001t0002g0210 a0001c0001t0003g0051 others(5): Show |
8 | HG02040.hp1 HG02135.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51+5463delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17644334 | ||||||
| chr22:17644534 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+5648G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644534 | |||||||
| chr22:17644558 | T | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-51+5672T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644558 | |||||||
| chr22:17644574 | C | T | 1 | a0006c0010t0001g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-51+5688C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644574 | |||||||
| chr22:17644610 | A | G | 3 | a0001c0001t0002g0134 a0001c0001t0002g0188 a0001c0001t0002g0210 |
3 | HG03927.hp1 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-51+5724A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644610 | |||||||
| chr22:17644671 | G | A | 86 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.-51+5785G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644671 | |||||||
| chr22:17644811 | T | C | 2 | a0001c0002t0001g0288 a0001c0002t0001g0289 |
2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-51+5925T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644811 | |||||||
| chr22:17644959 | G | A | 18 | a0002c0003t0001g0003 a0002c0003t0001g0005 a0002c0003t0001g0261 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.-51+6073G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17644959 | |||||||
| chr22:17645130 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+6244G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17645130 | |||||||
| chr22:17645225 | A | AT | 6 | a0001c0001t0028g0298 a0001c0002t0001g0286 a0001c0002t0001g0288 others(3): Show |
6 | HG00408.hp2 HG02572.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.-51+6360dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17645225 | ||||||
| chr22:17645225 | AT | A | 160 | a0001c0001t0002g0004 a0001c0001t0002g0114 a0001c0001t0002g0115 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-51+6360delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17645225 | ||||||
| chr22:17645225 | ATT | A | 60 | a0001c0001t0002g0100 a0001c0001t0002g0103 a0001c0001t0003g0001 others(57): Show |
61 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(58): Show |
intron_variant | MODIFIER | c.-51+6359_-51+6360d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17645225 | ||||||
| chr22:17645315 | C | T | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51+6429C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17645315 | |||||||
| chr22:17645895 | C | T | 1 | a0001c0002t0001g0284 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-51+7009C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17645895 | |||||||
| chr22:17645914 | AATACAAA others(810): Show |
A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+7029_-51+7845d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17645914 | |||||||
| chr22:17646117 | A | G | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51+7231A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646117 | |||||||
| chr22:17646194 | G | A | 245 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-51+7308G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646194 | |||||||
| chr22:17646227 | G | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+7341G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646227 | |||||||
| chr22:17646247 | T | A | 1 | a0001c0001t0036g0097 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-51+7361T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646247 | |||||||
| chr22:17646309 | C | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-51+7423C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646309 | |||||||
| chr22:17646369 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+7483C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646369 | |||||||
| chr22:17646438 | G | A | 1 | a0001c0001t0002g0159 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-51+7552G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646438 | |||||||
| chr22:17646494 | C | T | 2 | a0001c0001t0005g0062 a0001c0001t0005g0063 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-51+7608C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646494 | |||||||
| chr22:17646499 | G | T | 245 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-51+7613G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646499 | |||||||
| chr22:17646525 | A | G | 1 | a0001c0001t0002g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-51+7639A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646525 | |||||||
| chr22:17646558 | A | G | 2 | a0001c0002t0025g0069 a0001c0002t0025g0070 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-51+7672A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646558 | |||||||
| chr22:17646581 | TG | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-51+7696delG | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646581 | |||||||
| chr22:17646598 | G | T | 19 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(16): Show |
19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+7712G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646598 | |||||||
| chr22:17646599 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+7713G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646599 | |||||||
| chr22:17646714 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+7828G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646714 | |||||||
| chr22:17646716 | C | CTT | 13 | a0001c0001t0002g0114 a0001c0001t0002g0182 a0001c0001t0003g0035 others(10): Show |
13 | HG00099.hp2 HG00323.hp1 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+7850_-51+7851d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646716 | ||||||
| chr22:17646716 | C | CTTT | 154 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(151): Show |
155 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-51+7849_-51+7851d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646716 | ||||||
| chr22:17646716 | C | CTTTT | 57 | a0001c0001t0002g0133 a0001c0001t0002g0134 a0001c0001t0002g0153 others(54): Show |
58 | HG00140.hp2 HG00733.hp1 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.-51+7848_-51+7851d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646716 | ||||||
| chr22:17646716 | C | CTTTTT | 6 | a0001c0001t0003g0054 a0001c0001t0003g0110 a0001c0001t0007g0017 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+7847_-51+7851d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646716 | ||||||
| chr22:17646733 | T | C | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-51+7847T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646733 | |||||||
| chr22:17646885 | A | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+7999A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646885 | |||||||
| chr22:17646888 | T | TTG | 3 | a0001c0002t0035g0296 a0002c0003t0001g0290 a0002c0003t0001g0291 |
3 | HG01069.hp2 HG01071.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-51+8036_-51+8037d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | ||||||
| chr22:17646888 | TTG | T | 11 | a0001c0001t0003g0026 a0001c0001t0003g0055 a0001c0001t0003g0056 others(8): Show |
11 | HG01256.hp2 HG02280.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.-51+8036_-51+8037d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | ||||||
| chr22:17646888 | TTGTG | T | 55 | a0001c0001t0003g0001 a0001c0001t0003g0038 a0001c0001t0003g0042 others(52): Show |
56 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.-51+8034_-51+8037d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | ||||||
| chr22:17646888 | TTGTGTG | T | 172 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(169): Show |
173 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.-51+8032_-51+8037d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | ||||||
| chr22:17646888 | TTGTGTGT others(3): Show |
T | 9 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0002g0117 others(6): Show |
9 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+8028_-51+8037d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646888 | ||||||
| chr22:17646922 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+8036G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646922 | |||||||
| chr22:17646932 | C | CATATAT | 7 | a0001c0001t0002g0131 a0001c0001t0002g0133 a0001c0001t0002g0134 others(4): Show |
7 | HG01496.hp1 HG01934.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-51+8065_-51+8070d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646932 | ||||||
| chr22:17646948 | TA | T | 3 | a0004c0006t0001g0096 a0004c0006t0049g0094 a0004c0006t0062g0095 |
3 | HG02280.hp2 HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-51+8063delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646948 | |||||||
| chr22:17646951 | A | T | 7 | a0001c0002t0012g0009 a0001c0002t0026g0294 a0001c0002t0035g0296 others(4): Show |
7 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+8065A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646951 | |||||||
| chr22:17646951 | ATATAT | A | 21 | a0001c0001t0003g0001 a0001c0001t0003g0026 a0001c0001t0003g0038 others(18): Show |
21 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-51+8067_-51+8071d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646951 | ||||||
| chr22:17646953 | A | AT | 3 | a0001c0001t0008g0230 a0001c0001t0065g0016 a0001c0002t0068g0292 |
3 | HG00408.hp2 HG02109.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.-51+8068dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646953 | ||||||
| chr22:17646953 | A | T | 18 | a0001c0001t0038g0229 a0001c0002t0001g0098 a0001c0002t0001g0260 others(15): Show |
18 | HG01884.hp1 HG01981.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-51+8067A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646953 | |||||||
| chr22:17646953 | ATATTTTT others(1): Show |
A | 10 | a0001c0001t0003g0027 a0001c0001t0003g0030 a0001c0001t0003g0031 others(7): Show |
10 | HG02572.hp2 HG02630.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51+8069_-51+8076d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646953 | ||||||
| chr22:17646953 | ATATTTTT others(4): Show |
A | 1 | a0001c0001t0007g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-51+8069_-51+8079d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646953 | ||||||
| chr22:17646954 | TA | T | 7 | a0001c0002t0001g0259 a0001c0002t0001g0284 a0001c0002t0001g0285 others(4): Show |
7 | HG00639.hp2 HG02486.hp1 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.-51+8069delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646954 | |||||||
| chr22:17646955 | A | ATATATAT others(4): Show |
2 | a0001c0001t0005g0141 a0001c0001t0005g0183 |
2 | HG03540.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATAT others(7): Show |
2 | a0001c0001t0005g0143 a0001c0001t0005g0169 |
2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATAT others(4): Show |
1 | a0001c0001t0005g0220 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-51+8070_-51+8071i others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATAT others(5): Show |
2 | a0001c0001t0002g0004 a0001c0001t0005g0138 |
2 | HG01109.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATAT others(6): Show |
1 | a0001c0001t0002g0004 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-51+8070_-51+8071i others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATAT others(3): Show |
2 | a0001c0001t0002g0136 a0001c0001t0005g0181 |
2 | HG02071.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATAT others(4): Show |
4 | a0001c0001t0002g0186 a0001c0001t0004g0185 a0001c0001t0005g0145 others(1): Show |
4 | HG00735.hp1 HG02451.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATAT others(5): Show |
1 | a0001c0001t0005g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-51+8070_-51+8071i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATAT others(6): Show |
1 | a0001c0001t0004g0177 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-51+8070_-51+8071i others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATT | 15 | a0001c0001t0002g0117 a0001c0001t0002g0217 a0001c0001t0004g0102 others(12): Show |
15 | HG00423.hp2 HG00438.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATTT | 9 | a0001c0001t0002g0103 a0001c0001t0002g0123 a0001c0001t0002g0130 others(6): Show |
9 | HG00280.hp1 HG00639.hp1 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATTT others(1): Show |
8 | a0001c0001t0002g0151 a0001c0001t0004g0101 a0001c0001t0004g0213 others(5): Show |
8 | HG00544.hp1 HG01256.hp1 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATTT others(2): Show |
10 | a0001c0001t0002g0160 a0001c0001t0002g0182 a0001c0001t0004g0164 others(7): Show |
10 | HG00323.hp1 HG00408.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATATTT others(3): Show |
2 | a0001c0001t0002g0178 a0001c0001t0032g0146 |
2 | HG02004.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATTTT | 9 | a0001c0001t0002g0159 a0001c0001t0002g0165 a0001c0001t0002g0172 others(6): Show |
9 | HG01081.hp2 HG01167.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | ATATTTTT | 15 | a0001c0001t0002g0128 a0001c0001t0002g0144 a0001c0001t0002g0174 others(12): Show |
15 | HG00438.hp2 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | A | T | 49 | a0001c0001t0008g0223 a0001c0001t0008g0230 a0001c0001t0036g0097 others(46): Show |
50 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.-51+8069A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646955 | |||||||
| chr22:17646955 | ATTTT | A | 10 | a0001c0002t0006g0071 a0001c0002t0006g0072 a0001c0002t0006g0080 others(7): Show |
10 | HG00099.hp2 HG01175.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-51+8090_-51+8093d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | ATTTTT | A | 13 | a0001c0001t0007g0018 a0001c0002t0006g0074 a0001c0002t0025g0069 others(10): Show |
13 | HG00423.hp1 HG01109.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-51+8089_-51+8093d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646955 | ATTTTTTT | A | 12 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0017 others(9): Show |
12 | HG00738.hp1 HG02559.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-51+8087_-51+8093d others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17646955 | ||||||
| chr22:17646956 | T | TA | 3 | a0001c0002t0001g0198 a0002c0003t0001g0263 a0002c0003t0001g0264 |
3 | HG01168.hp1 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-51+8070_-51+8071i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646956 | |||||||
| chr22:17646957 | T | A | 3 | a0001c0001t0002g0131 a0005c0008t0019g0254 a0005c0008t0019g0255 |
3 | HG01496.hp1 HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+8071T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646957 | |||||||
| chr22:17646958 | T | A | 1 | a0001c0002t0037g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-51+8072T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646958 | |||||||
| chr22:17646959 | T | A | 3 | a0001c0001t0007g0111 a0005c0008t0019g0254 a0005c0008t0019g0255 |
3 | HG02965.hp2 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-51+8073T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646959 | |||||||
| chr22:17646960 | T | A | 2 | a0001c0002t0006g0082 a0001c0002t0037g0064 |
2 | NA19030.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-51+8074T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646960 | |||||||
| chr22:17646961 | T | A | 5 | a0001c0001t0007g0111 a0003c0004t0016g0092 a0003c0004t0030g0104 others(2): Show |
5 | HG01175.hp2 HG02055.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-51+8075T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646961 | |||||||
| chr22:17646962 | T | A | 10 | a0001c0001t0007g0018 a0001c0002t0025g0069 a0001c0002t0025g0070 others(7): Show |
10 | HG01109.hp2 HG01361.hp1 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.-51+8076T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646962 | |||||||
| chr22:17646963 | T | A | 6 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 others(3): Show |
6 | HG01175.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-51+8077T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646963 | |||||||
| chr22:17646964 | T | A | 13 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0017 others(10): Show |
13 | HG01934.hp2 HG02148.hp2 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.-51+8078T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646964 | |||||||
| chr22:17646965 | T | A | 3 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 |
3 | HG03195.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-51+8079T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646965 | |||||||
| chr22:17646966 | T | A | 3 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0003c0004t0015g0083 |
3 | HG02148.hp2 HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-51+8080T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646966 | |||||||
| chr22:17646971 | T | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-51+8085T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17646971 | |||||||
| chr22:17647004 | T | C | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-51+8118T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647004 | |||||||
| chr22:17647067 | G | A | 1 | a0001c0001t0009g0036 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-51+8181G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647067 | |||||||
| chr22:17647176 | G | A | 19 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(16): Show |
19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-51+8290G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647176 | |||||||
| chr22:17647372 | T | G | 27 | a0001c0001t0006g0077 a0001c0001t0065g0016 a0001c0002t0006g0071 others(24): Show |
27 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.-50-8290T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647372 | |||||||
| chr22:17647403 | G | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-8259G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647403 | |||||||
| chr22:17647441 | C | T | 1 | a0001c0001t0018g0195 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-50-8221C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647441 | |||||||
| chr22:17647443 | C | T | 12 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(9): Show |
12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-8219C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647443 | |||||||
| chr22:17647451 | A | G | 1 | a0001c0002t0001g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-50-8211A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647451 | |||||||
| chr22:17647749 | A | G | 4 | a0001c0001t0006g0077 a0001c0002t0006g0076 a0001c0002t0006g0078 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-7913A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647749 | |||||||
| chr22:17647801 | C | T | 1 | a0004c0006t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-50-7861C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647801 | |||||||
| chr22:17647854 | C | T | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-7808C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647854 | |||||||
| chr22:17647855 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50-7807G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647855 | |||||||
| chr22:17647954 | C | T | 1 | a0001c0001t0005g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-50-7708C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17647954 | |||||||
| chr22:17648033 | G | C | 1 | a0001c0001t0002g0136 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-50-7629G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648033 | |||||||
| chr22:17648103 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-7559C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648103 | |||||||
| chr22:17648106 | C | T | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-7556C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648106 | |||||||
| chr22:17648132 | A | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-7530A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648132 | |||||||
| chr22:17648166 | T | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-7496T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648166 | |||||||
| chr22:17648231 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50-7431C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648231 | |||||||
| chr22:17648312 | C | T | 254 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.-50-7350C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648312 | |||||||
| chr22:17648318 | A | C | 8 | a0001c0001t0003g0050 a0001c0001t0003g0051 a0001c0001t0003g0052 others(5): Show |
8 | HG02135.hp2 NA18968.hp2 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50-7344A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648318 | |||||||
| chr22:17648388 | T | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-7274T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648388 | |||||||
| chr22:17648435 | C | T | 1 | a0001c0001t0002g0123 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-50-7227C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648435 | |||||||
| chr22:17648460 | C | T | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-50-7202C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648460 | |||||||
| chr22:17648526 | C | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-7136C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648526 | |||||||
| chr22:17648603 | C | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50-7059C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648603 | |||||||
| chr22:17648657 | A | T | 3 | a0001c0001t0018g0214 a0001c0001t0018g0215 a0001c0001t0039g0194 |
3 | HG00438.hp2 HG00544.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.-50-7005A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648657 | |||||||
| chr22:17648665 | T | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-6997T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648665 | |||||||
| chr22:17648780 | A | G | 157 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.-50-6882A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648780 | |||||||
| chr22:17648830 | T | C | 1 | a0001c0001t0064g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-50-6832T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17648830 | |||||||
| chr22:17648933 | A | AT | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-6720dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17648933 | ||||||
| chr22:17649010 | A | T | 4 | a0001c0001t0002g0117 a0001c0001t0002g0130 a0001c0001t0002g0202 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-6652A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649010 | |||||||
| chr22:17649011 | C | T | 4 | a0001c0001t0002g0117 a0001c0001t0002g0130 a0001c0001t0002g0202 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-6651C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649011 | |||||||
| chr22:17649094 | C | T | 2 | a0001c0002t0035g0296 a0005c0008t0019g0295 |
2 | HG02258.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-50-6568C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649094 | |||||||
| chr22:17649101 | A | AT | 6 | a0001c0001t0002g0193 a0001c0001t0005g0063 a0001c0001t0013g0192 others(3): Show |
6 | HG00099.hp1 HG01255.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-50-6547dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17649101 | ||||||
| chr22:17649189 | C | T | 2 | a0001c0001t0022g0237 a0001c0001t0022g0238 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-50-6473C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649189 | |||||||
| chr22:17649231 | G | A | 1 | a0001c0002t0006g0105 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-50-6431G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649231 | |||||||
| chr22:17649238 | T | C | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.-50-6424T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649238 | |||||||
| chr22:17649348 | C | T | 1 | a0001c0001t0038g0229 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-50-6314C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649348 | |||||||
| chr22:17649472 | T | C | 1 | a0001c0001t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-50-6190T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649472 | |||||||
| chr22:17649526 | G | A | 1 | a0001c0002t0001g0284 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-50-6136G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649526 | |||||||
| chr22:17649871 | C | CTTT | 20 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(17): Show |
20 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.-50-5775_-50-5773d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17649871 | ||||||
| chr22:17649871 | CT | C | 209 | a0001c0001t0002g0004 a0001c0001t0002g0103 a0001c0001t0002g0114 others(206): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.-50-5773delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17649871 | ||||||
| chr22:17649871 | CTT | C | 12 | a0001c0001t0002g0100 a0001c0001t0002g0139 a0001c0001t0003g0055 others(9): Show |
12 | HG01069.hp1 HG01109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-50-5774_-50-5773d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17649871 | ||||||
| chr22:17649874 | T | TC | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50-5788_-50-5787i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649874 | |||||||
| chr22:17649877 | T | C | 2 | a0001c0001t0007g0013 a0001c0001t0007g0014 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-50-5785T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649877 | |||||||
| chr22:17649993 | C | T | 1 | a0001c0001t0004g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-50-5669C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17649993 | |||||||
| chr22:17650016 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50-5646G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650016 | |||||||
| chr22:17650046 | G | T | 178 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(175): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-50-5616G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650046 | |||||||
| chr22:17650056 | G | A | 1 | a0001c0002t0001g0200 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-50-5606G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650056 | |||||||
| chr22:17650162 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-5500G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650162 | |||||||
| chr22:17650164 | C | T | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-50-5498C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650164 | |||||||
| chr22:17650394 | A | G | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-5268A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650394 | |||||||
| chr22:17650443 | T | C | 1 | a0001c0001t0063g0299 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-50-5219T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650443 | |||||||
| chr22:17650469 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-5193C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650469 | |||||||
| chr22:17650724 | A | T | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.-50-4938A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650724 | |||||||
| chr22:17650734 | A | C | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-50-4928A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650734 | |||||||
| chr22:17650828 | C | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-50-4834C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650828 | |||||||
| chr22:17650964 | C | T | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-50-4698C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650964 | |||||||
| chr22:17650975 | C | T | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-4687C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650975 | |||||||
| chr22:17650979 | G | A | 1 | a0001c0001t0007g0111 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-50-4683G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17650979 | |||||||
| chr22:17650991 | C | CT | 151 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0114 others(148): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.-50-4651dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17650991 | ||||||
| chr22:17650991 | C | CTT | 28 | a0001c0001t0002g0103 a0001c0001t0002g0188 a0001c0001t0005g0062 others(25): Show |
28 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.-50-4652_-50-4651d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17650991 | ||||||
| chr22:17651042 | G | A | 133 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(130): Show |
134 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.-50-4620G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651042 | |||||||
| chr22:17651367 | C | CTATT | 19 | a0001c0001t0006g0077 a0001c0002t0001g0266 a0001c0002t0006g0071 others(16): Show |
19 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.-50-4265_-50-4262d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17651367 | ||||||
| chr22:17651367 | CTATT | C | 227 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0114 others(224): Show |
229 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.-50-4265_-50-4262d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17651367 | ||||||
| chr22:17651389 | A | T | 1 | a0001c0001t0013g0236 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-50-4273A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651389 | |||||||
| chr22:17651393 | A | T | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-4269A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651393 | |||||||
| chr22:17651397 | A | T | 177 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(174): Show |
178 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.-50-4265A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651397 | |||||||
| chr22:17651474 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-4188C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651474 | |||||||
| chr22:17651499 | C | T | 157 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.-50-4163C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651499 | |||||||
| chr22:17651705 | T | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-3957T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651705 | |||||||
| chr22:17651719 | C | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-3943C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651719 | |||||||
| chr22:17651721 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-3941C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651721 | |||||||
| chr22:17651722 | A | G | 19 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(16): Show |
19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50-3940A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651722 | |||||||
| chr22:17651729 | C | T | 1 | a0001c0001t0004g0213 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-50-3933C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651729 | |||||||
| chr22:17651730 | G | A | 1 | a0001c0001t0018g0195 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-50-3932G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651730 | |||||||
| chr22:17651845 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50-3817C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651845 | |||||||
| chr22:17651946 | T | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50-3716T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17651946 | |||||||
| chr22:17652084 | T | C | 245 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(242): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-50-3578T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652084 | |||||||
| chr22:17652090 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-3572G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652090 | |||||||
| chr22:17652127 | T | C | 8 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 others(5): Show |
8 | HG01255.hp2 HG02109.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50-3535T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652127 | |||||||
| chr22:17652162 | ACATAGCT others(4): Show |
A | 1 | a0001c0002t0027g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-50-3498_-50-3488d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17652162 | ||||||
| chr22:17652210 | A | T | 178 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(175): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-50-3452A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652210 | |||||||
| chr22:17652235 | G | A | 44 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(41): Show |
45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.-50-3427G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652235 | |||||||
| chr22:17652243 | G | A | 1 | a0002c0003t0001g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-50-3419G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652243 | |||||||
| chr22:17652418 | T | C | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-3244T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652418 | |||||||
| chr22:17652442 | A | G | 4 | a0001c0002t0014g0065 a0001c0002t0014g0066 a0001c0002t0014g0067 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-50-3220A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652442 | |||||||
| chr22:17652508 | G | A | 1 | a0001c0001t0051g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-50-3154G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652508 | |||||||
| chr22:17652978 | T | A | 1 | a0001c0001t0005g0141 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-50-2684T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17652978 | |||||||
| chr22:17653019 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-2643C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653019 | |||||||
| chr22:17653146 | A | G | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.-50-2516A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653146 | |||||||
| chr22:17653234 | A | G | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-2428A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653234 | |||||||
| chr22:17653267 | T | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-2395T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653267 | |||||||
| chr22:17653451 | T | C | 1 | a0001c0001t0002g0207 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-50-2211T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653451 | |||||||
| chr22:17653495 | A | AT | 14 | a0001c0001t0002g0186 a0001c0001t0002g0193 a0001c0001t0002g0202 others(11): Show |
14 | HG00099.hp1 HG00280.hp1 HG01123.hp2 others(11): Show |
intron_variant | MODIFIER | c.-50-2145dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | ||||||
| chr22:17653495 | A | ATT | 39 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0027 others(36): Show |
40 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(37): Show |
intron_variant | MODIFIER | c.-50-2146_-50-2145d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | ||||||
| chr22:17653495 | A | ATTT | 7 | a0001c0001t0002g0103 a0001c0001t0003g0026 a0001c0001t0003g0034 others(4): Show |
7 | HG02647.hp2 HG06807.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-2147_-50-2145d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | ||||||
| chr22:17653495 | AT | A | 40 | a0001c0001t0006g0077 a0001c0001t0007g0099 a0001c0001t0008g0223 others(37): Show |
40 | HG00099.hp2 HG00738.hp1 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.-50-2145delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | ||||||
| chr22:17653495 | ATT | A | 16 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0001c0002t0014g0065 others(13): Show |
16 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50-2146_-50-2145d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653495 | ||||||
| chr22:17653769 | G | T | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-50-1893G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653769 | |||||||
| chr22:17653808 | T | C | 2 | a0001c0001t0005g0138 a0001c0001t0005g0143 |
2 | HG01109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-50-1854T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653808 | |||||||
| chr22:17653856 | T | TAAAAATT others(1708): Show |
1 | a0001c0001t0003g0047 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1717): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1709): Show |
1 | a0001c0001t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1718): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1707): Show |
1 | a0001c0001t0009g0037 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1705): Show |
1 | a0001c0001t0003g0034 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1714): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1706): Show |
1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1715): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1707): Show |
1 | a0001c0001t0043g0006 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1707): Show |
1 | a0001c0001t0023g0108 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1708): Show |
1 | a0001c0001t0003g0026 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1717): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1706): Show |
1 | a0001c0001t0003g0056 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1715): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1703): Show |
1 | a0001c0001t0003g0061 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1712): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1704): Show |
2 | a0001c0001t0003g0032 a0001c0001t0003g0060 |
2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1713): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1705): Show |
7 | a0001c0001t0003g0029 a0001c0001t0003g0030 a0001c0001t0003g0031 others(4): Show |
7 | HG02572.hp2 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1714): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1705): Show |
9 | a0001c0001t0003g0001 a0001c0001t0003g0042 a0001c0001t0003g0043 others(6): Show |
10 | HG04199.hp1 NA18955.hp1 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1714): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1706): Show |
12 | a0001c0001t0003g0038 a0001c0001t0003g0048 a0001c0001t0003g0050 others(9): Show |
12 | HG00733.hp1 HG01168.hp2 HG01981.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1715): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1578): Show |
1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1587): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1706): Show |
1 | a0001c0007t0009g0059 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1715): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1707): Show |
1 | a0001c0001t0003g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653856 | T | TAAAAATT others(1707): Show |
2 | a0001c0001t0003g0045 a0001c0001t0003g0049 |
2 | NA18989.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-50-1792_-50-1791i others(1716): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17653856 | ||||||
| chr22:17653929 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-1733C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653929 | |||||||
| chr22:17653976 | T | C | 2 | a0001c0001t0005g0062 a0001c0001t0005g0063 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-50-1686T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653976 | |||||||
| chr22:17653992 | C | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-1670C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17653992 | |||||||
| chr22:17654008 | T | G | 1 | a0005c0008t0019g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-50-1654T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654008 | |||||||
| chr22:17654037 | A | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-50-1625A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654037 | |||||||
| chr22:17654223 | A | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-50-1439A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654223 | |||||||
| chr22:17654308 | T | TA | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50-1353dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17654308 | ||||||
| chr22:17654378 | T | C | 249 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.-50-1284T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654378 | |||||||
| chr22:17654397 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-50-1265C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654397 | |||||||
| chr22:17654461 | C | T | 3 | a0001c0001t0008g0227 a0001c0001t0024g0243 a0001c0001t0024g0244 |
3 | HG02895.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-50-1201C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654461 | |||||||
| chr22:17654508 | C | T | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-50-1154C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654508 | |||||||
| chr22:17654584 | G | A | 2 | a0001c0002t0012g0300 a0001c0002t0012g0301 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-50-1078G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654584 | |||||||
| chr22:17654589 | A | T | 1 | a0001c0001t0002g0212 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-50-1073A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654589 | |||||||
| chr22:17654857 | G | T | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50-805G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17654857 | |||||||
| chr22:17655022 | C | T | 1 | a0001c0001t0002g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-50-640C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17655022 | |||||||
| chr22:17655065 | CT | C | 249 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.-50-587delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17655065 | ||||||
| chr22:17655108 | A | T | 1 | a0001c0001t0055g0211 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-50-554A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17655108 | |||||||
| chr22:17655300 | C | CT | 12 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(9): Show |
12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.-50-347dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17655300 | ||||||
| chr22:17655300 | CT | C | 11 | a0001c0001t0002g0216 a0001c0001t0003g0038 a0001c0001t0004g0191 others(8): Show |
11 | HG02280.hp2 HG02886.hp1 HG03017.hp2 others(8): Show |
intron_variant | MODIFIER | c.-50-347delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17655300 | ||||||
| chr22:17655425 | CT | C | 7 | a0001c0001t0006g0077 a0001c0001t0007g0247 a0001c0001t0007g0248 others(4): Show |
7 | HG01168.hp2 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50-223delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr22 | 17655425 | ||||||
| chr22:17655480 | A | G | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50-182A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 1/6 | chr22 | 17655480 | |||||||
| chr22:17655960 | G | C | 5 | a0002c0003t0001g0269 a0002c0003t0001g0270 a0002c0003t0001g0271 others(2): Show |
5 | HG00280.hp2 HG01123.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+128G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17655960 | |||||||
| chr22:17656025 | G | A | 4 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 others(1): Show |
4 | HG02896.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+193G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656025 | |||||||
| chr22:17656091 | A | G | 1 | a0001c0001t0043g0006 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.121+259A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656091 | |||||||
| chr22:17656113 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+281C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656113 | |||||||
| chr22:17656154 | C | T | 1 | a0001c0001t0005g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.121+322C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656154 | |||||||
| chr22:17656165 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+333G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656165 | |||||||
| chr22:17656232 | T | A | 72 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(69): Show |
73 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.121+400T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656232 | |||||||
| chr22:17656239 | C | CA | 164 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(161): Show |
165 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.121+420dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656239 | ||||||
| chr22:17656251 | A | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+419A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656251 | |||||||
| chr22:17656253 | T | A | 1 | a0001c0001t0002g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.121+421T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656253 | |||||||
| chr22:17656304 | A | C | 1 | a0001c0001t0002g0182 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.121+472A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656304 | |||||||
| chr22:17656312 | A | G | 1 | a0001c0001t0007g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.121+480A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656312 | |||||||
| chr22:17656335 | C | CT | 55 | a0001c0001t0002g0117 a0001c0001t0002g0133 a0001c0001t0002g0159 others(52): Show |
55 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.121+536dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | C | CTT | 33 | a0001c0001t0002g0100 a0001c0001t0002g0103 a0001c0001t0002g0123 others(30): Show |
33 | HG00544.hp1 HG00639.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.121+535_121+536dup others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | C | CTTTT | 19 | a0001c0001t0002g0212 a0001c0001t0003g0001 a0001c0001t0003g0038 others(16): Show |
20 | HG00140.hp2 HG01168.hp2 HG02071.hp2 others(17): Show |
intron_variant | MODIFIER | c.121+533_121+536dup others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | C | CTTTTT | 13 | a0001c0001t0003g0026 a0001c0001t0003g0044 a0001c0001t0003g0045 others(10): Show |
13 | HG00733.hp1 HG01496.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+532_121+536dup others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CT | C | 15 | a0001c0001t0003g0251 a0001c0001t0005g0012 a0001c0001t0010g0239 others(12): Show |
15 | HG00639.hp2 HG00741.hp1 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.121+536delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTT | C | 9 | a0001c0001t0003g0250 a0001c0001t0008g0224 a0001c0001t0008g0228 others(6): Show |
9 | HG01433.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.121+535_121+536del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTT | C | 15 | a0001c0001t0008g0222 a0001c0001t0008g0230 a0001c0001t0008g0232 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.121+534_121+536del others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT | C | 7 | a0001c0001t0002g0144 a0001c0001t0046g0046 a0002c0003t0001g0273 others(4): Show |
7 | HG00140.hp1 HG00735.hp2 HG01069.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+530_121+536del others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT others(1): Show |
C | 13 | a0002c0003t0001g0003 a0002c0003t0001g0005 a0002c0003t0001g0261 others(10): Show |
14 | HG00280.hp2 HG00733.hp2 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.121+529_121+536del others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT others(3): Show |
C | 3 | a0001c0002t0006g0080 a0001c0002t0014g0068 a0001c0002t0027g0075 |
3 | HG02071.hp1 HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.121+527_121+536del others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT others(4): Show |
C | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.121+526_121+536del others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT others(5): Show |
C | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+525_121+536del others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0004g0101 a0003c0004t0016g0090 a0003c0004t0030g0104 |
3 | HG01175.hp2 HG01934.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.121+524_121+536del others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT others(7): Show |
C | 10 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0016g0091 others(7): Show |
10 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.121+523_121+536del others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT others(8): Show |
C | 1 | a0003c0004t0015g0252 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.121+522_121+536del others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT others(10): Show |
C | 5 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 others(2): Show |
5 | HG02683.hp2 HG02896.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+520_121+536del others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656335 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0004g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.121+518_121+536del others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17656335 | ||||||
| chr22:17656444 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.121+612C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656444 | |||||||
| chr22:17656445 | G | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+613G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656445 | |||||||
| chr22:17656582 | A | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+750A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656582 | |||||||
| chr22:17656636 | G | T | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.121+804G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656636 | |||||||
| chr22:17656744 | A | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+912A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656744 | |||||||
| chr22:17656825 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+993C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656825 | |||||||
| chr22:17656855 | G | C | 1 | a0001c0001t0002g0004 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.121+1023G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656855 | |||||||
| chr22:17656911 | C | T | 1 | a0001c0001t0018g0215 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.121+1079C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656911 | |||||||
| chr22:17656923 | A | G | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+1091A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656923 | |||||||
| chr22:17656976 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.121+1144G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656976 | |||||||
| chr22:17656979 | C | T | 1 | a0001c0002t0001g0277 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.121+1147C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17656979 | |||||||
| chr22:17657368 | TACTTA | T | 133 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(130): Show |
134 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.121+1540_121+1544d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657368 | ||||||
| chr22:17657423 | C | T | 1 | a0001c0001t0011g0157 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.121+1591C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657423 | |||||||
| chr22:17657521 | C | CT | 7 | a0001c0001t0002g0186 a0004c0006t0001g0093 a0004c0006t0001g0096 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+1701dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657521 | ||||||
| chr22:17657541 | A | T | 1 | a0001c0002t0006g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.121+1709A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657541 | |||||||
| chr22:17657575 | C | T | 1 | a0001c0002t0006g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.121+1743C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657575 | |||||||
| chr22:17657576 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+1744G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657576 | |||||||
| chr22:17657657 | A | G | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.121+1825A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657657 | |||||||
| chr22:17657664 | A | T | 1 | a0001c0001t0002g0217 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.121+1832A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657664 | |||||||
| chr22:17657810 | C | G | 1 | a0001c0001t0002g0217 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.121+1978C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657810 | |||||||
| chr22:17657823 | C | CT | 23 | a0001c0001t0020g0225 a0001c0001t0020g0233 a0001c0001t0036g0097 others(20): Show |
23 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.121+2012dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | ||||||
| chr22:17657823 | C | CTT | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0228 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.121+2011_121+2012d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | ||||||
| chr22:17657823 | C | CTTTTTT | 115 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(112): Show |
116 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.121+2007_121+2012d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | ||||||
| chr22:17657823 | C | CTTTTTTT | 13 | a0001c0001t0002g0117 a0001c0001t0002g0133 a0001c0001t0002g0210 others(10): Show |
13 | HG00544.hp1 HG01109.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+2006_121+2012d others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | ||||||
| chr22:17657823 | CTTTT | C | 68 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(65): Show |
69 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.121+2009_121+2012d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17657823 | ||||||
| chr22:17657854 | C | G | 1 | a0001c0001t0002g0217 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.121+2022C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657854 | |||||||
| chr22:17657878 | T | G | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.121+2046T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657878 | |||||||
| chr22:17657967 | C | T | 2 | a0001c0001t0005g0012 a0001c0001t0065g0016 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.121+2135C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657967 | |||||||
| chr22:17657979 | G | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+2147G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17657979 | |||||||
| chr22:17658005 | A | G | 134 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(131): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.121+2173A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658005 | |||||||
| chr22:17658012 | G | C | 5 | a0001c0001t0005g0138 a0001c0001t0005g0143 a0001c0001t0005g0145 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+2180G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658012 | |||||||
| chr22:17658050 | G | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+2218G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658050 | |||||||
| chr22:17658062 | C | T | 2 | a0001c0009t0004g0155 a0001c0009t0004g0156 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.121+2230C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658062 | |||||||
| chr22:17658096 | G | C | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+2264G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658096 | |||||||
| chr22:17658119 | C | T | 1 | a0001c0001t0003g0038 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.121+2287C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658119 | |||||||
| chr22:17658148 | T | TTCTTCAT others(2830): Show |
1 | a0001c0001t0024g0244 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.121+2331_121+2332i others(2839): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658148 | ||||||
| chr22:17658148 | T | TTCTTCAT others(2829): Show |
1 | a0001c0001t0024g0243 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.121+2331_121+2332i others(2838): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658148 | ||||||
| chr22:17658555 | A | G | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+2723A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658555 | |||||||
| chr22:17658696 | C | CA | 41 | a0001c0001t0003g0045 a0001c0001t0003g0107 a0001c0001t0006g0077 others(38): Show |
41 | HG00099.hp2 HG00423.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.121+2882dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658696 | ||||||
| chr22:17658696 | CA | C | 133 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(130): Show |
134 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.121+2882delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658696 | ||||||
| chr22:17658715 | T | G | 249 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.121+2883T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658715 | |||||||
| chr22:17658785 | A | G | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.121+2953A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17658785 | |||||||
| chr22:17658930 | GCACCTGT others(2925): Show |
G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+3119_121+6050d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17658930 | ||||||
| chr22:17659012 | C | T | 1 | a0001c0001t0007g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.121+3180C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659012 | |||||||
| chr22:17659018 | G | A | 4 | a0001c0002t0001g0260 a0001c0002t0001g0266 a0001c0002t0001g0268 others(1): Show |
4 | HG02155.hp2 HG04184.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+3186G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659018 | |||||||
| chr22:17659049 | C | T | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.121+3217C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659049 | |||||||
| chr22:17659056 | T | TA | 61 | a0001c0001t0002g0103 a0001c0001t0002g0117 a0001c0001t0002g0133 others(58): Show |
61 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.121+3251dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659056 | ||||||
| chr22:17659056 | T | TAA | 12 | a0001c0001t0005g0141 a0001c0001t0007g0122 a0001c0001t0008g0222 others(9): Show |
12 | HG02109.hp1 HG02257.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.121+3250_121+3251d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659056 | ||||||
| chr22:17659056 | TA | T | 30 | a0001c0001t0003g0001 a0001c0001t0003g0026 a0001c0001t0003g0047 others(27): Show |
30 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.121+3251delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659056 | ||||||
| chr22:17659056 | TAA | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0027 a0001c0001t0003g0029 others(42): Show |
45 | HG00140.hp2 HG00733.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.121+3250_121+3251d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659056 | ||||||
| chr22:17659181 | T | C | 1 | a0001c0001t0007g0018 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.121+3349T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659181 | |||||||
| chr22:17659221 | A | G | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.121+3389A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659221 | |||||||
| chr22:17659288 | T | C | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+3456T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659288 | |||||||
| chr22:17659345 | C | G | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+3513C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659345 | |||||||
| chr22:17659457 | C | T | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+3625C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659457 | |||||||
| chr22:17659488 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+3656C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659488 | |||||||
| chr22:17659656 | G | A | 1 | a0001c0001t0005g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.121+3824G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17659656 | |||||||
| chr22:17659660 | AAAAAC | A | 50 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(47): Show |
51 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.121+3848_121+3852d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659660 | ||||||
| chr22:17659783 | ACAG | A | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+3953_121+3955d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17659783 | ||||||
| chr22:17660103 | C | CA | 6 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(3): Show |
6 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+4272dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17660103 | ||||||
| chr22:17660270 | G | T | 2 | a0001c0002t0025g0069 a0001c0002t0025g0070 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.121+4438G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660270 | |||||||
| chr22:17660357 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.121+4525G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660357 | |||||||
| chr22:17660358 | A | T | 4 | a0001c0001t0006g0077 a0001c0002t0006g0076 a0001c0002t0006g0078 others(1): Show |
4 | HG02145.hp1 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+4526A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660358 | |||||||
| chr22:17660493 | C | T | 1 | a0001c0001t0005g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.121+4661C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660493 | |||||||
| chr22:17660523 | G | A | 1 | a0001c0001t0002g0159 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.121+4691G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660523 | |||||||
| chr22:17660544 | G | A | 13 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0017 others(10): Show |
13 | HG01192.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+4712G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660544 | |||||||
| chr22:17660572 | G | A | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+4740G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660572 | |||||||
| chr22:17660615 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.121+4783A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660615 | |||||||
| chr22:17660651 | C | T | 3 | a0001c0001t0002g0128 a0001c0001t0033g0127 a0001c0001t0053g0125 |
3 | HG00735.hp1 HG01081.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.121+4819C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660651 | |||||||
| chr22:17660718 | C | A | 5 | a0001c0001t0005g0138 a0001c0001t0005g0143 a0001c0001t0005g0145 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+4886C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660718 | |||||||
| chr22:17660814 | G | C | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+4982G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660814 | |||||||
| chr22:17660933 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.121+5101T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660933 | |||||||
| chr22:17660981 | G | A | 1 | a0002c0003t0001g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.121+5149G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17660981 | |||||||
| chr22:17661069 | C | T | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.121+5237C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661069 | |||||||
| chr22:17661113 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+5281C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661113 | |||||||
| chr22:17661326 | C | T | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+5494C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661326 | |||||||
| chr22:17661398 | T | C | 210 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(207): Show |
212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.121+5566T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661398 | |||||||
| chr22:17661504 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.121+5672G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661504 | |||||||
| chr22:17661549 | A | C | 165 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(162): Show |
166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.121+5717A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661549 | |||||||
| chr22:17661860 | G | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+6028G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17661860 | |||||||
| chr22:17661991 | C | CA | 6 | a0001c0001t0002g0136 a0001c0001t0005g0187 a0004c0006t0001g0093 others(3): Show |
6 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.121+6174dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17661991 | ||||||
| chr22:17661991 | CA | C | 7 | a0001c0001t0002g0208 a0001c0001t0004g0137 a0001c0001t0005g0242 others(4): Show |
7 | HG00408.hp1 HG01261.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.121+6174delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17661991 | ||||||
| chr22:17662058 | T | A | 254 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.121+6226T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662058 | |||||||
| chr22:17662205 | G | A | 2 | a0001c0001t0063g0299 a0001c0001t0064g0106 |
2 | HG01255.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.121+6373G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662205 | |||||||
| chr22:17662245 | A | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+6413A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662245 | |||||||
| chr22:17662304 | T | C | 1 | a0001c0002t0042g0010 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121+6472T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662304 | |||||||
| chr22:17662305 | C | A | 1 | a0001c0002t0042g0010 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.121+6473C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662305 | |||||||
| chr22:17662324 | A | G | 5 | a0001c0001t0009g0036 a0001c0001t0009g0037 a0001c0001t0009g0039 others(2): Show |
5 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.121+6492A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662324 | |||||||
| chr22:17662696 | A | G | 1 | a0001c0001t0011g0158 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.121+6864A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662696 | |||||||
| chr22:17662708 | A | C | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+6876A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662708 | |||||||
| chr22:17662725 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+6893G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17662725 | |||||||
| chr22:17663397 | A | G | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+7565A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17663397 | |||||||
| chr22:17663440 | G | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+7608G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17663440 | |||||||
| chr22:17663622 | T | C | 249 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.121+7790T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17663622 | |||||||
| chr22:17663683 | C | CT | 9 | a0001c0001t0008g0223 a0001c0001t0036g0097 a0001c0001t0039g0194 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.121+7869dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17663683 | ||||||
| chr22:17663683 | C | CTT | 157 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.121+7868_121+7869d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17663683 | ||||||
| chr22:17663683 | C | CTTT | 11 | a0001c0001t0005g0138 a0003c0004t0015g0083 a0003c0004t0016g0090 others(8): Show |
11 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.121+7867_121+7869d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17663683 | ||||||
| chr22:17663757 | G | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+7925G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17663757 | |||||||
| chr22:17663853 | AT | A | 14 | a0001c0001t0041g0240 a0003c0004t0015g0083 a0003c0004t0015g0084 others(11): Show |
14 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.121+8034delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17663853 | ||||||
| chr22:17664205 | G | A | 17 | a0001c0001t0003g0001 a0001c0001t0003g0038 a0001c0001t0003g0042 others(14): Show |
18 | HG02135.hp2 NA18955.hp1 NA18965.hp2 others(15): Show |
intron_variant | MODIFIER | c.121+8373G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664205 | |||||||
| chr22:17664223 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+8391G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664223 | |||||||
| chr22:17664260 | C | T | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.121+8428C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664260 | |||||||
| chr22:17664273 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.121+8441C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664273 | |||||||
| chr22:17664291 | C | T | 1 | a0001c0001t0005g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.121+8459C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664291 | |||||||
| chr22:17664305 | C | T | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.121+8473C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664305 | |||||||
| chr22:17664383 | T | C | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+8551T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664383 | |||||||
| chr22:17664415 | AC | A | 19 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(16): Show |
19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.121+8592delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17664415 | ||||||
| chr22:17664415 | ACC | A | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.121+8591_121+8592d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17664415 | ||||||
| chr22:17664445 | A | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+8613A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664445 | |||||||
| chr22:17664542 | A | C | 1 | a0001c0001t0011g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.121+8710A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664542 | |||||||
| chr22:17664657 | C | A | 157 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.121+8825C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664657 | |||||||
| chr22:17664761 | C | T | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+8929C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664761 | |||||||
| chr22:17664801 | C | T | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+8969C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664801 | |||||||
| chr22:17664802 | G | A | 23 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(20): Show |
23 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.121+8970G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664802 | |||||||
| chr22:17664861 | C | G | 1 | a0001c0001t0029g0168 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.121+9029C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17664861 | |||||||
| chr22:17665169 | C | G | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+9337C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665169 | |||||||
| chr22:17665445 | G | A | 1 | a0001c0001t0061g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.121+9613G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665445 | |||||||
| chr22:17665610 | G | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+9778G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665610 | |||||||
| chr22:17665625 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+9793G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665625 | |||||||
| chr22:17665688 | T | C | 249 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.121+9856T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665688 | |||||||
| chr22:17665688 | T | G | 1 | a0002c0003t0001g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.121+9856T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665688 | |||||||
| chr22:17665723 | T | C | 21 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(18): Show |
21 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.121+9891T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665723 | |||||||
| chr22:17665830 | A | G | 1 | a0001c0001t0004g0177 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121+9998A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665830 | |||||||
| chr22:17665884 | C | T | 1 | a0001c0001t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121+10052C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17665884 | |||||||
| chr22:17666200 | A | ATTTTTAT | 94 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(91): Show |
95 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.121+10381_121+1038 others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17666200 | ||||||
| chr22:17666221 | A | T | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+10389A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17666221 | |||||||
| chr22:17666271 | A | C | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+10439A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17666271 | |||||||
| chr22:17666678 | C | CT | 160 | a0001c0001t0002g0004 a0001c0001t0002g0103 a0001c0001t0002g0115 others(157): Show |
161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.121+10867dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17666678 | ||||||
| chr22:17666678 | CT | C | 10 | a0001c0001t0003g0034 a0001c0001t0003g0042 a0001c0001t0003g0053 others(7): Show |
10 | HG00280.hp2 HG01169.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.121+10867delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17666678 | ||||||
| chr22:17666998 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.121+11166G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17666998 | |||||||
| chr22:17667166 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+11334G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667166 | |||||||
| chr22:17667167 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+11335G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667167 | |||||||
| chr22:17667185 | T | C | 1 | a0001c0001t0060g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.121+11353T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667185 | |||||||
| chr22:17667204 | C | T | 1 | a0001c0001t0002g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.121+11372C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667204 | |||||||
| chr22:17667205 | C | G | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+11373C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667205 | |||||||
| chr22:17667376 | G | A | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.121+11544G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667376 | |||||||
| chr22:17667417 | C | T | 1 | a0001c0001t0034g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.121+11585C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667417 | |||||||
| chr22:17667418 | G | A | 2 | a0001c0002t0026g0293 a0001c0002t0026g0294 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.121+11586G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667418 | |||||||
| chr22:17667609 | A | G | 1 | a0001c0001t0005g0141 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.121+11777A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667609 | |||||||
| chr22:17667721 | C | G | 7 | a0001c0001t0002g0117 a0001c0001t0002g0128 a0001c0001t0002g0130 others(4): Show |
7 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.121+11889C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667721 | |||||||
| chr22:17667754 | C | G | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.121+11922C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667754 | |||||||
| chr22:17667754 | C | T | 1 | a0001c0001t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.121+11922C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667754 | |||||||
| chr22:17667854 | CATGATTG others(8): Show |
C | 1 | a0001c0001t0003g0058 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.121+12023_121+1203 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667854 | |||||||
| chr22:17667899 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.121+12067C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17667899 | |||||||
| chr22:17667963 | CT | C | 199 | a0001c0001t0002g0004 a0001c0001t0002g0103 a0001c0001t0002g0114 others(196): Show |
201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.121+12152delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17667963 | ||||||
| chr22:17667963 | CTT | C | 27 | a0001c0001t0002g0100 a0001c0001t0003g0049 a0001c0001t0004g0177 others(24): Show |
27 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.121+12151_121+1215 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17667963 | ||||||
| chr22:17668018 | C | CT | 43 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(40): Show |
44 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.121+12198dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17668018 | ||||||
| chr22:17668042 | G | A | 1 | a0002c0003t0057g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.121+12210G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668042 | |||||||
| chr22:17668075 | A | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+12243A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668075 | |||||||
| chr22:17668156 | G | T | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.121+12324G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668156 | |||||||
| chr22:17668302 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+12470C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668302 | |||||||
| chr22:17668487 | C | G | 4 | a0001c0001t0004g0101 a0001c0001t0004g0152 a0001c0001t0004g0185 others(1): Show |
4 | HG02738.hp1 HG03834.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.121+12655C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668487 | |||||||
| chr22:17668714 | C | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+12882C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668714 | |||||||
| chr22:17668745 | G | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.121+12913G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668745 | |||||||
| chr22:17668816 | A | C | 1 | a0001c0001t0002g0207 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.121+12984A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668816 | |||||||
| chr22:17668850 | C | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121+13018C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668850 | |||||||
| chr22:17668978 | C | T | 1 | a0001c0002t0068g0292 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.121+13146C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17668978 | |||||||
| chr22:17669030 | C | CT | 18 | a0001c0001t0002g0216 a0001c0001t0003g0250 a0001c0001t0004g0177 others(15): Show |
18 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.121+13218dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | ||||||
| chr22:17669030 | C | CTT | 136 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(133): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.121+13217_121+1321 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | ||||||
| chr22:17669030 | C | CTTT | 22 | a0001c0001t0002g0209 a0001c0001t0007g0013 a0001c0001t0008g0222 others(19): Show |
22 | HG01169.hp2 HG01175.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.121+13216_121+1321 others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | ||||||
| chr22:17669030 | CT | C | 23 | a0001c0001t0003g0026 a0001c0001t0003g0042 a0001c0001t0006g0077 others(20): Show |
23 | HG00099.hp2 HG00738.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.121+13218delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | ||||||
| chr22:17669030 | CTT | C | 6 | a0001c0002t0014g0065 a0001c0002t0014g0066 a0001c0002t0014g0067 others(3): Show |
6 | HG01261.hp2 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.121+13217_121+1321 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669030 | ||||||
| chr22:17669034 | T | C | 1 | a0001c0002t0001g0256 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.121+13202T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669034 | |||||||
| chr22:17669056 | G | A | 3 | a0001c0001t0002g0134 a0001c0001t0002g0188 a0001c0001t0002g0210 |
3 | HG03927.hp1 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.121+13224G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669056 | |||||||
| chr22:17669146 | C | T | 1 | a0001c0001t0004g0177 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.121+13314C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669146 | |||||||
| chr22:17669190 | AC | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+13361delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17669190 | ||||||
| chr22:17669278 | C | T | 5 | a0001c0001t0065g0016 a0004c0006t0001g0093 a0004c0006t0001g0096 others(2): Show |
5 | HG02109.hp2 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.121+13446C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669278 | |||||||
| chr22:17669412 | A | G | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.121+13580A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669412 | |||||||
| chr22:17669414 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.121+13582G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669414 | |||||||
| chr22:17669662 | G | T | 1 | a0006c0010t0001g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.122-13552G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669662 | |||||||
| chr22:17669712 | G | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.122-13502G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669712 | |||||||
| chr22:17669942 | A | G | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.122-13272A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669942 | |||||||
| chr22:17669950 | A | C | 1 | a0001c0001t0061g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.122-13264A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17669950 | |||||||
| chr22:17670076 | T | C | 2 | a0001c0001t0013g0179 a0001c0001t0013g0180 |
2 | NA18943.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.122-13138T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670076 | |||||||
| chr22:17670243 | T | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-12971T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670243 | |||||||
| chr22:17670373 | C | CT | 50 | a0001c0001t0002g0114 a0001c0001t0002g0147 a0001c0001t0003g0045 others(47): Show |
50 | HG00099.hp2 HG00738.hp1 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.122-12823dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17670373 | ||||||
| chr22:17670373 | C | CTT | 131 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(128): Show |
132 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.122-12824_122-1282 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17670373 | ||||||
| chr22:17670373 | C | CTTT | 6 | a0001c0001t0002g0209 a0001c0001t0002g0245 a0001c0001t0004g0175 others(3): Show |
6 | HG01175.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-12825_122-1282 others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17670373 | ||||||
| chr22:17670517 | G | A | 3 | a0001c0001t0020g0225 a0001c0001t0020g0231 a0001c0001t0020g0233 |
3 | HG02257.hp1 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122-12697G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670517 | |||||||
| chr22:17670566 | G | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-12648G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670566 | |||||||
| chr22:17670834 | A | G | 1 | a0001c0001t0003g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.122-12380A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17670834 | |||||||
| chr22:17671000 | C | T | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.122-12214C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671000 | |||||||
| chr22:17671142 | G | A | 1 | a0001c0001t0005g0241 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.122-12072G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671142 | |||||||
| chr22:17671146 | A | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-12068A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671146 | |||||||
| chr22:17671155 | G | C | 1 | a0001c0001t0004g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.122-12059G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671155 | |||||||
| chr22:17671287 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-11927G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671287 | |||||||
| chr22:17671318 | C | T | 5 | a0001c0001t0046g0046 a0004c0006t0001g0093 a0004c0006t0001g0096 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-11896C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671318 | |||||||
| chr22:17671350 | C | T | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.122-11864C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671350 | |||||||
| chr22:17671369 | G | C | 3 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0055g0211 |
3 | HG02132.hp1 NA18952.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.122-11845G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671369 | |||||||
| chr22:17671381 | G | C | 178 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(175): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.122-11833G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671381 | |||||||
| chr22:17671393 | CA | C | 35 | a0001c0001t0002g0130 a0001c0001t0002g0134 a0001c0001t0002g0188 others(32): Show |
35 | HG00423.hp1 HG00544.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.122-11797delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17671393 | ||||||
| chr22:17671393 | CAA | C | 206 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(203): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.122-11798_122-1179 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17671393 | ||||||
| chr22:17671393 | CAAA | C | 8 | a0001c0001t0003g0058 a0001c0001t0024g0244 a0001c0001t0046g0046 others(5): Show |
8 | HG01243.hp1 HG01884.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.122-11799_122-1179 others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17671393 | ||||||
| chr22:17671436 | G | A | 2 | a0001c0001t0005g0120 a0001c0001t0005g0161 |
2 | NA18956.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.122-11778G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671436 | |||||||
| chr22:17671519 | A | T | 178 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(175): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.122-11695A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671519 | |||||||
| chr22:17671565 | CA | C | 239 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(236): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.122-11634delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17671565 | ||||||
| chr22:17671612 | A | G | 1 | a0001c0001t0033g0127 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.122-11602A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671612 | |||||||
| chr22:17671630 | A | G | 1 | a0001c0001t0002g0212 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.122-11584A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671630 | |||||||
| chr22:17671632 | G | T | 18 | a0001c0002t0001g0203 a0001c0002t0001g0256 a0001c0002t0001g0257 others(15): Show |
18 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.122-11582G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671632 | |||||||
| chr22:17671712 | A | G | 1 | a0001c0007t0009g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.122-11502A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17671712 | |||||||
| chr22:17672008 | C | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.122-11206C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672008 | |||||||
| chr22:17672112 | A | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-11102A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672112 | |||||||
| chr22:17672202 | A | C | 1 | a0001c0001t0007g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.122-11012A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672202 | |||||||
| chr22:17672645 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.122-10569G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672645 | |||||||
| chr22:17672778 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.122-10436T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17672778 | |||||||
| chr22:17673255 | C | G | 13 | a0001c0001t0003g0007 a0001c0001t0003g0027 a0001c0001t0003g0029 others(10): Show |
13 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.122-9959C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673255 | |||||||
| chr22:17673300 | A | G | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122-9914A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673300 | |||||||
| chr22:17673333 | C | A | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.122-9881C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673333 | |||||||
| chr22:17673334 | A | G | 13 | a0001c0002t0001g0256 a0001c0002t0001g0257 a0001c0002t0001g0258 others(10): Show |
13 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.122-9880A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673334 | |||||||
| chr22:17673361 | CT | C | 120 | a0001c0001t0002g0165 a0001c0001t0003g0001 a0001c0001t0003g0007 others(117): Show |
121 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.122-9835delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673361 | ||||||
| chr22:17673361 | CTT | C | 107 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(104): Show |
108 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.122-9836_122-9835d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673361 | ||||||
| chr22:17673395 | T | C | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-9819T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673395 | |||||||
| chr22:17673398 | G | A | 1 | a0001c0001t0003g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.122-9816G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673398 | |||||||
| chr22:17673513 | G | A | 1 | a0001c0001t0011g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.122-9701G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673513 | |||||||
| chr22:17673533 | A | AT | 7 | a0001c0002t0001g0098 a0001c0002t0001g0288 a0001c0002t0012g0008 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-9664dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673533 | ||||||
| chr22:17673533 | AT | A | 204 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(201): Show |
206 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.122-9664delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673533 | ||||||
| chr22:17673533 | ATT | A | 12 | a0001c0001t0002g0182 a0001c0001t0003g0027 a0001c0001t0003g0029 others(9): Show |
12 | HG01070.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.122-9665_122-9664d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17673533 | ||||||
| chr22:17673619 | C | T | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.122-9595C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673619 | |||||||
| chr22:17673629 | G | A | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.122-9585G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673629 | |||||||
| chr22:17673861 | G | A | 1 | a0001c0001t0004g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.122-9353G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673861 | |||||||
| chr22:17673870 | A | G | 1 | a0001c0002t0001g0289 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.122-9344A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673870 | |||||||
| chr22:17673878 | A | G | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.122-9336A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17673878 | |||||||
| chr22:17674021 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-9193G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674021 | |||||||
| chr22:17674135 | G | A | 4 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 others(1): Show |
4 | HG02896.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-9079G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674135 | |||||||
| chr22:17674460 | G | A | 1 | a0001c0001t0010g0239 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.122-8754G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674460 | |||||||
| chr22:17674516 | A | G | 207 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(204): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.122-8698A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674516 | |||||||
| chr22:17674537 | C | T | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-8677C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674537 | |||||||
| chr22:17674605 | CAA | C | 234 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(231): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.122-8593_122-8592d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17674605 | ||||||
| chr22:17674605 | CAAA | C | 13 | a0001c0001t0003g0250 a0001c0001t0007g0111 a0001c0001t0007g0112 others(10): Show |
13 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-8594_122-8592d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17674605 | ||||||
| chr22:17674701 | A | G | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.122-8513A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674701 | |||||||
| chr22:17674886 | T | TATA | 250 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.122-8326_122-8325i others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17674886 | ||||||
| chr22:17674926 | A | T | 2 | a0001c0002t0026g0293 a0001c0002t0026g0294 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.122-8288A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17674926 | |||||||
| chr22:17675075 | TAC | T | 179 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(176): Show |
180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.122-8123_122-8122d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17675075 | ||||||
| chr22:17675279 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.122-7935G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675279 | |||||||
| chr22:17675346 | C | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.122-7868C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675346 | |||||||
| chr22:17675372 | T | C | 1 | a0001c0002t0027g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.122-7842T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675372 | |||||||
| chr22:17675403 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-7811G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675403 | |||||||
| chr22:17675435 | G | A | 3 | a0001c0001t0004g0101 a0001c0001t0004g0152 a0001c0001t0004g0185 |
3 | HG02738.hp1 HG03834.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.122-7779G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675435 | |||||||
| chr22:17675578 | C | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-7636C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675578 | |||||||
| chr22:17675605 | G | A | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-7609G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675605 | |||||||
| chr22:17675660 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.122-7554C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675660 | |||||||
| chr22:17675677 | T | C | 1 | a0001c0001t0050g0249 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.122-7537T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675677 | |||||||
| chr22:17675889 | A | C | 1 | a0001c0001t0010g0221 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.122-7325A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17675889 | |||||||
| chr22:17676119 | T | C | 1 | a0001c0001t0010g0239 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.122-7095T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676119 | |||||||
| chr22:17676276 | A | C | 1 | a0001c0001t0003g0058 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.122-6938A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676276 | |||||||
| chr22:17676305 | CA | C | 250 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.122-6900delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17676305 | ||||||
| chr22:17676336 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-6878G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676336 | |||||||
| chr22:17676545 | A | G | 1 | a0001c0001t0066g0189 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.122-6669A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676545 | |||||||
| chr22:17676641 | T | C | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.122-6573T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676641 | |||||||
| chr22:17676902 | A | G | 2 | a0001c0001t0002g0139 a0001c0001t0002g0174 |
2 | HG01069.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.122-6312A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676902 | |||||||
| chr22:17676902 | A | T | 1 | a0001c0001t0003g0058 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.122-6312A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676902 | |||||||
| chr22:17676938 | A | G | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.122-6276A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17676938 | |||||||
| chr22:17677154 | CAAAAAAT others(1): Show |
C | 4 | a0001c0001t0002g0117 a0001c0001t0002g0130 a0001c0001t0002g0202 others(1): Show |
4 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-6040_122-6033d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17677154 | ||||||
| chr22:17677156 | A | G | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-6058A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677156 | |||||||
| chr22:17677163 | A | G | 1 | a0001c0001t0020g0225 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.122-6051A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677163 | |||||||
| chr22:17677180 | A | G | 157 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(154): Show |
158 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.122-6034A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677180 | |||||||
| chr22:17677247 | T | C | 2 | a0002c0003t0001g0290 a0002c0003t0001g0291 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.122-5967T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677247 | |||||||
| chr22:17677258 | T | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-5956T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677258 | |||||||
| chr22:17677533 | A | G | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-5681A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677533 | |||||||
| chr22:17677688 | A | C | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-5526A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677688 | |||||||
| chr22:17677837 | A | G | 1 | a0001c0001t0021g0023 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.122-5377A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677837 | |||||||
| chr22:17677838 | T | C | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.122-5376T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677838 | |||||||
| chr22:17677867 | C | CA | 20 | a0001c0001t0005g0140 a0001c0001t0005g0169 a0001c0001t0007g0099 others(17): Show |
20 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-5337dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17677867 | ||||||
| chr22:17677878 | C | A | 5 | a0001c0002t0012g0008 a0004c0006t0001g0093 a0004c0006t0001g0096 others(2): Show |
5 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-5336C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677878 | |||||||
| chr22:17677886 | C | A | 4 | a0001c0001t0002g0100 a0001c0001t0002g0123 a0001c0001t0002g0176 others(1): Show |
4 | NA18984.hp1 NA19056.hp2 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-5328C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677886 | |||||||
| chr22:17677989 | T | C | 1 | a0001c0001t0007g0122 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.122-5225T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17677989 | |||||||
| chr22:17678115 | C | T | 134 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(131): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.122-5099C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678115 | |||||||
| chr22:17678148 | G | A | 1 | a0002c0003t0001g0269 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.122-5066G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678148 | |||||||
| chr22:17678263 | A | G | 2 | a0001c0001t0005g0190 a0001c0001t0005g0242 |
2 | HG00408.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.122-4951A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678263 | |||||||
| chr22:17678302 | G | A | 1 | a0001c0001t0002g0182 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.122-4912G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678302 | |||||||
| chr22:17678377 | C | T | 1 | a0001c0001t0039g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.122-4837C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678377 | |||||||
| chr22:17678410 | A | G | 1 | a0001c0001t0007g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.122-4804A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678410 | |||||||
| chr22:17678693 | T | G | 1 | a0001c0001t0002g0139 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.122-4521T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678693 | |||||||
| chr22:17678703 | C | T | 1 | a0001c0001t0011g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.122-4511C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678703 | |||||||
| chr22:17678777 | G | A | 20 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(17): Show |
20 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.122-4437G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678777 | |||||||
| chr22:17678878 | A | T | 1 | a0001c0002t0001g0284 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.122-4336A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678878 | |||||||
| chr22:17678996 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.122-4218A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17678996 | |||||||
| chr22:17679213 | G | A | 71 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(68): Show |
72 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.122-4001G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679213 | |||||||
| chr22:17679226 | G | A | 1 | a0001c0001t0005g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.122-3988G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679226 | |||||||
| chr22:17679248 | GTCAATTG others(2905): Show |
G | 1 | a0001c0002t0037g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.122-3963_122-1052d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679248 | ||||||
| chr22:17679264 | C | CT | 9 | a0001c0001t0003g0027 a0001c0001t0003g0058 a0001c0001t0009g0036 others(6): Show |
9 | HG01256.hp2 HG01517.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-3926dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | ||||||
| chr22:17679264 | C | CTT | 19 | a0001c0001t0006g0077 a0001c0001t0065g0016 a0001c0002t0006g0071 others(16): Show |
19 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.122-3927_122-3926d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | ||||||
| chr22:17679264 | CT | C | 12 | a0001c0001t0002g0182 a0001c0001t0002g0209 a0001c0001t0002g0210 others(9): Show |
12 | HG01070.hp2 HG01109.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.122-3926delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | ||||||
| chr22:17679264 | CTT | C | 159 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(156): Show |
160 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.122-3927_122-3926d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | ||||||
| chr22:17679264 | CTTT | C | 7 | a0001c0001t0005g0140 a0001c0001t0011g0116 a0001c0001t0066g0189 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.122-3928_122-3926d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17679264 | ||||||
| chr22:17679290 | A | G | 2 | a0001c0001t0003g0250 a0001c0001t0003g0251 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.122-3924A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679290 | |||||||
| chr22:17679296 | T | C | 1 | a0001c0002t0035g0296 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.122-3918T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679296 | |||||||
| chr22:17679312 | C | T | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-3902C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679312 | |||||||
| chr22:17679414 | C | T | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-3800C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679414 | |||||||
| chr22:17679539 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-3675G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679539 | |||||||
| chr22:17679932 | G | A | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-3282G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679932 | |||||||
| chr22:17679960 | C | G | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-3254C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17679960 | |||||||
| chr22:17680016 | C | A | 4 | a0001c0002t0006g0071 a0001c0002t0006g0072 a0001c0002t0006g0079 others(1): Show |
4 | HG02071.hp1 HG02602.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-3198C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680016 | |||||||
| chr22:17680071 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-3143G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680071 | |||||||
| chr22:17680137 | C | T | 1 | a0001c0001t0005g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.122-3077C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680137 | |||||||
| chr22:17680188 | C | T | 6 | a0001c0001t0017g0019 a0001c0001t0017g0020 a0001c0001t0017g0025 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-3026C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680188 | |||||||
| chr22:17680200 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.122-3014G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680200 | |||||||
| chr22:17680215 | C | CAA | 44 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(41): Show |
45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.122-2986_122-2985d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | ||||||
| chr22:17680215 | C | CAAAAAAA others(1): Show |
8 | a0001c0001t0002g0103 a0001c0001t0007g0247 a0001c0001t0007g0248 others(5): Show |
8 | HG02717.hp2 HG03041.hp1 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.122-2992_122-2985d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | ||||||
| chr22:17680215 | C | CAAAAAAA others(2): Show |
140 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0114 others(137): Show |
141 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.122-2993_122-2985d others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | ||||||
| chr22:17680215 | C | CAAAAAAA others(3): Show |
10 | a0001c0001t0002g0133 a0001c0001t0002g0212 a0001c0001t0005g0063 others(7): Show |
10 | HG01255.hp2 HG02148.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.122-2994_122-2985d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | ||||||
| chr22:17680215 | C | CAAAAAAA others(4): Show |
13 | a0003c0004t0015g0084 a0003c0004t0015g0252 a0003c0004t0016g0090 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-2995_122-2985d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | ||||||
| chr22:17680215 | C | CAAAAAAA others(5): Show |
7 | a0001c0001t0005g0140 a0003c0004t0015g0083 a0003c0004t0016g0092 others(4): Show |
7 | HG01361.hp1 HG02055.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.122-2996_122-2985d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | ||||||
| chr22:17680215 | C | CAAAAAAA others(6): Show |
1 | a0005c0008t0019g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.122-2997_122-2985d others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680215 | ||||||
| chr22:17680240 | G | A | 3 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 |
3 | HG02886.hp1 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.122-2974G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680240 | |||||||
| chr22:17680311 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.122-2903C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680311 | |||||||
| chr22:17680370 | A | C | 249 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(246): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.122-2844A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680370 | |||||||
| chr22:17680379 | G | A | 6 | a0001c0001t0017g0019 a0001c0001t0017g0020 a0001c0001t0017g0025 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.122-2835G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680379 | |||||||
| chr22:17680392 | C | T | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.122-2822C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680392 | |||||||
| chr22:17680511 | C | CA | 37 | a0001c0001t0002g0174 a0001c0001t0003g0001 a0001c0001t0003g0029 others(34): Show |
38 | HG00140.hp2 HG00544.hp2 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.122-2673dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680511 | ||||||
| chr22:17680511 | C | CAAAAAAA others(20): Show |
1 | a0001c0001t0028g0298 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.122-2699_122-2673d others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680511 | ||||||
| chr22:17680518 | AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.122-2688_122-2665d others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680518 | ||||||
| chr22:17680521 | AAAAAAAA others(14): Show |
A | 9 | a0001c0001t0002g0100 a0001c0001t0002g0176 a0001c0001t0007g0111 others(6): Show |
9 | HG01255.hp2 HG02717.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.122-2685_122-2665d others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680521 | ||||||
| chr22:17680522 | AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0063g0299 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.122-2684_122-2665d others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680522 | ||||||
| chr22:17680523 | AAAAAAAA others(12): Show |
A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.122-2683_122-2665d others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680523 | ||||||
| chr22:17680524 | AAAAAAAA others(11): Show |
A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.122-2682_122-2665d others(20): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680524 | ||||||
| chr22:17680525 | AAAAAAAA others(10): Show |
A | 1 | a0001c0001t0002g0147 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.122-2681_122-2665d others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680525 | ||||||
| chr22:17680527 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0005g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.122-2679_122-2665d others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680527 | ||||||
| chr22:17680528 | AAAAAAAA others(7): Show |
A | 21 | a0001c0001t0006g0077 a0001c0001t0008g0230 a0001c0001t0021g0024 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.122-2678_122-2665d others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680528 | ||||||
| chr22:17680529 | AAAAAAAA others(6): Show |
A | 5 | a0001c0002t0014g0065 a0001c0002t0014g0066 a0001c0002t0014g0067 others(2): Show |
5 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.122-2677_122-2665d others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680529 | ||||||
| chr22:17680531 | AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0003g0030 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.122-2675_122-2665d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680531 | ||||||
| chr22:17680532 | AAAAAAAA others(3): Show |
A | 4 | a0001c0001t0003g0035 a0001c0001t0003g0060 a0001c0001t0003g0061 others(1): Show |
4 | HG02630.hp2 HG02922.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-2674_122-2665d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680532 | ||||||
| chr22:17680538 | AAAAG | A | 42 | a0001c0001t0002g0004 a0001c0001t0002g0114 a0001c0001t0002g0115 others(39): Show |
43 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.122-2672_122-2669d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680538 | ||||||
| chr22:17680539 | AAAG | A | 43 | a0001c0001t0002g0103 a0001c0001t0002g0117 a0001c0001t0002g0123 others(40): Show |
43 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.122-2672_122-2670d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680539 | ||||||
| chr22:17680540 | AAG | A | 31 | a0001c0001t0002g0128 a0001c0001t0002g0131 a0001c0001t0002g0139 others(28): Show |
31 | HG00609.hp1 HG00609.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.122-2672_122-2671d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17680540 | ||||||
| chr22:17680541 | AG | A | 19 | a0001c0001t0002g0134 a0001c0001t0002g0210 a0001c0001t0003g0250 others(16): Show |
19 | HG00423.hp2 HG01168.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.122-2672delG | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680541 | |||||||
| chr22:17680542 | G | A | 47 | a0001c0001t0002g0133 a0001c0001t0002g0174 a0001c0001t0003g0001 others(44): Show |
48 | HG00140.hp2 HG00733.hp1 HG01496.hp2 others(45): Show |
intron_variant | MODIFIER | c.122-2672G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680542 | |||||||
| chr22:17680773 | G | A | 156 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(153): Show |
157 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.122-2441G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680773 | |||||||
| chr22:17680990 | G | A | 2 | a0001c0001t0013g0179 a0001c0001t0013g0192 |
2 | NA19007.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.122-2224G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17680990 | |||||||
| chr22:17681029 | C | T | 20 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(17): Show |
20 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.122-2185C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681029 | |||||||
| chr22:17681142 | A | C | 1 | a0001c0002t0035g0296 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.122-2072A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681142 | |||||||
| chr22:17681159 | G | A | 1 | a0001c0001t0007g0017 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.122-2055G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681159 | |||||||
| chr22:17681161 | A | T | 3 | a0001c0007t0009g0040 a0001c0007t0009g0059 a0001c0007t0044g0033 |
3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.122-2053A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681161 | |||||||
| chr22:17681315 | G | C | 1 | a0001c0001t0005g0143 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.122-1899G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681315 | |||||||
| chr22:17681386 | G | C | 1 | a0002c0003t0001g0271 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.122-1828G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681386 | |||||||
| chr22:17681498 | G | GA | 49 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(46): Show |
50 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.122-1703dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17681498 | ||||||
| chr22:17681535 | A | C | 1 | a0001c0001t0005g0140 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.122-1679A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681535 | |||||||
| chr22:17681622 | A | G | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-1592A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681622 | |||||||
| chr22:17681763 | C | T | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-1451C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681763 | |||||||
| chr22:17681812 | T | A | 3 | a0001c0001t0020g0225 a0001c0001t0020g0231 a0001c0001t0020g0233 |
3 | HG02257.hp1 HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.122-1402T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681812 | |||||||
| chr22:17681836 | G | A | 15 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(12): Show |
15 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.122-1378G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681836 | |||||||
| chr22:17681899 | G | A | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-1315G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681899 | |||||||
| chr22:17681909 | A | G | 5 | a0001c0001t0005g0138 a0001c0001t0005g0143 a0001c0001t0005g0145 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.122-1305A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681909 | |||||||
| chr22:17681928 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.122-1286G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681928 | |||||||
| chr22:17681976 | G | C | 4 | a0001c0002t0014g0065 a0001c0002t0014g0066 a0001c0002t0014g0067 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-1238G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17681976 | |||||||
| chr22:17682007 | T | C | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.122-1207T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682007 | |||||||
| chr22:17682098 | A | G | 134 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(131): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.122-1116A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682098 | |||||||
| chr22:17682100 | T | C | 20 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(17): Show |
20 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.122-1114T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682100 | |||||||
| chr22:17682310 | T | C | 4 | a0001c0001t0008g0224 a0001c0001t0010g0135 a0001c0001t0010g0235 others(1): Show |
4 | NA18946.hp2 NA18953.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.122-904T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682310 | |||||||
| chr22:17682604 | T | C | 2 | a0001c0001t0002g0134 a0001c0001t0002g0210 |
2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.122-610T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682604 | |||||||
| chr22:17682872 | G | A | 44 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(41): Show |
45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.122-342G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682872 | |||||||
| chr22:17682964 | C | T | 1 | a0001c0001t0005g0181 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.122-250C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17682964 | |||||||
| chr22:17683119 | C | T | 2 | a0001c0001t0005g0190 a0001c0001t0005g0242 |
2 | HG00408.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.122-95C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | chr22 | 17683119 | |||||||
| chr22:17683132 | C | CAA | 15 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.122-67_122-66dupAA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17683132 | ||||||
| chr22:17683132 | CA | C | 26 | a0001c0001t0002g0123 a0001c0001t0003g0055 a0001c0001t0006g0077 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.122-66delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr22 | 17683132 | ||||||
| chr22:17683360 | G | T | 1 | a0001c0001t0003g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.229+39G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683360 | |||||||
| chr22:17683539 | A | G | 1 | a0001c0001t0018g0195 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.229+218A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683539 | |||||||
| chr22:17683728 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+407C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683728 | |||||||
| chr22:17683729 | A | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+408A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683729 | |||||||
| chr22:17683731 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+410C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683731 | |||||||
| chr22:17683734 | TATA | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+414_229+416del others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683734 | |||||||
| chr22:17683735 | A | T | 9 | a0001c0001t0002g0100 a0001c0001t0002g0123 a0001c0001t0002g0151 others(6): Show |
9 | HG01192.hp2 HG01978.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.229+414A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683735 | |||||||
| chr22:17683801 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+480G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683801 | |||||||
| chr22:17683844 | C | CATT | 63 | a0001c0001t0002g0174 a0001c0001t0003g0001 a0001c0001t0003g0026 others(60): Show |
64 | HG00140.hp2 HG00733.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.229+561_229+563dup others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | ||||||
| chr22:17683844 | C | CATTATT | 3 | a0001c0001t0003g0030 a0001c0002t0001g0256 a0001c0002t0012g0008 |
3 | HG02970.hp2 HG03486.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.229+558_229+563dup others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | ||||||
| chr22:17683844 | CATT | C | 14 | a0001c0001t0013g0236 a0001c0001t0065g0016 a0001c0002t0001g0203 others(11): Show |
14 | HG00423.hp1 HG01109.hp2 HG01175.hp2 others(11): Show |
intron_variant | MODIFIER | c.229+561_229+563del others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | ||||||
| chr22:17683844 | CATTATT | C | 16 | a0001c0001t0002g0100 a0001c0001t0002g0123 a0001c0001t0002g0151 others(13): Show |
16 | HG00438.hp2 HG00544.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.229+558_229+563del others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | ||||||
| chr22:17683844 | CATTATTA others(2): Show |
C | 143 | a0001c0001t0002g0004 a0001c0001t0002g0103 a0001c0001t0002g0114 others(140): Show |
144 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.229+555_229+563del others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17683844 | ||||||
| chr22:17683914 | G | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.229+593G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683914 | |||||||
| chr22:17683975 | T | C | 21 | a0001c0002t0035g0296 a0003c0004t0015g0083 a0003c0004t0015g0084 others(18): Show |
21 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(18): Show |
intron_variant | MODIFIER | c.229+654T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683975 | |||||||
| chr22:17683981 | C | G | 1 | a0001c0001t0005g0181 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.229+660C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17683981 | |||||||
| chr22:17684040 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+719C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684040 | |||||||
| chr22:17684071 | C | T | 4 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 others(1): Show |
4 | HG02896.hp1 HG03195.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+750C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684071 | |||||||
| chr22:17684078 | A | G | 1 | a0001c0001t0006g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.229+757A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684078 | |||||||
| chr22:17684187 | T | G | 1 | a0001c0001t0002g0172 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.229+866T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684187 | |||||||
| chr22:17684194 | A | G | 1 | a0001c0001t0056g0204 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.229+873A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684194 | |||||||
| chr22:17684569 | T | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.229+1248T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684569 | |||||||
| chr22:17684591 | T | G | 1 | a0002c0003t0001g0271 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.229+1270T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684591 | |||||||
| chr22:17684712 | T | C | 192 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.229+1391T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684712 | |||||||
| chr22:17684726 | GCTAATTT others(162): Show |
G | 1 | a0003c0004t0016g0092 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.229+1424_229+1592d others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17684726 | ||||||
| chr22:17684739 | A | AT | 18 | a0001c0001t0002g0117 a0001c0001t0003g0043 a0001c0001t0005g0190 others(15): Show |
18 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.229+1432dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17684739 | ||||||
| chr22:17684765 | G | A | 1 | a0003c0005t0006g0086 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.229+1444G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684765 | |||||||
| chr22:17684848 | T | G | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.229+1527T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684848 | |||||||
| chr22:17684860 | G | A | 136 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(133): Show |
137 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.229+1539G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684860 | |||||||
| chr22:17684881 | T | C | 4 | a0001c0001t0003g0035 a0001c0001t0008g0228 a0002c0003t0001g0270 others(1): Show |
4 | HG00280.hp2 HG00423.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+1560T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684881 | |||||||
| chr22:17684882 | G | A | 1 | a0001c0001t0003g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.229+1561G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684882 | |||||||
| chr22:17684923 | G | A | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.229+1602G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684923 | |||||||
| chr22:17684934 | G | A | 1 | a0001c0001t0004g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.229+1613G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684934 | |||||||
| chr22:17684939 | A | G | 1 | a0001c0001t0004g0164 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.229+1618A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684939 | |||||||
| chr22:17684940 | G | A | 1 | a0001c0001t0004g0213 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.229+1619G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17684940 | |||||||
| chr22:17685015 | A | G | 25 | a0001c0001t0002g0144 a0001c0001t0002g0245 a0001c0001t0004g0175 others(22): Show |
25 | HG01123.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.229+1694A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685015 | |||||||
| chr22:17685093 | T | C | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.229+1772T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685093 | |||||||
| chr22:17685110 | G | C | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.229+1789G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685110 | |||||||
| chr22:17685301 | C | G | 2 | a0001c0001t0002g0207 a0001c0001t0002g0212 |
2 | NA18964.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.229+1980C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685301 | |||||||
| chr22:17685366 | C | T | 3 | a0001c0001t0008g0223 a0001c0001t0008g0227 a0001c0001t0038g0229 |
3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.229+2045C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685366 | |||||||
| chr22:17685416 | G | T | 3 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 |
3 | HG03195.hp2 HG03471.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.229+2095G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685416 | |||||||
| chr22:17685445 | A | G | 1 | a0001c0001t0002g0193 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.229+2124A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685445 | |||||||
| chr22:17685512 | C | T | 1 | a0001c0001t0004g0150 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.229+2191C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685512 | |||||||
| chr22:17685557 | T | C | 3 | a0001c0002t0026g0293 a0001c0002t0026g0294 a0001c0002t0035g0296 |
3 | HG02258.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.229+2236T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685557 | |||||||
| chr22:17685671 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.229+2350A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685671 | |||||||
| chr22:17685692 | A | T | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.229+2371A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685692 | |||||||
| chr22:17685736 | A | G | 1 | a0001c0001t0010g0239 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.229+2415A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685736 | |||||||
| chr22:17685754 | CTTTTTCT others(3): Show |
C | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.229+2439_229+2448d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685754 | ||||||
| chr22:17685754 | CTTTTTCT others(6): Show |
C | 1 | a0001c0001t0005g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.229+2439_229+2451d others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685754 | ||||||
| chr22:17685760 | C | CT | 21 | a0001c0001t0003g0027 a0001c0001t0003g0031 a0001c0001t0003g0043 others(18): Show |
21 | HG00140.hp1 HG00735.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.229+2468dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTT | 14 | a0001c0001t0002g0153 a0001c0001t0002g0209 a0001c0001t0004g0102 others(11): Show |
14 | HG01074.hp1 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.229+2464_229+2468d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTCT others(2): Show |
11 | a0001c0001t0008g0227 a0001c0001t0008g0230 a0001c0001t0010g0235 others(8): Show |
11 | HG01167.hp1 HG01169.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.229+2444_229+2445i others(11): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTCT others(3): Show |
4 | a0001c0001t0008g0224 a0001c0001t0008g0228 a0001c0001t0008g0234 others(1): Show |
4 | HG01433.hp1 HG02257.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+2444_229+2445i others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTCT others(4): Show |
3 | a0001c0001t0010g0239 a0001c0001t0028g0297 a0001c0001t0041g0240 |
3 | HG01978.hp2 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.229+2444_229+2445i others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTCT others(5): Show |
1 | a0001c0001t0028g0298 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.229+2444_229+2445i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTCT others(6): Show |
2 | a0001c0001t0010g0221 a0001c0001t0010g0226 |
2 | NA18952.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.229+2444_229+2445i others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTT | 48 | a0001c0001t0002g0004 a0001c0001t0002g0117 a0001c0001t0002g0123 others(45): Show |
48 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.229+2463_229+2468d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTTT | 30 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(27): Show |
30 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.229+2462_229+2468d others(9): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTTT others(1): Show |
19 | a0001c0001t0002g0114 a0001c0001t0002g0128 a0001c0001t0002g0131 others(16): Show |
19 | HG00423.hp2 HG00438.hp1 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.229+2461_229+2468d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0063g0299 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.229+2459_229+2468d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0064g0106 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.229+2458_229+2468d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0007g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.229+2446_229+2468d others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | CT | C | 28 | a0001c0001t0003g0026 a0001c0001t0003g0053 a0001c0001t0009g0037 others(25): Show |
28 | HG00099.hp2 HG00738.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.229+2468delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | CTT | C | 9 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0016g0090 others(6): Show |
9 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.229+2467_229+2468d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0008g0222 a0001c0001t0021g0023 |
2 | HG02486.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.229+2459_229+2468d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685760 | CTTTTTTT others(4): Show |
C | 12 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0017 others(9): Show |
12 | HG01192.hp1 HG02615.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.229+2458_229+2468d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17685760 | ||||||
| chr22:17685776 | T | C | 1 | a0001c0001t0008g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.229+2455T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685776 | |||||||
| chr22:17685828 | G | A | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.229+2507G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685828 | |||||||
| chr22:17685832 | C | T | 2 | a0001c0001t0053g0125 a0004c0006t0001g0093 |
2 | HG01081.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.229+2511C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685832 | |||||||
| chr22:17685857 | C | T | 1 | a0001c0002t0001g0284 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.229+2536C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685857 | |||||||
| chr22:17685902 | G | A | 1 | a0001c0001t0004g0246 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.229+2581G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685902 | |||||||
| chr22:17685937 | C | A | 22 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(19): Show |
22 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.229+2616C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685937 | |||||||
| chr22:17685962 | C | T | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.229+2641C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17685962 | |||||||
| chr22:17686008 | A | G | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.229+2687A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686008 | |||||||
| chr22:17686010 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.229+2689G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686010 | |||||||
| chr22:17686100 | A | G | 1 | a0001c0001t0004g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.229+2779A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686100 | |||||||
| chr22:17686183 | C | T | 1 | a0001c0001t0011g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.230-2803C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686183 | |||||||
| chr22:17686224 | G | A | 1 | a0001c0002t0014g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.230-2762G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686224 | |||||||
| chr22:17686237 | C | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-2749C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686237 | |||||||
| chr22:17686246 | T | G | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.230-2740T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686246 | |||||||
| chr22:17686446 | T | A | 1 | a0001c0001t0003g0043 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.230-2540T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686446 | |||||||
| chr22:17686446 | T | G | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.230-2540T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686446 | |||||||
| chr22:17686455 | T | A | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.230-2531T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686455 | |||||||
| chr22:17686503 | ATTTCTTT others(3): Show |
A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-2469_230-2460d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17686503 | ||||||
| chr22:17686517 | C | CTT | 153 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(150): Show |
154 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.230-2459_230-2458d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17686517 | ||||||
| chr22:17686517 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.230-2469C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686517 | |||||||
| chr22:17686518 | T | C | 1 | a0001c0001t0003g0043 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.230-2468T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686518 | |||||||
| chr22:17686657 | C | G | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.230-2329C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686657 | |||||||
| chr22:17686743 | T | C | 1 | a0001c0001t0034g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.230-2243T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686743 | |||||||
| chr22:17686756 | G | A | 6 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 others(3): Show |
6 | HG01255.hp2 HG02109.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.230-2230G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686756 | |||||||
| chr22:17686761 | G | A | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.230-2225G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686761 | |||||||
| chr22:17686906 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.230-2080G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686906 | |||||||
| chr22:17686962 | C | T | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.230-2024C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17686962 | |||||||
| chr22:17687134 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.230-1852C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687134 | |||||||
| chr22:17687209 | C | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.230-1777C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687209 | |||||||
| chr22:17687291 | G | A | 2 | a0001c0001t0003g0060 a0001c0001t0003g0061 |
2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.230-1695G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687291 | |||||||
| chr22:17687317 | GTTTTATT others(4): Show |
G | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.230-1660_230-1650d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17687317 | ||||||
| chr22:17687360 | GAGACAGA others(5): Show |
G | 1 | a0001c0001t0003g0026 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.230-1624_230-1613d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17687360 | ||||||
| chr22:17687390 | G | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.230-1596G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687390 | |||||||
| chr22:17687441 | A | G | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.230-1545A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687441 | |||||||
| chr22:17687538 | C | A | 1 | a0001c0001t0061g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.230-1448C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687538 | |||||||
| chr22:17687586 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.230-1400G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687586 | |||||||
| chr22:17687612 | G | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.230-1374G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687612 | |||||||
| chr22:17687678 | A | G | 2 | a0001c0009t0004g0155 a0001c0009t0004g0156 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.230-1308A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687678 | |||||||
| chr22:17687739 | G | A | 1 | a0001c0002t0001g0257 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.230-1247G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687739 | |||||||
| chr22:17687818 | C | A | 1 | a0001c0001t0003g0026 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.230-1168C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687818 | |||||||
| chr22:17687818 | C | CT | 165 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(162): Show |
166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.230-1152dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17687818 | ||||||
| chr22:17687818 | C | CTT | 9 | a0001c0001t0002g0139 a0001c0001t0002g0245 a0001c0001t0004g0175 others(6): Show |
9 | HG01069.hp1 HG01934.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-1153_230-1152d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17687818 | ||||||
| chr22:17687819 | T | C | 7 | a0001c0001t0006g0077 a0001c0002t0006g0076 a0001c0002t0006g0081 others(4): Show |
7 | HG02145.hp1 HG02280.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.230-1167T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687819 | |||||||
| chr22:17687979 | G | A | 1 | a0001c0001t0010g0135 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.230-1007G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17687979 | |||||||
| chr22:17688030 | C | T | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.230-956C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688030 | |||||||
| chr22:17688252 | C | T | 2 | a0001c0001t0002g0207 a0001c0001t0002g0212 |
2 | NA18964.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.230-734C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688252 | |||||||
| chr22:17688323 | A | G | 12 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(9): Show |
12 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.230-663A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688323 | |||||||
| chr22:17688336 | T | A | 1 | a0001c0001t0004g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.230-650T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688336 | |||||||
| chr22:17688345 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.230-641C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688345 | |||||||
| chr22:17688457 | A | T | 1 | a0001c0001t0005g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.230-529A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688457 | |||||||
| chr22:17688534 | A | G | 1 | a0001c0002t0001g0275 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.230-452A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688534 | |||||||
| chr22:17688535 | T | A | 1 | a0001c0002t0001g0275 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.230-451T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688535 | |||||||
| chr22:17688646 | A | G | 1 | a0001c0001t0005g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.230-340A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688646 | |||||||
| chr22:17688722 | G | A | 1 | a0001c0001t0054g0173 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.230-264G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688722 | |||||||
| chr22:17688762 | A | G | 1 | a0001c0001t0004g0163 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.230-224A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688762 | |||||||
| chr22:17688768 | G | GT | 22 | a0001c0001t0002g0117 a0001c0001t0002g0186 a0001c0001t0003g0007 others(19): Show |
22 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.230-202dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr22 | 17688768 | ||||||
| chr22:17688768 | G | T | 2 | a0001c0002t0012g0300 a0001c0002t0012g0301 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.230-218G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688768 | |||||||
| chr22:17688791 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.230-195G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688791 | |||||||
| chr22:17688801 | C | T | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.230-185C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688801 | |||||||
| chr22:17688824 | G | A | 22 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(19): Show |
22 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.230-162G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688824 | |||||||
| chr22:17688884 | C | T | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.230-102C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 3/6 | chr22 | 17688884 | |||||||
| chr22:17689328 | G | A | 1 | a0001c0001t0003g0050 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.386+186G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689328 | |||||||
| chr22:17689421 | C | G | 1 | a0002c0003t0001g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.386+279C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689421 | |||||||
| chr22:17689470 | C | G | 180 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(177): Show |
181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.386+328C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689470 | |||||||
| chr22:17689571 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.386+429G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689571 | |||||||
| chr22:17689619 | C | T | 1 | a0001c0001t0008g0230 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.386+477C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689619 | |||||||
| chr22:17689768 | G | A | 160 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(157): Show |
161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.386+626G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689768 | |||||||
| chr22:17689770 | G | C | 1 | a0001c0001t0003g0026 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.386+628G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689770 | |||||||
| chr22:17689842 | C | CA | 12 | a0001c0001t0002g0216 a0001c0002t0001g0198 a0001c0002t0001g0258 others(9): Show |
12 | HG00544.hp2 HG01256.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.386+718dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17689842 | ||||||
| chr22:17689842 | CA | C | 205 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(202): Show |
207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.386+718delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17689842 | ||||||
| chr22:17689859 | A | C | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.386+717A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689859 | |||||||
| chr22:17689860 | A | C | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+718A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689860 | |||||||
| chr22:17689863 | C | A | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.386+721C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689863 | |||||||
| chr22:17689872 | G | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.386+730G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17689872 | |||||||
| chr22:17690091 | C | T | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.386+949C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690091 | |||||||
| chr22:17690124 | G | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.386+982G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690124 | |||||||
| chr22:17690200 | C | T | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.386+1058C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690200 | |||||||
| chr22:17690241 | G | A | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+1099G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690241 | |||||||
| chr22:17690329 | G | GA | 155 | a0001c0001t0002g0100 a0001c0001t0002g0114 a0001c0001t0002g0115 others(152): Show |
155 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.386+1194dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17690329 | ||||||
| chr22:17690337 | T | A | 92 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0027 others(89): Show |
93 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.386+1195T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690337 | |||||||
| chr22:17690338 | T | A | 43 | a0001c0001t0003g0001 a0001c0001t0003g0026 a0001c0001t0003g0038 others(40): Show |
44 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(41): Show |
intron_variant | MODIFIER | c.386+1196T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690338 | |||||||
| chr22:17690339 | T | A | 1 | a0001c0001t0003g0026 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.386+1197T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690339 | |||||||
| chr22:17690391 | G | A | 1 | a0001c0001t0004g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.386+1249G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690391 | |||||||
| chr22:17690581 | A | G | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+1439A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690581 | |||||||
| chr22:17690743 | G | A | 28 | a0001c0001t0003g0001 a0001c0001t0003g0026 a0001c0001t0003g0038 others(25): Show |
29 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.386+1601G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690743 | |||||||
| chr22:17690815 | A | G | 1 | a0001c0001t0011g0166 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.386+1673A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690815 | |||||||
| chr22:17690920 | A | G | 1 | a0002c0003t0001g0267 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.386+1778A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690920 | |||||||
| chr22:17690981 | T | C | 13 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(10): Show |
13 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.386+1839T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17690981 | |||||||
| chr22:17691205 | G | A | 1 | a0001c0001t0032g0146 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.386+2063G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691205 | |||||||
| chr22:17691224 | A | G | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.386+2082A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691224 | |||||||
| chr22:17691336 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0202 |
2 | HG00280.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.386+2194G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691336 | |||||||
| chr22:17691350 | T | G | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.386+2208T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691350 | |||||||
| chr22:17691358 | TTG | T | 180 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(177): Show |
181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.386+2218_386+2219d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17691358 | ||||||
| chr22:17691372 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.386+2230C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691372 | |||||||
| chr22:17691532 | G | T | 2 | a0001c0001t0007g0247 a0001c0001t0007g0248 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.386+2390G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691532 | |||||||
| chr22:17691585 | G | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+2443G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691585 | |||||||
| chr22:17691595 | G | A | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+2453G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691595 | |||||||
| chr22:17691612 | C | T | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.386+2470C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691612 | |||||||
| chr22:17691651 | C | CA | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.386+2519dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17691651 | ||||||
| chr22:17691689 | T | G | 1 | a0001c0001t0007g0013 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.386+2547T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691689 | |||||||
| chr22:17691752 | T | C | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+2610T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691752 | |||||||
| chr22:17691763 | A | C | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.386+2621A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691763 | |||||||
| chr22:17691765 | A | G | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+2623A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691765 | |||||||
| chr22:17691819 | C | T | 1 | a0001c0002t0001g0203 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.386+2677C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691819 | |||||||
| chr22:17691868 | A | AT | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.386+2729dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17691868 | ||||||
| chr22:17691892 | A | G | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.386+2750A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691892 | |||||||
| chr22:17691945 | G | A | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.386+2803G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17691945 | |||||||
| chr22:17692015 | T | C | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.386+2873T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692015 | |||||||
| chr22:17692137 | A | G | 1 | a0001c0001t0010g0239 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.386+2995A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692137 | |||||||
| chr22:17692230 | A | G | 3 | a0001c0001t0002g0117 a0001c0001t0002g0130 a0001c0001t0002g0202 |
3 | HG00280.hp1 HG00639.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.386+3088A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692230 | |||||||
| chr22:17692264 | A | G | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.386+3122A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692264 | |||||||
| chr22:17692605 | T | C | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.386+3463T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692605 | |||||||
| chr22:17692784 | G | A | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.387-3357G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692784 | |||||||
| chr22:17692792 | A | T | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.387-3349A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692792 | |||||||
| chr22:17692915 | A | G | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-3226A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692915 | |||||||
| chr22:17692954 | G | A | 3 | a0001c0001t0002g0134 a0001c0001t0002g0188 a0001c0001t0002g0210 |
3 | HG03927.hp1 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.387-3187G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692954 | |||||||
| chr22:17692964 | C | T | 1 | a0001c0001t0005g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.387-3177C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17692964 | |||||||
| chr22:17693176 | G | A | 1 | a0001c0001t0017g0019 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.387-2965G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693176 | |||||||
| chr22:17693333 | G | GTTTA | 16 | a0001c0001t0002g0165 a0001c0001t0005g0241 a0001c0001t0007g0013 others(13): Show |
16 | HG00738.hp2 HG01192.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2779_387-2776d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693333 | ||||||
| chr22:17693333 | GTTTA | G | 13 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 others(10): Show |
13 | HG01255.hp2 HG02109.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.387-2779_387-2776d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693333 | ||||||
| chr22:17693333 | GTTTATTT others(5): Show |
G | 16 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0001c0002t0001g0203 others(13): Show |
16 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.387-2787_387-2776d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693333 | ||||||
| chr22:17693343 | T | G | 1 | a0005c0008t0019g0254 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.387-2798T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693343 | |||||||
| chr22:17693362 | T | G | 43 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(40): Show |
44 | HG00140.hp2 HG01243.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.387-2779T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693362 | |||||||
| chr22:17693364 | T | G | 43 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(40): Show |
44 | HG00140.hp2 HG01243.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.387-2777T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693364 | |||||||
| chr22:17693365 | A | G | 2 | a0001c0001t0009g0039 a0001c0001t0009g0041 |
2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.387-2776A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693365 | |||||||
| chr22:17693365 | A | T | 43 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(40): Show |
44 | HG00140.hp2 HG01243.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.387-2776A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693365 | |||||||
| chr22:17693365 | AGTG | A | 3 | a0001c0002t0006g0079 a0001c0002t0006g0082 a0001c0002t0014g0066 |
3 | HG03710.hp2 NA19240.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.387-2775_387-2773d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693365 | |||||||
| chr22:17693365 | AGTGTT | A | 16 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(13): Show |
16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2775_387-2771d others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693365 | |||||||
| chr22:17693366 | G | T | 43 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(40): Show |
44 | HG00140.hp2 HG01243.hp1 HG01496.hp2 others(41): Show |
intron_variant | MODIFIER | c.387-2775G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693366 | |||||||
| chr22:17693368 | G | T | 2 | a0001c0001t0009g0039 a0001c0001t0009g0041 |
2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.387-2773G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693368 | |||||||
| chr22:17693368 | GTTTGTTT others(3): Show |
G | 11 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(8): Show |
11 | HG00423.hp1 HG01109.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.387-2769_387-2760d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693368 | ||||||
| chr22:17693368 | GTTTGTTT others(6): Show |
G | 2 | a0001c0002t0006g0081 a0004c0006t0001g0096 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.387-2769_387-2757d others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693368 | ||||||
| chr22:17693368 | GTTTGTTT others(7): Show |
G | 3 | a0004c0006t0001g0093 a0004c0006t0049g0094 a0004c0006t0062g0095 |
3 | HG02280.hp2 HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.387-2769_387-2756d others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693368 | ||||||
| chr22:17693372 | G | A | 3 | a0001c0002t0006g0079 a0001c0002t0006g0082 a0001c0002t0014g0066 |
3 | HG03710.hp2 NA19240.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.387-2769G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | |||||||
| chr22:17693372 | G | GGTTT | 3 | a0001c0001t0003g0035 a0001c0001t0003g0250 a0007c0013t0003g0028 |
3 | HG02922.hp1 HG02965.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.387-2769_387-2768i others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | |||||||
| chr22:17693372 | G | GGTTTT | 15 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0029 others(12): Show |
15 | HG00140.hp2 HG01496.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.387-2769_387-2768i others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | |||||||
| chr22:17693372 | G | GGTTTTT | 24 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0031 others(21): Show |
25 | HG01981.hp1 HG02135.hp2 HG02572.hp2 others(22): Show |
intron_variant | MODIFIER | c.387-2769_387-2768i others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | |||||||
| chr22:17693372 | G | GT | 11 | a0001c0001t0007g0248 a0001c0002t0001g0098 a0001c0002t0001g0201 others(8): Show |
11 | HG00408.hp2 HG00639.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.387-2745dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693372 | ||||||
| chr22:17693372 | G | T | 24 | a0001c0001t0006g0077 a0001c0001t0009g0039 a0001c0001t0009g0041 others(21): Show |
24 | HG00099.hp2 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.387-2769G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693372 | |||||||
| chr22:17693372 | GT | G | 53 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0115 others(50): Show |
54 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.387-2745delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693372 | ||||||
| chr22:17693372 | GTT | G | 96 | a0001c0001t0002g0103 a0001c0001t0002g0114 a0001c0001t0002g0128 others(93): Show |
96 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.387-2746_387-2745d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17693372 | ||||||
| chr22:17693374 | T | A | 16 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(13): Show |
16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2767T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693374 | |||||||
| chr22:17693374 | T | G | 1 | a0001c0002t0052g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.387-2767T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693374 | |||||||
| chr22:17693376 | T | A | 3 | a0001c0002t0006g0079 a0001c0002t0006g0082 a0001c0002t0014g0066 |
3 | HG03710.hp2 NA19240.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.387-2765T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693376 | |||||||
| chr22:17693377 | T | A | 1 | a0001c0002t0037g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.387-2764T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693377 | |||||||
| chr22:17693377 | T | G | 2 | a0001c0001t0022g0237 a0001c0001t0022g0238 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.387-2764T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693377 | |||||||
| chr22:17693378 | T | A | 16 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(13): Show |
16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2763T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693378 | |||||||
| chr22:17693378 | T | G | 20 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(17): Show |
20 | HG01433.hp1 HG01978.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.387-2763T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693378 | |||||||
| chr22:17693379 | T | G | 16 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(13): Show |
16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.387-2762T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693379 | |||||||
| chr22:17693379 | T | TAG | 3 | a0001c0002t0006g0079 a0001c0002t0006g0082 a0001c0002t0014g0066 |
3 | HG03710.hp2 NA19240.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.387-2762_387-2761i others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693379 | |||||||
| chr22:17693380 | T | G | 1 | a0001c0002t0037g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.387-2761T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693380 | |||||||
| chr22:17693381 | T | G | 19 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(16): Show |
19 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.387-2760T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693381 | |||||||
| chr22:17693384 | T | G | 1 | a0001c0001t0034g0167 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387-2757T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693384 | |||||||
| chr22:17693526 | T | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-2615T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693526 | |||||||
| chr22:17693646 | C | G | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.387-2495C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693646 | |||||||
| chr22:17693670 | G | T | 1 | a0006c0010t0001g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.387-2471G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17693670 | |||||||
| chr22:17694033 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.387-2108C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694033 | |||||||
| chr22:17694098 | G | A | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.387-2043G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694098 | |||||||
| chr22:17694147 | T | A | 27 | a0001c0001t0006g0077 a0001c0001t0029g0168 a0001c0002t0006g0071 others(24): Show |
27 | HG00099.hp2 HG00609.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.387-1994T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694147 | |||||||
| chr22:17694326 | A | G | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.387-1815A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694326 | |||||||
| chr22:17694382 | T | C | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.387-1759T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694382 | |||||||
| chr22:17694506 | TA | T | 54 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(51): Show |
55 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.387-1624delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17694506 | ||||||
| chr22:17694517 | A | T | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.387-1624A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694517 | |||||||
| chr22:17694518 | T | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.387-1623T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694518 | |||||||
| chr22:17694553 | C | T | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-1588C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694553 | |||||||
| chr22:17694872 | T | G | 1 | a0001c0001t0002g0217 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.387-1269T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17694872 | |||||||
| chr22:17695011 | G | A | 1 | a0001c0001t0007g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.387-1130G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695011 | |||||||
| chr22:17695035 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1106G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695035 | |||||||
| chr22:17695036 | GC | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1103delC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr22 | 17695036 | ||||||
| chr22:17695040 | C | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1101C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695040 | |||||||
| chr22:17695042 | T | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1099T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695042 | |||||||
| chr22:17695044 | G | C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1097G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695044 | |||||||
| chr22:17695045 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1096C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695045 | |||||||
| chr22:17695046 | A | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1095A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695046 | |||||||
| chr22:17695049 | G | GGTTCC | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1092_387-1091i others(7): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695049 | |||||||
| chr22:17695050 | C | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.387-1091C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695050 | |||||||
| chr22:17695097 | G | A | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.387-1044G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695097 | |||||||
| chr22:17695216 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.387-925C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695216 | |||||||
| chr22:17695341 | G | A | 3 | a0001c0001t0008g0230 a0001c0001t0010g0221 a0001c0001t0010g0226 |
3 | NA18952.hp2 NA18956.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.387-800G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695341 | |||||||
| chr22:17695413 | C | T | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.387-728C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695413 | |||||||
| chr22:17695531 | A | C | 1 | a0001c0001t0003g0050 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.387-610A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695531 | |||||||
| chr22:17695571 | C | T | 1 | a0001c0001t0061g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.387-570C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695571 | |||||||
| chr22:17695627 | A | T | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.387-514A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695627 | |||||||
| chr22:17695682 | A | C | 1 | a0003c0004t0015g0083 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.387-459A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695682 | |||||||
| chr22:17695692 | T | C | 2 | a0001c0001t0007g0247 a0001c0001t0007g0248 |
2 | HG02717.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.387-449T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695692 | |||||||
| chr22:17695756 | C | T | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.387-385C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695756 | |||||||
| chr22:17695929 | T | G | 1 | a0001c0001t0004g0102 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.387-212T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695929 | |||||||
| chr22:17695983 | T | A | 1 | a0001c0001t0004g0102 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.387-158T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17695983 | |||||||
| chr22:17696019 | A | G | 2 | a0001c0002t0001g0288 a0001c0002t0001g0289 |
2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.387-122A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17696019 | |||||||
| chr22:17696071 | T | A | 1 | a0001c0001t0004g0102 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.387-70T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17696071 | |||||||
| chr22:17696093 | C | T | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.387-48C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 4/6 | chr22 | 17696093 | |||||||
| chr22:17696334 | T | C | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.456+124T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696334 | |||||||
| chr22:17696366 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.456+156C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696366 | |||||||
| chr22:17696367 | G | A | 2 | a0001c0001t0003g0050 a0001c0001t0003g0051 |
2 | NA18986.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.456+157G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696367 | |||||||
| chr22:17696449 | C | G | 1 | a0001c0002t0027g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.456+239C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696449 | |||||||
| chr22:17696623 | G | A | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.456+413G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696623 | |||||||
| chr22:17696633 | C | T | 71 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(68): Show |
72 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.456+423C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696633 | |||||||
| chr22:17696636 | T | A | 1 | a0001c0001t0004g0102 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.456+426T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696636 | |||||||
| chr22:17696706 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+496G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696706 | |||||||
| chr22:17696847 | G | T | 1 | a0001c0001t0003g0054 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.456+637G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696847 | |||||||
| chr22:17696883 | G | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.456+673G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696883 | |||||||
| chr22:17696983 | T | G | 1 | a0007c0013t0003g0028 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.456+773T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17696983 | |||||||
| chr22:17697137 | T | TA | 19 | a0001c0001t0020g0225 a0001c0001t0020g0231 a0001c0001t0020g0233 others(16): Show |
19 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.456+942dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17697137 | ||||||
| chr22:17697137 | TA | T | 11 | a0001c0001t0002g0130 a0001c0001t0002g0218 a0001c0001t0003g0051 others(8): Show |
11 | HG00323.hp1 HG00639.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.456+942delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17697137 | ||||||
| chr22:17697475 | G | A | 1 | a0001c0001t0007g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.456+1265G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697475 | |||||||
| chr22:17697631 | A | G | 44 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(41): Show |
45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.456+1421A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697631 | |||||||
| chr22:17697801 | G | C | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.456+1591G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697801 | |||||||
| chr22:17697826 | T | TTTTA | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.456+1632_456+1635d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17697826 | ||||||
| chr22:17697846 | T | A | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.456+1636T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697846 | |||||||
| chr22:17697932 | G | A | 1 | a0001c0002t0037g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.456+1722G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17697932 | |||||||
| chr22:17698094 | G | A | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.456+1884G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698094 | |||||||
| chr22:17698145 | T | C | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.456+1935T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698145 | |||||||
| chr22:17698179 | C | T | 1 | a0001c0002t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.456+1969C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698179 | |||||||
| chr22:17698368 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+2158G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698368 | |||||||
| chr22:17698487 | A | C | 1 | a0001c0001t0013g0179 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.456+2277A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698487 | |||||||
| chr22:17698506 | C | T | 5 | a0001c0001t0002g0117 a0001c0001t0002g0130 a0001c0001t0002g0202 others(2): Show |
5 | HG00280.hp1 HG00323.hp1 HG00639.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+2296C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698506 | |||||||
| chr22:17698507 | G | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.456+2297G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698507 | |||||||
| chr22:17698511 | A | G | 3 | a0001c0001t0008g0223 a0001c0001t0008g0227 a0001c0001t0038g0229 |
3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.456+2301A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698511 | |||||||
| chr22:17698554 | CT | C | 7 | a0001c0001t0003g0053 a0004c0006t0001g0093 a0004c0006t0001g0096 others(4): Show |
7 | HG02280.hp2 HG02965.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.456+2346delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17698554 | ||||||
| chr22:17698555 | T | TA | 135 | a0001c0001t0002g0100 a0001c0001t0002g0103 a0001c0001t0002g0114 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.456+2345_456+2346i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698555 | |||||||
| chr22:17698555 | T | TAA | 42 | a0001c0001t0002g0134 a0001c0001t0002g0151 a0001c0001t0002g0172 others(39): Show |
42 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.456+2345_456+2346i others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698555 | |||||||
| chr22:17698555 | T | TAAA | 3 | a0001c0001t0004g0137 a0001c0001t0013g0236 a0003c0004t0016g0090 |
3 | HG01934.hp2 NA18957.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.456+2345_456+2346i others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698555 | |||||||
| chr22:17698556 | T | A | 244 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(241): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.456+2346T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698556 | |||||||
| chr22:17698667 | T | A | 2 | a0001c0001t0005g0062 a0001c0001t0005g0063 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.456+2457T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698667 | |||||||
| chr22:17698725 | T | G | 3 | a0001c0001t0002g0103 a0001c0001t0002g0216 a0001c0001t0002g0218 |
3 | NA18968.hp1 NA18974.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.456+2515T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698725 | |||||||
| chr22:17698855 | T | C | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.456+2645T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698855 | |||||||
| chr22:17698979 | A | G | 1 | a0001c0001t0018g0214 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.456+2769A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17698979 | |||||||
| chr22:17699103 | A | G | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.456+2893A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699103 | |||||||
| chr22:17699218 | T | G | 44 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(41): Show |
45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.456+3008T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699218 | |||||||
| chr22:17699445 | CAA | C | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.457-2796_457-2795d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17699445 | ||||||
| chr22:17699542 | A | G | 1 | a0001c0001t0007g0017 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.457-2701A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699542 | |||||||
| chr22:17699588 | A | G | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.457-2655A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699588 | |||||||
| chr22:17699595 | G | A | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.457-2648G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699595 | |||||||
| chr22:17699811 | T | C | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.457-2432T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699811 | |||||||
| chr22:17699889 | T | C | 1 | a0005c0008t0019g0255 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.457-2354T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699889 | |||||||
| chr22:17699890 | C | T | 3 | a0001c0002t0001g0284 a0001c0002t0001g0288 a0001c0002t0001g0289 |
3 | HG02683.hp2 HG03831.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.457-2353C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17699890 | |||||||
| chr22:17700055 | T | A | 1 | a0001c0001t0004g0102 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.457-2188T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700055 | |||||||
| chr22:17700073 | A | G | 2 | a0002c0003t0001g0290 a0002c0003t0001g0291 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.457-2170A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700073 | |||||||
| chr22:17700321 | G | T | 1 | a0002c0003t0001g0003 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.457-1922G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700321 | |||||||
| chr22:17700326 | A | G | 1 | a0001c0001t0002g0182 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.457-1917A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700326 | |||||||
| chr22:17700737 | G | C | 1 | a0001c0001t0053g0125 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.457-1506G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700737 | |||||||
| chr22:17700857 | G | C | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.457-1386G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700857 | |||||||
| chr22:17700908 | T | C | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.457-1335T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700908 | |||||||
| chr22:17700958 | G | T | 12 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0030 others(9): Show |
12 | HG02572.hp2 HG02630.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.457-1285G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17700958 | |||||||
| chr22:17701018 | A | G | 1 | a0001c0001t0004g0132 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.457-1225A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701018 | |||||||
| chr22:17701245 | G | A | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.457-998G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701245 | |||||||
| chr22:17701268 | A | C | 1 | a0001c0001t0010g0226 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.457-975A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701268 | |||||||
| chr22:17701403 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.457-840C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701403 | |||||||
| chr22:17701404 | G | A | 1 | a0001c0001t0013g0192 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.457-839G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701404 | |||||||
| chr22:17701447 | A | G | 1 | a0001c0002t0027g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.457-796A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701447 | |||||||
| chr22:17701482 | A | G | 1 | a0001c0001t0011g0116 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.457-761A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701482 | |||||||
| chr22:17701524 | T | C | 254 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.457-719T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701524 | |||||||
| chr22:17701529 | T | C | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.457-714T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701529 | |||||||
| chr22:17701757 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.457-486C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701757 | |||||||
| chr22:17701851 | G | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.457-392G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701851 | |||||||
| chr22:17701863 | G | A | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.457-380G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701863 | |||||||
| chr22:17701882 | C | T | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.457-361C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17701882 | |||||||
| chr22:17701915 | C | CAA | 43 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(40): Show |
44 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(41): Show |
intron_variant | MODIFIER | c.457-311_457-310dup others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17701915 | ||||||
| chr22:17701915 | CA | C | 166 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(163): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.457-310delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17701915 | ||||||
| chr22:17701915 | CAA | C | 6 | a0001c0001t0005g0140 a0001c0001t0005g0242 a0001c0001t0028g0297 others(3): Show |
6 | HG00408.hp1 HG02572.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.457-311_457-310del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr22 | 17701915 | ||||||
| chr22:17702075 | C | G | 3 | a0001c0001t0008g0223 a0001c0001t0008g0227 a0001c0001t0038g0229 |
3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.457-168C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 5/6 | chr22 | 17702075 | |||||||
| chr22:17702592 | A | G | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+206A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17702592 | |||||||
| chr22:17702803 | G | A | 2 | a0001c0001t0022g0237 a0001c0001t0022g0238 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.600+417G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17702803 | |||||||
| chr22:17702953 | G | T | 3 | a0001c0001t0008g0223 a0001c0001t0008g0227 a0001c0001t0038g0229 |
3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.600+567G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17702953 | |||||||
| chr22:17703032 | G | A | 1 | a0001c0002t0006g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.600+646G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703032 | |||||||
| chr22:17703053 | G | A | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+667G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703053 | |||||||
| chr22:17703162 | AAT | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.600+786_600+787del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703162 | ||||||
| chr22:17703168 | T | TACACACA others(7): Show |
3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+783_600+784ins others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703168 | ||||||
| chr22:17703168 | T | TACACACA others(9): Show |
4 | a0001c0002t0012g0008 a0001c0002t0012g0300 a0001c0002t0012g0301 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+783_600+784ins others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703168 | ||||||
| chr22:17703168 | T | TACACACA others(11): Show |
1 | a0001c0002t0012g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.600+783_600+784ins others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703168 | ||||||
| chr22:17703170 | T | C | 12 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(9): Show |
12 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.600+784T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703170 | |||||||
| chr22:17703172 | T | C | 15 | a0001c0001t0003g0026 a0001c0001t0003g0056 a0001c0001t0003g0057 others(12): Show |
15 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+786T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703172 | |||||||
| chr22:17703172 | T | TACACACA others(5): Show |
18 | a0001c0001t0006g0077 a0001c0001t0024g0243 a0001c0001t0024g0244 others(15): Show |
18 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.600+792_600+803dup others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703172 | ||||||
| chr22:17703172 | T | TACACACA others(7): Show |
5 | a0001c0002t0006g0071 a0001c0002t0006g0072 a0001c0002t0006g0079 others(2): Show |
5 | HG01261.hp2 HG02071.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.600+790_600+803dup others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703172 | ||||||
| chr22:17703190 | T | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+804T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703190 | |||||||
| chr22:17703191 | ATG | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+807_600+808del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703191 | ||||||
| chr22:17703194 | T | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+808T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703194 | |||||||
| chr22:17703355 | A | G | 2 | a0001c0001t0002g0153 a0001c0001t0002g0209 |
2 | HG01074.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.600+969A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703355 | |||||||
| chr22:17703413 | G | A | 23 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(20): Show |
23 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.600+1027G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703413 | |||||||
| chr22:17703475 | C | CTCTT | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+1099_600+1102d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17703475 | ||||||
| chr22:17703683 | C | T | 3 | a0001c0007t0009g0040 a0001c0007t0009g0059 a0001c0007t0044g0033 |
3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.600+1297C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703683 | |||||||
| chr22:17703919 | A | G | 2 | a0001c0002t0001g0279 a0001c0002t0001g0283 |
2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.600+1533A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17703919 | |||||||
| chr22:17704039 | C | T | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.600+1653C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704039 | |||||||
| chr22:17704257 | T | C | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+1871T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704257 | |||||||
| chr22:17704282 | C | T | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+1896C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704282 | |||||||
| chr22:17704431 | A | G | 1 | a0001c0001t0002g0217 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.600+2045A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704431 | |||||||
| chr22:17704450 | C | T | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+2064C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704450 | |||||||
| chr22:17704464 | C | T | 1 | a0001c0001t0023g0108 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.600+2078C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704464 | |||||||
| chr22:17704551 | G | A | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.600+2165G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704551 | |||||||
| chr22:17704563 | G | A | 1 | a0006c0010t0001g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.600+2177G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704563 | |||||||
| chr22:17704670 | GT | G | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+2285delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17704670 | |||||||
| chr22:17704987 | C | CA | 7 | a0001c0001t0005g0012 a0001c0001t0007g0111 a0001c0001t0007g0112 others(4): Show |
7 | HG01255.hp2 HG02109.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+2615dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17704987 | ||||||
| chr22:17704987 | CA | C | 33 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(30): Show |
33 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.600+2615delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17704987 | ||||||
| chr22:17705113 | T | TA | 147 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0114 others(144): Show |
148 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.600+2737dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17705113 | ||||||
| chr22:17705113 | TA | T | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.600+2737delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17705113 | ||||||
| chr22:17705127 | T | C | 1 | a0001c0002t0027g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.600+2741T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705127 | |||||||
| chr22:17705300 | AT | A | 24 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(21): Show |
24 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(21): Show |
intron_variant | MODIFIER | c.600+2929delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17705300 | ||||||
| chr22:17705699 | C | T | 1 | a0001c0001t0018g0195 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.600+3313C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705699 | |||||||
| chr22:17705703 | T | A | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+3317T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705703 | |||||||
| chr22:17705759 | T | C | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+3373T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705759 | |||||||
| chr22:17705784 | C | T | 1 | a0001c0001t0006g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.600+3398C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17705784 | |||||||
| chr22:17706058 | G | A | 1 | a0001c0001t0007g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.600+3672G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706058 | |||||||
| chr22:17706135 | C | G | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.600+3749C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706135 | |||||||
| chr22:17706158 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.600+3772G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706158 | |||||||
| chr22:17706210 | A | G | 1 | a0001c0001t0039g0194 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.600+3824A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706210 | |||||||
| chr22:17706223 | T | C | 134 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(131): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.600+3837T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706223 | |||||||
| chr22:17706279 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+3893G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706279 | |||||||
| chr22:17706329 | GT | G | 9 | a0001c0001t0003g0027 a0001c0001t0003g0030 a0001c0001t0003g0031 others(6): Show |
9 | HG02572.hp2 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+3958delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17706329 | ||||||
| chr22:17706414 | C | G | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+4028C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706414 | |||||||
| chr22:17706530 | T | C | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+4144T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706530 | |||||||
| chr22:17706584 | G | A | 6 | a0001c0001t0007g0111 a0001c0001t0007g0112 a0001c0001t0007g0121 others(3): Show |
6 | HG01255.hp2 HG02109.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+4198G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706584 | |||||||
| chr22:17706703 | G | A | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+4317G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706703 | |||||||
| chr22:17706751 | T | C | 1 | a0001c0001t0011g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.600+4365T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706751 | |||||||
| chr22:17706778 | G | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.600+4392G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706778 | |||||||
| chr22:17706998 | A | G | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0048g0126 |
3 | HG01070.hp1 HG01071.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.600+4612A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17706998 | |||||||
| chr22:17707181 | GA | G | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.600+4799delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17707181 | ||||||
| chr22:17707259 | C | T | 2 | a0001c0002t0012g0300 a0001c0002t0012g0301 |
2 | HG02055.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.600+4873C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707259 | |||||||
| chr22:17707359 | G | A | 1 | a0001c0002t0037g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.600+4973G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707359 | |||||||
| chr22:17707397 | G | A | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+5011G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707397 | |||||||
| chr22:17707548 | T | C | 4 | a0001c0002t0014g0065 a0001c0002t0014g0066 a0001c0002t0014g0067 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+5162T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707548 | |||||||
| chr22:17707623 | G | A | 2 | a0001c0001t0022g0237 a0001c0001t0022g0238 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.600+5237G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17707623 | |||||||
| chr22:17708011 | G | A | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.600+5625G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17708011 | |||||||
| chr22:17708323 | A | G | 1 | a0001c0002t0014g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.600+5937A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17708323 | |||||||
| chr22:17708329 | T | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+5943T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17708329 | |||||||
| chr22:17708654 | C | T | 1 | a0001c0001t0004g0101 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.600+6268C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17708654 | |||||||
| chr22:17709062 | C | T | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+6676C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709062 | |||||||
| chr22:17709152 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+6766C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709152 | |||||||
| chr22:17709185 | A | G | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.600+6799A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709185 | |||||||
| chr22:17709305 | A | G | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+6919A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709305 | |||||||
| chr22:17709370 | A | G | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.600+6984A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709370 | |||||||
| chr22:17709385 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.600+6999C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709385 | |||||||
| chr22:17709641 | C | G | 3 | a0001c0007t0009g0040 a0001c0007t0009g0059 a0001c0007t0044g0033 |
3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.600+7255C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709641 | |||||||
| chr22:17709750 | C | G | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.600+7364C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709750 | |||||||
| chr22:17709767 | G | A | 5 | a0001c0001t0003g0026 a0001c0001t0003g0055 a0001c0001t0003g0056 others(2): Show |
5 | NA18963.hp2 NA18974.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+7381G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17709767 | |||||||
| chr22:17710053 | G | A | 1 | a0001c0002t0001g0201 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.600+7667G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710053 | |||||||
| chr22:17710067 | T | TA | 40 | a0001c0001t0002g0114 a0001c0001t0002g0128 a0001c0001t0002g0144 others(37): Show |
40 | HG01070.hp1 HG01109.hp1 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.600+7706dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | ||||||
| chr22:17710067 | T | TAA | 131 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.600+7705_600+7706d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | ||||||
| chr22:17710067 | T | TAAA | 16 | a0001c0001t0002g0134 a0001c0001t0002g0188 a0001c0001t0002g0207 others(13): Show |
16 | HG00738.hp2 HG01192.hp1 HG02602.hp1 others(13): Show |
intron_variant | MODIFIER | c.600+7704_600+7706d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | ||||||
| chr22:17710067 | TA | T | 44 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(41): Show |
45 | HG00140.hp2 HG00733.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.600+7706delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | ||||||
| chr22:17710067 | TAAAAAAA others(5): Show |
T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+7695_600+7706d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17710067 | ||||||
| chr22:17710302 | C | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.600+7916C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710302 | |||||||
| chr22:17710350 | G | A | 16 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(13): Show |
16 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.600+7964G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710350 | |||||||
| chr22:17710395 | T | C | 1 | a0001c0001t0007g0099 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.600+8009T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710395 | |||||||
| chr22:17710433 | C | A | 2 | a0001c0001t0005g0062 a0001c0001t0005g0063 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.600+8047C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710433 | |||||||
| chr22:17710448 | C | T | 1 | a0001c0002t0012g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.600+8062C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710448 | |||||||
| chr22:17710449 | G | A | 1 | a0004c0006t0001g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.600+8063G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710449 | |||||||
| chr22:17710454 | C | G | 1 | a0001c0002t0006g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.600+8068C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710454 | |||||||
| chr22:17710474 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.600+8088G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710474 | |||||||
| chr22:17710520 | C | T | 1 | a0001c0002t0001g0289 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.600+8134C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710520 | |||||||
| chr22:17710540 | A | T | 13 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0017 others(10): Show |
13 | HG01192.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.600+8154A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710540 | |||||||
| chr22:17710583 | A | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.600+8197A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710583 | |||||||
| chr22:17710615 | G | A | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+8229G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710615 | |||||||
| chr22:17710642 | C | A | 3 | a0001c0001t0008g0223 a0001c0001t0008g0227 a0001c0001t0038g0229 |
3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.600+8256C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710642 | |||||||
| chr22:17710656 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.600+8270C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710656 | |||||||
| chr22:17710753 | C | T | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.600+8367C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710753 | |||||||
| chr22:17710794 | A | G | 250 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.600+8408A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710794 | |||||||
| chr22:17710824 | T | C | 1 | a0001c0002t0014g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.600+8438T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710824 | |||||||
| chr22:17710872 | G | A | 1 | a0001c0001t0002g0208 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.600+8486G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710872 | |||||||
| chr22:17710897 | A | T | 6 | a0001c0007t0009g0040 a0001c0007t0009g0059 a0001c0007t0044g0033 others(3): Show |
6 | HG02965.hp2 HG03130.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.600+8511A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710897 | |||||||
| chr22:17710901 | T | A | 15 | a0001c0001t0002g0139 a0002c0003t0001g0261 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG00733.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.600+8515T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710901 | |||||||
| chr22:17710941 | C | T | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+8555C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710941 | |||||||
| chr22:17710984 | G | A | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.600+8598G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17710984 | |||||||
| chr22:17711066 | A | T | 1 | a0001c0002t0027g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.600+8680A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711066 | |||||||
| chr22:17711067 | A | T | 1 | a0001c0002t0027g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.600+8681A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711067 | |||||||
| chr22:17711304 | C | CCTTTTTT others(7): Show |
1 | a0001c0001t0003g0055 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.600+8918_600+8919i others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711304 | |||||||
| chr22:17711304 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0003g0032 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.600+8919_600+8929d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | ||||||
| chr22:17711304 | C | CTTTTTTT others(5): Show |
35 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(32): Show |
36 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(33): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | ||||||
| chr22:17711304 | C | CTTTTTTT others(6): Show |
13 | a0001c0001t0003g0027 a0001c0001t0003g0042 a0001c0001t0003g0052 others(10): Show |
13 | HG01243.hp1 HG01496.hp2 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | ||||||
| chr22:17711304 | C | CTTTTTTT others(7): Show |
24 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(21): Show |
24 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | ||||||
| chr22:17711304 | C | CTTTTTTT others(8): Show |
14 | a0001c0002t0006g0082 a0001c0002t0012g0300 a0003c0004t0015g0083 others(11): Show |
14 | HG01074.hp2 HG01081.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | ||||||
| chr22:17711304 | C | CTTTTTTT others(9): Show |
4 | a0003c0004t0016g0090 a0003c0004t0016g0092 a0003c0005t0006g0085 others(1): Show |
4 | HG00423.hp1 HG01361.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+8929_600+8930i others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | ||||||
| chr22:17711304 | C | CTTTTTTT others(10): Show |
1 | a0003c0004t0030g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.600+8929_600+8930i others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17711304 | ||||||
| chr22:17711344 | C | T | 2 | a0001c0001t0022g0237 a0001c0001t0022g0238 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.600+8958C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711344 | |||||||
| chr22:17711422 | T | C | 94 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(91): Show |
95 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.600+9036T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711422 | |||||||
| chr22:17711604 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.600+9218G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711604 | |||||||
| chr22:17711848 | T | G | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+9462T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711848 | |||||||
| chr22:17711898 | A | G | 1 | a0001c0001t0003g0048 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.600+9512A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17711898 | |||||||
| chr22:17712024 | G | GT | 9 | a0001c0001t0002g0134 a0001c0001t0002g0188 a0001c0001t0004g0185 others(6): Show |
9 | HG02683.hp1 HG02738.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.600+9650dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17712024 | ||||||
| chr22:17712305 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.600+9919C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712305 | |||||||
| chr22:17712339 | A | G | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.600+9953A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712339 | |||||||
| chr22:17712792 | T | C | 1 | a0001c0001t0007g0017 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.600+10406T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712792 | |||||||
| chr22:17712817 | T | G | 4 | a0001c0001t0004g0164 a0001c0001t0013g0179 a0001c0001t0013g0180 others(1): Show |
4 | HG02132.hp2 NA18943.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+10431T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712817 | |||||||
| chr22:17712922 | C | T | 3 | a0001c0001t0003g0049 a0001c0001t0009g0039 a0001c0001t0009g0041 |
3 | HG00733.hp1 HG01168.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.600+10536C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712922 | |||||||
| chr22:17712994 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.600+10608G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17712994 | |||||||
| chr22:17713039 | C | T | 1 | a0006c0010t0001g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.600+10653C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713039 | |||||||
| chr22:17713238 | A | G | 3 | a0001c0002t0026g0293 a0001c0002t0026g0294 a0001c0002t0035g0296 |
3 | HG02258.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.600+10852A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713238 | |||||||
| chr22:17713240 | A | G | 1 | a0001c0001t0011g0158 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.600+10854A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713240 | |||||||
| chr22:17713282 | G | C | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+10896G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713282 | |||||||
| chr22:17713310 | A | G | 2 | a0001c0001t0005g0120 a0001c0001t0005g0161 |
2 | NA18956.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.600+10924A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713310 | |||||||
| chr22:17713359 | T | C | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+10973T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713359 | |||||||
| chr22:17713362 | T | G | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.600+10976T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713362 | |||||||
| chr22:17713460 | A | AT | 138 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0114 others(135): Show |
139 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.600+11092dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17713460 | ||||||
| chr22:17713460 | A | ATT | 20 | a0001c0001t0002g0134 a0001c0001t0002g0186 a0001c0001t0002g0205 others(17): Show |
20 | HG00408.hp1 HG00438.hp2 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.600+11091_600+1109 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17713460 | ||||||
| chr22:17713460 | AT | A | 57 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(54): Show |
58 | HG00140.hp2 HG00423.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.600+11092delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17713460 | ||||||
| chr22:17713460 | ATT | A | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+11091_600+1109 others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17713460 | ||||||
| chr22:17713473 | T | G | 18 | a0002c0003t0001g0003 a0002c0003t0001g0005 a0002c0003t0001g0261 others(15): Show |
19 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.600+11087T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713473 | |||||||
| chr22:17713500 | C | T | 1 | a0001c0001t0005g0187 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.600+11114C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713500 | |||||||
| chr22:17713571 | C | G | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+11185C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713571 | |||||||
| chr22:17713740 | A | G | 1 | a0001c0001t0041g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.600+11354A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713740 | |||||||
| chr22:17713752 | G | A | 1 | a0002c0003t0001g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.600+11366G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713752 | |||||||
| chr22:17713913 | G | A | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+11527G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713913 | |||||||
| chr22:17713993 | A | T | 4 | a0001c0002t0014g0068 a0001c0007t0009g0040 a0001c0007t0009g0059 others(1): Show |
4 | HG02717.hp1 HG03130.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.600+11607A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17713993 | |||||||
| chr22:17714019 | C | T | 3 | a0001c0002t0026g0293 a0001c0002t0026g0294 a0001c0002t0035g0296 |
3 | HG02258.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.600+11633C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714019 | |||||||
| chr22:17714020 | G | A | 1 | a0001c0001t0007g0122 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.600+11634G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714020 | |||||||
| chr22:17714060 | G | A | 3 | a0001c0001t0008g0223 a0001c0001t0008g0227 a0001c0001t0038g0229 |
3 | HG03041.hp1 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.600+11674G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714060 | |||||||
| chr22:17714065 | A | G | 46 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(43): Show |
47 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(44): Show |
intron_variant | MODIFIER | c.600+11679A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714065 | |||||||
| chr22:17714109 | T | C | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.600+11723T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714109 | |||||||
| chr22:17714147 | G | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+11761G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714147 | |||||||
| chr22:17714157 | G | A | 12 | a0001c0002t0001g0256 a0001c0002t0001g0257 a0001c0002t0001g0258 others(9): Show |
12 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(9): Show |
intron_variant | MODIFIER | c.600+11771G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714157 | |||||||
| chr22:17714287 | C | T | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+11901C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714287 | |||||||
| chr22:17714346 | G | A | 1 | a0001c0001t0047g0129 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.600+11960G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714346 | |||||||
| chr22:17714366 | C | T | 1 | a0001c0001t0007g0247 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.600+11980C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714366 | |||||||
| chr22:17714395 | C | T | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.600+12009C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714395 | |||||||
| chr22:17714406 | G | C | 250 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(247): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.600+12020G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714406 | |||||||
| chr22:17714406 | G | T | 1 | a0001c0001t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.600+12020G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714406 | |||||||
| chr22:17714412 | A | G | 2 | a0001c0001t0003g0042 a0001c0001t0003g0043 |
2 | NA18955.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.600+12026A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714412 | |||||||
| chr22:17714434 | A | C | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.600+12048A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714434 | |||||||
| chr22:17714497 | A | G | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.600+12111A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714497 | |||||||
| chr22:17714571 | G | A | 1 | a0001c0001t0005g0162 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.601-12106G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714571 | |||||||
| chr22:17714590 | C | T | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.601-12087C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714590 | |||||||
| chr22:17714858 | A | G | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-11819A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714858 | |||||||
| chr22:17714970 | G | A | 1 | a0001c0001t0005g0220 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.601-11707G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17714970 | |||||||
| chr22:17715121 | TTTATATA others(8): Show |
T | 1 | a0001c0001t0010g0235 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.601-11554_601-1154 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715121 | ||||||
| chr22:17715122 | T | A | 1 | a0001c0001t0003g0007 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601-11555T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715122 | |||||||
| chr22:17715122 | T | TTATATAT others(3): Show |
1 | a0002c0003t0001g0269 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.601-11515_601-1150 others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | T | TTATATAT others(5): Show |
1 | a0002c0003t0001g0271 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.601-11517_601-1150 others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | T | TTATATAT others(11): Show |
1 | a0001c0002t0001g0257 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.601-11523_601-1150 others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | T | TTATATAT others(13): Show |
1 | a0001c0002t0001g0278 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.601-11525_601-1150 others(24): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | T | TTATATAT others(19): Show |
1 | a0001c0002t0001g0268 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.601-11531_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | TTATATAT others(3): Show |
T | 1 | a0001c0001t0046g0046 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.601-11515_601-1150 others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | TTATATAT others(7): Show |
T | 1 | a0001c0002t0026g0293 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.601-11519_601-1150 others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | TTATATAT others(13): Show |
T | 2 | a0001c0001t0003g0052 a0001c0001t0010g0221 |
2 | HG02135.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.601-11525_601-1150 others(24): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | TTATATAT others(15): Show |
T | 3 | a0001c0001t0010g0226 a0004c0006t0001g0096 a0007c0013t0003g0028 |
3 | HG02922.hp1 HG03516.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.601-11527_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | TTATATAT others(17): Show |
T | 2 | a0001c0002t0035g0296 a0001c0007t0044g0033 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.601-11529_601-1150 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | TTATATAT others(19): Show |
T | 4 | a0001c0001t0002g0134 a0001c0001t0002g0210 a0001c0001t0032g0146 others(1): Show |
4 | HG00423.hp2 HG03927.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11531_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | TTATATAT others(21): Show |
T | 15 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0191 others(12): Show |
15 | HG01109.hp1 HG01255.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-11533_601-1150 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715122 | TTATATAT others(23): Show |
T | 4 | a0001c0001t0005g0161 a0001c0001t0007g0013 a0001c0001t0007g0014 others(1): Show |
4 | HG01256.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11535_601-1150 others(34): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715122 | ||||||
| chr22:17715136 | ATATATAT others(31): Show |
A | 1 | a0001c0001t0003g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.601-11539_601-1150 others(42): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715136 | ||||||
| chr22:17715140 | ATATATAT others(34): Show |
A | 1 | a0001c0014t0007g0015 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.601-11535_601-1149 others(45): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715140 | ||||||
| chr22:17715141 | TATATATA others(18): Show |
T | 1 | a0001c0001t0004g0152 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.601-11535_601-1151 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715141 | |||||||
| chr22:17715141 | TATATATA others(20): Show |
T | 7 | a0001c0001t0004g0102 a0001c0001t0004g0132 a0001c0001t0004g0163 others(4): Show |
7 | HG00438.hp1 HG02135.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-11535_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715141 | |||||||
| chr22:17715141 | TATATATA others(22): Show |
T | 2 | a0001c0001t0005g0120 a0001c0001t0011g0166 |
2 | NA18979.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.601-11535_601-1150 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715141 | |||||||
| chr22:17715142 | ATATATAT others(22): Show |
A | 2 | a0001c0001t0017g0019 a0001c0001t0017g0020 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.601-11533_601-1150 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715142 | ||||||
| chr22:17715143 | TATATATA others(18): Show |
T | 2 | a0001c0001t0004g0185 a0001c0007t0009g0059 |
2 | HG02738.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.601-11533_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715143 | |||||||
| chr22:17715143 | TATATATA others(20): Show |
T | 6 | a0001c0001t0004g0101 a0001c0001t0004g0148 a0001c0001t0004g0150 others(3): Show |
6 | HG01256.hp1 HG01258.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-11533_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715143 | |||||||
| chr22:17715144 | ATATATAT others(20): Show |
A | 9 | a0001c0001t0002g0160 a0001c0001t0004g0137 a0001c0001t0005g0143 others(6): Show |
9 | HG00609.hp2 HG00738.hp2 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-11531_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | ||||||
| chr22:17715144 | ATATATAT others(21): Show |
A | 8 | a0001c0001t0004g0124 a0001c0001t0004g0177 a0001c0001t0005g0169 others(5): Show |
8 | HG01516.hp1 HG02071.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-11531_601-1150 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | ||||||
| chr22:17715144 | ATATATAT others(22): Show |
A | 3 | a0001c0001t0005g0183 a0001c0001t0017g0025 a0001c0001t0063g0299 |
3 | HG02109.hp1 HG03130.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.601-11531_601-1150 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | ||||||
| chr22:17715144 | ATATATAT others(23): Show |
A | 1 | a0001c0001t0007g0248 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.601-11531_601-1150 others(34): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | ||||||
| chr22:17715144 | ATATATAT others(28): Show |
A | 1 | a0005c0008t0019g0295 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.601-11531_601-1149 others(39): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715144 | ||||||
| chr22:17715145 | TATATATA others(18): Show |
T | 1 | a0001c0007t0009g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.601-11531_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715145 | |||||||
| chr22:17715146 | ATATATAT others(18): Show |
A | 1 | a0001c0001t0002g0159 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.601-11529_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | ||||||
| chr22:17715146 | ATATATAT others(19): Show |
A | 10 | a0001c0001t0002g0205 a0001c0001t0002g0207 a0001c0001t0002g0212 others(7): Show |
10 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-11529_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | ||||||
| chr22:17715146 | ATATATAT others(20): Show |
A | 24 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0117 others(21): Show |
25 | HG00099.hp1 HG00544.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.601-11529_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | ||||||
| chr22:17715146 | ATATATAT others(21): Show |
A | 8 | a0001c0001t0002g0123 a0001c0001t0005g0012 a0001c0001t0007g0112 others(5): Show |
8 | HG02559.hp1 HG02622.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-11529_601-1150 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | ||||||
| chr22:17715146 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0005g0145 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.601-11529_601-1150 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | ||||||
| chr22:17715146 | ATATATAT others(27): Show |
A | 1 | a0001c0002t0012g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.601-11529_601-1149 others(38): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715146 | ||||||
| chr22:17715148 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0005g0242 a0003c0004t0031g0253 |
2 | HG00408.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.601-11527_601-1150 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715148 | ATATATAT others(17): Show |
A | 4 | a0001c0001t0003g0031 a0001c0001t0003g0032 a0001c0001t0003g0045 others(1): Show |
4 | HG01981.hp1 HG02572.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-11527_601-1150 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715148 | ATATATAT others(18): Show |
A | 5 | a0001c0001t0004g0164 a0001c0001t0047g0129 a0002c0003t0001g0005 others(2): Show |
5 | HG00323.hp1 HG01361.hp1 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-11527_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715148 | ATATATAT others(19): Show |
A | 4 | a0001c0001t0002g0103 a0001c0001t0002g0186 a0001c0001t0007g0111 others(1): Show |
4 | HG03492.hp2 HG03831.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11527_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715148 | ATATATAT others(20): Show |
A | 7 | a0001c0001t0002g0130 a0001c0001t0002g0147 a0001c0001t0002g0174 others(4): Show |
7 | HG00280.hp1 HG00639.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-11527_601-1150 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715148 | ATATATAT others(21): Show |
A | 2 | a0001c0001t0005g0170 a0001c0001t0007g0121 |
2 | HG03017.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.601-11527_601-1150 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715148 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0056g0204 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.601-11527_601-1149 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715148 | ATATATAT others(24): Show |
A | 1 | a0001c0001t0022g0237 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.601-11527_601-1149 others(35): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715148 | ATATATAT others(25): Show |
A | 1 | a0001c0001t0022g0238 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.601-11527_601-1149 others(36): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715148 | ATATATAT others(27): Show |
A | 2 | a0001c0002t0012g0300 a0001c0002t0042g0010 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.601-11527_601-1149 others(38): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715148 | ||||||
| chr22:17715150 | ATATATAT others(14): Show |
A | 3 | a0001c0001t0008g0228 a0001c0001t0008g0230 a0001c0001t0020g0225 |
3 | HG02698.hp2 HG02818.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.601-11525_601-1150 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715150 | ATATATAT others(15): Show |
A | 4 | a0001c0001t0003g0054 a0001c0001t0013g0179 a0001c0001t0013g0236 others(1): Show |
4 | NA18979.hp2 NA19077.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11525_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715150 | ATATATAT others(16): Show |
A | 8 | a0001c0001t0003g0026 a0001c0001t0003g0027 a0001c0001t0003g0050 others(5): Show |
8 | HG01109.hp2 HG03098.hp1 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-11525_601-1150 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715150 | ATATATAT others(17): Show |
A | 19 | a0001c0001t0003g0001 a0001c0001t0003g0030 a0001c0001t0003g0038 others(16): Show |
20 | HG00140.hp2 HG00733.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.601-11525_601-1150 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715150 | ATATATAT others(18): Show |
A | 6 | a0001c0001t0002g0208 a0001c0001t0009g0039 a0003c0004t0015g0083 others(3): Show |
6 | HG01168.hp2 HG01175.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-11525_601-1150 others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715150 | ATATATAT others(19): Show |
A | 3 | a0001c0001t0002g0139 a0001c0001t0008g0227 a0003c0005t0006g0087 |
3 | HG00423.hp1 HG01069.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.601-11525_601-1150 others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715150 | ATATATAT others(20): Show |
A | 2 | a0001c0001t0002g0136 a0001c0001t0008g0223 |
2 | HG03041.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.601-11525_601-1149 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715150 | ATATATAT others(21): Show |
A | 2 | a0001c0001t0002g0209 a0001c0001t0038g0229 |
2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.601-11525_601-1149 others(32): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715150 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0002g0153 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.601-11525_601-1149 others(33): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715150 | ATATATAT others(27): Show |
A | 1 | a0001c0002t0012g0301 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.601-11525_601-1149 others(38): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715150 | ||||||
| chr22:17715152 | ATATATAT others(13): Show |
A | 3 | a0001c0001t0002g0115 a0001c0001t0008g0222 a0001c0001t0010g0239 |
3 | HG01071.hp2 HG01978.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.601-11523_601-1150 others(24): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | ||||||
| chr22:17715152 | ATATATAT others(14): Show |
A | 4 | a0001c0001t0002g0114 a0001c0001t0002g0182 a0001c0001t0013g0192 others(1): Show |
4 | HG01070.hp1 HG01070.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-11523_601-1150 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | ||||||
| chr22:17715152 | ATATATAT others(15): Show |
A | 4 | a0001c0001t0003g0034 a0001c0001t0008g0234 a0001c0001t0010g0135 others(1): Show |
4 | HG01433.hp1 HG02647.hp2 NA19089.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-11523_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | ||||||
| chr22:17715152 | ATATATAT others(16): Show |
A | 2 | a0001c0001t0003g0007 a0004c0006t0049g0094 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.601-11523_601-1150 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | ||||||
| chr22:17715152 | ATATATAT others(17): Show |
A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0051 a0001c0001t0003g0107 |
3 | HG04199.hp1 NA18967.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.601-11523_601-1150 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | ||||||
| chr22:17715152 | ATATATAT others(20): Show |
A | 2 | a0001c0001t0002g0128 a0001c0001t0033g0127 |
2 | HG00735.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.601-11523_601-1149 others(31): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | ||||||
| chr22:17715152 | ATATATAT others(23): Show |
A | 1 | a0001c0002t0012g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601-11523_601-1149 others(34): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715152 | ||||||
| chr22:17715154 | ATATATAT others(12): Show |
A | 1 | a0001c0001t0024g0244 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.601-11521_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | ||||||
| chr22:17715154 | ATATATAT others(14): Show |
A | 1 | a0001c0002t0006g0080 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.601-11521_601-1150 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | ||||||
| chr22:17715154 | ATATATAT others(15): Show |
A | 3 | a0001c0001t0003g0055 a0001c0001t0003g0058 a0001c0002t0027g0075 |
3 | HG02145.hp2 NA18974.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.601-11521_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | ||||||
| chr22:17715154 | ATATATAT others(16): Show |
A | 5 | a0001c0001t0003g0029 a0001c0001t0003g0250 a0001c0001t0003g0251 others(2): Show |
5 | HG00099.hp2 HG02809.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-11521_601-1149 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | ||||||
| chr22:17715154 | ATATATAT others(17): Show |
A | 1 | a0001c0002t0027g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.601-11521_601-1149 others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715154 | ||||||
| chr22:17715156 | ATATATAT others(11): Show |
A | 2 | a0001c0001t0024g0243 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.601-11519_601-1150 others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715156 | ||||||
| chr22:17715156 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0041g0240 a0001c0002t0037g0064 |
2 | HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.601-11519_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715156 | ||||||
| chr22:17715156 | ATATATAT others(14): Show |
A | 2 | a0001c0001t0008g0224 a0001c0002t0006g0079 |
2 | HG03710.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.601-11519_601-1149 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715156 | ||||||
| chr22:17715156 | ATATATAT others(16): Show |
A | 3 | a0001c0002t0006g0073 a0001c0002t0025g0069 a0001c0002t0025g0070 |
3 | HG00738.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.601-11519_601-1149 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715156 | ||||||
| chr22:17715157 | TATATATA others(6): Show |
T | 1 | a0001c0002t0026g0294 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.601-11519_601-1150 others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715157 | |||||||
| chr22:17715158 | ATATATAT others(8): Show |
A | 1 | a0001c0001t0028g0297 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.601-11517_601-1150 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715158 | ||||||
| chr22:17715158 | ATATATAT others(14): Show |
A | 1 | a0004c0006t0001g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-11517_601-1149 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715158 | ||||||
| chr22:17715158 | ATATATAT others(15): Show |
A | 2 | a0001c0002t0006g0071 a0001c0002t0014g0068 |
2 | HG02602.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.601-11517_601-1149 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715158 | ||||||
| chr22:17715158 | ATATATAT others(16): Show |
A | 2 | a0001c0002t0006g0074 a0004c0006t0062g0095 |
2 | HG02280.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.601-11517_601-1149 others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715158 | ||||||
| chr22:17715160 | ATATATAT others(4): Show |
A | 1 | a0001c0002t0001g0277 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.601-11515_601-1150 others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715160 | ||||||
| chr22:17715160 | ATATATAT others(12): Show |
A | 2 | a0001c0002t0006g0072 a0001c0002t0006g0082 |
2 | HG03654.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.601-11515_601-1149 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715160 | ||||||
| chr22:17715160 | ATATATAT others(13): Show |
A | 2 | a0001c0002t0014g0065 a0001c0002t0014g0067 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.601-11515_601-1149 others(24): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715160 | ||||||
| chr22:17715162 | ATATATAT others(3): Show |
A | 1 | a0001c0002t0001g0260 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.601-11513_601-1150 others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715162 | ||||||
| chr22:17715162 | ATATATAT others(12): Show |
A | 1 | a0001c0002t0006g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.601-11513_601-1149 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715162 | ||||||
| chr22:17715164 | ATATATAT others(10): Show |
A | 1 | a0001c0002t0006g0081 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.601-11511_601-1149 others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715164 | ||||||
| chr22:17715168 | A | T | 5 | a0001c0001t0004g0118 a0001c0001t0004g0119 a0001c0001t0004g0152 others(2): Show |
5 | HG00735.hp2 HG02040.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-11509A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715168 | |||||||
| chr22:17715170 | A | ATATATAT others(8): Show |
1 | a0002c0003t0058g0005 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(12): Show |
2 | a0001c0002t0001g0284 a0001c0002t0068g0292 |
2 | HG00408.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.601-11506_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(14): Show |
1 | a0001c0002t0052g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(11): Show |
1 | a0002c0003t0001g0265 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(15): Show |
1 | a0001c0002t0001g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(12): Show |
1 | a0002c0003t0057g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(7): Show |
3 | a0002c0003t0001g0273 a0002c0003t0001g0290 a0002c0003t0001g0291 |
3 | HG01069.hp2 HG01071.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.601-11506_601-1150 others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(8): Show |
1 | a0006c0010t0001g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(5): Show |
1 | a0001c0002t0001g0276 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.601-11506_601-1150 others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(10): Show |
1 | a0001c0002t0001g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(4): Show |
2 | a0002c0003t0001g0263 a0002c0003t0001g0264 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.601-11506_601-1150 others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | ATATATAT others(6): Show |
1 | a0001c0002t0001g0285 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | A | T | 30 | a0001c0001t0004g0102 a0001c0001t0004g0118 a0001c0001t0004g0119 others(27): Show |
30 | HG00423.hp2 HG00438.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.601-11507A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715170 | |||||||
| chr22:17715170 | ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0006g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.601-11488_601-1147 others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715170 | ATTTTTTT others(10): Show |
A | 1 | a0001c0002t0006g0076 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.601-11490_601-1147 others(21): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715170 | ||||||
| chr22:17715171 | T | TATATATA others(4): Show |
1 | a0002c0003t0001g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(15): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715171 | |||||||
| chr22:17715171 | T | TATATATA others(12): Show |
1 | a0001c0002t0001g0288 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.601-11506_601-1150 others(23): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715171 | |||||||
| chr22:17715172 | T | A | 2 | a0001c0002t0001g0278 a0002c0003t0001g0269 |
2 | HG01981.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.601-11505T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715172 | |||||||
| chr22:17715173 | T | A | 3 | a0001c0002t0001g0279 a0002c0003t0001g0270 a0002c0003t0001g0282 |
3 | HG00280.hp2 HG01123.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.601-11504T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715173 | |||||||
| chr22:17715174 | T | A | 1 | a0002c0003t0001g0003 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.601-11503T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715174 | |||||||
| chr22:17715227 | G | GC | 5 | a0001c0001t0005g0138 a0001c0001t0005g0143 a0001c0001t0005g0145 others(2): Show |
5 | HG01109.hp1 HG02451.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-11449dupC | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17715227 | ||||||
| chr22:17715331 | G | A | 1 | a0001c0001t0004g0137 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.601-11346G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715331 | |||||||
| chr22:17715335 | C | A | 1 | a0001c0002t0001g0278 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.601-11342C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715335 | |||||||
| chr22:17715343 | G | A | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.601-11334G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715343 | |||||||
| chr22:17715500 | C | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.601-11177C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715500 | |||||||
| chr22:17715561 | C | G | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.601-11116C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715561 | |||||||
| chr22:17715980 | T | A | 2 | a0001c0001t0004g0118 a0001c0001t0004g0119 |
2 | HG02040.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.601-10697T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715980 | |||||||
| chr22:17715992 | A | T | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-10685A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17715992 | |||||||
| chr22:17716337 | G | T | 3 | a0001c0007t0009g0040 a0001c0007t0009g0059 a0001c0007t0044g0033 |
3 | HG03130.hp2 HG03225.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.601-10340G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17716337 | |||||||
| chr22:17716477 | A | C | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-10200A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17716477 | |||||||
| chr22:17716717 | A | G | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.601-9960A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17716717 | |||||||
| chr22:17716779 | T | G | 1 | a0001c0001t0050g0249 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.601-9898T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17716779 | |||||||
| chr22:17717210 | A | G | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-9467A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717210 | |||||||
| chr22:17717283 | C | T | 7 | a0001c0001t0004g0102 a0001c0001t0004g0118 a0001c0001t0004g0119 others(4): Show |
7 | HG00423.hp2 HG02040.hp1 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-9394C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717283 | |||||||
| chr22:17717284 | G | A | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-9393G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717284 | |||||||
| chr22:17717354 | TG | T | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-9319delG | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717354 | ||||||
| chr22:17717380 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-9291_601-9290i others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(9): Show |
12 | a0003c0004t0015g0083 a0003c0004t0015g0252 a0003c0004t0016g0090 others(9): Show |
12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(10): Show |
1 | a0003c0004t0015g0084 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.601-9291_601-9290i others(19): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(16): Show |
16 | a0001c0001t0006g0077 a0001c0001t0009g0039 a0001c0002t0006g0071 others(13): Show |
16 | HG01168.hp2 HG01261.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(25): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(17): Show |
32 | a0001c0001t0003g0001 a0001c0001t0003g0026 a0001c0001t0003g0038 others(29): Show |
33 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(18): Show |
12 | a0001c0001t0003g0007 a0001c0001t0003g0049 a0001c0001t0003g0051 others(9): Show |
12 | HG00738.hp1 HG01243.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(27): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(19): Show |
9 | a0001c0001t0003g0027 a0001c0001t0003g0030 a0001c0001t0003g0031 others(6): Show |
9 | HG02572.hp2 HG02630.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(28): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(20): Show |
5 | a0001c0001t0003g0029 a0001c0001t0003g0034 a0001c0001t0003g0251 others(2): Show |
5 | HG02647.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.601-9291_601-9290i others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(26): Show |
1 | a0004c0006t0001g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-9291_601-9290i others(35): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(27): Show |
1 | a0004c0006t0049g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.601-9291_601-9290i others(36): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(28): Show |
1 | a0004c0006t0001g0096 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.601-9291_601-9290i others(37): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717380 | C | CAAAAAAA others(38): Show |
1 | a0004c0006t0062g0095 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.601-9291_601-9290i others(47): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17717380 | ||||||
| chr22:17717439 | C | T | 1 | a0001c0002t0012g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.601-9238C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717439 | |||||||
| chr22:17717459 | T | G | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-9218T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717459 | |||||||
| chr22:17717464 | T | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.601-9213T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717464 | |||||||
| chr22:17717500 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-9177G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717500 | |||||||
| chr22:17717586 | C | T | 1 | a0001c0002t0006g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.601-9091C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717586 | |||||||
| chr22:17717620 | G | A | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.601-9057G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717620 | |||||||
| chr22:17717706 | A | G | 2 | a0001c0001t0063g0299 a0001c0001t0064g0106 |
2 | HG01255.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.601-8971A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717706 | |||||||
| chr22:17717737 | T | C | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-8940T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717737 | |||||||
| chr22:17717914 | C | T | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-8763C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717914 | |||||||
| chr22:17717947 | C | T | 5 | a0001c0001t0003g0001 a0001c0001t0003g0042 a0001c0001t0003g0043 others(2): Show |
6 | NA18955.hp1 NA18989.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-8730C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717947 | |||||||
| chr22:17717960 | G | A | 1 | a0004c0006t0001g0093 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.601-8717G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17717960 | |||||||
| chr22:17718044 | G | A | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.601-8633G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718044 | |||||||
| chr22:17718112 | G | T | 15 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(12): Show |
15 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.601-8565G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718112 | |||||||
| chr22:17718438 | C | T | 71 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(68): Show |
72 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.601-8239C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718438 | |||||||
| chr22:17718529 | C | T | 1 | a0001c0002t0027g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.601-8148C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718529 | |||||||
| chr22:17718730 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-7947C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718730 | |||||||
| chr22:17718732 | T | G | 22 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(19): Show |
22 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.601-7945T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718732 | |||||||
| chr22:17718760 | G | C | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.601-7917G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718760 | |||||||
| chr22:17718835 | G | C | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-7842G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718835 | |||||||
| chr22:17718839 | C | G | 1 | a0001c0001t0061g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.601-7838C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718839 | |||||||
| chr22:17718875 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-7802G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718875 | |||||||
| chr22:17718875 | G | T | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-7802G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718875 | |||||||
| chr22:17718947 | T | C | 134 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(131): Show |
135 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.601-7730T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718947 | |||||||
| chr22:17718988 | G | A | 1 | a0001c0001t0005g0241 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.601-7689G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17718988 | |||||||
| chr22:17719003 | C | T | 1 | a0006c0010t0001g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601-7674C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719003 | |||||||
| chr22:17719021 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.601-7656G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719021 | |||||||
| chr22:17719153 | C | CA | 52 | a0001c0001t0002g0144 a0001c0001t0002g0172 a0001c0001t0002g0209 others(49): Show |
52 | HG00140.hp2 HG00733.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.601-7500dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719153 | ||||||
| chr22:17719153 | C | CAA | 38 | a0001c0001t0003g0027 a0001c0001t0003g0047 a0001c0001t0003g0049 others(35): Show |
38 | HG00099.hp2 HG00423.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.601-7501_601-7500d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719153 | ||||||
| chr22:17719153 | C | CAAA | 9 | a0001c0002t0006g0072 a0001c0002t0006g0073 a0001c0002t0006g0076 others(6): Show |
9 | HG00738.hp1 HG01361.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.601-7502_601-7500d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719153 | ||||||
| chr22:17719153 | CA | C | 14 | a0001c0001t0002g0208 a0001c0001t0005g0120 a0001c0001t0007g0099 others(11): Show |
14 | HG01081.hp2 HG01169.hp1 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.601-7500delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719153 | ||||||
| chr22:17719206 | A | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-7471A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719206 | |||||||
| chr22:17719266 | A | G | 2 | a0001c0009t0004g0155 a0001c0009t0004g0156 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.601-7411A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719266 | |||||||
| chr22:17719273 | A | C | 1 | a0001c0001t0002g0178 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.601-7404A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719273 | |||||||
| chr22:17719363 | A | G | 254 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.601-7314A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719363 | |||||||
| chr22:17719370 | G | A | 1 | a0006c0010t0001g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601-7307G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719370 | |||||||
| chr22:17719384 | C | T | 21 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(18): Show |
21 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(18): Show |
intron_variant | MODIFIER | c.601-7293C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719384 | |||||||
| chr22:17719441 | A | G | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.601-7236A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719441 | |||||||
| chr22:17719541 | G | A | 2 | a0001c0001t0005g0062 a0001c0001t0005g0063 |
2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.601-7136G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719541 | |||||||
| chr22:17719549 | C | G | 4 | a0001c0001t0004g0101 a0001c0001t0004g0152 a0001c0001t0004g0185 others(1): Show |
4 | HG02738.hp1 HG03834.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-7128C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719549 | |||||||
| chr22:17719701 | C | T | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-6976C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719701 | |||||||
| chr22:17719764 | G | C | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.601-6913G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719764 | |||||||
| chr22:17719827 | C | CAA | 20 | a0001c0001t0008g0222 a0001c0001t0008g0223 a0001c0001t0008g0224 others(17): Show |
20 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.601-6828_601-6827d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719827 | ||||||
| chr22:17719827 | CAAAAAAA others(3): Show |
C | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.601-6836_601-6827d others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719827 | ||||||
| chr22:17719827 | CAAAAAAA others(4): Show |
C | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-6837_601-6827d others(13): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719827 | ||||||
| chr22:17719827 | CAAAAAAA others(8): Show |
C | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-6841_601-6827d others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719827 | ||||||
| chr22:17719846 | A | AAAC | 58 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(55): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.601-6829_601-6828i others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719846 | ||||||
| chr22:17719846 | A | AAC | 70 | a0001c0001t0002g0182 a0001c0001t0002g0208 a0001c0001t0002g0216 others(67): Show |
70 | HG00408.hp1 HG00423.hp2 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.601-6830_601-6829i others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719846 | ||||||
| chr22:17719846 | A | C | 4 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0048g0126 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-6831A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719846 | |||||||
| chr22:17719868 | A | ATGC | 13 | a0001c0001t0007g0013 a0001c0001t0007g0014 a0001c0001t0007g0017 others(10): Show |
13 | HG01192.hp1 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-6807_601-6805d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17719868 | ||||||
| chr22:17719882 | G | A | 1 | a0001c0002t0027g0011 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.601-6795G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719882 | |||||||
| chr22:17719897 | A | G | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-6780A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17719897 | |||||||
| chr22:17720084 | A | G | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-6593A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720084 | |||||||
| chr22:17720090 | G | A | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-6587G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720090 | |||||||
| chr22:17720135 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-6542C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720135 | |||||||
| chr22:17720154 | T | TTTCTTTC others(8): Show |
1 | a0001c0001t0059g0149 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.601-6521_601-6520i others(17): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTCTTTC others(20): Show |
1 | a0001c0001t0011g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.601-6521_601-6520i others(29): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTCTTTC others(32): Show |
1 | a0001c0001t0010g0239 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.601-6521_601-6520i others(41): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTC | 7 | a0001c0001t0003g0001 a0001c0001t0003g0042 a0001c0001t0003g0043 others(4): Show |
8 | HG02965.hp1 NA18955.hp1 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-6498_601-6495d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(5): Show |
6 | a0001c0001t0002g0139 a0001c0001t0002g0174 a0001c0001t0005g0169 others(3): Show |
6 | HG01069.hp1 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-6506_601-6495d others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(9): Show |
56 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(53): Show |
57 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.601-6510_601-6495d others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(13): Show |
35 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0172 others(32): Show |
35 | HG00099.hp1 HG00438.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.601-6514_601-6495d others(22): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(17): Show |
25 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0133 others(22): Show |
25 | HG00323.hp1 HG00408.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.601-6518_601-6495d others(26): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(21): Show |
14 | a0001c0001t0002g0117 a0001c0001t0002g0144 a0001c0001t0002g0202 others(11): Show |
14 | HG00280.hp1 HG01261.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.601-6522_601-6495d others(30): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(25): Show |
10 | a0001c0001t0002g0205 a0001c0001t0008g0228 a0001c0001t0028g0298 others(7): Show |
10 | HG00738.hp1 HG01934.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(34): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(29): Show |
3 | a0001c0001t0008g0223 a0001c0002t0006g0074 a0001c0002t0012g0300 |
3 | HG02055.hp2 HG03041.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.601-6495_601-6494i others(38): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(33): Show |
12 | a0001c0001t0008g0222 a0001c0001t0008g0227 a0001c0001t0008g0232 others(9): Show |
12 | HG01169.hp2 HG01261.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(42): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(37): Show |
12 | a0001c0001t0010g0135 a0001c0001t0022g0238 a0001c0001t0024g0243 others(9): Show |
12 | HG00099.hp2 HG01167.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(46): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(41): Show |
6 | a0001c0001t0008g0230 a0001c0001t0020g0233 a0001c0001t0036g0097 others(3): Show |
6 | HG02257.hp1 HG02717.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(50): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(45): Show |
4 | a0001c0001t0008g0224 a0001c0001t0010g0235 a0001c0002t0014g0066 others(1): Show |
4 | HG02965.hp2 NA18953.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.601-6495_601-6494i others(54): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720154 | T | TTTTCTTT others(53): Show |
1 | a0001c0001t0010g0221 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.601-6495_601-6494i others(62): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720154 | ||||||
| chr22:17720349 | T | A | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.601-6328T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720349 | |||||||
| chr22:17720411 | C | T | 2 | a0001c0001t0028g0297 a0001c0001t0028g0298 |
2 | HG02572.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.601-6266C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720411 | |||||||
| chr22:17720413 | C | G | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.601-6264C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720413 | |||||||
| chr22:17720556 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-6121G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720556 | |||||||
| chr22:17720584 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-6093C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720584 | |||||||
| chr22:17720668 | A | AT | 8 | a0001c0001t0002g0103 a0001c0001t0004g0196 a0001c0001t0008g0224 others(5): Show |
8 | HG01192.hp1 HG04184.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.601-5993dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17720668 | ||||||
| chr22:17720690 | C | T | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-5987C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720690 | |||||||
| chr22:17720692 | G | A | 1 | a0001c0001t0004g0213 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.601-5985G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720692 | |||||||
| chr22:17720766 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0038 a0001c0001t0003g0042 others(4): Show |
8 | NA18955.hp1 NA18965.hp2 NA18989.hp2 others(5): Show |
intron_variant | MODIFIER | c.601-5911T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720766 | |||||||
| chr22:17720904 | C | T | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.601-5773C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720904 | |||||||
| chr22:17720958 | A | G | 6 | a0001c0002t0006g0073 a0001c0002t0006g0074 a0001c0002t0006g0082 others(3): Show |
6 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-5719A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720958 | |||||||
| chr22:17720992 | C | T | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-5685C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17720992 | |||||||
| chr22:17721035 | C | T | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-5642C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721035 | |||||||
| chr22:17721095 | G | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-5582G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721095 | |||||||
| chr22:17721104 | A | G | 44 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(41): Show |
45 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(42): Show |
intron_variant | MODIFIER | c.601-5573A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721104 | |||||||
| chr22:17721125 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-5552G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721125 | |||||||
| chr22:17721169 | CA | C | 158 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(155): Show |
159 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.601-5496delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17721169 | ||||||
| chr22:17721176 | A | T | 22 | a0001c0001t0003g0053 a0001c0001t0006g0077 a0001c0002t0006g0071 others(19): Show |
22 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.601-5501A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721176 | |||||||
| chr22:17721178 | A | T | 94 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(91): Show |
95 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(92): Show |
intron_variant | MODIFIER | c.601-5499A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721178 | |||||||
| chr22:17721180 | A | AT | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-5497_601-5496i others(3): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721180 | |||||||
| chr22:17721180 | A | T | 111 | a0001c0001t0002g0128 a0001c0001t0003g0001 a0001c0001t0003g0007 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.601-5497A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721180 | |||||||
| chr22:17721182 | T | A | 16 | a0001c0002t0026g0293 a0001c0002t0026g0294 a0001c0002t0035g0296 others(13): Show |
16 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-5495T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721182 | |||||||
| chr22:17721184 | T | A | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-5493T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721184 | |||||||
| chr22:17721208 | G | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.601-5469G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721208 | |||||||
| chr22:17721285 | G | A | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-5392G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721285 | |||||||
| chr22:17721325 | A | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-5352A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721325 | |||||||
| chr22:17721381 | A | G | 1 | a0001c0001t0004g0191 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.601-5296A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721381 | |||||||
| chr22:17721452 | C | G | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.601-5225C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721452 | |||||||
| chr22:17721492 | G | GT | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-5174dupT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17721492 | ||||||
| chr22:17721525 | A | ATTT | 199 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0114 others(196): Show |
201 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.601-5136_601-5134d others(5): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17721525 | ||||||
| chr22:17721525 | A | ATTTT | 45 | a0001c0001t0002g0103 a0001c0001t0002g0136 a0001c0001t0002g0186 others(42): Show |
45 | HG00099.hp2 HG00323.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.601-5137_601-5134d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17721525 | ||||||
| chr22:17721550 | T | G | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-5127T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721550 | |||||||
| chr22:17721650 | A | G | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.601-5027A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721650 | |||||||
| chr22:17721707 | G | A | 2 | a0001c0001t0022g0237 a0001c0001t0022g0238 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.601-4970G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721707 | |||||||
| chr22:17721756 | C | G | 15 | a0001c0001t0024g0243 a0001c0001t0024g0244 a0003c0004t0015g0083 others(12): Show |
15 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-4921C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721756 | |||||||
| chr22:17721821 | C | T | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-4856C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721821 | |||||||
| chr22:17721853 | G | A | 1 | a0001c0001t0008g0222 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.601-4824G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721853 | |||||||
| chr22:17721860 | C | T | 1 | a0001c0001t0004g0124 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.601-4817C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721860 | |||||||
| chr22:17721879 | C | G | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.601-4798C>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721879 | |||||||
| chr22:17721882 | G | A | 1 | a0001c0002t0027g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.601-4795G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721882 | |||||||
| chr22:17721908 | G | C | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-4769G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17721908 | |||||||
| chr22:17722061 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.601-4616A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722061 | |||||||
| chr22:17722076 | T | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-4601T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722076 | |||||||
| chr22:17722090 | AATAAGTA others(7): Show |
A | 1 | a0001c0001t0005g0141 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.601-4583_601-4570d others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722090 | ||||||
| chr22:17722109 | A | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-4568A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722109 | |||||||
| chr22:17722122 | A | G | 1 | a0003c0004t0030g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.601-4555A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722122 | |||||||
| chr22:17722158 | T | C | 1 | a0001c0001t0004g0175 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.601-4519T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722158 | |||||||
| chr22:17722289 | C | T | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-4388C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722289 | |||||||
| chr22:17722314 | A | G | 1 | a0001c0002t0012g0009 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.601-4363A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722314 | |||||||
| chr22:17722375 | AGG | A | 30 | a0001c0001t0002g0128 a0001c0001t0003g0030 a0001c0001t0003g0031 others(27): Show |
30 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.601-4299_601-4298d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722375 | ||||||
| chr22:17722376 | G | GGT | 16 | a0001c0001t0002g0103 a0001c0001t0002g0151 a0001c0001t0002g0178 others(13): Show |
16 | HG02004.hp1 HG02300.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | G | GGTGC | 28 | a0001c0001t0003g0001 a0001c0001t0003g0026 a0001c0001t0003g0038 others(25): Show |
29 | HG00140.hp2 HG01168.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | G | GGTGCGT | 10 | a0001c0001t0003g0110 a0001c0001t0004g0148 a0001c0001t0004g0164 others(7): Show |
10 | HG00733.hp1 HG01243.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | G | GGTGCGTG others(3): Show |
9 | a0003c0004t0015g0083 a0003c0004t0015g0252 a0003c0004t0030g0104 others(6): Show |
9 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(12): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | G | GGTGCGTG others(5): Show |
5 | a0003c0004t0015g0084 a0003c0004t0016g0091 a0004c0006t0001g0096 others(2): Show |
5 | HG02280.hp2 HG02300.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-4300_601-4299i others(14): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | G | GGTGCGTG others(7): Show |
2 | a0003c0004t0016g0092 a0004c0006t0001g0093 |
2 | HG02055.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.601-4300_601-4299i others(16): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | G | GGTGCGTG others(9): Show |
1 | a0003c0004t0016g0090 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.601-4300_601-4299i others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | GGGGT | G | 13 | a0001c0001t0005g0190 a0001c0001t0005g0242 a0001c0001t0007g0014 others(10): Show |
13 | HG00408.hp1 HG01192.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.601-4299_601-4296d others(6): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | GGGGTGT | G | 32 | a0001c0001t0005g0012 a0001c0001t0007g0013 a0001c0001t0007g0017 others(29): Show |
32 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(29): Show |
intron_variant | MODIFIER | c.601-4299_601-4294d others(8): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | GGGGTGTG others(1): Show |
G | 7 | a0001c0001t0005g0241 a0001c0001t0064g0106 a0001c0002t0012g0008 others(4): Show |
7 | HG00738.hp2 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-4299_601-4292d others(10): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722376 | GGGGTGTG others(9): Show |
G | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601-4299_601-4284d others(18): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722376 | ||||||
| chr22:17722378 | G | C | 16 | a0001c0001t0002g0103 a0001c0001t0002g0151 a0001c0001t0002g0178 others(13): Show |
16 | HG02004.hp1 HG02300.hp1 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-4299G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722378 | |||||||
| chr22:17722378 | G | GGT | 3 | a0001c0002t0001g0199 a0002c0003t0001g0265 a0002c0003t0001g0273 |
3 | HG01258.hp2 HG02698.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.601-4258_601-4257d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17722378 | ||||||
| chr22:17722378 | G | T | 156 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0114 others(153): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.601-4299G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722378 | |||||||
| chr22:17722380 | T | C | 98 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0114 others(95): Show |
99 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.601-4297T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722380 | |||||||
| chr22:17722382 | T | C | 30 | a0001c0001t0002g0128 a0001c0001t0003g0030 a0001c0001t0003g0031 others(27): Show |
30 | HG00099.hp2 HG00738.hp1 HG01516.hp2 others(27): Show |
intron_variant | MODIFIER | c.601-4295T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722382 | |||||||
| chr22:17722384 | T | C | 13 | a0001c0001t0005g0190 a0001c0001t0005g0242 a0001c0001t0007g0014 others(10): Show |
13 | HG00408.hp1 HG01192.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.601-4293T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722384 | |||||||
| chr22:17722386 | T | C | 29 | a0001c0001t0005g0012 a0001c0001t0007g0013 a0001c0001t0007g0017 others(26): Show |
29 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(26): Show |
intron_variant | MODIFIER | c.601-4291T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722386 | |||||||
| chr22:17722388 | T | C | 7 | a0001c0001t0005g0241 a0001c0001t0064g0106 a0001c0002t0012g0008 others(4): Show |
7 | HG00738.hp2 HG01255.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.601-4289T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722388 | |||||||
| chr22:17722396 | T | C | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601-4281T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722396 | |||||||
| chr22:17722417 | G | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-4260G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722417 | |||||||
| chr22:17722421 | A | G | 26 | a0001c0001t0006g0077 a0001c0002t0006g0071 a0001c0002t0006g0072 others(23): Show |
26 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.601-4256A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722421 | |||||||
| chr22:17722664 | A | T | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.601-4013A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722664 | |||||||
| chr22:17722791 | C | T | 93 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.601-3886C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722791 | |||||||
| chr22:17722911 | G | C | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-3766G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17722911 | |||||||
| chr22:17723154 | C | T | 2 | a0001c0001t0002g0186 a0001c0001t0002g0245 |
2 | HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.601-3523C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723154 | |||||||
| chr22:17723173 | C | T | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-3504C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723173 | |||||||
| chr22:17723181 | CCT | C | 3 | a0001c0002t0026g0293 a0001c0002t0026g0294 a0001c0002t0035g0296 |
3 | HG02258.hp1 HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.601-3489_601-3488d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17723181 | ||||||
| chr22:17723232 | G | T | 1 | a0001c0002t0052g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.601-3445G>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723232 | |||||||
| chr22:17723560 | A | G | 1 | a0001c0001t0002g0159 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.601-3117A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723560 | |||||||
| chr22:17723570 | T | C | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-3107T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723570 | |||||||
| chr22:17723639 | A | G | 7 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(4): Show |
7 | HG02280.hp2 HG02886.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-3038A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723639 | |||||||
| chr22:17723656 | C | T | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-3021C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723656 | |||||||
| chr22:17723701 | G | A | 1 | a0001c0001t0061g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.601-2976G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723701 | |||||||
| chr22:17723734 | A | C | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-2943A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723734 | |||||||
| chr22:17723750 | T | C | 1 | a0001c0001t0003g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.601-2927T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723750 | |||||||
| chr22:17723762 | G | A | 2 | a0005c0008t0019g0254 a0005c0008t0019g0255 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.601-2915G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723762 | |||||||
| chr22:17723772 | A | G | 13 | a0003c0004t0015g0083 a0003c0004t0015g0084 a0003c0004t0015g0252 others(10): Show |
13 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.601-2905A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723772 | |||||||
| chr22:17723777 | A | G | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-2900A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723777 | |||||||
| chr22:17723887 | T | C | 254 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.601-2790T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723887 | |||||||
| chr22:17723888 | G | A | 1 | a0001c0001t0002g0151 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.601-2789G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723888 | |||||||
| chr22:17723931 | C | CA | 25 | a0001c0001t0004g0132 a0001c0001t0004g0185 a0001c0001t0006g0077 others(22): Show |
25 | HG00099.hp2 HG00738.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.601-2736dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17723931 | ||||||
| chr22:17723931 | C | CAA | 12 | a0003c0004t0015g0083 a0003c0004t0015g0252 a0003c0004t0016g0090 others(9): Show |
12 | HG00423.hp1 HG01074.hp2 HG01081.hp1 others(9): Show |
intron_variant | MODIFIER | c.601-2737_601-2736d others(4): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17723931 | ||||||
| chr22:17723983 | G | C | 2 | a0001c0002t0001g0279 a0001c0002t0001g0283 |
2 | HG00741.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.601-2694G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17723983 | |||||||
| chr22:17724003 | T | A | 2 | a0001c0001t0024g0243 a0001c0001t0024g0244 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.601-2674T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724003 | |||||||
| chr22:17724025 | C | T | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-2652C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724025 | |||||||
| chr22:17724259 | C | T | 1 | a0001c0001t0005g0242 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.601-2418C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724259 | |||||||
| chr22:17724372 | C | T | 1 | a0001c0001t0065g0016 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.601-2305C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724372 | |||||||
| chr22:17724447 | T | A | 1 | a0008c0011t0023g0109 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.601-2230T>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724447 | |||||||
| chr22:17724454 | C | T | 15 | a0001c0001t0008g0224 a0001c0001t0008g0228 a0001c0001t0008g0230 others(12): Show |
15 | HG01167.hp1 HG01169.hp2 HG01433.hp1 others(12): Show |
intron_variant | MODIFIER | c.601-2223C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724454 | |||||||
| chr22:17724485 | T | C | 79 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(76): Show |
80 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.601-2192T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724485 | |||||||
| chr22:17724750 | T | C | 1 | a0001c0001t0003g0031 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.601-1927T>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724750 | |||||||
| chr22:17724961 | C | A | 1 | a0001c0002t0001g0277 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.601-1716C>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724961 | |||||||
| chr22:17724964 | G | C | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-1713G>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17724964 | |||||||
| chr22:17725014 | C | CA | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-1662dupA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17725014 | ||||||
| chr22:17725045 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.601-1632G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725045 | |||||||
| chr22:17725161 | T | G | 254 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(251): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(253): Show |
intron_variant | MODIFIER | c.601-1516T>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725161 | |||||||
| chr22:17725278 | G | A | 1 | a0001c0001t0005g0012 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.601-1399G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725278 | |||||||
| chr22:17725300 | A | C | 1 | a0001c0002t0052g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.601-1377A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725300 | |||||||
| chr22:17725649 | C | T | 6 | a0001c0001t0017g0019 a0001c0001t0017g0020 a0001c0001t0017g0025 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.601-1028C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725649 | |||||||
| chr22:17725762 | AT | A | 6 | a0001c0001t0002g0100 a0001c0001t0003g0054 a0001c0001t0005g0241 others(3): Show |
6 | HG00738.hp2 HG01255.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.601-902delT | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17725762 | ||||||
| chr22:17725870 | A | G | 1 | a0001c0001t0047g0129 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.601-807A>G | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725870 | |||||||
| chr22:17725875 | G | A | 110 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(107): Show |
111 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.601-802G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725875 | |||||||
| chr22:17725998 | C | T | 251 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(248): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.601-679C>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17725998 | |||||||
| chr22:17726110 | G | A | 45 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(42): Show |
46 | HG00140.hp2 HG00733.hp1 HG01168.hp2 others(43): Show |
intron_variant | MODIFIER | c.601-567G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726110 | |||||||
| chr22:17726212 | G | A | 4 | a0004c0006t0001g0093 a0004c0006t0001g0096 a0004c0006t0049g0094 others(1): Show |
4 | HG02280.hp2 HG02886.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-465G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726212 | |||||||
| chr22:17726350 | TA | T | 155 | a0001c0001t0002g0004 a0001c0001t0002g0100 a0001c0001t0002g0103 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.601-308delA | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17726350 | ||||||
| chr22:17726350 | TAA | T | 91 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0026 others(88): Show |
92 | HG00140.hp2 HG00733.hp1 HG01167.hp1 others(89): Show |
intron_variant | MODIFIER | c.601-309_601-308del others(2): Show |
BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr22 | 17726350 | ||||||
| chr22:17726351 | A | T | 1 | a0006c0010t0001g0262 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.601-326A>T | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726351 | |||||||
| chr22:17726363 | A | C | 3 | a0005c0008t0019g0254 a0005c0008t0019g0255 a0005c0008t0019g0295 |
3 | HG02965.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.601-314A>C | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726363 | |||||||
| chr22:17726545 | G | A | 5 | a0001c0002t0012g0008 a0001c0002t0012g0009 a0001c0002t0012g0300 others(2): Show |
5 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.601-132G>A | BCL2L13 | ENSG00000099968.18 | transcript | ENST00000317582.10 | protein_coding | 6/6 | chr22 | 17726545 |