Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 122060 |
| ensemblid | ENSG00000139737.23 |
| hgncid | 26387 |
| symbol | SLAIN1 |
| name | SLAIN motif family member 1 |
| refseq_nuc | NM_001242868.2 |
| refseq_prot | NP_001229797.1 |
| ensembl_nuc | ENST00000418532.6 |
| ensembl_prot | ENSP00000400921.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 77697687 |
| end | 77764229 |
| strand | + |
| ver | v1.2 |
| region | chr13:77697687-77764229 |
| region5000 | chr13:77692687-77769229 |
| regionname0 | SLAIN1_chr13_77697687_77764229 |
| regionname5000 | SLAIN1_chr13_77692687_77769229 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 590 | 290 | 73 | 58 | 108 | 14 | 36 | 78 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | MMAEQ others(585): Show |
chr13 | 77692687 | 77769229 |
| a0002 | 0/0 | 591 | 8 | 7 | 0 | 1 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | MMAEQ others(586): Show |
chr13 | 77692687 | 77769229 |
| a0003 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | MMAEQ others(585): Show |
chr13 | 77692687 | 77769229 |
| a0004 | 0/1 | 591 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | MMAEQ others(586): Show |
chr13 | 77692687 | 77769229 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1770 | 285 | 70 | 56 | 108 | 14 | 36 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | ATGAT others(1765): Show |
chr13 | 77692687 | 77769229 | ||
| a0001c0003 | 0/0 | 1770 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | ATGAT others(1765): Show |
chr13 | 77692687 | 77769229 | ||
| a0001c0004 | 0/0 | 1770 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | ATGAT others(1765): Show |
chr13 | 77692687 | 77769229 | ||
| a0002c0002 | 0/0 | 1773 | 8 | 7 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | ATGAT others(1768): Show |
chr13 | 77692687 | 77769229 | ||
| a0003c0005 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | ATGAT others(1765): Show |
chr13 | 77692687 | 77769229 | ||
| a0004c0006 | 0/1 | 1773 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | ATGAT others(1768): Show |
chr13 | 77692687 | 77769229 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3009 | 208 | 39 | 44 | 91 | 7 | 26 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3004): Show |
chr13 | 77692687 | 77769229 |
| a0001c0001t0002 | 0/0 | 3009 | 62 | 19 | 9 | 17 | 7 | 10 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3004): Show |
chr13 | 77692687 | 77769229 |
| a0001c0001t0003 | 0/0 | 3008 | 10 | 9 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3003): Show |
chr13 | 77692687 | 77769229 |
| a0001c0001t0004 | 0/0 | 3009 | 2 | 1 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3004): Show |
chr13 | 77692687 | 77769229 |
| a0001c0001t0005 | 0/0 | 3009 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3004): Show |
chr13 | 77692687 | 77769229 |
| a0001c0001t0006 | 0/0 | 3009 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3004): Show |
chr13 | 77692687 | 77769229 |
| a0001c0001t0007 | 0/0 | 3008 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3003): Show |
chr13 | 77692687 | 77769229 |
| a0001c0003t0001 | 0/0 | 3009 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3004): Show |
chr13 | 77692687 | 77769229 |
| a0001c0004t0001 | 0/0 | 3009 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3004): Show |
chr13 | 77692687 | 77769229 |
| a0002c0002t0001 | 0/0 | 3012 | 7 | 6 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3007): Show |
chr13 | 77692687 | 77769229 |
| a0002c0002t0002 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3007): Show |
chr13 | 77692687 | 77769229 |
| a0003c0005t0001 | 0/0 | 3009 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3004): Show |
chr13 | 77692687 | 77769229 |
| a0004c0006t0001 | 0/1 | 3012 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | GGGGA others(3007): Show |
chr13 | 77692687 | 77769229 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0274 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0006g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0001c0004t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0002c0002t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0002c0002t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0003c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| a0004c0006t0001g0085 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0231 | EUR | GBR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0245 | EUR | GBR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0120 | EUR | FIN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0116 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01169 | hp2 | a0001 | c0004 | t0001 | g0015 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0124 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0123 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01934 | hp2 | a0001 | c0001 | t0006 | g0083 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CDX | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | CDX | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02630 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0170 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0171 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0073 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0156 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0167 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | BEB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | YRI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | YRI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18944 | hp1 | a0003 | c0005 | t0001 | g0052 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0159 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0168 | AFR | YRI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | YRI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | ASW | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ASW | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0258 | EUR | TSI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0128 | EUR | TSI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0178 | EUR | TSI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | GIH | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | GIH | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0072 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0158 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0151 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | USA | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0169 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| homoSapiens | chm13v2 | a0004 | c0006 | t0001 | g0085 | REF | REF | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0274 | REF | REF | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77698098 | T | TGCC | 1 | a0002 | 8 | HG02559.hp2 HG02818.hp1 HG02886.hp2 others(5): Show |
disruptive_inframe_insertion | MODERATE | c.198_200dupGCC | p.Pro67dup | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/7 | 428/3009 | 201/1773 | 67/590 | INFO_REALIGN_3_PRIME | chr13 | 77698098 | ||
| chr13:77746676 | G | A | 1 | a0003 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1079G>A | p.Arg360His | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/7 | 1306/3009 | 1079/1773 | 360/590 | chr13 | 77746676 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77753279 | G | A | 1 | a0001c0003 | 3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.1335G>A | p.Pro445Pro | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/7 | 1562/3009 | 1335/1773 | 445/590 | chr13 | 77753279 | |||
| chr13:77761012 | A | G | 1 | a0001c0004 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1599A>G | p.Ala533Ala | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/7 | 1826/3009 | 1599/1773 | 533/590 | chr13 | 77761012 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77697898 | GC | G | 2 | a0001c0001t0003 a0001c0001t0007 |
11 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-13delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/7 | 13 | INFO_REALIGN_3_PRIME | chr13 | 77697898 | |||||
| chr13:77763356 | A | G | 1 | a0001c0001t0006 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 7/7 | 136 | chr13 | 77763356 | ||||||
| chr13:77763784 | C | T | 1 | a0001c0001t0005 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 7/7 | 564 | chr13 | 77763784 | ||||||
| chr13:77763826 | C | G | 1 | a0001c0001t0004 | 2 | HG01109.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*606C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 7/7 | 606 | chr13 | 77763826 | ||||||
| chr13:77763881 | A | G | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(1): Show |
66 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*661A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 7/7 | 661 | chr13 | 77763881 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:77698541 | T | G | 1 | a0001c0001t0001g0016 | 1 | NA19064.hp1 | splice_donor_variant&intron_variant | HIGH | c.626+2T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698541 | |||||||
| chr13:77698619 | C | G | 1 | a0001c0001t0001g0283 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.626+80C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698619 | |||||||
| chr13:77698771 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.626+232G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698771 | |||||||
| chr13:77698909 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 |
3 | NA18974.hp1 NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.626+370G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698909 | |||||||
| chr13:77698910 | A | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 |
3 | NA18974.hp1 NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.626+371A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698910 | |||||||
| chr13:77698918 | C | T | 1 | a0001c0001t0002g0282 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.626+379C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698918 | |||||||
| chr13:77698921 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.626+382G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698921 | |||||||
| chr13:77699039 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | NA18951.hp2 NA18979.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.626+500G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699039 | |||||||
| chr13:77699152 | A | C | 1 | a0001c0001t0001g0016 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.626+613A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699152 | |||||||
| chr13:77699253 | A | T | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.626+714A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699253 | |||||||
| chr13:77699260 | T | C | 1 | a0001c0001t0001g0025 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.626+721T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699260 | |||||||
| chr13:77699536 | T | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
95 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.626+997T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699536 | |||||||
| chr13:77699555 | A | G | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
95 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.626+1016A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699555 | |||||||
| chr13:77699796 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.626+1257A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699796 | |||||||
| chr13:77699815 | G | T | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.626+1276G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699815 | |||||||
| chr13:77699859 | A | AGCCCAGG others(7): Show |
145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.626+1321_626+1322i others(16): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77699859 | ||||||
| chr13:77700179 | AG | A | 8 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.626+1641delG | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700179 | |||||||
| chr13:77700409 | C | A | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.626+1870C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700409 | |||||||
| chr13:77700591 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+2052G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700591 | |||||||
| chr13:77700799 | A | G | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+2260A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700799 | |||||||
| chr13:77700852 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.626+2313A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700852 | |||||||
| chr13:77700897 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.626+2358C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700897 | |||||||
| chr13:77701240 | TA | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.626+2706delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77701240 | ||||||
| chr13:77701481 | A | G | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+2942A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701481 | |||||||
| chr13:77701589 | A | G | 1 | a0001c0001t0002g0277 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.626+3050A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701589 | |||||||
| chr13:77701597 | A | T | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.626+3058A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701597 | |||||||
| chr13:77701670 | A | G | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+3131A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701670 | |||||||
| chr13:77701714 | G | A | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+3175G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701714 | |||||||
| chr13:77701731 | ATTCT | A | 32 | a0001c0001t0001g0016 a0001c0001t0001g0122 a0001c0001t0001g0132 others(29): Show |
35 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.626+3215_626+3218d others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77701731 | ||||||
| chr13:77701948 | T | C | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+3409T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701948 | |||||||
| chr13:77702161 | C | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
92 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.626+3622C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702161 | |||||||
| chr13:77702168 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+3629T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702168 | |||||||
| chr13:77702169 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+3630G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702169 | |||||||
| chr13:77702239 | A | G | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+3700A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702239 | |||||||
| chr13:77702550 | A | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.626+4011A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702550 | |||||||
| chr13:77702629 | G | A | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG01175.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.626+4090G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702629 | |||||||
| chr13:77702716 | A | AT | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
121 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.626+4186dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77702716 | ||||||
| chr13:77703258 | T | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.626+4719T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703258 | |||||||
| chr13:77703279 | C | T | 27 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(24): Show |
27 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.626+4740C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703279 | |||||||
| chr13:77703286 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.626+4747A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703286 | |||||||
| chr13:77703333 | T | C | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.626+4794T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703333 | |||||||
| chr13:77703400 | T | A | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.626+4861T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703400 | |||||||
| chr13:77703420 | A | G | 1 | a0002c0002t0002g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.626+4881A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703420 | |||||||
| chr13:77703462 | T | C | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+4923T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703462 | |||||||
| chr13:77703489 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.626+4950C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703489 | |||||||
| chr13:77703889 | T | TTA | 4 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
4 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+5365_626+5366d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703889 | ||||||
| chr13:77703904 | TAC | T | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
95 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.626+5375_626+5376d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703904 | ||||||
| chr13:77703948 | T | TAAAATAT others(528): Show |
1 | a0002c0002t0001g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(537): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(566): Show |
2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(575): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(528): Show |
1 | a0001c0001t0001g0174 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(537): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(612): Show |
2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG03098.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(621): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(572): Show |
1 | a0001c0001t0002g0178 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(581): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(612): Show |
1 | a0001c0001t0001g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(621): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(572): Show |
47 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
52 | HG00423.hp2 HG00735.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(581): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(860): Show |
1 | a0001c0001t0001g0227 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(869): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(533): Show |
1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(542): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(532): Show |
13 | a0001c0001t0001g0166 a0001c0001t0001g0232 a0001c0001t0001g0251 others(10): Show |
13 | HG00741.hp1 HG01070.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(541): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(534): Show |
1 | a0001c0001t0002g0263 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(543): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(616): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0264 a0001c0001t0001g0265 others(4): Show |
7 | HG00558.hp2 HG02080.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(625): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(656): Show |
1 | a0001c0001t0001g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(665): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(744): Show |
1 | a0001c0001t0001g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(753): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(574): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | NA18951.hp2 NA18979.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(583): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(570): Show |
1 | a0001c0001t0001g0273 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(579): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(758): Show |
1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(767): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(802): Show |
1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(811): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(831): Show |
1 | a0001c0001t0003g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(840): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(661): Show |
2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(670): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(697): Show |
1 | a0001c0001t0001g0112 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(706): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(699): Show |
1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(708): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(785): Show |
3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02615.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(794): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(791): Show |
1 | a0001c0001t0003g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(800): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(753): Show |
1 | a0001c0001t0003g0150 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(762): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(795): Show |
3 | a0001c0001t0003g0010 a0001c0001t0003g0148 a0001c0001t0003g0149 |
4 | HG02647.hp2 HG02717.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(804): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(791): Show |
1 | a0001c0001t0003g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(800): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(833): Show |
1 | a0001c0001t0003g0151 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(842): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(540): Show |
3 | a0001c0001t0002g0120 a0001c0001t0002g0138 a0001c0001t0002g0139 |
3 | HG00280.hp2 HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(549): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(582): Show |
20 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0137 others(17): Show |
23 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(591): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(797): Show |
1 | a0001c0001t0001g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(806): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(584): Show |
1 | a0001c0001t0002g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(593): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(628): Show |
1 | a0001c0001t0002g0142 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(637): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(879): Show |
1 | a0001c0001t0007g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(888): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(797): Show |
1 | a0001c0001t0001g0157 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(806): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(494): Show |
1 | a0001c0001t0002g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.626+5437_626+5438i others(503): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TAAAATAT others(616): Show |
1 | a0001c0001t0001g0275 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.626+5422_626+5423i others(625): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | ||||||
| chr13:77703948 | T | TTAAAATA others(583): Show |
1 | a0001c0001t0002g0143 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.626+5409_626+5410i others(592): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703948 | |||||||
| chr13:77703949 | A | AAAATATA others(530): Show |
1 | a0001c0001t0001g0179 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(539): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703949 | ||||||
| chr13:77703950 | A | AAATATAT others(697): Show |
1 | a0001c0001t0004g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(706): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | ||||||
| chr13:77703950 | A | AAATATAT others(657): Show |
1 | a0001c0001t0004g0116 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(666): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | ||||||
| chr13:77703950 | A | AAATATAT others(579): Show |
1 | a0001c0001t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(588): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | ||||||
| chr13:77703950 | A | AAATATAT others(498): Show |
1 | a0001c0001t0002g0140 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(507): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | ||||||
| chr13:77703950 | A | AAATATAT others(789): Show |
1 | a0001c0001t0001g0154 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(798): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | ||||||
| chr13:77703950 | A | AAATATAT others(709): Show |
1 | a0001c0001t0001g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(718): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | ||||||
| chr13:77703963 | T | TATGTTTT others(812): Show |
1 | a0002c0002t0001g0167 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(821): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(814): Show |
3 | a0002c0002t0001g0168 a0002c0002t0001g0169 a0002c0002t0001g0170 |
3 | HG02818.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(823): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(812): Show |
1 | a0001c0001t0001g0175 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(821): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(612): Show |
4 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(1): Show |
4 | HG01928.hp2 HG01934.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(621): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(856): Show |
1 | a0001c0001t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(865): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(858): Show |
4 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
4 | HG02572.hp2 HG02717.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(867): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(858): Show |
1 | a0002c0002t0001g0228 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(867): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(818): Show |
1 | a0001c0001t0001g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(827): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(898): Show |
1 | a0001c0001t0001g0231 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(907): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(818): Show |
20 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0160 others(17): Show |
23 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(827): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(858): Show |
3 | a0001c0001t0001g0248 a0001c0001t0002g0246 a0001c0001t0002g0277 |
3 | HG00558.hp1 HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(867): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(898): Show |
2 | a0001c0001t0002g0249 a0001c0001t0002g0250 |
2 | HG02135.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(907): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(816): Show |
1 | a0001c0001t0001g0259 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(825): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(818): Show |
1 | a0001c0001t0001g0165 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(827): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(816): Show |
1 | a0001c0001t0002g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(825): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(816): Show |
1 | a0001c0001t0001g0262 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(825): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(948): Show |
1 | a0001c0001t0001g0271 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(957): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TATGTTTT others(858): Show |
1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(867): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | ||||||
| chr13:77703963 | T | TGTTTTAT others(812): Show |
1 | a0001c0004t0001g0015 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.626+5424_626+5425i others(821): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703963 | |||||||
| chr13:77703973 | A | AAG | 50 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(47): Show |
50 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703973 | |||||||
| chr13:77703973 | A | AAGTGTAT others(127): Show |
38 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(35): Show |
42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(136): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703973 | |||||||
| chr13:77703973 | A | AAGTGTAT others(215): Show |
5 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(224): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703973 | |||||||
| chr13:77703977 | A | ATATATAC others(776): Show |
1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5444_626+5445i others(785): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703977 | ||||||
| chr13:77703977 | A | ATATATAC others(653): Show |
1 | a0001c0001t0001g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.626+5444_626+5445i others(662): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703977 | ||||||
| chr13:77703983 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5444A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703983 | |||||||
| chr13:77703984 | T | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
95 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.626+5445T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703984 | |||||||
| chr13:77703990 | G | T | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
95 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.626+5451G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703990 | |||||||
| chr13:77704003 | C | CAT | 129 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(126): Show |
137 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.626+5465_626+5466d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | ||||||
| chr13:77704003 | C | CATATGTT others(88): Show |
2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.626+5466_626+5467i others(97): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | ||||||
| chr13:77704003 | C | CATATGTT others(90): Show |
1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.626+5466_626+5467i others(99): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | ||||||
| chr13:77704003 | C | CATATGTT others(308): Show |
1 | a0001c0001t0002g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.626+5466_626+5467i others(317): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | ||||||
| chr13:77704003 | C | CATATGTT others(255): Show |
7 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(4): Show |
7 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5466_626+5467i others(264): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | ||||||
| chr13:77704003 | C | CATATGTT others(310): Show |
6 | a0001c0001t0002g0074 a0001c0001t0002g0075 a0001c0001t0002g0076 others(3): Show |
6 | HG02630.hp2 HG02896.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.626+5466_626+5467i others(319): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | ||||||
| chr13:77704003 | C | CATGTTTT others(308): Show |
1 | a0001c0001t0002g0082 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.626+5474_626+5475i others(317): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | ||||||
| chr13:77704013 | A | AAG | 30 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0086 others(27): Show |
30 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.626+5474_626+5475i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704013 | |||||||
| chr13:77704013 | A | ATG | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+5476_626+5477d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704013 | ||||||
| chr13:77704015 | GTA | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
62 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.626+5485_626+5486d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704015 | ||||||
| chr13:77704017 | A | ATATATAC others(161): Show |
1 | a0001c0001t0001g0081 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.626+5484_626+5485i others(170): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704017 | ||||||
| chr13:77704024 | T | C | 32 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(29): Show |
32 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.626+5485T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704024 | |||||||
| chr13:77704030 | G | T | 32 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(29): Show |
32 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.626+5491G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704030 | |||||||
| chr13:77704040 | A | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
62 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.626+5501A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704040 | |||||||
| chr13:77704043 | C | CAT | 149 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(146): Show |
157 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.626+5505_626+5506d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704043 | ||||||
| chr13:77704051 | A | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): Show |
50 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.626+5512A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704051 | |||||||
| chr13:77704053 | A | ATG | 28 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(25): Show |
28 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.626+5516_626+5517d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704053 | ||||||
| chr13:77704055 | G | GTGTATAT others(167): Show |
1 | a0001c0001t0006g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.626+5517_626+5518i others(176): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704055 | ||||||
| chr13:77704055 | GTA | G | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
66 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.626+5525_626+5526d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704055 | ||||||
| chr13:77704057 | A | G | 1 | a0001c0001t0006g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.626+5518A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704057 | |||||||
| chr13:77704064 | T | C | 28 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(25): Show |
28 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.626+5525T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704064 | |||||||
| chr13:77704070 | G | T | 28 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(25): Show |
28 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.626+5531G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704070 | |||||||
| chr13:77704080 | A | ATACATAT others(251): Show |
22 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(19): Show |
22 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.626+5559_626+5560i others(260): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704080 | ||||||
| chr13:77704080 | A | ATACATAT others(249): Show |
2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.626+5559_626+5560i others(258): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704080 | ||||||
| chr13:77704080 | A | ATACATAT others(295): Show |
2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.626+5559_626+5560i others(304): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704080 | ||||||
| chr13:77704080 | A | ATACATAT others(220): Show |
1 | a0001c0001t0002g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.626+5559_626+5560i others(229): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704080 | ||||||
| chr13:77704080 | A | G | 25 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(22): Show |
25 | HG01099.hp1 HG01934.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.626+5541A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704080 | |||||||
| chr13:77704084 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.626+5545A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704084 | |||||||
| chr13:77704093 | A | C | 14 | a0001c0001t0001g0006 a0001c0001t0001g0058 a0001c0001t0001g0059 others(11): Show |
15 | HG00639.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5554A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704093 | |||||||
| chr13:77704097 | GTA | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
94 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.626+5567_626+5568d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704097 | ||||||
| chr13:77704099 | A | G | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5560A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704099 | |||||||
| chr13:77704108 | C | CACATATA others(52): Show |
1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5570_626+5571i others(61): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704108 | ||||||
| chr13:77704112 | G | T | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5573G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704112 | |||||||
| chr13:77704117 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5578T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704117 | |||||||
| chr13:77704122 | A | G | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(73): Show |
80 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.626+5583A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704122 | |||||||
| chr13:77704125 | CAT | C | 15 | a0001c0001t0002g0030 a0001c0001t0002g0062 a0001c0001t0002g0063 others(12): Show |
15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5589_626+5590d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704125 | ||||||
| chr13:77704126 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01981.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.626+5587A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704126 | |||||||
| chr13:77704127 | T | TACGTTTT others(193): Show |
1 | a0002c0002t0001g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.626+5589_626+5590i others(202): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704127 | ||||||
| chr13:77704127 | T | TACGTTTT others(195): Show |
1 | a0001c0001t0001g0166 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.626+5589_626+5590i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704127 | ||||||
| chr13:77704129 | T | C | 13 | a0001c0001t0001g0232 a0001c0001t0001g0251 a0001c0001t0001g0254 others(10): Show |
13 | HG00741.hp1 HG01070.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.626+5590T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704129 | |||||||
| chr13:77704135 | A | C | 29 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(26): Show |
29 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.626+5596A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704135 | |||||||
| chr13:77704139 | GTA | G | 90 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(87): Show |
94 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.626+5609_626+5610d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704139 | ||||||
| chr13:77704148 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5609T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704148 | |||||||
| chr13:77704154 | G | T | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5615G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704154 | |||||||
| chr13:77704164 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(74): Show |
81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.626+5625A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704164 | |||||||
| chr13:77704167 | CAT | C | 5 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5631_626+5632d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704167 | ||||||
| chr13:77704168 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5629A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704168 | |||||||
| chr13:77704171 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.626+5632T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704171 | |||||||
| chr13:77704177 | A | C | 28 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(25): Show |
28 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.626+5638A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704177 | |||||||
| chr13:77704181 | GTA | G | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(72): Show |
79 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.626+5651_626+5652d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704181 | ||||||
| chr13:77704183 | A | ATATATAT others(117): Show |
1 | a0001c0001t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.626+5666_626+5667i others(126): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704183 | ||||||
| chr13:77704188 | TATAC | T | 15 | a0001c0001t0002g0030 a0001c0001t0002g0062 a0001c0001t0002g0063 others(12): Show |
15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5653_626+5656d others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704188 | ||||||
| chr13:77704190 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5651T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704190 | |||||||
| chr13:77704196 | G | T | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5657G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704196 | |||||||
| chr13:77704199 | AAT | A | 15 | a0001c0001t0002g0030 a0001c0001t0002g0062 a0001c0001t0002g0063 others(12): Show |
15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5668_626+5669d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704199 | ||||||
| chr13:77704206 | A | ATACATAT others(405): Show |
1 | a0001c0001t0001g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(414): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704206 | ||||||
| chr13:77704206 | A | ATACATAT others(523): Show |
1 | a0001c0001t0001g0185 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704206 | ||||||
| chr13:77704206 | A | ATACATAT others(363): Show |
1 | a0001c0001t0002g0247 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(372): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704206 | ||||||
| chr13:77704206 | A | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0117 others(77): Show |
88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.626+5667A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704206 | |||||||
| chr13:77704209 | C | CGTATGTT others(153): Show |
1 | a0001c0001t0001g0154 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5670_626+5671i others(162): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704209 | |||||||
| chr13:77704209 | CAT | C | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
74 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.626+5673_626+5674d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704209 | ||||||
| chr13:77704211 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5672T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704211 | |||||||
| chr13:77704211 | T | TATGTTTT others(111): Show |
1 | a0001c0001t0001g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(120): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(521): Show |
2 | a0001c0001t0002g0253 a0001c0001t0002g0282 |
2 | HG00741.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(530): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(483): Show |
1 | a0001c0001t0002g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(492): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(441): Show |
3 | a0001c0001t0002g0178 a0001c0001t0002g0255 a0001c0001t0002g0263 |
3 | HG01255.hp2 HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(450): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(521): Show |
2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(530): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(481): Show |
1 | a0001c0001t0001g0177 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(523): Show |
1 | a0001c0001t0001g0199 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(477): Show |
1 | a0001c0001t0001g0013 | 2 | NA18998.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(486): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(481): Show |
28 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0018 others(25): Show |
28 | HG00408.hp2 HG00741.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(519): Show |
1 | a0001c0001t0001g0214 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(528): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(557): Show |
2 | a0001c0001t0001g0213 a0001c0001t0003g0188 |
2 | HG00735.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(566): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(481): Show |
10 | a0001c0001t0001g0012 a0001c0001t0001g0189 a0001c0001t0001g0192 others(7): Show |
11 | HG00438.hp1 HG02074.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(519): Show |
1 | a0001c0001t0001g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(528): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(481): Show |
1 | a0001c0001t0001g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(481): Show |
1 | a0001c0001t0001g0212 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(355): Show |
1 | a0001c0001t0001g0179 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(364): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(481): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0193 |
3 | HG01258.hp1 HG01261.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(479): Show |
1 | a0001c0001t0001g0208 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(488): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(193): Show |
1 | a0002c0002t0001g0170 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.626+5734_626+5735i others(202): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(523): Show |
3 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG01433.hp2 HG01952.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.626+5692_626+5693i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(523): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0195 a0001c0001t0001g0264 others(1): Show |
5 | HG02257.hp2 HG02809.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5692_626+5693i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(523): Show |
1 | a0001c0001t0001g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(523): Show |
1 | a0001c0001t0001g0020 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(481): Show |
1 | a0001c0001t0001g0265 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(195): Show |
1 | a0001c0001t0002g0140 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.626+5692_626+5693i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(485): Show |
1 | a0001c0001t0001g0224 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(494): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(195): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0160 others(21): Show |
28 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.626+5692_626+5693i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(235): Show |
1 | a0001c0001t0001g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(244): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(237): Show |
1 | a0002c0002t0001g0169 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(246): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(279): Show |
1 | a0001c0001t0001g0227 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.626+5692_626+5693i others(288): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(237): Show |
3 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0001c0001t0001g0278 |
3 | HG02572.hp2 NA18946.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.626+5692_626+5693i others(246): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(239): Show |
1 | a0001c0001t0001g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.626+5692_626+5693i others(248): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(195): Show |
2 | a0001c0001t0001g0243 a0002c0002t0001g0228 |
2 | HG04115.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.626+5692_626+5693i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(195): Show |
1 | a0001c0001t0001g0259 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704211 | T | TATGTTTT others(155): Show |
2 | a0001c0001t0001g0112 a0001c0001t0001g0115 |
2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.626+5692_626+5693i others(164): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | ||||||
| chr13:77704219 | A | C | 1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5680A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704219 | |||||||
| chr13:77704223 | G | GTA | 23 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0155 others(20): Show |
23 | HG00140.hp2 HG00558.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.626+5691_626+5692d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | ||||||
| chr13:77704223 | G | GTATATAT others(113): Show |
3 | a0001c0001t0001g0176 a0001c0001t0001g0186 a0001c0001t0001g0251 |
3 | HG02148.hp2 HG03098.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(122): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | ||||||
| chr13:77704223 | G | GTATATAT others(155): Show |
3 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 |
3 | NA18951.hp2 NA18979.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(164): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | ||||||
| chr13:77704223 | G | GTATATAT others(239): Show |
1 | a0001c0001t0001g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(248): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | ||||||
| chr13:77704223 | G | GTATATAT others(153): Show |
1 | a0001c0001t0001g0223 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(162): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | ||||||
| chr13:77704230 | TAC | T | 5 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5693_626+5694d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704230 | ||||||
| chr13:77704240 | A | C | 15 | a0001c0001t0002g0030 a0001c0001t0002g0062 a0001c0001t0002g0063 others(12): Show |
15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5701A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704240 | |||||||
| chr13:77704242 | A | G | 15 | a0001c0001t0002g0030 a0001c0001t0002g0062 a0001c0001t0002g0063 others(12): Show |
15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5703A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704242 | |||||||
| chr13:77704244 | ATG | A | 5 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0001t0002g0071 others(2): Show |
5 | HG02257.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5707_626+5708d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704244 | ||||||
| chr13:77704246 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(105): Show |
112 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.626+5707G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704246 | |||||||
| chr13:77704249 | CAT | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG01123.hp1 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.626+5713_626+5714d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704249 | ||||||
| chr13:77704251 | T | TGTTTTAT others(31): Show |
1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+5712_626+5713i others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704251 | |||||||
| chr13:77704253 | T | G | 15 | a0001c0001t0002g0030 a0001c0001t0002g0062 a0001c0001t0002g0063 others(12): Show |
15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5714T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704253 | |||||||
| chr13:77704258 | T | C | 3 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0002g0140 |
3 | HG01069.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.626+5719T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704258 | |||||||
| chr13:77704258 | T | TATATGTA others(111): Show |
11 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(8): Show |
11 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.626+5732_626+5733i others(120): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704258 | ||||||
| chr13:77704258 | T | TATATGTA others(149): Show |
1 | a0001c0001t0002g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.626+5732_626+5733i others(158): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704258 | ||||||
| chr13:77704270 | T | TAC | 63 | a0001c0001t0001g0017 a0001c0001t0001g0114 a0001c0001t0001g0132 others(60): Show |
67 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.626+5732_626+5733i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704270 | ||||||
| chr13:77704270 | T | TACATAGA others(157): Show |
2 | a0001c0001t0001g0221 a0001c0001t0001g0232 |
2 | HG03471.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.626+5732_626+5733i others(166): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704270 | ||||||
| chr13:77704270 | T | TATAC | 24 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
24 | HG00140.hp2 HG00558.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.626+5734_626+5735i others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704270 | ||||||
| chr13:77704274 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5735G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704274 | |||||||
| chr13:77704277 | A | AAT | 38 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(35): Show |
41 | HG00438.hp2 HG00544.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.626+5744_626+5745d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704277 | ||||||
| chr13:77704277 | A | ACT | 21 | a0001c0001t0001g0185 a0001c0001t0002g0030 a0001c0001t0002g0062 others(18): Show |
21 | HG00423.hp2 HG01099.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.626+5738_626+5739i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704277 | |||||||
| chr13:77704277 | A | C | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5738A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704277 | |||||||
| chr13:77704278 | A | ATATATAC others(33): Show |
6 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+5749_626+5750i others(42): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | ||||||
| chr13:77704278 | A | ATATATAT others(189): Show |
1 | a0001c0001t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.626+5745_626+5746i others(198): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | ||||||
| chr13:77704278 | A | ATATATAT others(149): Show |
2 | a0001c0001t0001g0145 a0001c0001t0002g0007 |
3 | HG02055.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.626+5745_626+5746i others(158): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | ||||||
| chr13:77704278 | A | ATATATAT others(189): Show |
1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.626+5745_626+5746i others(198): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | ||||||
| chr13:77704278 | A | ATATATGT others(267): Show |
1 | a0002c0002t0002g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.626+5744_626+5745i others(276): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | ||||||
| chr13:77704278 | A | ATATATGT others(545): Show |
1 | a0002c0002t0001g0158 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.626+5744_626+5745i others(554): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | ||||||
| chr13:77704278 | A | ATATATGT others(227): Show |
1 | a0001c0001t0002g0031 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5744_626+5745i others(236): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | ||||||
| chr13:77704278 | A | G | 21 | a0001c0001t0001g0185 a0001c0001t0002g0030 a0001c0001t0002g0062 others(18): Show |
21 | HG00423.hp2 HG01099.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.626+5739A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704278 | |||||||
| chr13:77704282 | A | ATG | 24 | a0001c0001t0001g0114 a0001c0001t0001g0155 a0001c0001t0001g0157 others(21): Show |
24 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.626+5744_626+5745i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704282 | ||||||
| chr13:77704282 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5743A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704282 | |||||||
| chr13:77704284 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.626+5745A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704284 | |||||||
| chr13:77704285 | C | T | 6 | a0001c0001t0001g0161 a0001c0001t0001g0180 a0001c0001t0001g0219 others(3): Show |
6 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+5746C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704285 | |||||||
| chr13:77704287 | T | C | 6 | a0001c0001t0001g0161 a0001c0001t0001g0180 a0001c0001t0001g0219 others(3): Show |
6 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+5748T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704287 | |||||||
| chr13:77704287 | T | G | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+5748T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704287 | |||||||
| chr13:77704287 | T | TAGGTTTT others(33): Show |
64 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(61): Show |
69 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.626+6491_626+6530d others(42): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704287 | ||||||
| chr13:77704287 | T | TAGGTTTT others(73): Show |
15 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0174 others(12): Show |
16 | HG00735.hp2 HG01243.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.626+6451_626+6530d others(82): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704287 | ||||||
| chr13:77704287 | T | TAGGTTTT others(113): Show |
4 | a0001c0001t0001g0019 a0001c0001t0001g0183 a0001c0001t0001g0218 others(1): Show |
4 | HG00408.hp2 HG02723.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+6411_626+6530d others(122): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704287 | ||||||
| chr13:77704289 | G | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.626+5750G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704289 | |||||||
| chr13:77704294 | T | C | 7 | a0001c0001t0001g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5755T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704294 | |||||||
| chr13:77704295 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.626+5756A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704295 | |||||||
| chr13:77704299 | G | GTA | 19 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(16): Show |
19 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.626+5767_626+5768d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704299 | ||||||
| chr13:77704306 | TAC | T | 7 | a0001c0001t0001g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5769_626+5770d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704306 | ||||||
| chr13:77704315 | ACT | A | 7 | a0001c0001t0001g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5777_626+5778d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704315 | |||||||
| chr13:77704316 | C | A | 62 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(59): Show |
65 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.626+5777C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704316 | |||||||
| chr13:77704317 | T | TATATATA others(107): Show |
2 | a0001c0001t0002g0120 a0001c0001t0002g0139 |
2 | HG00280.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.626+5778_626+5779i others(116): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704317 | |||||||
| chr13:77704317 | T | TATATATA others(67): Show |
15 | a0001c0001t0001g0132 a0001c0001t0001g0137 a0001c0001t0002g0008 others(12): Show |
17 | HG00438.hp2 HG00544.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.626+5778_626+5779i others(76): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704317 | |||||||
| chr13:77704317 | T | TATATATA others(513): Show |
1 | a0001c0001t0005g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.626+5778_626+5779i others(522): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704317 | |||||||
| chr13:77704318 | G | A | 69 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(66): Show |
72 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.626+5779G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704318 | |||||||
| chr13:77704322 | A | G | 24 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
24 | HG00140.hp2 HG00558.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.626+5783A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704322 | |||||||
| chr13:77704325 | CAG | C | 11 | a0001c0001t0001g0157 a0001c0001t0001g0184 a0001c0001t0001g0231 others(8): Show |
12 | HG00140.hp1 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.626+5789_626+5790d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704325 | ||||||
| chr13:77704327 | G | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
168 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.626+5788G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704327 | |||||||
| chr13:77704329 | G | T | 70 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(67): Show |
73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.626+5790G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704329 | |||||||
| chr13:77704335 | A | C | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.626+5796A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704335 | |||||||
| chr13:77704339 | G | GTA | 15 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5807_626+5808d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704339 | ||||||
| chr13:77704356 | C | A | 43 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(40): Show |
44 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.626+5817C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704356 | |||||||
| chr13:77704357 | T | TATATATA others(67): Show |
2 | a0001c0001t0001g0155 a0001c0001t0003g0150 |
2 | HG00735.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.626+5818_626+5819i others(76): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704357 | |||||||
| chr13:77704357 | T | TATATGTA others(107): Show |
1 | a0001c0001t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.626+5818_626+5819i others(116): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704357 | |||||||
| chr13:77704358 | G | A | 44 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(41): Show |
45 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.626+5819G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704358 | |||||||
| chr13:77704358 | G | GTATATAC others(31): Show |
1 | a0001c0001t0002g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.626+5821_626+5858d others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704358 | ||||||
| chr13:77704362 | A | G | 24 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(21): Show |
24 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.626+5823A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704362 | |||||||
| chr13:77704367 | G | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.626+5828G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704367 | |||||||
| chr13:77704369 | G | T | 42 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(39): Show |
43 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.626+5830G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704369 | |||||||
| chr13:77704379 | G | GTA | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(10): Show |
13 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.626+5847_626+5848d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704379 | ||||||
| chr13:77704386 | TAC | T | 11 | a0001c0001t0001g0157 a0001c0001t0001g0184 a0001c0001t0001g0231 others(8): Show |
12 | HG00140.hp1 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.626+5849_626+5850d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704386 | ||||||
| chr13:77704395 | ACT | A | 11 | a0001c0001t0001g0157 a0001c0001t0001g0184 a0001c0001t0001g0231 others(8): Show |
12 | HG00140.hp1 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.626+5857_626+5858d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704395 | |||||||
| chr13:77704396 | C | A | 29 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
29 | HG00140.hp2 HG00558.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.626+5857C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704396 | |||||||
| chr13:77704396 | CTG | C | 15 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0062 others(12): Show |
15 | HG01099.hp1 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5859_626+5860d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704396 | ||||||
| chr13:77704397 | T | TATATATA others(67): Show |
1 | a0001c0001t0001g0245 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.626+5858_626+5859i others(76): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704397 | |||||||
| chr13:77704398 | G | A | 40 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(37): Show |
41 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.626+5859G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704398 | |||||||
| chr13:77704398 | G | GTATATAC others(31): Show |
2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.626+5861_626+5898d others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704398 | ||||||
| chr13:77704398 | G | GTATATAC others(31): Show |
1 | a0001c0001t0002g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.626+5867_626+5868i others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704398 | ||||||
| chr13:77704402 | A | G | 18 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
18 | HG00558.hp1 HG02135.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.626+5863A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704402 | |||||||
| chr13:77704405 | CAG | C | 5 | a0001c0001t0002g0249 a0001c0001t0002g0272 a0001c0001t0002g0277 others(2): Show |
5 | HG01109.hp2 HG02080.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5869_626+5870d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704405 | ||||||
| chr13:77704407 | G | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(121): Show |
132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.626+5868G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704407 | |||||||
| chr13:77704409 | G | T | 39 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(36): Show |
40 | HG00558.hp1 HG00735.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.626+5870G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704409 | |||||||
| chr13:77704414 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.626+5875T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704414 | |||||||
| chr13:77704415 | A | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02622.hp2 HG02976.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5876A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704415 | |||||||
| chr13:77704419 | G | GTA | 8 | a0001c0001t0001g0161 a0001c0001t0001g0176 a0001c0001t0001g0186 others(5): Show |
8 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.626+5887_626+5888d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704419 | ||||||
| chr13:77704427 | A | T | 2 | a0001c0001t0002g0246 a0001c0001t0002g0250 |
2 | HG00558.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.626+5888A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704427 | |||||||
| chr13:77704436 | C | A | 26 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(23): Show |
26 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.626+5897C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704436 | |||||||
| chr13:77704436 | CTG | C | 9 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+5899_626+5900d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704436 | ||||||
| chr13:77704438 | G | A | 28 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
28 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.626+5899G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704438 | |||||||
| chr13:77704438 | G | GTATATAC others(31): Show |
39 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(36): Show |
43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.626+5901_626+5938d others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704438 | ||||||
| chr13:77704438 | G | GTATATAC others(33): Show |
1 | a0001c0001t0001g0187 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.626+5938_626+5939i others(42): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704438 | ||||||
| chr13:77704442 | A | G | 18 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
18 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.626+5903A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704442 | |||||||
| chr13:77704445 | CAG | C | 6 | a0001c0001t0001g0229 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG00558.hp1 HG02135.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+5909_626+5910d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704445 | ||||||
| chr13:77704447 | G | T | 35 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(32): Show |
36 | HG00735.hp1 HG01109.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.626+5908G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704447 | |||||||
| chr13:77704449 | G | T | 36 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(33): Show |
37 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.626+5910G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704449 | |||||||
| chr13:77704454 | T | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.626+5915T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704454 | |||||||
| chr13:77704455 | A | C | 3 | a0001c0001t0001g0176 a0001c0001t0001g0186 a0001c0001t0001g0221 |
3 | HG03098.hp1 HG03704.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.626+5916A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704455 | |||||||
| chr13:77704459 | G | GTA | 4 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+5927_626+5928d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704459 | ||||||
| chr13:77704466 | TAC | T | 3 | a0001c0001t0002g0249 a0001c0001t0002g0272 a0001c0001t0002g0277 |
3 | HG02080.hp1 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.626+5929_626+5930d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704466 | ||||||
| chr13:77704468 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.626+5929C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704468 | |||||||
| chr13:77704473 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+5934A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704473 | |||||||
| chr13:77704475 | ACT | A | 5 | a0001c0001t0002g0249 a0001c0001t0002g0272 a0001c0001t0002g0277 others(2): Show |
5 | HG01109.hp2 HG02080.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5937_626+5938d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704475 | |||||||
| chr13:77704476 | C | A | 21 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(18): Show |
21 | HG00558.hp1 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.626+5937C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704476 | |||||||
| chr13:77704476 | CTG | C | 25 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(22): Show |
25 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.626+5939_626+5940d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704476 | ||||||
| chr13:77704477 | T | TATATGTA others(29): Show |
1 | a0001c0001t0002g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.626+5938_626+5939i others(38): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704477 | |||||||
| chr13:77704478 | G | A | 26 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(23): Show |
26 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.626+5939G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704478 | |||||||
| chr13:77704478 | G | GTATATAC others(71): Show |
1 | a0001c0001t0003g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.626+5941_626+6018d others(80): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704478 | ||||||
| chr13:77704482 | A | G | 18 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(15): Show |
18 | HG00558.hp1 HG01123.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.626+5943A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704482 | |||||||
| chr13:77704487 | G | T | 35 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(32): Show |
36 | HG00558.hp1 HG00735.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.626+5948G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704487 | |||||||
| chr13:77704489 | G | T | 22 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(19): Show |
22 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.626+5950G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704489 | |||||||
| chr13:77704495 | A | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0221 |
2 | HG03704.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.626+5956A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704495 | |||||||
| chr13:77704499 | G | GTA | 4 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+5967_626+5968d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704499 | ||||||
| chr13:77704506 | TAC | T | 5 | a0001c0001t0001g0229 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG00558.hp1 HG02135.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5969_626+5970d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704506 | ||||||
| chr13:77704515 | ACT | A | 5 | a0001c0001t0001g0229 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG00558.hp1 HG02135.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5977_626+5978d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704515 | |||||||
| chr13:77704516 | C | A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5977C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704516 | |||||||
| chr13:77704518 | G | A | 20 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(17): Show |
20 | HG00558.hp1 HG01123.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.626+5979G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704518 | |||||||
| chr13:77704522 | A | G | 10 | a0001c0001t0001g0161 a0001c0001t0001g0166 a0001c0001t0001g0176 others(7): Show |
10 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.626+5983A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704522 | |||||||
| chr13:77704525 | CAG | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02148.hp2 HG02622.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5989_626+5990d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704525 | ||||||
| chr13:77704527 | G | T | 27 | a0001c0001t0001g0157 a0001c0001t0001g0161 a0001c0001t0001g0166 others(24): Show |
28 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.626+5988G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704527 | |||||||
| chr13:77704529 | G | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5990G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704529 | |||||||
| chr13:77704535 | A | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG01123.hp1 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.626+5996A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704535 | |||||||
| chr13:77704556 | C | A | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(10): Show |
13 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.626+6017C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704556 | |||||||
| chr13:77704558 | G | A | 15 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+6019G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704558 | |||||||
| chr13:77704562 | A | G | 8 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(5): Show |
8 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.626+6023A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704562 | |||||||
| chr13:77704565 | CAG | C | 5 | a0001c0001t0001g0176 a0001c0001t0001g0186 a0001c0001t0001g0221 others(2): Show |
5 | HG02622.hp2 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+6029_626+6030d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704565 | ||||||
| chr13:77704567 | G | T | 10 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(7): Show |
10 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.626+6028G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704567 | |||||||
| chr13:77704569 | G | T | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(10): Show |
13 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.626+6030G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704569 | |||||||
| chr13:77704586 | TAC | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG02148.hp2 NA18951.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+6049_626+6050d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704586 | ||||||
| chr13:77704589 | A | T | 1 | a0001c0001t0003g0150 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.626+6050A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704589 | |||||||
| chr13:77704595 | ACT | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG02148.hp2 NA18951.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+6057_626+6058d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704595 | |||||||
| chr13:77704596 | C | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0176 a0001c0001t0001g0186 others(6): Show |
9 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6057C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704596 | |||||||
| chr13:77704598 | G | A | 13 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(10): Show |
13 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.626+6059G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704598 | |||||||
| chr13:77704602 | A | G | 9 | a0001c0001t0001g0161 a0001c0001t0001g0176 a0001c0001t0001g0186 others(6): Show |
9 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6063A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704602 | |||||||
| chr13:77704607 | G | GAGGTTTT others(33): Show |
1 | a0002c0002t0002g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.626+6107_626+6108i others(42): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704607 | ||||||
| chr13:77704607 | G | T | 15 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+6068G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704607 | |||||||
| chr13:77704609 | G | T | 9 | a0001c0001t0001g0161 a0001c0001t0001g0176 a0001c0001t0001g0186 others(6): Show |
9 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6070G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704609 | |||||||
| chr13:77704626 | TAC | T | 5 | a0001c0001t0001g0176 a0001c0001t0001g0186 a0001c0001t0001g0221 others(2): Show |
5 | HG02622.hp2 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+6089_626+6090d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704626 | ||||||
| chr13:77704629 | A | T | 8 | a0001c0001t0003g0010 a0001c0001t0003g0146 a0001c0001t0003g0147 others(5): Show |
9 | HG02647.hp2 HG02717.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6090A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704629 | |||||||
| chr13:77704635 | ACT | A | 5 | a0001c0001t0001g0176 a0001c0001t0001g0186 a0001c0001t0001g0221 others(2): Show |
5 | HG02622.hp2 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+6097_626+6098d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704635 | |||||||
| chr13:77704636 | C | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6097C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704636 | |||||||
| chr13:77704638 | G | A | 9 | a0001c0001t0001g0161 a0001c0001t0001g0176 a0001c0001t0001g0186 others(6): Show |
9 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6099G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704638 | |||||||
| chr13:77704642 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6103A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704642 | |||||||
| chr13:77704645 | CAG | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG01123.hp1 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.626+6109_626+6110d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704645 | ||||||
| chr13:77704647 | G | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0176 a0001c0001t0001g0221 others(4): Show |
7 | HG02622.hp2 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+6108G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704647 | |||||||
| chr13:77704649 | G | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6110G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704649 | |||||||
| chr13:77704676 | C | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6137C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704676 | |||||||
| chr13:77704677 | T | TATATGTA others(29): Show |
3 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | HG01123.hp1 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.626+6138_626+6139i others(38): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704677 | |||||||
| chr13:77704678 | G | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0219 a0001c0001t0001g0220 others(1): Show |
4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6139G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704678 | |||||||
| chr13:77704678 | G | GTATATAC others(31): Show |
5 | a0001c0001t0001g0014 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
6 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.626+6141_626+6178d others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704678 | ||||||
| chr13:77704687 | G | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0161 a0001c0001t0001g0219 others(1): Show |
4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6148G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704687 | |||||||
| chr13:77704689 | G | T | 1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6150G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704689 | |||||||
| chr13:77704716 | C | A | 1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6177C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704716 | |||||||
| chr13:77704718 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6179G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704718 | |||||||
| chr13:77704722 | A | G | 1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6183A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704722 | |||||||
| chr13:77704727 | G | T | 1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6188G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704727 | |||||||
| chr13:77704729 | G | T | 1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6190G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704729 | |||||||
| chr13:77704758 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6219G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704758 | |||||||
| chr13:77704767 | G | T | 1 | a0001c0001t0002g0252 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6228G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704767 | |||||||
| chr13:77704819 | G | GTATATAT others(35): Show |
1 | a0001c0001t0001g0020 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.626+6287_626+6328d others(44): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704819 | ||||||
| chr13:77704967 | G | T | 63 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(60): Show |
67 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.626+6428G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704967 | |||||||
| chr13:77705007 | G | T | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
83 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.626+6468G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705007 | |||||||
| chr13:77705047 | G | GAGGTTTT others(153): Show |
1 | a0001c0001t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.626+6530_626+6531i others(162): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77705047 | ||||||
| chr13:77705047 | G | GAGGTTTT others(113): Show |
12 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(9): Show |
12 | HG01099.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.626+6530_626+6531i others(122): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77705047 | ||||||
| chr13:77705047 | G | T | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
125 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.626+6508G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705047 | |||||||
| chr13:77705097 | C | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.626+6558C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705097 | |||||||
| chr13:77705202 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.626+6663A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705202 | |||||||
| chr13:77705243 | A | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0243 |
2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.626+6704A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705243 | |||||||
| chr13:77705393 | A | G | 1 | a0001c0001t0001g0018 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.626+6854A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705393 | |||||||
| chr13:77705615 | A | T | 1 | a0002c0002t0001g0158 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.626+7076A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705615 | |||||||
| chr13:77705644 | A | AT | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
75 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.626+7120dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77705644 | ||||||
| chr13:77705644 | A | ATT | 15 | a0001c0001t0001g0056 a0001c0001t0002g0062 a0001c0001t0002g0063 others(12): Show |
15 | HG01099.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+7119_626+7120d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77705644 | ||||||
| chr13:77705660 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.626+7121A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705660 | |||||||
| chr13:77706124 | T | C | 1 | a0002c0002t0001g0158 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.626+7585T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77706124 | |||||||
| chr13:77706671 | AT | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
146 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.626+8140delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77706671 | ||||||
| chr13:77707490 | T | G | 14 | a0001c0001t0001g0017 a0001c0001t0001g0153 a0001c0001t0001g0154 others(11): Show |
15 | HG00735.hp1 HG01884.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.626+8951T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707490 | |||||||
| chr13:77707584 | A | G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.626+9045A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707584 | |||||||
| chr13:77707753 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
88 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.626+9214A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707753 | |||||||
| chr13:77707794 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.626+9255G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707794 | |||||||
| chr13:77707878 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0243 |
2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.626+9339C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707878 | |||||||
| chr13:77707917 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.626+9378G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707917 | |||||||
| chr13:77707957 | G | C | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 |
3 | HG01175.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.626+9418G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707957 | |||||||
| chr13:77707957 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.626+9418G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707957 | |||||||
| chr13:77708020 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.626+9481T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708020 | |||||||
| chr13:77708054 | C | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0244 |
2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.626+9515C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708054 | |||||||
| chr13:77708058 | A | G | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.626+9519A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708058 | |||||||
| chr13:77708107 | A | T | 1 | a0001c0001t0001g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.626+9568A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708107 | |||||||
| chr13:77708486 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0221 |
2 | NA18747.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.626+9947T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708486 | |||||||
| chr13:77708794 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.626+10255C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708794 | |||||||
| chr13:77708871 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.626+10332A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708871 | |||||||
| chr13:77708944 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0153 a0001c0001t0001g0154 others(11): Show |
15 | HG00735.hp1 HG01884.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.626+10405G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708944 | |||||||
| chr13:77708967 | G | A | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
88 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.626+10428G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708967 | |||||||
| chr13:77708980 | A | G | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02615.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.626+10441A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708980 | |||||||
| chr13:77709046 | C | T | 8 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-10486C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709046 | |||||||
| chr13:77709048 | A | G | 38 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(35): Show |
41 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.627-10484A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709048 | |||||||
| chr13:77709061 | A | G | 5 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0001g0117 others(2): Show |
5 | HG02615.hp1 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-10471A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709061 | |||||||
| chr13:77709163 | C | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.627-10369C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709163 | |||||||
| chr13:77709197 | T | C | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-10335T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709197 | |||||||
| chr13:77709367 | C | T | 33 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(30): Show |
36 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.627-10165C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709367 | |||||||
| chr13:77709383 | A | G | 11 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0003g0010 others(8): Show |
12 | HG00735.hp1 HG01884.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.627-10149A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709383 | |||||||
| chr13:77709833 | C | T | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.627-9699C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709833 | |||||||
| chr13:77709856 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.627-9676C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709856 | |||||||
| chr13:77709960 | C | T | 9 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(6): Show |
9 | HG01109.hp2 HG02602.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.627-9572C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709960 | |||||||
| chr13:77710008 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.627-9524A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710008 | |||||||
| chr13:77710062 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627-9470G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710062 | |||||||
| chr13:77710073 | T | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01981.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.627-9459T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710073 | |||||||
| chr13:77710102 | C | T | 1 | a0001c0001t0004g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.627-9430C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710102 | |||||||
| chr13:77710116 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.627-9416G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710116 | |||||||
| chr13:77710410 | A | C | 4 | a0001c0001t0001g0248 a0001c0001t0001g0254 a0002c0002t0001g0158 others(1): Show |
4 | HG02559.hp2 HG03831.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-9122A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710410 | |||||||
| chr13:77710564 | C | G | 28 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0137 others(25): Show |
31 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.627-8968C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710564 | |||||||
| chr13:77710723 | G | C | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.627-8809G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710723 | |||||||
| chr13:77710775 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.627-8757C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710775 | |||||||
| chr13:77710796 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | HG00558.hp2 HG02080.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-8736C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710796 | |||||||
| chr13:77710839 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.627-8693T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710839 | |||||||
| chr13:77711447 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.627-8085C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711447 | |||||||
| chr13:77711461 | AC | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-8070delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711461 | |||||||
| chr13:77711586 | A | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.627-7946A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711586 | |||||||
| chr13:77711604 | G | C | 1 | a0001c0001t0001g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.627-7928G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711604 | |||||||
| chr13:77711660 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.627-7872G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711660 | |||||||
| chr13:77711669 | C | T | 1 | a0002c0002t0002g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.627-7863C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711669 | |||||||
| chr13:77711738 | A | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.627-7794A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711738 | |||||||
| chr13:77711888 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.627-7644G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711888 | |||||||
| chr13:77711945 | T | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0193 |
3 | HG01258.hp1 HG01261.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.627-7587T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711945 | |||||||
| chr13:77711999 | C | T | 5 | a0001c0001t0003g0010 a0001c0001t0003g0147 a0001c0001t0003g0148 others(2): Show |
6 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-7533C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711999 | |||||||
| chr13:77712003 | G | A | 12 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(9): Show |
12 | HG01099.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.627-7529G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712003 | |||||||
| chr13:77712121 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.627-7411T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712121 | |||||||
| chr13:77712156 | C | T | 1 | a0001c0001t0002g0263 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.627-7376C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712156 | |||||||
| chr13:77712316 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.627-7216A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712316 | |||||||
| chr13:77712693 | T | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.627-6839T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712693 | |||||||
| chr13:77712730 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.627-6802A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712730 | |||||||
| chr13:77712980 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.627-6552A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712980 | |||||||
| chr13:77712988 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6544G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712988 | |||||||
| chr13:77712989 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6543G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712989 | |||||||
| chr13:77712990 | G | T | 1 | a0001c0001t0001g0231 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6542G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712990 | |||||||
| chr13:77712991 | A | T | 1 | a0001c0001t0001g0231 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6541A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712991 | |||||||
| chr13:77712993 | A | ATAAATGG others(10): Show |
1 | a0001c0001t0001g0231 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6539_627-6538i others(19): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712993 | |||||||
| chr13:77712995 | C | A | 1 | a0001c0001t0001g0231 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6537C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712995 | |||||||
| chr13:77713082 | C | T | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01981.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.627-6450C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713082 | |||||||
| chr13:77713108 | T | A | 37 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(34): Show |
37 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.627-6424T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713108 | |||||||
| chr13:77713287 | C | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(142): Show |
153 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.627-6245C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713287 | |||||||
| chr13:77713811 | C | T | 13 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0180 others(10): Show |
14 | HG00558.hp2 HG02080.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.627-5721C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713811 | |||||||
| chr13:77713835 | T | G | 87 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
90 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.627-5697T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713835 | |||||||
| chr13:77713966 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.627-5566G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713966 | |||||||
| chr13:77714028 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.627-5504G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714028 | |||||||
| chr13:77714087 | G | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-5445G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714087 | |||||||
| chr13:77714174 | TA | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
88 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.627-5351delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77714174 | ||||||
| chr13:77714183 | A | G | 8 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-5349A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714183 | |||||||
| chr13:77714230 | G | T | 3 | a0001c0003t0001g0067 a0001c0003t0001g0072 a0001c0003t0001g0073 |
3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.627-5302G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714230 | |||||||
| chr13:77714285 | C | T | 7 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.627-5247C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714285 | |||||||
| chr13:77714376 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.627-5156C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714376 | |||||||
| chr13:77714792 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0216 |
2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.627-4740T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714792 | |||||||
| chr13:77714804 | A | T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0236 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.627-4728A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714804 | |||||||
| chr13:77714811 | C | T | 8 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(5): Show |
8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-4721C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714811 | |||||||
| chr13:77714860 | C | A | 28 | a0001c0001t0001g0122 a0001c0001t0001g0132 a0001c0001t0001g0137 others(25): Show |
31 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.627-4672C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714860 | |||||||
| chr13:77715020 | A | T | 1 | a0001c0001t0002g0263 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.627-4512A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715020 | |||||||
| chr13:77715057 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.627-4475A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715057 | |||||||
| chr13:77715440 | T | C | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-4092T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715440 | |||||||
| chr13:77715551 | TA | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-3979delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77715551 | ||||||
| chr13:77715633 | A | G | 2 | a0002c0002t0001g0158 a0002c0002t0002g0159 |
2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.627-3899A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715633 | |||||||
| chr13:77715896 | A | G | 33 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(30): Show |
36 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.627-3636A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715896 | |||||||
| chr13:77716244 | A | AT | 12 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(9): Show |
12 | HG01099.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.627-3281dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77716244 | ||||||
| chr13:77716331 | A | AT | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(254): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.627-3189dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77716331 | ||||||
| chr13:77716331 | A | ATT | 20 | a0001c0001t0001g0034 a0001c0001t0001g0213 a0001c0001t0001g0214 others(17): Show |
20 | HG00735.hp2 HG01099.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.627-3190_627-3189d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77716331 | ||||||
| chr13:77716359 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.627-3173A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716359 | |||||||
| chr13:77716664 | A | G | 1 | a0002c0002t0002g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.627-2868A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716664 | |||||||
| chr13:77716672 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | NA18952.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.627-2860G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716672 | |||||||
| chr13:77716679 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.627-2853G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716679 | |||||||
| chr13:77716915 | C | T | 4 | a0001c0001t0001g0238 a0001c0001t0001g0241 a0001c0001t0001g0242 others(1): Show |
4 | HG02486.hp1 HG03453.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-2617C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716915 | |||||||
| chr13:77716916 | G | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-2616G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716916 | |||||||
| chr13:77716953 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0036 others(3): Show |
7 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.627-2579G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716953 | |||||||
| chr13:77717134 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.627-2398T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717134 | |||||||
| chr13:77717360 | T | C | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-2172T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717360 | |||||||
| chr13:77717457 | G | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0265 a0001c0001t0001g0266 others(3): Show |
6 | HG00558.hp2 HG02080.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-2075G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717457 | |||||||
| chr13:77717519 | T | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-2013T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717519 | |||||||
| chr13:77717551 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.627-1981A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717551 | |||||||
| chr13:77717752 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0191 |
4 | HG00741.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-1780C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717752 | |||||||
| chr13:77718098 | GA | G | 6 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 others(3): Show |
6 | HG00423.hp1 HG01261.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.627-1423delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77718098 | ||||||
| chr13:77718107 | A | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-1425A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718107 | |||||||
| chr13:77718205 | C | T | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
146 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.627-1327C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718205 | |||||||
| chr13:77718353 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.627-1179A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718353 | |||||||
| chr13:77718545 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.627-987C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718545 | |||||||
| chr13:77718987 | A | G | 52 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(49): Show |
56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-545A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718987 | |||||||
| chr13:77719258 | T | TA | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
126 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.627-259dupA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77719258 | ||||||
| chr13:77719311 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.627-221G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77719311 | |||||||
| chr13:77720032 | A | G | 51 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(48): Show |
55 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.766+361A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720032 | |||||||
| chr13:77720316 | G | C | 51 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(48): Show |
55 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.766+645G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720316 | |||||||
| chr13:77720362 | A | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.766+691A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720362 | |||||||
| chr13:77720392 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0267 |
3 | HG02735.hp2 HG03492.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.766+721C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720392 | |||||||
| chr13:77720414 | G | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(143): Show |
154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.766+743G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720414 | |||||||
| chr13:77720471 | T | C | 50 | a0001c0001t0001g0017 a0001c0001t0001g0112 a0001c0001t0001g0114 others(47): Show |
54 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.766+800T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720471 | |||||||
| chr13:77720517 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.766+846A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720517 | |||||||
| chr13:77720565 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.766+894T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720565 | |||||||
| chr13:77720667 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.766+996C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720667 | |||||||
| chr13:77720830 | C | T | 36 | a0001c0001t0001g0084 a0001c0001t0001g0087 a0001c0001t0001g0088 others(33): Show |
36 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.766+1159C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720830 | |||||||
| chr13:77720831 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.766+1160G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720831 | |||||||
| chr13:77720931 | T | C | 1 | a0002c0002t0001g0158 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.766+1260T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720931 | |||||||
| chr13:77720952 | G | T | 1 | a0001c0001t0006g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.766+1281G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720952 | |||||||
| chr13:77720957 | A | G | 7 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG01928.hp2 HG01934.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.766+1286A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720957 | |||||||
| chr13:77721132 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.766+1461G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721132 | |||||||
| chr13:77721154 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.766+1483C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721154 | |||||||
| chr13:77721203 | T | C | 57 | a0001c0001t0001g0027 a0001c0001t0001g0039 a0001c0001t0001g0086 others(54): Show |
60 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.766+1532T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721203 | |||||||
| chr13:77721240 | TGCCACCA others(6): Show |
T | 1 | a0001c0001t0001g0087 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.766+1571_766+1583d others(15): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77721240 | ||||||
| chr13:77721369 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.766+1698C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721369 | |||||||
| chr13:77721388 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.766+1717A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721388 | |||||||
| chr13:77721515 | A | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0281 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.766+1844A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721515 | |||||||
| chr13:77721779 | G | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(32): Show |
37 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.766+2108G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721779 | |||||||
| chr13:77721812 | TA | T | 35 | a0001c0001t0001g0122 a0001c0001t0002g0007 a0001c0001t0002g0008 others(32): Show |
38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.766+2148delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77721812 | ||||||
| chr13:77721817 | A | C | 36 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(33): Show |
38 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.766+2146A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721817 | |||||||
| chr13:77721907 | G | A | 17 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0036 others(14): Show |
18 | HG01109.hp2 HG01168.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.766+2236G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721907 | |||||||
| chr13:77721916 | T | C | 37 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(34): Show |
37 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.766+2245T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721916 | |||||||
| chr13:77721955 | T | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+2284T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721955 | |||||||
| chr13:77721996 | G | GT | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+2334dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77721996 | ||||||
| chr13:77721996 | GTTTTT | G | 26 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(23): Show |
26 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.766+2330_766+2334d others(7): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77721996 | ||||||
| chr13:77722049 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.766+2378T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722049 | |||||||
| chr13:77722071 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.766+2400C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722071 | |||||||
| chr13:77722106 | A | T | 1 | a0001c0001t0005g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.766+2435A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722106 | |||||||
| chr13:77722147 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0243 |
2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.766+2476T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722147 | |||||||
| chr13:77722420 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.766+2749C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722420 | |||||||
| chr13:77722420 | CA | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+2752delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77722420 | ||||||
| chr13:77722502 | A | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+2831A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722502 | |||||||
| chr13:77723645 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.766+3974A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77723645 | |||||||
| chr13:77723652 | T | C | 15 | a0001c0001t0001g0229 a0001c0001t0002g0178 a0001c0001t0002g0246 others(12): Show |
15 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.766+3981T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77723652 | |||||||
| chr13:77723851 | A | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+4180A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77723851 | |||||||
| chr13:77723932 | TA | T | 159 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(156): Show |
169 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.766+4276delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77723932 | ||||||
| chr13:77723932 | TAA | T | 40 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0026 others(37): Show |
42 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.766+4275_766+4276d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77723932 | ||||||
| chr13:77723977 | T | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+4306T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77723977 | |||||||
| chr13:77724040 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+4369G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724040 | |||||||
| chr13:77724171 | T | C | 1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.766+4500T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724171 | |||||||
| chr13:77724320 | G | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+4649G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724320 | |||||||
| chr13:77724327 | C | T | 1 | a0001c0001t0002g0277 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.766+4656C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724327 | |||||||
| chr13:77724445 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.766+4774G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724445 | |||||||
| chr13:77724744 | CT | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+5081delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77724744 | ||||||
| chr13:77724855 | A | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+5184A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724855 | |||||||
| chr13:77725263 | C | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(86): Show |
91 | HG00558.hp1 HG00642.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.766+5592C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725263 | |||||||
| chr13:77725311 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0184 |
2 | NA18747.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.766+5640C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725311 | |||||||
| chr13:77725576 | C | T | 1 | a0001c0001t0001g0275 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.766+5905C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725576 | |||||||
| chr13:77725602 | G | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+5931G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725602 | |||||||
| chr13:77725962 | G | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0242 |
2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.766+6291G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725962 | |||||||
| chr13:77725963 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 |
3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.766+6292C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725963 | |||||||
| chr13:77725991 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.766+6320A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725991 | |||||||
| chr13:77726232 | C | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(35): Show |
40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+6561C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726232 | |||||||
| chr13:77726344 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.766+6673G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726344 | |||||||
| chr13:77726374 | A | G | 37 | a0001c0001t0001g0122 a0001c0001t0002g0007 a0001c0001t0002g0008 others(34): Show |
40 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.766+6703A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726374 | |||||||
| chr13:77726378 | G | C | 3 | a0001c0003t0001g0067 a0001c0003t0001g0072 a0001c0003t0001g0073 |
3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.766+6707G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726378 | |||||||
| chr13:77726488 | G | A | 26 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(23): Show |
26 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.766+6817G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726488 | |||||||
| chr13:77726625 | G | T | 1 | a0001c0001t0002g0277 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.766+6954G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726625 | |||||||
| chr13:77727157 | T | G | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.766+7486T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727157 | |||||||
| chr13:77727168 | C | G | 3 | a0001c0001t0001g0014 a0001c0001t0001g0233 a0001c0001t0001g0234 |
4 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+7497C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727168 | |||||||
| chr13:77727431 | G | A | 3 | a0001c0001t0001g0104 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | HG01167.hp2 HG01169.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.766+7760G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727431 | |||||||
| chr13:77727437 | C | CA | 37 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(34): Show |
41 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.766+7777dupA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77727437 | ||||||
| chr13:77727448 | AC | A | 32 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(29): Show |
32 | HG00642.hp2 HG01081.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.766+7778delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727448 | |||||||
| chr13:77727449 | C | A | 5 | a0001c0001t0001g0084 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
5 | HG01123.hp2 HG02109.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.766+7778C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727449 | |||||||
| chr13:77727504 | C | CAA | 37 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(34): Show |
37 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.766+7844_766+7845d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77727504 | ||||||
| chr13:77727522 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.766+7851A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727522 | |||||||
| chr13:77727728 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.766+8057G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727728 | |||||||
| chr13:77727812 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.766+8141T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727812 | |||||||
| chr13:77727824 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0002g0131 a0001c0001t0002g0135 |
3 | NA18956.hp1 NA18998.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.766+8153T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727824 | |||||||
| chr13:77727923 | A | T | 25 | a0001c0001t0001g0040 a0001c0001t0002g0007 a0001c0001t0002g0008 others(22): Show |
28 | HG00280.hp2 HG00438.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.766+8252A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727923 | |||||||
| chr13:77728011 | C | T | 1 | a0001c0001t0003g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.766+8340C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728011 | |||||||
| chr13:77728052 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.766+8381T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728052 | |||||||
| chr13:77728055 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.766+8384A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728055 | |||||||
| chr13:77728166 | C | G | 1 | a0002c0002t0001g0171 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.766+8495C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728166 | |||||||
| chr13:77728712 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.766+9041G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728712 | |||||||
| chr13:77729001 | A | G | 8 | a0001c0001t0001g0026 a0001c0001t0002g0031 a0001c0001t0002g0074 others(5): Show |
8 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.766+9330A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77729001 | |||||||
| chr13:77729054 | A | C | 1 | a0001c0001t0001g0206 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.766+9383A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77729054 | |||||||
| chr13:77729135 | G | GT | 14 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+9465dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77729135 | ||||||
| chr13:77729468 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.766+9797C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77729468 | |||||||
| chr13:77729503 | CT | C | 48 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(45): Show |
51 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.766+9845delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77729503 | ||||||
| chr13:77729505 | T | A | 1 | a0001c0001t0001g0097 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.766+9834T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77729505 | |||||||
| chr13:77729901 | C | CTG | 41 | a0001c0001t0001g0100 a0001c0001t0001g0243 a0001c0001t0001g0280 others(38): Show |
44 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.766+10248_766+1024 others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77729901 | ||||||
| chr13:77730093 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766+10422T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730093 | |||||||
| chr13:77730295 | A | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0105 a0001c0001t0001g0106 |
3 | NA18962.hp2 NA18966.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.766+10624A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730295 | |||||||
| chr13:77730300 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.766+10629C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730300 | |||||||
| chr13:77730516 | C | T | 1 | a0001c0003t0001g0073 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.766+10845C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730516 | |||||||
| chr13:77730671 | A | G | 1 | a0001c0001t0002g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.766+11000A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730671 | |||||||
| chr13:77730821 | C | T | 84 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(81): Show |
87 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.766+11150C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730821 | |||||||
| chr13:77731162 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.766+11491A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731162 | |||||||
| chr13:77731510 | T | C | 1 | a0001c0001t0002g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.766+11839T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731510 | |||||||
| chr13:77731667 | G | A | 25 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(22): Show |
28 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.766+11996G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731667 | |||||||
| chr13:77731746 | A | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0036 others(14): Show |
18 | HG01109.hp2 HG01168.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.766+12075A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731746 | |||||||
| chr13:77731934 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.766+12263G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731934 | |||||||
| chr13:77732205 | C | T | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-12078C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77732205 | |||||||
| chr13:77732499 | G | GT | 35 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(32): Show |
38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.767-11781dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77732499 | ||||||
| chr13:77732763 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.767-11520A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77732763 | |||||||
| chr13:77732801 | T | C | 3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG02615.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.767-11482T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77732801 | |||||||
| chr13:77732918 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-11365G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77732918 | |||||||
| chr13:77733390 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.767-10893T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733390 | |||||||
| chr13:77733395 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.767-10888T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733395 | |||||||
| chr13:77733396 | T | G | 3 | a0001c0003t0001g0067 a0001c0003t0001g0072 a0001c0003t0001g0073 |
3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.767-10887T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733396 | |||||||
| chr13:77733408 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.767-10875T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733408 | |||||||
| chr13:77733428 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.767-10855A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733428 | |||||||
| chr13:77733584 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.767-10699A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733584 | |||||||
| chr13:77733595 | T | C | 4 | a0001c0001t0001g0025 a0001c0001t0001g0177 a0001c0001t0001g0210 others(1): Show |
4 | HG02074.hp1 NA18961.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-10688T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733595 | |||||||
| chr13:77733768 | A | G | 1 | a0001c0001t0001g0013 | 2 | NA18998.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.767-10515A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733768 | |||||||
| chr13:77733808 | G | A | 3 | a0001c0001t0003g0010 a0001c0001t0003g0149 a0001c0001t0003g0150 |
4 | HG00735.hp1 HG02717.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.767-10475G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733808 | |||||||
| chr13:77733850 | A | G | 1 | a0001c0001t0002g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.767-10433A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733850 | |||||||
| chr13:77734105 | G | T | 1 | a0001c0001t0002g0138 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.767-10178G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734105 | |||||||
| chr13:77734156 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.767-10127G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734156 | |||||||
| chr13:77734612 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.767-9671G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734612 | |||||||
| chr13:77734659 | A | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0029 others(24): Show |
29 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.767-9624A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734659 | |||||||
| chr13:77734682 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.767-9601A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734682 | |||||||
| chr13:77735001 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.767-9282C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735001 | |||||||
| chr13:77735078 | A | G | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-9205A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735078 | |||||||
| chr13:77735185 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.767-9098A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735185 | |||||||
| chr13:77735366 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.767-8917G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735366 | |||||||
| chr13:77735471 | C | T | 35 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(32): Show |
38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.767-8812C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735471 | |||||||
| chr13:77735472 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0115 |
2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.767-8811G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735472 | |||||||
| chr13:77735647 | C | T | 1 | a0002c0002t0001g0170 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.767-8636C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735647 | |||||||
| chr13:77735739 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0101 |
2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.767-8544T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735739 | |||||||
| chr13:77735815 | G | A | 14 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-8468G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735815 | |||||||
| chr13:77735991 | C | T | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-8292C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735991 | |||||||
| chr13:77736025 | A | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.767-8258A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736025 | |||||||
| chr13:77736090 | G | C | 35 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(32): Show |
38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.767-8193G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736090 | |||||||
| chr13:77736134 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.767-8149A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736134 | |||||||
| chr13:77736216 | C | T | 1 | a0001c0001t0002g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.767-8067C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736216 | |||||||
| chr13:77736414 | C | G | 62 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(59): Show |
65 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.767-7869C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736414 | |||||||
| chr13:77736758 | A | G | 14 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-7525A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736758 | |||||||
| chr13:77736792 | C | CT | 36 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(33): Show |
36 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.767-7478dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77736792 | ||||||
| chr13:77736806 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.767-7477G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736806 | |||||||
| chr13:77736819 | T | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(119): Show |
127 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.767-7464T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736819 | |||||||
| chr13:77736949 | G | A | 68 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(65): Show |
71 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.767-7334G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736949 | |||||||
| chr13:77736981 | T | A | 16 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(13): Show |
16 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.767-7302T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736981 | |||||||
| chr13:77737092 | A | AT | 62 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.767-7181dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77737092 | ||||||
| chr13:77737099 | T | G | 5 | a0001c0001t0001g0186 a0001c0001t0001g0243 a0001c0001t0001g0248 others(2): Show |
5 | HG01433.hp2 HG03704.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-7184T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737099 | |||||||
| chr13:77737485 | G | A | 1 | a0001c0001t0001g0040 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.767-6798G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737485 | |||||||
| chr13:77737671 | C | T | 1 | a0001c0001t0002g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.767-6612C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737671 | |||||||
| chr13:77737681 | C | G | 1 | a0001c0001t0002g0130 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.767-6602C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737681 | |||||||
| chr13:77737800 | G | T | 6 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG02615.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-6483G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737800 | |||||||
| chr13:77737813 | AC | A | 35 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(32): Show |
35 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.767-6468delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77737813 | ||||||
| chr13:77738057 | G | C | 14 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-6226G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738057 | |||||||
| chr13:77738157 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01981.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.767-6126G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738157 | |||||||
| chr13:77738200 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.767-6083A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738200 | |||||||
| chr13:77738202 | A | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.767-6081A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738202 | |||||||
| chr13:77738221 | T | TACATATA others(3): Show |
189 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(186): Show |
201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.767-6060_767-6051d others(12): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77738221 | ||||||
| chr13:77738221 | T | TACATATA others(3): Show |
2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-6054_767-6053i others(12): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77738221 | ||||||
| chr13:77738274 | A | T | 3 | a0001c0001t0001g0001 a0001c0001t0001g0191 a0001c0001t0001g0244 |
5 | HG00741.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.767-6009A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738274 | |||||||
| chr13:77738943 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.767-5340A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738943 | |||||||
| chr13:77738955 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.767-5328C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738955 | |||||||
| chr13:77738956 | G | A | 14 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-5327G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738956 | |||||||
| chr13:77738962 | T | C | 50 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(47): Show |
53 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.767-5321T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738962 | |||||||
| chr13:77738994 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.767-5289C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738994 | |||||||
| chr13:77739284 | A | G | 1 | a0001c0001t0001g0005 | 2 | NA18953.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.767-4999A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739284 | |||||||
| chr13:77739415 | C | T | 59 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(56): Show |
62 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.767-4868C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739415 | |||||||
| chr13:77739765 | G | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-4518G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739765 | |||||||
| chr13:77739928 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.767-4355C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739928 | |||||||
| chr13:77739936 | A | T | 1 | a0001c0001t0001g0037 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.767-4347A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739936 | |||||||
| chr13:77739973 | A | G | 25 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(22): Show |
25 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.767-4310A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739973 | |||||||
| chr13:77740054 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.767-4229A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740054 | |||||||
| chr13:77740250 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.767-4033G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740250 | |||||||
| chr13:77740284 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(103): Show |
110 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.767-3999A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740284 | |||||||
| chr13:77740418 | C | T | 25 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(22): Show |
25 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.767-3865C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740418 | |||||||
| chr13:77740515 | A | G | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.767-3768A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740515 | |||||||
| chr13:77740528 | G | GC | 32 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0025 others(29): Show |
33 | HG00438.hp1 HG00558.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.767-3744dupC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77740528 | ||||||
| chr13:77740528 | GC | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(81): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.767-3744delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77740528 | ||||||
| chr13:77740528 | GCC | G | 76 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0084 others(73): Show |
79 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.767-3745_767-3744d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77740528 | ||||||
| chr13:77740538 | C | A | 1 | a0001c0001t0001g0245 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.767-3745C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740538 | |||||||
| chr13:77740861 | C | G | 58 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(55): Show |
61 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.767-3422C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740861 | |||||||
| chr13:77740928 | A | G | 6 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(3): Show |
6 | HG01099.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.767-3355A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740928 | |||||||
| chr13:77741000 | G | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0036 others(4): Show |
8 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.767-3283G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741000 | |||||||
| chr13:77741119 | G | A | 1 | a0001c0001t0002g0143 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.767-3164G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741119 | |||||||
| chr13:77741151 | G | A | 1 | a0001c0001t0002g0133 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.767-3132G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741151 | |||||||
| chr13:77741252 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.767-3031A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741252 | |||||||
| chr13:77741372 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.767-2911A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741372 | |||||||
| chr13:77741450 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.767-2833G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741450 | |||||||
| chr13:77741532 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0254 a0001c0001t0001g0256 |
3 | HG01433.hp2 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.767-2751G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741532 | |||||||
| chr13:77741570 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.767-2713C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741570 | |||||||
| chr13:77741572 | C | T | 2 | a0001c0001t0001g0230 a0001c0001t0001g0276 |
2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.767-2711C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741572 | |||||||
| chr13:77741646 | AT | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(107): Show |
115 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.767-2618delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77741646 | ||||||
| chr13:77741745 | G | GT | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.767-2526dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77741745 | ||||||
| chr13:77742028 | A | G | 1 | a0001c0001t0002g0074 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.767-2255A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742028 | |||||||
| chr13:77742060 | G | A | 1 | a0001c0001t0003g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.767-2223G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742060 | |||||||
| chr13:77742187 | G | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0131 a0001c0001t0002g0134 others(2): Show |
6 | HG00438.hp2 HG02015.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-2096G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742187 | |||||||
| chr13:77742314 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.767-1969G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742314 | |||||||
| chr13:77742357 | C | T | 1 | a0001c0001t0002g0134 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.767-1926C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742357 | |||||||
| chr13:77742418 | C | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.767-1865C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742418 | |||||||
| chr13:77742543 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | NA18974.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.767-1740C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742543 | |||||||
| chr13:77742806 | T | TTCAAAAT others(5): Show |
2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-1476_767-1475i others(14): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77742806 | ||||||
| chr13:77742808 | A | C | 14 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-1475A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742808 | |||||||
| chr13:77742809 | A | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-1474A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742809 | |||||||
| chr13:77742814 | G | A | 3 | a0001c0003t0001g0067 a0001c0003t0001g0072 a0001c0003t0001g0073 |
3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.767-1469G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742814 | |||||||
| chr13:77742919 | CT | C | 24 | a0001c0001t0001g0108 a0001c0001t0002g0178 a0001c0001t0002g0246 others(21): Show |
25 | HG00558.hp1 HG00735.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.767-1349delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77742919 | ||||||
| chr13:77742934 | T | A | 1 | a0001c0001t0001g0219 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.767-1349T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742934 | |||||||
| chr13:77743327 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.767-956A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743327 | |||||||
| chr13:77743368 | A | G | 49 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(46): Show |
52 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.767-915A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743368 | |||||||
| chr13:77743495 | A | AT | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.767-780dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77743495 | ||||||
| chr13:77743510 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.767-773T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743510 | |||||||
| chr13:77743596 | C | A | 11 | a0001c0001t0001g0155 a0001c0001t0001g0157 a0001c0001t0003g0010 others(8): Show |
12 | HG00735.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767-687C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743596 | |||||||
| chr13:77743667 | T | TGAAGCCA others(15): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG02135.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.767-615_767-594dup others(22): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77743667 | ||||||
| chr13:77743932 | T | C | 105 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0036 others(102): Show |
109 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.767-351T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743932 | |||||||
| chr13:77744254 | G | A | 14 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-29G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77744254 | |||||||
| chr13:77744464 | G | T | 10 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0074 others(7): Show |
10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.916+32G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77744464 | |||||||
| chr13:77744665 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.916+233G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77744665 | |||||||
| chr13:77744830 | T | G | 14 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+398T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77744830 | |||||||
| chr13:77745040 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.916+608G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745040 | |||||||
| chr13:77745263 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.916+831G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745263 | |||||||
| chr13:77745376 | G | T | 8 | a0001c0001t0001g0012 a0001c0001t0001g0185 a0001c0001t0001g0189 others(5): Show |
9 | HG00423.hp2 HG00438.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.916+944G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745376 | |||||||
| chr13:77745468 | A | G | 14 | a0001c0001t0002g0178 a0001c0001t0002g0246 a0001c0001t0002g0247 others(11): Show |
14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+1036A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745468 | |||||||
| chr13:77745475 | A | G | 1 | a0001c0004t0001g0015 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.917-1039A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745475 | |||||||
| chr13:77745488 | G | C | 25 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(22): Show |
28 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.917-1026G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745488 | |||||||
| chr13:77745526 | A | G | 8 | a0001c0001t0001g0012 a0001c0001t0001g0185 a0001c0001t0001g0189 others(5): Show |
9 | HG00423.hp2 HG00438.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.917-988A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745526 | |||||||
| chr13:77745866 | T | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0007g0156 |
3 | HG01256.hp1 HG01261.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.917-648T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745866 | |||||||
| chr13:77746087 | T | C | 3 | a0001c0003t0001g0067 a0001c0003t0001g0072 a0001c0003t0001g0073 |
3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.917-427T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77746087 | |||||||
| chr13:77746251 | A | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0281 |
2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.917-263A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77746251 | |||||||
| chr13:77746990 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1258+135G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77746990 | |||||||
| chr13:77747029 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1258+174C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77747029 | |||||||
| chr13:77747507 | A | G | 1 | a0001c0001t0005g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1258+652A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77747507 | |||||||
| chr13:77748186 | TAAG | T | 35 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(32): Show |
38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1258+1333_1258+133 others(7): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77748186 | ||||||
| chr13:77748277 | A | C | 1 | a0001c0001t0001g0084 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1258+1422A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748277 | |||||||
| chr13:77748292 | A | C | 1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1258+1437A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748292 | |||||||
| chr13:77748342 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1258+1487G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748342 | |||||||
| chr13:77748398 | C | CT | 28 | a0001c0001t0001g0019 a0001c0001t0001g0024 a0001c0001t0001g0034 others(25): Show |
29 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1258+1569dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77748398 | ||||||
| chr13:77748398 | C | CTTTT | 11 | a0001c0001t0002g0031 a0001c0001t0002g0074 a0001c0001t0002g0075 others(8): Show |
11 | HG02486.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1258+1566_1258+156 others(8): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77748398 | ||||||
| chr13:77748398 | CT | C | 42 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0036 others(39): Show |
43 | HG01167.hp1 HG01167.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.1258+1569delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77748398 | ||||||
| chr13:77748674 | C | T | 11 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0074 others(8): Show |
11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1258+1819C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748674 | |||||||
| chr13:77748855 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1258+2000T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748855 | |||||||
| chr13:77748902 | C | A | 4 | a0002c0002t0001g0167 a0002c0002t0001g0168 a0002c0002t0001g0169 others(1): Show |
4 | HG02818.hp1 HG03516.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258+2047C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748902 | |||||||
| chr13:77749211 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1258+2356G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749211 | |||||||
| chr13:77749342 | T | A | 45 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(42): Show |
48 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1258+2487T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749342 | |||||||
| chr13:77749363 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1258+2508A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749363 | |||||||
| chr13:77749608 | C | A | 1 | a0001c0001t0002g0071 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1258+2753C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749608 | |||||||
| chr13:77749660 | T | C | 3 | a0001c0003t0001g0067 a0001c0003t0001g0072 a0001c0003t0001g0073 |
3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1258+2805T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749660 | |||||||
| chr13:77749673 | C | A | 66 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(63): Show |
69 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1258+2818C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749673 | |||||||
| chr13:77750101 | T | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0053 others(1): Show |
4 | HG00423.hp1 NA18944.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259-3102T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750101 | |||||||
| chr13:77750124 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1259-3079T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750124 | |||||||
| chr13:77750255 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1259-2948C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750255 | |||||||
| chr13:77750396 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1259-2807T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750396 | |||||||
| chr13:77750918 | A | G | 2 | a0001c0001t0002g0255 a0001c0001t0002g0258 |
2 | HG01255.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1259-2285A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750918 | |||||||
| chr13:77751188 | C | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0187 |
2 | NA18946.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1259-2015C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751188 | |||||||
| chr13:77751189 | G | A | 3 | a0001c0001t0002g0030 a0001c0001t0002g0077 a0001c0001t0002g0078 |
3 | HG02970.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1259-2014G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751189 | |||||||
| chr13:77751320 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1259-1883G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751320 | |||||||
| chr13:77751623 | A | G | 10 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0074 others(7): Show |
10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1259-1580A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751623 | |||||||
| chr13:77751632 | A | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(126): Show |
135 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.1259-1571A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751632 | |||||||
| chr13:77751901 | C | T | 6 | a0001c0001t0001g0112 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG02615.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1259-1302C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751901 | |||||||
| chr13:77751992 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1259-1211A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751992 | |||||||
| chr13:77752123 | G | A | 7 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1259-1080G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752123 | |||||||
| chr13:77752160 | T | G | 1 | a0001c0001t0004g0116 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1259-1043T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752160 | |||||||
| chr13:77752238 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1259-965A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752238 | |||||||
| chr13:77752288 | C | CT | 10 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0084 others(7): Show |
10 | HG00423.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1259-897dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77752288 | ||||||
| chr13:77752288 | C | CTTTT | 46 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(43): Show |
49 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1259-900_1259-897d others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77752288 | ||||||
| chr13:77752288 | C | CTTTTT | 13 | a0001c0001t0002g0076 a0001c0001t0002g0080 a0001c0001t0002g0135 others(10): Show |
13 | HG00558.hp1 HG02080.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1259-901_1259-897d others(7): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77752288 | ||||||
| chr13:77752288 | CT | C | 15 | a0001c0001t0001g0038 a0001c0001t0001g0054 a0001c0001t0001g0090 others(12): Show |
15 | HG01081.hp1 HG01081.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1259-897delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77752288 | ||||||
| chr13:77752307 | A | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1259-896A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752307 | |||||||
| chr13:77752416 | T | C | 1 | a0001c0001t0002g0140 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1259-787T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752416 | |||||||
| chr13:77752543 | G | T | 66 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(63): Show |
69 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1259-660G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752543 | |||||||
| chr13:77752626 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0036 others(12): Show |
16 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1259-577G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752626 | |||||||
| chr13:77752657 | G | T | 1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1259-546G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752657 | |||||||
| chr13:77752687 | G | A | 10 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0074 others(7): Show |
10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1259-516G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752687 | |||||||
| chr13:77752821 | C | T | 3 | a0001c0003t0001g0067 a0001c0003t0001g0072 a0001c0003t0001g0073 |
3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1259-382C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752821 | |||||||
| chr13:77752854 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1259-349G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752854 | |||||||
| chr13:77752868 | A | G | 10 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(7): Show |
10 | HG01099.hp1 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1259-335A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752868 | |||||||
| chr13:77752919 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1259-284C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752919 | |||||||
| chr13:77753171 | G | A | 10 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0074 others(7): Show |
10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1259-32G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77753171 | |||||||
| chr13:77753194 | C | A | 1 | a0001c0001t0002g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1259-9C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77753194 | |||||||
| chr13:77753598 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1414+240A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753598 | |||||||
| chr13:77753608 | G | A | 36 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(33): Show |
39 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1414+250G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753608 | |||||||
| chr13:77753615 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1414+257T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753615 | |||||||
| chr13:77753709 | T | C | 10 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0074 others(7): Show |
10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1414+351T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753709 | |||||||
| chr13:77753799 | G | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0259 |
2 | HG00738.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1414+441G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753799 | |||||||
| chr13:77754179 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1414+821C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754179 | |||||||
| chr13:77754321 | T | G | 3 | a0001c0001t0001g0090 a0001c0001t0001g0093 a0001c0001t0001g0099 |
3 | NA18940.hp2 NA18961.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1414+963T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754321 | |||||||
| chr13:77754695 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1414+1337C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754695 | |||||||
| chr13:77754747 | A | G | 12 | a0001c0001t0001g0192 a0001c0001t0001g0197 a0001c0001t0001g0198 others(9): Show |
12 | HG01928.hp2 HG01934.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1414+1389A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754747 | |||||||
| chr13:77754794 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1414+1436T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754794 | |||||||
| chr13:77754820 | A | G | 1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1414+1462A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754820 | |||||||
| chr13:77754833 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1414+1475T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754833 | |||||||
| chr13:77754860 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1414+1502A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754860 | |||||||
| chr13:77754944 | A | G | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1414+1586A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754944 | |||||||
| chr13:77755058 | T | C | 1 | a0002c0002t0001g0158 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1414+1700T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755058 | |||||||
| chr13:77755204 | A | T | 1 | a0002c0002t0002g0159 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1414+1846A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755204 | |||||||
| chr13:77755330 | GA | G | 25 | a0001c0001t0001g0084 a0001c0001t0001g0086 a0001c0001t0001g0087 others(22): Show |
25 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.1414+1983delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 77755330 | ||||||
| chr13:77755337 | A | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1414+1979A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755337 | |||||||
| chr13:77755362 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1414+2004G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755362 | |||||||
| chr13:77755567 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1414+2209T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755567 | |||||||
| chr13:77755731 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0036 others(10): Show |
14 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1414+2373G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755731 | |||||||
| chr13:77755759 | A | G | 1 | a0001c0001t0001g0264 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1414+2401A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755759 | |||||||
| chr13:77756073 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1414+2715T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77756073 | |||||||
| chr13:77756180 | C | G | 4 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0044 others(1): Show |
4 | HG00544.hp1 NA18956.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414+2822C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77756180 | |||||||
| chr13:77756721 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1414+3363T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77756721 | |||||||
| chr13:77756995 | A | C | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1414+3637A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77756995 | |||||||
| chr13:77757050 | A | G | 2 | a0001c0001t0002g0077 a0001c0001t0002g0078 |
2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1414+3692A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757050 | |||||||
| chr13:77757201 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1415-3627G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757201 | |||||||
| chr13:77757584 | C | A | 35 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(32): Show |
38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1415-3244C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757584 | |||||||
| chr13:77757656 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1415-3172C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757656 | |||||||
| chr13:77757760 | A | T | 3 | a0002c0002t0001g0167 a0002c0002t0001g0169 a0002c0002t0001g0170 |
3 | HG02818.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1415-3068A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757760 | |||||||
| chr13:77757907 | T | A | 11 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0074 others(8): Show |
11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1415-2921T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757907 | |||||||
| chr13:77758087 | C | T | 9 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(6): Show |
9 | HG01099.hp1 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1415-2741C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758087 | |||||||
| chr13:77758140 | G | A | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1415-2688G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758140 | |||||||
| chr13:77758185 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0101 |
2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1415-2643T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758185 | |||||||
| chr13:77758278 | G | GT | 15 | a0001c0001t0001g0099 a0001c0001t0002g0178 a0001c0001t0002g0246 others(12): Show |
15 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1415-2542dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 77758278 | ||||||
| chr13:77758421 | G | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(127): Show |
136 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1415-2407G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758421 | |||||||
| chr13:77758810 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1415-2018G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758810 | |||||||
| chr13:77758960 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1415-1868A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758960 | |||||||
| chr13:77758976 | A | C | 1 | a0001c0001t0001g0026 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1415-1852A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758976 | |||||||
| chr13:77759116 | T | G | 2 | a0001c0001t0002g0125 a0001c0001t0002g0127 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1415-1712T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77759116 | |||||||
| chr13:77759485 | A | G | 1 | a0001c0001t0002g0066 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1415-1343A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77759485 | |||||||
| chr13:77759803 | A | G | 36 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0009 others(33): Show |
39 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1415-1025A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77759803 | |||||||
| chr13:77759835 | T | C | 1 | a0001c0001t0007g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1415-993T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77759835 | |||||||
| chr13:77760082 | T | G | 108 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0027 others(105): Show |
112 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.1415-746T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760082 | |||||||
| chr13:77760088 | G | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0036 others(4): Show |
8 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1415-740G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760088 | |||||||
| chr13:77760183 | T | C | 10 | a0001c0001t0002g0062 a0001c0001t0002g0063 a0001c0001t0002g0064 others(7): Show |
10 | HG01099.hp1 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1415-645T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760183 | |||||||
| chr13:77760188 | C | A | 3 | a0001c0001t0001g0001 a0001c0001t0001g0191 a0001c0001t0001g0244 |
5 | HG00741.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1415-640C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760188 | |||||||
| chr13:77760439 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1415-389A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760439 | |||||||
| chr13:77761121 | G | A | 1 | a0001c0001t0002g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1697+11G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761121 | |||||||
| chr13:77761173 | C | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG00558.hp2 HG02080.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1697+63C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761173 | |||||||
| chr13:77761483 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1697+373C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761483 | |||||||
| chr13:77761948 | A | G | 2 | a0001c0001t0002g0064 a0001c0001t0002g0069 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1697+838A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761948 | |||||||
| chr13:77761969 | G | A | 11 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0074 others(8): Show |
11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1697+859G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761969 | |||||||
| chr13:77762211 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1698-934T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762211 | |||||||
| chr13:77762277 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1698-868T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762277 | |||||||
| chr13:77762283 | C | A | 2 | a0001c0001t0002g0064 a0001c0001t0002g0069 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1698-862C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762283 | |||||||
| chr13:77762405 | A | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
6 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1698-740A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762405 | |||||||
| chr13:77762426 | T | G | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1698-719T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762426 | |||||||
| chr13:77762689 | T | C | 2 | a0001c0001t0004g0113 a0001c0001t0004g0116 |
2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1698-456T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762689 | |||||||
| chr13:77762911 | A | T | 1 | a0001c0001t0007g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1698-234A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762911 | |||||||
| chr13:77763018 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1698-127G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77763018 | |||||||
| chr13:77763059 | A | G | 5 | a0001c0001t0003g0010 a0001c0001t0003g0147 a0001c0001t0003g0148 others(2): Show |
6 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1698-86A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77763059 |