Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 387755 |
| ensemblid | ENSG00000188487.12 |
| hgncid | 33116 |
| symbol | INSC |
| name | INSC spindle orientation adaptor protein |
| refseq_nuc | NM_001042536.3 |
| refseq_prot | NP_001036001.1 |
| ensembl_nuc | ENST00000379556.8 |
| ensembl_prot | ENSP00000368874.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 15114923 |
| end | 15247208 |
| strand | + |
| ver | v1.2 |
| region | chr11:15114923-15247208 |
| region5000 | chr11:15109923-15252208 |
| regionname0 | INSC_chr11_15114923_15247208 |
| regionname5000 | INSC_chr11_15109923_15252208 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 532 | 243 | 76 | 46 | 83 | 9 | 27 | 61 | INSC_chr11_15109923_15252208 | INSC | MMALP others(527): Show |
chr11 | 15109923 | 15252208 |
| a0002 | 0/0 | 532 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | MMALP others(527): Show |
chr11 | 15109923 | 15252208 |
| a0003 | 0/0 | 532 | 6 | 0 | 1 | 0 | 1 | 4 | 0 | INSC_chr11_15109923_15252208 | INSC | MMALP others(527): Show |
chr11 | 15109923 | 15252208 |
| a0004 | 0/0 | 532 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | MMALP others(527): Show |
chr11 | 15109923 | 15252208 |
| a0005 | 0/0 | 532 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | MMALP others(527): Show |
chr11 | 15109923 | 15252208 |
| a0006 | 0/0 | 532 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | MMALP others(527): Show |
chr11 | 15109923 | 15252208 |
| a0007 | 0/0 | 532 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | MMALP others(527): Show |
chr11 | 15109923 | 15252208 |
| a0008 | 0/0 | 532 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | MMALP others(527): Show |
chr11 | 15109923 | 15252208 |
| a0009 | 0/0 | 532 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | MMALP others(527): Show |
chr11 | 15109923 | 15252208 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1596 | 183 | 50 | 38 | 65 | 7 | 23 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0001c0002 | 0/0 | 1596 | 34 | 16 | 4 | 12 | 1 | 1 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0001c0003 | 1/1 | 1596 | 20 | 7 | 3 | 4 | 1 | 3 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0001c0009 | 0/0 | 1596 | 2 | 2 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0001c0012 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0001c0013 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0001c0016 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0001c0018 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0002c0004 | 0/0 | 1596 | 8 | 8 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0002c0011 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0002c0017 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0003c0005 | 0/0 | 1596 | 6 | 0 | 1 | 0 | 1 | 4 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0004c0006 | 0/0 | 1596 | 3 | 3 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0004c0008 | 0/0 | 1596 | 2 | 2 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0005c0007 | 0/0 | 1596 | 2 | 0 | 1 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0006c0019 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0007c0014 | 0/0 | 1596 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0008c0015 | 0/0 | 1596 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 | ||
| a0009c0010 | 0/0 | 1596 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ATGAT others(1591): Show |
chr11 | 15109923 | 15252208 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2893 | 72 | 2 | 19 | 34 | 0 | 17 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0002 | 0/0 | 2893 | 44 | 13 | 11 | 15 | 3 | 2 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0003 | 0/0 | 2894 | 13 | 4 | 2 | 7 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0004 | 0/0 | 2891 | 12 | 3 | 3 | 2 | 2 | 2 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2886): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0005 | 0/0 | 2894 | 19 | 14 | 0 | 4 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0006 | 0/0 | 2893 | 6 | 3 | 0 | 0 | 2 | 1 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0007 | 0/0 | 2893 | 2 | 0 | 1 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0008 | 0/0 | 2894 | 4 | 4 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0011 | 0/0 | 2893 | 2 | 1 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0012 | 0/0 | 2894 | 2 | 1 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0014 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0016 | 0/0 | 2893 | 2 | 2 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0018 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0021 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0022 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0001t0024 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0001 | 0/0 | 2893 | 6 | 1 | 0 | 4 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0002 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0003 | 0/0 | 2894 | 11 | 6 | 1 | 4 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0004 | 0/0 | 2891 | 3 | 0 | 2 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2886): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0005 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0006 | 0/0 | 2893 | 5 | 5 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0007 | 0/0 | 2893 | 4 | 0 | 1 | 3 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0008 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0013 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0002t0023 | 0/0 | 2894 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0003t0001 | 0/0 | 2893 | 3 | 0 | 2 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0003t0002 | 1/1 | 2893 | 9 | 4 | 0 | 1 | 1 | 1 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0003t0003 | 0/0 | 2894 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0003t0004 | 0/0 | 2891 | 3 | 2 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2886): Show |
chr11 | 15109923 | 15252208 |
| a0001c0003t0006 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0003t0013 | 0/0 | 2894 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0003t0019 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0003t0020 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0009t0010 | 0/0 | 2894 | 2 | 2 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0012t0001 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0013t0017 | 0/0 | 2894 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2889): Show |
chr11 | 15109923 | 15252208 |
| a0001c0016t0002 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0001c0018t0006 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0002c0004t0001 | 0/0 | 2893 | 7 | 7 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0002c0004t0002 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0002c0011t0002 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0002c0017t0001 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0003c0005t0001 | 0/0 | 2893 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0003c0005t0004 | 0/0 | 2891 | 2 | 0 | 0 | 0 | 0 | 2 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2886): Show |
chr11 | 15109923 | 15252208 |
| a0003c0005t0009 | 0/0 | 2893 | 3 | 0 | 0 | 0 | 1 | 2 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0004c0006t0001 | 0/0 | 2893 | 3 | 3 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0004c0008t0015 | 0/0 | 2893 | 2 | 2 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0005c0007t0001 | 0/0 | 2893 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0005c0007t0014 | 0/0 | 2893 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0006c0019t0001 | 0/0 | 2893 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0007c0014t0004 | 0/0 | 2891 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2886): Show |
chr11 | 15109923 | 15252208 |
| a0008c0015t0001 | 0/0 | 2893 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| a0009c0010t0001 | 0/0 | 2893 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | ACTTT others(2888): Show |
chr11 | 15109923 | 15252208 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0007g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0008g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0011g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0011g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0012g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0012g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0016g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0016g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0018g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0021g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0022g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0001t0024g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0004g0007 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0004g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0005g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0006g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0006g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0006g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0007g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0007g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0007g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0008g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0013g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0002t0023g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0002g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0002g0220 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0004g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0013g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0019g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0003t0020g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0009t0010g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0009t0010g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0012t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0013t0017g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0016t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0001c0018t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0004t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0004t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0004t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0011t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0002c0017t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0003c0005t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0003c0005t0004g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0003c0005t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0003c0005t0009g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0003c0005t0009g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0003c0005t0009g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0004c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0004c0006t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0004c0006t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0004c0008t0015g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0004c0008t0015g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0005c0007t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0005c0007t0014g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0006c0019t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0007c0014t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0008c0015t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| a0009c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | GBR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00099 | hp2 | a0003 | c0005 | t0009 | g0171 | EUR | GBR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00408 | hp1 | a0001 | c0002 | t0003 | g0251 | EAS | CHS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | CHS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00621 | hp2 | a0001 | c0002 | t0013 | g0159 | EAS | CHS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0063 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00639 | hp2 | a0001 | c0013 | t0017 | g0081 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0236 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0106 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0234 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01081 | hp1 | a0001 | c0002 | t0004 | g0103 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01106 | hp1 | a0006 | c0019 | t0001 | g0084 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0260 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01192 | hp2 | a0001 | c0001 | t0012 | g0129 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01257 | hp1 | a0001 | c0001 | t0007 | g0030 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0025 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01346 | hp2 | a0001 | c0003 | t0001 | g0066 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01361 | hp2 | a0003 | c0005 | t0001 | g0216 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01433 | hp1 | a0007 | c0014 | t0004 | g0026 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01433 | hp2 | a0001 | c0001 | t0011 | g0181 | AMR | CLM | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | IBS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01515 | hp2 | a0001 | c0003 | t0002 | g0237 | EUR | IBS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01516 | hp1 | a0001 | c0002 | t0004 | g0007 | EUR | IBS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0086 | EUR | IBS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | IBS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0087 | EUR | IBS | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0217 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01884 | hp2 | a0001 | c0003 | t0004 | g0225 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG01993 | hp2 | a0001 | c0003 | t0004 | g0192 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0247 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02055 | hp1 | a0001 | c0002 | t0003 | g0239 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02055 | hp2 | a0001 | c0003 | t0002 | g0158 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02056 | hp2 | a0001 | c0003 | t0013 | g0104 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02129 | hp2 | a0001 | c0003 | t0020 | g0101 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | KHV | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02145 | hp1 | a0001 | c0002 | t0005 | g0077 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02257 | hp1 | a0001 | c0003 | t0002 | g0114 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02257 | hp2 | a0001 | c0002 | t0006 | g0033 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0187 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02273 | hp1 | a0001 | c0002 | t0007 | g0068 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02280 | hp1 | a0001 | c0001 | t0012 | g0169 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02293 | hp1 | a0005 | c0007 | t0014 | g0155 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02451 | hp2 | a0001 | c0003 | t0006 | g0226 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02572 | hp1 | a0001 | c0002 | t0003 | g0076 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02572 | hp2 | a0001 | c0002 | t0006 | g0179 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0243 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02615 | hp2 | a0002 | c0017 | t0001 | g0199 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0148 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0147 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02647 | hp1 | a0001 | c0018 | t0006 | g0228 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02647 | hp2 | a0001 | c0002 | t0023 | g0010 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02698 | hp2 | a0003 | c0005 | t0009 | g0249 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0178 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02818 | hp2 | a0008 | c0015 | t0001 | g0093 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02896 | hp1 | a0004 | c0008 | t0015 | g0035 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02896 | hp2 | a0001 | c0003 | t0004 | g0240 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02897 | hp2 | a0004 | c0008 | t0015 | g0034 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02922 | hp1 | a0002 | c0004 | t0001 | g0142 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02922 | hp2 | a0001 | c0002 | t0003 | g0222 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0183 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02970 | hp1 | a0001 | c0002 | t0006 | g0252 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0221 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0195 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02976 | hp2 | a0001 | c0002 | t0006 | g0257 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03017 | hp1 | a0003 | c0005 | t0004 | g0082 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03017 | hp2 | a0001 | c0003 | t0001 | g0065 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0229 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03041 | hp2 | a0001 | c0003 | t0002 | g0185 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03098 | hp1 | a0002 | c0004 | t0001 | g0231 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03130 | hp1 | a0002 | c0004 | t0001 | g0233 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03139 | hp1 | a0002 | c0004 | t0001 | g0031 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03139 | hp2 | a0001 | c0001 | t0024 | g0143 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0150 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0253 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03486 | hp2 | a0001 | c0001 | t0021 | g0263 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03490 | hp1 | a0003 | c0005 | t0009 | g0097 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03491 | hp1 | a0001 | c0003 | t0003 | g0254 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0186 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03540 | hp1 | a0002 | c0004 | t0002 | g0218 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03540 | hp2 | a0004 | c0006 | t0001 | g0244 | AFR | GWD | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03579 | hp1 | a0004 | c0006 | t0001 | g0245 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03654 | hp1 | a0001 | c0003 | t0002 | g0137 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03654 | hp2 | a0005 | c0007 | t0001 | g0215 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | BEB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0071 | SAS | BEB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG04115 | hp2 | a0003 | c0005 | t0004 | g0064 | SAS | STU | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | STU | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0080 | SAS | STU | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0175 | SAS | STU | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | YRI | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18522 | hp2 | a0001 | c0001 | t0005 | g0022 | AFR | YRI | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | CHB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CHB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0167 | AFR | YRI | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18944 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18954 | hp1 | a0001 | c0001 | t0018 | g0098 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18959 | hp1 | a0001 | c0003 | t0002 | g0194 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18959 | hp2 | a0009 | c0010 | t0001 | g0111 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18960 | hp1 | a0001 | c0016 | t0002 | g0201 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18967 | hp1 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18969 | hp2 | a0001 | c0002 | t0007 | g0165 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18981 | hp1 | a0001 | c0002 | t0007 | g0205 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18982 | hp1 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18987 | hp1 | a0001 | c0002 | t0003 | g0157 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18987 | hp2 | a0001 | c0001 | t0022 | g0128 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18989 | hp2 | a0001 | c0012 | t0001 | g0204 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0107 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19005 | hp2 | a0001 | c0002 | t0007 | g0050 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19006 | hp1 | a0001 | c0003 | t0019 | g0172 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19030 | hp1 | a0001 | c0009 | t0010 | g0258 | AFR | LWK | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0153 | AFR | LWK | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0149 | AFR | LWK | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19043 | hp2 | a0001 | c0009 | t0010 | g0262 | AFR | LWK | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0177 | AFR | YRI | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0255 | AFR | YRI | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA20129 | hp1 | a0002 | c0004 | t0001 | g0219 | AFR | ASW | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA20129 | hp2 | a0001 | c0002 | t0006 | g0256 | AFR | ASW | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | TSI | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | TSI | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0059 | SAS | GIH | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | GIH | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02109 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02109 | hp2 | a0002 | c0011 | t0002 | g0017 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02486 | hp1 | a0001 | c0002 | t0008 | g0040 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02486 | hp2 | a0004 | c0006 | t0001 | g0136 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0213 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG02559 | hp2 | a0002 | c0004 | t0001 | g0242 | AFR | ACB | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0089 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG03471 | hp2 | a0001 | c0001 | t0016 | g0261 | AFR | MSL | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG06807 | hp1 | a0001 | c0001 | t0016 | g0042 | AFR | USA | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| HG06807 | hp2 | a0001 | c0002 | t0003 | g0016 | AFR | USA | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0121 | AFR | LWK | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0002 | g0011 | REF | REF | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0002 | g0220 | REF | REF | INSC_chr11_15109923_15252208 | INSC | chr11 | 15109923 | 15252208 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:15149197 | G | A | 1 | a0009 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.23G>A | p.Arg8His | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/13 | 149/2893 | 23/1599 | 8/532 | chr11 | 15149197 | |||
| chr11:15176060 | A | G | 1 | a0006 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.376A>G | p.Arg126Gly | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 3/13 | 502/2893 | 376/1599 | 126/532 | chr11 | 15176060 | |||
| chr11:15200836 | G | A | 1 | a0002 | 10 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
missense_variant | MODERATE | c.706G>A | p.Val236Ile | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/13 | 832/2893 | 706/1599 | 236/532 | chr11 | 15200836 | |||
| chr11:15221501 | G | A | 1 | a0005 | 2 | HG02293.hp1 HG03654.hp2 |
missense_variant | MODERATE | c.844G>A | p.Asp282Asn | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/13 | 970/2893 | 844/1599 | 282/532 | chr11 | 15221501 | |||
| chr11:15221513 | G | A | 1 | a0003 | 6 | HG00099.hp2 HG01361.hp2 HG02698.hp2 others(3): Show |
missense_variant | MODERATE | c.856G>A | p.Asp286Asn | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/13 | 982/2893 | 856/1599 | 286/532 | chr11 | 15221513 | |||
| chr11:15221576 | C | T | 1 | a0008 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.919C>T | p.Pro307Ser | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/13 | 1045/2893 | 919/1599 | 307/532 | chr11 | 15221576 | |||
| chr11:15225767 | G | A | 2 | a0004 a0008 |
6 | HG02486.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.1109G>A | p.Arg370His | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/13 | 1235/2893 | 1109/1599 | 370/532 | chr11 | 15225767 | |||
| chr11:15240506 | G | A | 1 | a0007 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.1453G>A | p.Val485Met | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/13 | 1579/2893 | 1453/1599 | 485/532 | chr11 | 15240506 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:15175801 | C | T | 1 | a0001c0009 | 2 | NA19030.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.117C>T | p.Thr39Thr | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 3/13 | 243/2893 | 117/1599 | 39/532 | chr11 | 15175801 | |||
| chr11:15178411 | T | C | 14 | a0001c0001 a0001c0002 a0001c0009 others(11): Show |
238 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(235): Show |
synonymous_variant | LOW | c.543T>C | p.Gly181Gly | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/13 | 669/2893 | 543/1599 | 181/532 | chr11 | 15178411 | |||
| chr11:15190787 | G | T | 1 | a0001c0016 | 1 | NA18960.hp1 | synonymous_variant | LOW | c.666G>T | p.Gly222Gly | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/13 | 792/2893 | 666/1599 | 222/532 | chr11 | 15190787 | |||
| chr11:15221551 | G | A | 1 | a0001c0012 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.894G>A | p.Ala298Ala | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/13 | 1020/2893 | 894/1599 | 298/532 | chr11 | 15221551 | |||
| chr11:15221644 | C | T | 3 | a0001c0002 a0001c0018 a0002c0017 |
36 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(33): Show |
synonymous_variant | LOW | c.987C>T | p.Leu329Leu | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/13 | 1113/2893 | 987/1599 | 329/532 | chr11 | 15221644 | |||
| chr11:15225699 | G | A | 1 | a0001c0013 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.1041G>A | p.Ala347Ala | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/13 | 1167/2893 | 1041/1599 | 347/532 | chr11 | 15225699 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:15114961 | C | T | 1 | a0001c0001t0024 | 1 | HG03139.hp2 | 5_prime_UTR_variant | MODIFIER | c.-88C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/13 | 34214 | chr11 | 15114961 | ||||||
| chr11:15149136 | G | A | 1 | a0001c0009t0010 | 2 | NA19030.hp1 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-39G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/13 | 39 | chr11 | 15149136 | ||||||
| chr11:15149140 | G | A | 4 | a0001c0001t0007 a0001c0001t0011 a0001c0001t0012 others(1): Show |
10 | HG01192.hp2 HG01257.hp1 HG01433.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-35G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/13 | 35 | chr11 | 15149140 | ||||||
| chr11:15246048 | G | T | 1 | a0001c0002t0023 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 8 | chr11 | 15246048 | ||||||
| chr11:15246051 | C | A | 19 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(16): Show |
72 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*11C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 11 | chr11 | 15246051 | ||||||
| chr11:15246066 | G | T | 1 | a0001c0001t0022 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 26 | chr11 | 15246066 | ||||||
| chr11:15246180 | C | T | 1 | a0001c0001t0021 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*140C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 140 | chr11 | 15246180 | ||||||
| chr11:15246181 | A | G | 47 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(44): Show |
211 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
3_prime_UTR_variant | MODIFIER | c.*141A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 141 | chr11 | 15246181 | ||||||
| chr11:15246275 | G | A | 4 | a0001c0001t0014 a0001c0002t0013 a0001c0003t0013 others(1): Show |
4 | HG00621.hp2 HG02056.hp2 HG02293.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*235G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 235 | chr11 | 15246275 | ||||||
| chr11:15246289 | T | G | 1 | a0001c0013t0017 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 249 | chr11 | 15246289 | ||||||
| chr11:15246355 | A | C | 1 | a0001c0003t0020 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*315A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 315 | chr11 | 15246355 | ||||||
| chr11:15246355 | A | G | 1 | a0003c0005t0009 | 3 | HG00099.hp2 HG02698.hp2 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*315A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 315 | chr11 | 15246355 | ||||||
| chr11:15246378 | T | C | 1 | a0004c0008t0015 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*338T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 338 | chr11 | 15246378 | ||||||
| chr11:15246381 | G | C | 5 | a0001c0001t0004 a0001c0002t0004 a0001c0003t0004 others(2): Show |
21 | HG00639.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*341G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 341 | chr11 | 15246381 | ||||||
| chr11:15246409 | G | GT | 2 | a0001c0001t0008 a0001c0002t0008 |
5 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*379dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 380 | INFO_REALIGN_3_PRIME | chr11 | 15246409 | |||||
| chr11:15246475 | A | C | 1 | a0001c0001t0022 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 435 | chr11 | 15246475 | ||||||
| chr11:15246514 | CAT | C | 5 | a0001c0001t0004 a0001c0002t0004 a0001c0003t0004 others(2): Show |
21 | HG00639.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*478_*479delTA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 478 | INFO_REALIGN_3_PRIME | chr11 | 15246514 | |||||
| chr11:15246632 | G | T | 1 | a0001c0003t0019 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*592G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 592 | chr11 | 15246632 | ||||||
| chr11:15246670 | C | T | 20 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0006 others(17): Show |
74 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*630C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 630 | chr11 | 15246670 | ||||||
| chr11:15246755 | A | G | 5 | a0001c0001t0006 a0001c0002t0006 a0001c0003t0006 others(2): Show |
16 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*715A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 715 | chr11 | 15246755 | ||||||
| chr11:15246759 | C | T | 2 | a0001c0001t0018 a0001c0001t0022 |
2 | NA18954.hp1 NA18987.hp2 |
3_prime_UTR_variant | MODIFIER | c.*719C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 719 | chr11 | 15246759 | ||||||
| chr11:15246869 | C | G | 5 | a0001c0001t0006 a0001c0002t0006 a0001c0003t0006 others(2): Show |
16 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*829C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 829 | chr11 | 15246869 | ||||||
| chr11:15246973 | A | G | 1 | a0001c0001t0022 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*933A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 933 | chr11 | 15246973 | ||||||
| chr11:15247025 | C | T | 1 | a0001c0002t0023 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*985C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 985 | chr11 | 15247025 | ||||||
| chr11:15247027 | C | CT | 14 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0012 others(11): Show |
56 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1000dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 1001 | INFO_REALIGN_3_PRIME | chr11 | 15247027 | |||||
| chr11:15247159 | T | C | 1 | a0004c0008t0015 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1119T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 13/13 | 1119 | chr11 | 15247159 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:15115105 | A | C | 1 | a0001c0001t0002g0264 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-46+102A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115105 | |||||||
| chr11:15115212 | C | T | 12 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0016g0261 others(9): Show |
12 | HG01106.hp2 HG02970.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46+209C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115212 | |||||||
| chr11:15115291 | G | A | 1 | a0001c0002t0004g0007 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-46+288G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115291 | |||||||
| chr11:15115309 | C | T | 20 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(17): Show |
20 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.-46+306C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115309 | |||||||
| chr11:15115342 | G | A | 1 | a0001c0001t0006g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-46+339G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115342 | |||||||
| chr11:15115482 | G | T | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-46+479G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115482 | |||||||
| chr11:15115526 | G | A | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-46+523G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115526 | |||||||
| chr11:15115565 | G | C | 1 | a0001c0001t0004g0001 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-46+562G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115565 | |||||||
| chr11:15115567 | G | A | 12 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0016g0261 others(9): Show |
12 | HG01106.hp2 HG02970.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46+564G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115567 | |||||||
| chr11:15115583 | A | G | 25 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(22): Show |
25 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(22): Show |
intron_variant | MODIFIER | c.-46+580A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115583 | |||||||
| chr11:15115644 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-46+641G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115644 | |||||||
| chr11:15115666 | G | A | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+663G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115666 | |||||||
| chr11:15115699 | A | G | 8 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0250 others(5): Show |
8 | HG00408.hp1 HG02040.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+696A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115699 | |||||||
| chr11:15115816 | G | A | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+813G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115816 | |||||||
| chr11:15115854 | C | T | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+851C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115854 | |||||||
| chr11:15115874 | C | T | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+871C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15115874 | |||||||
| chr11:15116023 | G | A | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-46+1020G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116023 | |||||||
| chr11:15116039 | G | A | 2 | a0004c0006t0001g0244 a0004c0006t0001g0245 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-46+1036G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116039 | |||||||
| chr11:15116078 | G | C | 1 | a0001c0001t0003g0013 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-46+1075G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116078 | |||||||
| chr11:15116087 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-46+1084C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116087 | |||||||
| chr11:15116149 | C | T | 8 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0250 others(5): Show |
8 | HG00408.hp1 HG02040.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+1146C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116149 | |||||||
| chr11:15116177 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-46+1174T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116177 | |||||||
| chr11:15116189 | G | A | 10 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(7): Show |
10 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46+1186G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116189 | |||||||
| chr11:15116204 | C | A | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0002g0025 others(3): Show |
6 | HG01256.hp2 HG01257.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+1201C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116204 | |||||||
| chr11:15116317 | A | G | 4 | a0001c0001t0001g0235 a0001c0001t0004g0234 a0001c0001t0004g0236 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46+1314A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116317 | |||||||
| chr11:15116441 | T | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-46+1438T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116441 | |||||||
| chr11:15116462 | C | CT | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+1466dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116462 | ||||||
| chr11:15116532 | G | C | 3 | a0001c0001t0002g0032 a0001c0002t0006g0033 a0002c0004t0001g0031 |
3 | HG01243.hp1 HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-46+1529G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116532 | |||||||
| chr11:15116742 | T | TTTCC | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+1756_-46+1759d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116742 | ||||||
| chr11:15116770 | CT | C | 12 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0016g0261 others(9): Show |
12 | HG01106.hp2 HG02970.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46+1774delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116770 | ||||||
| chr11:15116785 | CCTTTCTT others(7): Show |
C | 1 | a0004c0008t0015g0034 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-46+1796_-46+1809d others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116785 | ||||||
| chr11:15116786 | C | CTTTCT | 9 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0083 others(6): Show |
9 | HG00099.hp1 HG00733.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46+1796_-46+1800d others(7): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116786 | ||||||
| chr11:15116786 | C | CTTTCTTT others(3): Show |
1 | a0001c0001t0002g0060 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-46+1791_-46+1800d others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116786 | ||||||
| chr11:15116786 | C | T | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-46+1783C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116786 | |||||||
| chr11:15116796 | T | TTTCTTTT others(5): Show |
2 | a0001c0001t0002g0241 a0001c0001t0016g0042 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-46+1795_-46+1796i others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116796 | ||||||
| chr11:15116796 | T | TTTCTTTT others(9): Show |
3 | a0001c0002t0003g0239 a0001c0002t0003g0243 a0002c0004t0001g0242 |
3 | HG02055.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-46+1795_-46+1796i others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116796 | ||||||
| chr11:15116796 | T | TTTTCTTT others(2): Show |
7 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0061 others(4): Show |
8 | HG00741.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46+1800_-46+1801i others(11): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116796 | ||||||
| chr11:15116796 | T | TTTTCTTT others(6): Show |
1 | a0001c0001t0001g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-46+1800_-46+1801i others(15): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116796 | ||||||
| chr11:15116796 | TTTTC | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0056 others(4): Show |
8 | HG01070.hp2 HG01071.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.-46+1801_-46+1804d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116796 | ||||||
| chr11:15116798 | T | TCTTTTCT others(15): Show |
1 | a0001c0003t0004g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-46+1795_-46+1796i others(24): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116798 | |||||||
| chr11:15116800 | C | CT | 12 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(9): Show |
13 | HG01346.hp1 HG01361.hp2 HG01515.hp1 others(10): Show |
intron_variant | MODIFIER | c.-46+1800dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116800 | ||||||
| chr11:15116801 | TTTCTTTT others(1): Show |
T | 3 | a0001c0001t0003g0203 a0001c0002t0007g0205 a0001c0012t0001g0204 |
3 | NA18954.hp2 NA18981.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.-46+1801_-46+1808d others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116801 | ||||||
| chr11:15116801 | TTTCTTTT others(5): Show |
T | 1 | a0001c0001t0001g0202 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-46+1801_-46+1812d others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116801 | ||||||
| chr11:15116804 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0053 others(16): Show |
20 | HG00609.hp2 HG00738.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.-46+1801C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116804 | |||||||
| chr11:15116805 | T | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0053 others(17): Show |
21 | HG00609.hp2 HG00738.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-46+1802T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116805 | |||||||
| chr11:15116805 | T | TTTC | 31 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0001g0049 others(28): Show |
33 | HG00099.hp1 HG00733.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-46+1804_-46+1805i others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116805 | ||||||
| chr11:15116805 | T | TTTTC | 18 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0067 others(15): Show |
18 | HG01070.hp1 HG01081.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.-46+1844_-46+1847d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116805 | ||||||
| chr11:15116805 | T | TTTTCTTT others(1): Show |
12 | a0001c0001t0001g0100 a0001c0001t0001g0138 a0001c0001t0002g0062 others(9): Show |
12 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.-46+1840_-46+1847d others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116805 | ||||||
| chr11:15116805 | T | TTTTCTTT others(5): Show |
7 | a0001c0001t0001g0073 a0001c0001t0001g0099 a0001c0001t0003g0020 others(4): Show |
7 | HG01516.hp2 HG01517.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46+1836_-46+1847d others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116805 | ||||||
| chr11:15116805 | T | TTTTCTTT others(9): Show |
9 | a0001c0001t0002g0075 a0001c0002t0001g0089 a0001c0002t0004g0007 others(6): Show |
9 | HG00639.hp1 HG01074.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46+1832_-46+1847d others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116805 | ||||||
| chr11:15116805 | T | TTTTCTTT others(13): Show |
2 | a0001c0002t0001g0095 a0001c0002t0005g0077 |
2 | HG02071.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-46+1828_-46+1847d others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116805 | ||||||
| chr11:15116805 | T | TTTTCTTT others(17): Show |
2 | a0001c0001t0001g0079 a0001c0001t0003g0096 |
2 | HG02074.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-46+1824_-46+1847d others(26): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116805 | ||||||
| chr11:15116843 | TTCTTTCT others(5): Show |
T | 1 | a0001c0002t0003g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-46+1844_-46+1855d others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116843 | ||||||
| chr11:15116845 | C | CTTTCTTT others(5): Show |
3 | a0001c0001t0001g0146 a0001c0001t0008g0147 a0001c0001t0008g0148 |
3 | HG01069.hp2 HG02622.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116845 | ||||||
| chr11:15116846 | T | TTTCTTTC others(4): Show |
1 | a0001c0002t0003g0157 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(13): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116846 | ||||||
| chr11:15116847 | T | C | 1 | a0004c0008t0015g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-46+1844T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116847 | |||||||
| chr11:15116847 | T | TTCTCTCT others(3): Show |
1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-46+1865_-46+1874d others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTCTCT others(5): Show |
1 | a0001c0001t0001g0028 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-46+1863_-46+1874d others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(3): Show |
1 | a0001c0001t0003g0144 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(7): Show |
1 | a0001c0001t0001g0029 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(11): Show |
1 | a0001c0001t0002g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(20): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(3): Show |
1 | a0005c0007t0014g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(7): Show |
2 | a0001c0001t0002g0032 a0001c0001t0007g0030 |
2 | HG01243.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(9): Show |
3 | a0001c0001t0001g0156 a0001c0001t0004g0236 a0001c0002t0006g0033 |
3 | HG00733.hp1 HG02257.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(7): Show |
3 | a0001c0001t0001g0168 a0001c0001t0008g0170 a0001c0001t0012g0169 |
3 | HG00738.hp2 HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(11): Show |
1 | a0002c0004t0001g0233 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(20): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(15): Show |
1 | a0003c0005t0009g0171 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(24): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(12): Show |
1 | a0001c0003t0019g0172 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(21): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(11): Show |
5 | a0001c0001t0001g0184 a0001c0001t0003g0188 a0001c0001t0005g0187 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(20): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(13): Show |
1 | a0001c0001t0001g0189 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0001g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(24): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(14): Show |
1 | a0001c0001t0001g0191 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(23): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(15): Show |
2 | a0001c0001t0001g0200 a0002c0017t0001g0199 |
2 | HG01993.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(24): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(17): Show |
1 | a0001c0003t0002g0237 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(26): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | T | TTCTTTCT others(23): Show |
1 | a0001c0016t0002g0201 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(32): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116847 | TTC | T | 3 | a0001c0001t0001g0202 a0001c0001t0002g0037 a0001c0001t0004g0006 |
4 | HG01952.hp1 HG02293.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+1873_-46+1874d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116847 | ||||||
| chr11:15116849 | C | CTT | 16 | a0001c0001t0001g0012 a0001c0001t0001g0141 a0001c0001t0001g0154 others(13): Show |
16 | HG00609.hp2 HG00621.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTCT others(5): Show |
1 | a0001c0002t0001g0247 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTT | 6 | a0001c0001t0002g0151 a0001c0001t0002g0153 a0001c0001t0002g0230 others(3): Show |
6 | HG01243.hp2 HG02055.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTTT others(25): Show |
1 | a0004c0006t0001g0244 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(34): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTTT others(3): Show |
10 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0002g0166 others(7): Show |
10 | HG02698.hp1 HG02717.hp1 HG03098.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTTT others(25): Show |
1 | a0001c0001t0001g0248 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(34): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTTT others(33): Show |
1 | a0004c0006t0001g0245 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(42): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTTT others(7): Show |
6 | a0001c0001t0001g0182 a0001c0001t0002g0180 a0001c0001t0005g0178 others(3): Show |
6 | HG01433.hp2 HG02572.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTTT others(11): Show |
6 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0005g0193 others(3): Show |
6 | HG02258.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46+1847_-46+1848i others(20): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTTT others(33): Show |
1 | a0001c0001t0002g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(42): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTTT others(37): Show |
1 | a0003c0005t0009g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(46): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116849 | C | CTTTCTTT others(37): Show |
1 | a0001c0002t0003g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-46+1847_-46+1848i others(46): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116849 | ||||||
| chr11:15116851 | C | T | 126 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(123): Show |
131 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.-46+1848C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116851 | |||||||
| chr11:15116853 | C | T | 20 | a0001c0001t0001g0012 a0001c0001t0001g0154 a0001c0001t0001g0160 others(17): Show |
20 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-46+1850C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116853 | |||||||
| chr11:15116854 | T | TTTCTTTC others(18): Show |
1 | a0001c0001t0001g0140 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-46+1851_-46+1852i others(27): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116854 | |||||||
| chr11:15116855 | C | CTTTCTTT others(19): Show |
1 | a0001c0001t0001g0246 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-46+1853_-46+1854i others(28): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116855 | ||||||
| chr11:15116855 | C | T | 47 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0112 others(44): Show |
48 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-46+1852C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116855 | |||||||
| chr11:15116857 | C | T | 18 | a0001c0001t0001g0012 a0001c0001t0001g0160 a0001c0001t0001g0161 others(15): Show |
18 | HG00621.hp2 HG00735.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-46+1854C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116857 | |||||||
| chr11:15116859 | C | T | 21 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0126 others(18): Show |
21 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.-46+1856C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116859 | |||||||
| chr11:15116861 | C | T | 16 | a0001c0001t0001g0174 a0001c0001t0001g0259 a0001c0001t0002g0173 others(13): Show |
16 | HG00735.hp1 HG01106.hp2 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.-46+1858C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116861 | |||||||
| chr11:15116863 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0138 a0001c0002t0001g0139 others(3): Show |
6 | HG00621.hp1 HG02040.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+1860C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116863 | |||||||
| chr11:15116864 | T | C | 2 | a0003c0005t0009g0249 a0004c0006t0001g0245 |
2 | HG02698.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-46+1861T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116864 | |||||||
| chr11:15116865 | C | T | 13 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0016g0261 others(10): Show |
13 | HG01106.hp2 HG01993.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.-46+1862C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116865 | |||||||
| chr11:15116868 | T | C | 6 | a0001c0001t0001g0248 a0001c0001t0002g0250 a0001c0002t0003g0251 others(3): Show |
6 | HG00408.hp1 HG02698.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+1865T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116868 | |||||||
| chr11:15116868 | T | TTTCTTTC others(17): Show |
1 | a0001c0002t0006g0256 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-46+1865_-46+1866i others(26): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116868 | |||||||
| chr11:15116869 | C | T | 10 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0016g0261 others(7): Show |
10 | HG01106.hp2 HG02970.hp1 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.-46+1866C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116869 | |||||||
| chr11:15116870 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-46+1867T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116870 | |||||||
| chr11:15116872 | T | C | 9 | a0001c0001t0001g0248 a0001c0001t0002g0250 a0001c0002t0003g0251 others(6): Show |
9 | HG00408.hp1 HG02698.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46+1869T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116872 | |||||||
| chr11:15116873 | C | T | 4 | a0001c0001t0003g0255 a0001c0002t0006g0252 a0001c0003t0003g0254 others(1): Show |
4 | HG02970.hp1 HG03453.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+1870C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116873 | |||||||
| chr11:15116874 | T | C | 2 | a0001c0001t0001g0036 a0001c0001t0001g0246 |
2 | NA18956.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-46+1871T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116874 | |||||||
| chr11:15116876 | T | C | 17 | a0001c0001t0001g0036 a0001c0001t0001g0248 a0001c0001t0001g0259 others(14): Show |
17 | HG00408.hp1 HG01106.hp2 HG02698.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46+1873T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116876 | |||||||
| chr11:15116876 | TCCCC | T | 7 | a0001c0001t0001g0105 a0001c0001t0001g0125 a0001c0001t0002g0025 others(4): Show |
7 | HG00609.hp1 HG00741.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46+1875_-46+1878d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116876 | ||||||
| chr11:15116876 | TCCCCCTC others(1): Show |
T | 5 | a0001c0001t0001g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 others(2): Show |
6 | HG01074.hp2 HG02129.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46+1875_-46+1882d others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116876 | ||||||
| chr11:15116876 | TCCCCCTC others(5): Show |
T | 2 | a0001c0001t0007g0107 a0001c0003t0001g0106 |
2 | HG00738.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-46+1875_-46+1886d others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116876 | ||||||
| chr11:15116877 | C | T | 1 | a0001c0001t0003g0255 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-46+1874C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116877 | |||||||
| chr11:15116878 | C | T | 63 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0036 others(60): Show |
63 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-46+1875C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116878 | |||||||
| chr11:15116878 | CCCCTCCC others(1): Show |
C | 4 | a0001c0001t0001g0090 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
4 | HG01081.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+1914_-46+1921d others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116878 | ||||||
| chr11:15116878 | CCCCTCCC others(5): Show |
C | 1 | a0001c0001t0001g0156 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-46+1910_-46+1921d others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116878 | ||||||
| chr11:15116878 | CCCCTCCC others(9): Show |
C | 43 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0092 others(40): Show |
43 | HG00099.hp2 HG00733.hp1 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.-46+1906_-46+1921d others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116878 | ||||||
| chr11:15116878 | CCCCTCCC others(13): Show |
C | 2 | a0001c0001t0005g0167 a0001c0001t0005g0183 |
2 | HG02965.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-46+1902_-46+1921d others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116878 | ||||||
| chr11:15116878 | CCCCTCCC others(17): Show |
C | 1 | a0001c0003t0013g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-46+1898_-46+1921d others(26): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116878 | ||||||
| chr11:15116880 | C | T | 40 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0112 others(37): Show |
40 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(37): Show |
intron_variant | MODIFIER | c.-46+1877C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116880 | |||||||
| chr11:15116881 | CTCCCTCC others(6): Show |
C | 1 | a0001c0001t0002g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-46+1879_-46+1891d others(15): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116881 | |||||||
| chr11:15116882 | T | C | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-46+1879T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116882 | |||||||
| chr11:15116884 | C | T | 39 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0105 others(36): Show |
39 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-46+1881C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116884 | |||||||
| chr11:15116884 | CCTCCCTC others(3): Show |
C | 4 | a0001c0001t0001g0113 a0001c0001t0006g0008 a0001c0001t0012g0129 others(1): Show |
4 | HG01192.hp2 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46+1883_-46+1892d others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116884 | ||||||
| chr11:15116884 | CCTCCCTC others(11): Show |
C | 2 | a0001c0001t0005g0109 a0009c0010t0001g0111 |
2 | NA18959.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-46+1883_-46+1900d others(20): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116884 | ||||||
| chr11:15116886 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0115 a0001c0001t0005g0117 others(1): Show |
4 | HG02132.hp2 NA18960.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+1883T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116886 | |||||||
| chr11:15116888 | C | T | 34 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0112 others(31): Show |
35 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-46+1885C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116888 | |||||||
| chr11:15116888 | CCTCCCT | C | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0131 others(1): Show |
4 | HG02056.hp1 HG02630.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46+1887_-46+1892d others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116888 | ||||||
| chr11:15116888 | CCTCCCTC others(7): Show |
C | 1 | a0001c0001t0005g0110 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-46+1887_-46+1900d others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116888 | ||||||
| chr11:15116890 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-46+1887T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116890 | |||||||
| chr11:15116891 | CCCT | C | 3 | a0001c0001t0001g0154 a0001c0001t0002g0132 a0001c0001t0004g0133 |
3 | HG00735.hp2 NA18949.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-46+1891_-46+1893d others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116891 | ||||||
| chr11:15116892 | C | T | 28 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0112 others(25): Show |
29 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.-46+1889C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116892 | |||||||
| chr11:15116892 | CCT | C | 5 | a0001c0001t0001g0134 a0001c0001t0002g0027 a0001c0001t0002g0135 others(2): Show |
5 | HG00408.hp2 HG00621.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46+1891_-46+1892d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116892 | ||||||
| chr11:15116894 | T | C | 27 | a0001c0001t0001g0014 a0001c0001t0001g0105 a0001c0001t0001g0112 others(24): Show |
28 | HG00609.hp1 HG00621.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-46+1891T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116894 | |||||||
| chr11:15116897 | C | CTCCTTCC others(9): Show |
1 | a0002c0004t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-46+1897_-46+1898i others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116897 | ||||||
| chr11:15116897 | C | T | 1 | a0001c0003t0004g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-46+1894C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116897 | |||||||
| chr11:15116901 | C | T | 4 | a0001c0002t0003g0239 a0001c0003t0004g0240 a0002c0004t0001g0242 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46+1898C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116901 | |||||||
| chr11:15116905 | C | CTCCTTCC others(13): Show |
1 | a0001c0002t0003g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-46+1905_-46+1906i others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116905 | ||||||
| chr11:15116905 | C | CTCCTTCC others(17): Show |
1 | a0001c0001t0002g0241 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-46+1905_-46+1906i others(26): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116905 | ||||||
| chr11:15116905 | C | T | 10 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0250 others(7): Show |
11 | HG00408.hp1 HG01515.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.-46+1902C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116905 | |||||||
| chr11:15116909 | C | T | 13 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0241 others(10): Show |
14 | HG00408.hp1 HG01515.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.-46+1906C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116909 | |||||||
| chr11:15116913 | C | CTCCT | 4 | a0001c0001t0001g0164 a0001c0001t0001g0197 a0001c0001t0006g0086 others(1): Show |
4 | HG01516.hp2 HG01517.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46+1913_-46+1914i others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116913 | ||||||
| chr11:15116913 | C | CTCCTTCC others(1): Show |
5 | a0001c0001t0001g0085 a0001c0001t0001g0168 a0001c0001t0011g0181 others(2): Show |
5 | HG00738.hp2 HG00741.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+1913_-46+1914i others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116913 | ||||||
| chr11:15116913 | C | CTCCTTCC others(5): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0083 a0001c0001t0001g0146 others(5): Show |
9 | HG00733.hp2 HG01069.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46+1913_-46+1914i others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116913 | ||||||
| chr11:15116913 | C | T | 23 | a0001c0001t0001g0012 a0001c0001t0001g0246 a0001c0001t0001g0248 others(20): Show |
24 | HG00408.hp1 HG01081.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.-46+1910C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116913 | |||||||
| chr11:15116917 | C | CTCCT | 7 | a0001c0001t0002g0032 a0001c0001t0002g0180 a0001c0001t0003g0152 others(4): Show |
7 | HG01243.hp1 HG02257.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46+1917_-46+1918i others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116917 | ||||||
| chr11:15116917 | C | CTCCTTCC others(1): Show |
13 | a0001c0001t0001g0079 a0001c0001t0001g0162 a0001c0001t0001g0196 others(10): Show |
13 | HG00639.hp2 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-46+1917_-46+1918i others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116917 | ||||||
| chr11:15116917 | C | CTCCTTCC others(5): Show |
26 | a0001c0001t0001g0061 a0001c0001t0001g0067 a0001c0001t0001g0072 others(23): Show |
27 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46+1917_-46+1918i others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116917 | ||||||
| chr11:15116917 | C | CTCCTTCC others(9): Show |
32 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0047 others(29): Show |
33 | HG00609.hp2 HG01257.hp2 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.-46+1917_-46+1918i others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116917 | ||||||
| chr11:15116917 | C | CTCCTTCC others(13): Show |
3 | a0001c0001t0001g0238 a0001c0001t0002g0206 a0001c0001t0004g0041 |
3 | HG02148.hp2 NA18969.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-46+1917_-46+1918i others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116917 | ||||||
| chr11:15116917 | C | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0083 others(43): Show |
48 | HG00408.hp1 HG00733.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.-46+1914C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116917 | |||||||
| chr11:15116921 | C | CTCCCTCC others(13): Show |
1 | a0001c0001t0003g0255 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-46+1921_-46+1922i others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116921 | ||||||
| chr11:15116921 | C | CTCCCTCC others(9): Show |
2 | a0001c0002t0006g0252 a0002c0004t0001g0253 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-46+1921_-46+1922i others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116921 | ||||||
| chr11:15116921 | C | CTCCCTCC others(13): Show |
1 | a0001c0002t0003g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-46+1921_-46+1922i others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116921 | ||||||
| chr11:15116921 | C | CTCCCTCC others(5): Show |
1 | a0001c0002t0006g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-46+1921_-46+1922i others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116921 | ||||||
| chr11:15116921 | C | CTCCCTCC others(9): Show |
1 | a0001c0001t0005g0178 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-46+1921_-46+1922i others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116921 | ||||||
| chr11:15116921 | C | CTCCTTCC others(1): Show |
6 | a0001c0001t0001g0259 a0001c0002t0006g0179 a0001c0002t0008g0040 others(3): Show |
6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46+1937_-46+1944d others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116921 | ||||||
| chr11:15116921 | C | CTCCTTCC others(5): Show |
5 | a0001c0001t0001g0039 a0001c0001t0002g0018 a0001c0001t0002g0038 others(2): Show |
5 | HG00099.hp1 HG02135.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46+1933_-46+1944d others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116921 | ||||||
| chr11:15116921 | C | CTCCTTCC others(9): Show |
2 | a0001c0001t0005g0193 a0002c0011t0002g0017 |
2 | HG02109.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-46+1929_-46+1944d others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116921 | ||||||
| chr11:15116921 | C | CTCCTTCC others(13): Show |
1 | a0001c0001t0001g0202 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-46+1925_-46+1944d others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116921 | ||||||
| chr11:15116921 | C | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(126): Show |
133 | HG00408.hp1 HG00609.hp2 HG00639.hp1 others(130): Show |
intron_variant | MODIFIER | c.-46+1918C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116921 | |||||||
| chr11:15116932 | C | CTTCCTTC others(9): Show |
1 | a0001c0001t0002g0264 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-46+1941_-46+1956d others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15116932 | ||||||
| chr11:15116984 | C | T | 20 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(17): Show |
20 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.-46+1981C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15116984 | |||||||
| chr11:15117030 | C | T | 8 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0250 others(5): Show |
8 | HG00408.hp1 HG02040.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+2027C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117030 | |||||||
| chr11:15117203 | T | A | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
149 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.-46+2200T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117203 | |||||||
| chr11:15117429 | A | G | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
149 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.-46+2426A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117429 | |||||||
| chr11:15117555 | T | C | 1 | a0001c0001t0008g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-46+2552T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117555 | |||||||
| chr11:15117624 | A | T | 10 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(7): Show |
10 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46+2621A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117624 | |||||||
| chr11:15117635 | C | T | 1 | a0001c0001t0005g0178 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-46+2632C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117635 | |||||||
| chr11:15117742 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(104): Show |
111 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.-46+2739T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117742 | |||||||
| chr11:15117771 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-46+2768A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117771 | |||||||
| chr11:15117773 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-46+2770G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117773 | |||||||
| chr11:15117785 | C | T | 1 | a0001c0003t0002g0158 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-46+2782C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117785 | |||||||
| chr11:15117807 | T | C | 1 | a0001c0003t0004g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-46+2804T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15117807 | |||||||
| chr11:15118027 | C | T | 1 | a0001c0001t0004g0176 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-46+3024C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15118027 | |||||||
| chr11:15118038 | C | T | 1 | a0001c0002t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-46+3035C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15118038 | |||||||
| chr11:15118353 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(104): Show |
111 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.-46+3350T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15118353 | |||||||
| chr11:15118483 | T | G | 26 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(23): Show |
26 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46+3480T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15118483 | |||||||
| chr11:15118487 | A | G | 26 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(23): Show |
26 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46+3484A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15118487 | |||||||
| chr11:15118533 | T | C | 1 | a0001c0001t0001g0191 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-46+3530T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15118533 | |||||||
| chr11:15118653 | T | C | 145 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(142): Show |
149 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.-46+3650T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15118653 | |||||||
| chr11:15118943 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-46+3940T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15118943 | |||||||
| chr11:15119303 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-46+4300C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15119303 | |||||||
| chr11:15119379 | G | A | 11 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0193 others(8): Show |
11 | HG01106.hp2 HG02258.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.-46+4376G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15119379 | |||||||
| chr11:15119406 | C | T | 6 | a0001c0001t0008g0195 a0001c0001t0024g0143 a0001c0002t0003g0076 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46+4403C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15119406 | |||||||
| chr11:15119423 | C | G | 21 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(18): Show |
21 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.-46+4420C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15119423 | |||||||
| chr11:15119562 | C | G | 26 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(23): Show |
26 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46+4559C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15119562 | |||||||
| chr11:15119574 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-46+4571T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15119574 | |||||||
| chr11:15119595 | G | A | 5 | a0001c0001t0002g0153 a0001c0001t0005g0167 a0001c0001t0005g0183 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46+4592G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15119595 | |||||||
| chr11:15120068 | C | T | 1 | a0001c0001t0002g0214 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-46+5065C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15120068 | |||||||
| chr11:15120225 | C | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(104): Show |
111 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.-46+5222C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15120225 | |||||||
| chr11:15120247 | T | C | 1 | a0001c0003t0002g0194 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-46+5244T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15120247 | |||||||
| chr11:15120400 | A | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(104): Show |
111 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.-46+5397A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15120400 | |||||||
| chr11:15120526 | A | G | 10 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(7): Show |
10 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46+5523A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15120526 | |||||||
| chr11:15120539 | C | T | 10 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(7): Show |
10 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46+5536C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15120539 | |||||||
| chr11:15120738 | T | C | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+5735T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15120738 | |||||||
| chr11:15120936 | TA | T | 26 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(23): Show |
26 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46+5935delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15120936 | ||||||
| chr11:15120954 | A | G | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-46+5951A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15120954 | |||||||
| chr11:15120983 | G | T | 4 | a0001c0001t0003g0144 a0001c0001t0005g0102 a0004c0008t0015g0034 others(1): Show |
4 | HG02886.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+5980G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15120983 | |||||||
| chr11:15121066 | T | TA | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-46+6063_-46+6064i others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121066 | |||||||
| chr11:15121180 | G | A | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+6177G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121180 | |||||||
| chr11:15121216 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-46+6213A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121216 | |||||||
| chr11:15121240 | C | T | 1 | a0001c0003t0003g0254 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-46+6237C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121240 | |||||||
| chr11:15121315 | A | AT | 5 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(2): Show |
5 | HG01074.hp1 HG01081.hp2 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46+6318dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15121315 | ||||||
| chr11:15121407 | G | T | 1 | a0001c0001t0007g0107 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-46+6404G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121407 | |||||||
| chr11:15121424 | A | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0196 others(4): Show |
7 | HG02132.hp2 HG02135.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46+6421A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121424 | |||||||
| chr11:15121571 | T | C | 1 | a0001c0002t0006g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-46+6568T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121571 | |||||||
| chr11:15121607 | G | T | 10 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(7): Show |
10 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-46+6604G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121607 | |||||||
| chr11:15121877 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(104): Show |
111 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.-46+6874A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121877 | |||||||
| chr11:15121905 | T | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-46+6902T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121905 | |||||||
| chr11:15121938 | C | T | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+6935C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15121938 | |||||||
| chr11:15122011 | C | G | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+7008C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122011 | |||||||
| chr11:15122024 | A | C | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-46+7021A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122024 | |||||||
| chr11:15122216 | A | G | 1 | a0001c0003t0002g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-46+7213A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122216 | |||||||
| chr11:15122220 | G | A | 1 | a0001c0003t0002g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-46+7217G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122220 | |||||||
| chr11:15122326 | G | A | 11 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0193 others(8): Show |
11 | HG01106.hp2 HG02258.hp1 HG02970.hp1 others(8): Show |
intron_variant | MODIFIER | c.-46+7323G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122326 | |||||||
| chr11:15122378 | G | A | 1 | a0001c0001t0004g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-46+7375G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122378 | |||||||
| chr11:15122443 | A | C | 1 | a0001c0013t0017g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-46+7440A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122443 | |||||||
| chr11:15122474 | C | A | 5 | a0001c0001t0001g0196 a0001c0001t0002g0180 a0001c0001t0003g0013 others(2): Show |
5 | NA18981.hp2 NA18985.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+7471C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122474 | |||||||
| chr11:15122845 | C | T | 41 | a0001c0001t0001g0014 a0001c0001t0001g0090 a0001c0001t0001g0099 others(38): Show |
41 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.-46+7842C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122845 | |||||||
| chr11:15122904 | C | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-46+7901C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15122904 | |||||||
| chr11:15123120 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(103): Show |
110 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.-46+8117C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15123120 | |||||||
| chr11:15123435 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-46+8432G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15123435 | |||||||
| chr11:15123953 | A | C | 2 | a0001c0001t0005g0229 a0001c0018t0006g0228 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-46+8950A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15123953 | |||||||
| chr11:15123959 | T | C | 26 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(23): Show |
26 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46+8956T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15123959 | |||||||
| chr11:15124317 | A | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(140): Show |
147 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.-46+9314A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15124317 | |||||||
| chr11:15124325 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(105): Show |
112 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.-46+9322C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15124325 | |||||||
| chr11:15124333 | G | A | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-46+9330G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15124333 | |||||||
| chr11:15124652 | G | A | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-46+9649G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15124652 | |||||||
| chr11:15124986 | T | A | 1 | a0001c0001t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-46+9983T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15124986 | |||||||
| chr11:15125011 | G | A | 3 | a0001c0001t0002g0032 a0001c0002t0006g0179 a0002c0004t0001g0031 |
3 | HG01243.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-46+10008G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125011 | |||||||
| chr11:15125065 | C | T | 1 | a0001c0001t0002g0264 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-46+10062C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125065 | |||||||
| chr11:15125209 | G | A | 1 | a0001c0001t0005g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46+10206G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125209 | |||||||
| chr11:15125369 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-46+10366G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125369 | |||||||
| chr11:15125382 | G | A | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(101): Show |
108 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.-46+10379G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125382 | |||||||
| chr11:15125401 | A | G | 1 | a0001c0001t0005g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46+10398A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125401 | |||||||
| chr11:15125404 | A | T | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-46+10401A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125404 | |||||||
| chr11:15125719 | T | C | 1 | a0001c0001t0002g0043 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-46+10716T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125719 | |||||||
| chr11:15125744 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-46+10741G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125744 | |||||||
| chr11:15125803 | A | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(101): Show |
108 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.-46+10800A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15125803 | |||||||
| chr11:15126039 | T | C | 103 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(100): Show |
104 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-46+11036T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126039 | |||||||
| chr11:15126072 | A | G | 14 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0163 others(11): Show |
14 | HG01106.hp2 HG02258.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-46+11069A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126072 | |||||||
| chr11:15126085 | G | A | 1 | a0001c0003t0002g0137 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-46+11082G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126085 | |||||||
| chr11:15126171 | G | T | 141 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(138): Show |
145 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.-46+11168G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126171 | |||||||
| chr11:15126246 | CCTTT | C | 3 | a0002c0004t0001g0219 a0002c0004t0001g0231 a0002c0004t0002g0218 |
3 | HG03098.hp1 HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-46+11244_-46+1124 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126246 | |||||||
| chr11:15126278 | G | T | 1 | a0001c0001t0002g0180 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-46+11275G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126278 | |||||||
| chr11:15126303 | C | G | 1 | a0001c0001t0005g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46+11300C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126303 | |||||||
| chr11:15126418 | T | C | 95 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(92): Show |
96 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-46+11415T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126418 | |||||||
| chr11:15126429 | G | T | 3 | a0001c0001t0002g0070 a0001c0001t0003g0069 a0001c0002t0007g0068 |
3 | HG01952.hp2 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.-46+11426G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126429 | |||||||
| chr11:15126778 | A | T | 14 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0163 others(11): Show |
14 | HG01106.hp2 HG02258.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.-46+11775A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126778 | |||||||
| chr11:15126794 | C | G | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(101): Show |
108 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.-46+11791C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126794 | |||||||
| chr11:15126846 | G | A | 2 | a0001c0002t0003g0045 a0001c0002t0003g0046 |
2 | NA18944.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-46+11843G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15126846 | |||||||
| chr11:15127165 | A | G | 248 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(245): Show |
254 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-46+12162A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15127165 | |||||||
| chr11:15127268 | T | C | 7 | a0001c0001t0001g0047 a0001c0001t0002g0048 a0001c0001t0002g0060 others(4): Show |
7 | NA18956.hp2 NA18959.hp1 NA18973.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46+12265T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15127268 | |||||||
| chr11:15127378 | T | A | 1 | a0001c0001t0005g0217 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-46+12375T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15127378 | |||||||
| chr11:15127454 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-46+12451G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15127454 | |||||||
| chr11:15127586 | T | G | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(140): Show |
147 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.-46+12583T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15127586 | |||||||
| chr11:15127786 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-46+12783A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15127786 | |||||||
| chr11:15127813 | A | C | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+12810A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15127813 | |||||||
| chr11:15127902 | G | T | 1 | a0001c0003t0006g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-46+12899G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15127902 | |||||||
| chr11:15127955 | G | A | 2 | a0001c0001t0001g0090 a0001c0001t0001g0115 |
2 | NA18949.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-46+12952G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15127955 | |||||||
| chr11:15128026 | T | C | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+13023T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128026 | |||||||
| chr11:15128032 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-46+13029T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128032 | |||||||
| chr11:15128231 | C | T | 1 | a0001c0003t0020g0101 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-46+13228C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128231 | |||||||
| chr11:15128238 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(140): Show |
147 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.-46+13235T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128238 | |||||||
| chr11:15128265 | A | G | 2 | a0001c0001t0002g0145 a0001c0003t0002g0114 |
2 | HG02257.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-46+13262A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128265 | |||||||
| chr11:15128273 | C | A | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+13270C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128273 | |||||||
| chr11:15128430 | G | T | 1 | a0001c0001t0002g0043 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-46+13427G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128430 | |||||||
| chr11:15128515 | T | C | 8 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0250 others(5): Show |
8 | HG00408.hp1 HG02040.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+13512T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128515 | |||||||
| chr11:15128588 | C | T | 2 | a0001c0001t0005g0117 a0001c0002t0001g0116 |
2 | NA18960.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-46+13585C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128588 | |||||||
| chr11:15128600 | G | C | 2 | a0001c0002t0008g0040 a0002c0017t0001g0199 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-46+13597G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128600 | |||||||
| chr11:15128780 | G | A | 3 | a0001c0001t0001g0061 a0001c0001t0002g0062 a0001c0001t0006g0149 |
3 | HG01261.hp1 NA19043.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-46+13777G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15128780 | |||||||
| chr11:15129179 | G | A | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-46+14176G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15129179 | |||||||
| chr11:15129920 | C | A | 1 | a0001c0016t0002g0201 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-46+14917C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15129920 | |||||||
| chr11:15129924 | C | A | 4 | a0001c0001t0002g0009 a0001c0001t0016g0261 a0001c0001t0021g0263 others(1): Show |
4 | HG02647.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46+14921C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15129924 | |||||||
| chr11:15130000 | T | C | 3 | a0001c0001t0002g0060 a0001c0001t0002g0208 a0001c0001t0002g0264 |
3 | NA18973.hp1 NA19065.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.-46+14997T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15130000 | |||||||
| chr11:15130038 | A | G | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+15035A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15130038 | |||||||
| chr11:15130283 | G | C | 9 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(6): Show |
9 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46+15280G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15130283 | |||||||
| chr11:15130367 | T | C | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46+15364T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15130367 | |||||||
| chr11:15130531 | G | A | 2 | a0004c0006t0001g0244 a0004c0006t0001g0245 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-46+15528G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15130531 | |||||||
| chr11:15130693 | G | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0115 |
2 | NA18949.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-46+15690G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15130693 | |||||||
| chr11:15130884 | C | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(102): Show |
109 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.-46+15881C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15130884 | |||||||
| chr11:15130939 | GTTTAT | G | 15 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0004g0001 others(12): Show |
16 | HG01106.hp2 HG01515.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46+15942_-46+1594 others(9): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15130939 | ||||||
| chr11:15131057 | T | C | 2 | a0001c0001t0016g0261 a0001c0001t0021g0263 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-46+16054T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15131057 | |||||||
| chr11:15131091 | A | G | 21 | a0001c0001t0001g0057 a0001c0001t0001g0067 a0001c0001t0001g0072 others(18): Show |
21 | HG00639.hp1 HG01074.hp1 HG01081.hp2 others(18): Show |
intron_variant | MODIFIER | c.-46+16088A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15131091 | |||||||
| chr11:15131405 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(140): Show |
147 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.-46+16402T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15131405 | |||||||
| chr11:15131470 | A | G | 2 | a0001c0001t0001g0164 a0001c0001t0001g0197 |
2 | NA18982.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-46+16467A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15131470 | |||||||
| chr11:15131544 | A | G | 2 | a0001c0001t0002g0151 a0001c0001t0005g0150 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-46+16541A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15131544 | |||||||
| chr11:15131654 | A | G | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-46+16651A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15131654 | |||||||
| chr11:15131655 | T | C | 9 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(6): Show |
9 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-46+16652T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15131655 | |||||||
| chr11:15131870 | T | G | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-46+16867T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15131870 | |||||||
| chr11:15132003 | G | C | 12 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0163 others(9): Show |
12 | HG01106.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-46+17000G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15132003 | |||||||
| chr11:15132008 | GATTA | G | 3 | a0001c0001t0005g0178 a0001c0002t0008g0040 a0002c0017t0001g0199 |
3 | HG02486.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-46+17009_-46+1701 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15132008 | ||||||
| chr11:15132322 | G | A | 12 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0163 others(9): Show |
12 | HG01106.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-45-16808G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15132322 | |||||||
| chr11:15132533 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0016g0261 a0001c0001t0021g0263 others(1): Show |
4 | HG02647.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45-16597T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15132533 | |||||||
| chr11:15132570 | A | C | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-45-16560A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15132570 | |||||||
| chr11:15133080 | C | T | 12 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0163 others(9): Show |
12 | HG01106.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-45-16050C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133080 | |||||||
| chr11:15133096 | T | G | 1 | a0001c0001t0002g0078 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-45-16034T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133096 | |||||||
| chr11:15133219 | G | A | 2 | a0001c0002t0008g0040 a0002c0017t0001g0199 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-45-15911G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133219 | |||||||
| chr11:15133245 | C | T | 1 | a0001c0002t0003g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-45-15885C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133245 | |||||||
| chr11:15133256 | C | A | 1 | a0001c0001t0002g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-45-15874C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133256 | |||||||
| chr11:15133335 | TATTTGGT others(10): Show |
T | 1 | a0001c0001t0006g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-45-15790_-45-1577 others(21): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15133335 | ||||||
| chr11:15133389 | A | G | 1 | a0001c0001t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-45-15741A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133389 | |||||||
| chr11:15133416 | T | C | 4 | a0001c0001t0001g0154 a0001c0001t0001g0191 a0001c0001t0003g0005 others(1): Show |
5 | HG02129.hp1 HG02132.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45-15714T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133416 | |||||||
| chr11:15133484 | C | T | 2 | a0001c0001t0002g0120 a0001c0001t0002g0135 |
2 | HG01074.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-45-15646C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133484 | |||||||
| chr11:15133593 | CCT | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(101): Show |
108 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.-45-15536_-45-1553 others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133593 | |||||||
| chr11:15133875 | T | G | 12 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0163 others(9): Show |
12 | HG01106.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-45-15255T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15133875 | |||||||
| chr11:15134024 | A | AG | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(130): Show |
137 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.-45-15106_-45-1510 others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134024 | |||||||
| chr11:15134154 | T | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(110): Show |
117 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(114): Show |
intron_variant | MODIFIER | c.-45-14976T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134154 | |||||||
| chr11:15134213 | T | C | 1 | a0001c0002t0004g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-45-14917T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134213 | |||||||
| chr11:15134285 | G | A | 1 | a0001c0001t0005g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-45-14845G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134285 | |||||||
| chr11:15134554 | C | A | 102 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(99): Show |
103 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.-45-14576C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134554 | |||||||
| chr11:15134618 | G | A | 1 | a0001c0002t0003g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-45-14512G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134618 | |||||||
| chr11:15134685 | A | C | 2 | a0001c0001t0006g0088 a0001c0002t0001g0089 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-45-14445A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134685 | |||||||
| chr11:15134733 | T | C | 1 | a0001c0002t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-45-14397T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134733 | |||||||
| chr11:15134767 | G | A | 1 | a0001c0003t0020g0101 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-45-14363G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134767 | |||||||
| chr11:15134776 | T | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(101): Show |
108 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.-45-14354T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134776 | |||||||
| chr11:15134827 | C | CTTTA | 7 | a0001c0001t0002g0241 a0001c0001t0016g0042 a0001c0002t0003g0239 others(4): Show |
7 | HG02055.hp1 HG02056.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-45-14275_-45-1427 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15134827 | ||||||
| chr11:15134827 | C | CTTTATTT others(5): Show |
1 | a0001c0001t0016g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-45-14283_-45-1427 others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15134827 | ||||||
| chr11:15134827 | C | CTTTATTT others(9): Show |
16 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0015 others(13): Show |
16 | HG00408.hp1 HG02040.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.-45-14287_-45-1427 others(20): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15134827 | ||||||
| chr11:15134827 | C | CTTTATTT others(13): Show |
4 | a0001c0001t0002g0009 a0001c0001t0003g0020 a0001c0001t0005g0022 others(1): Show |
4 | HG02647.hp2 HG03209.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45-14291_-45-1427 others(24): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15134827 | ||||||
| chr11:15134827 | CTTTA | C | 12 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0163 others(9): Show |
12 | HG01106.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-45-14275_-45-1427 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15134827 | ||||||
| chr11:15134827 | CTTTATTT others(5): Show |
C | 1 | a0002c0004t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-45-14283_-45-1427 others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15134827 | ||||||
| chr11:15134894 | C | G | 1 | a0001c0002t0006g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-45-14236C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15134894 | |||||||
| chr11:15135088 | A | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(97): Show |
104 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.-45-14042A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15135088 | |||||||
| chr11:15135117 | A | G | 2 | a0001c0001t0016g0261 a0001c0001t0021g0263 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-45-14013A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15135117 | |||||||
| chr11:15135142 | C | A | 2 | a0004c0006t0001g0244 a0004c0006t0001g0245 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-45-13988C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15135142 | |||||||
| chr11:15135239 | G | A | 1 | a0001c0003t0003g0254 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-45-13891G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15135239 | |||||||
| chr11:15135403 | A | G | 20 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(17): Show |
20 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.-45-13727A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15135403 | |||||||
| chr11:15135416 | C | T | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-45-13714C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15135416 | |||||||
| chr11:15135430 | A | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0067 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-45-13700A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15135430 | |||||||
| chr11:15135465 | T | A | 5 | a0001c0001t0003g0255 a0001c0002t0006g0252 a0001c0002t0006g0256 others(2): Show |
5 | HG02970.hp1 HG02976.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45-13665T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15135465 | |||||||
| chr11:15135581 | G | C | 1 | a0001c0003t0003g0254 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-45-13549G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15135581 | |||||||
| chr11:15136231 | A | T | 1 | a0001c0001t0002g0180 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-45-12899A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15136231 | |||||||
| chr11:15136290 | C | T | 40 | a0001c0001t0001g0014 a0001c0001t0001g0090 a0001c0001t0001g0099 others(37): Show |
40 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-45-12840C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15136290 | |||||||
| chr11:15136334 | A | G | 8 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0250 others(5): Show |
8 | HG00408.hp1 HG02040.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-45-12796A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15136334 | |||||||
| chr11:15136335 | T | C | 2 | a0001c0001t0016g0261 a0001c0001t0021g0263 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-45-12795T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15136335 | |||||||
| chr11:15136427 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0168 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.-45-12703C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15136427 | |||||||
| chr11:15136461 | T | C | 29 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(26): Show |
29 | HG00408.hp1 HG00639.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-45-12669T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15136461 | |||||||
| chr11:15136563 | A | G | 2 | a0001c0001t0002g0075 a0001c0003t0001g0066 |
2 | HG01074.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.-45-12567A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15136563 | |||||||
| chr11:15136963 | G | A | 9 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(6): Show |
9 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45-12167G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15136963 | |||||||
| chr11:15136978 | T | C | 9 | a0001c0001t0001g0012 a0001c0001t0001g0039 a0001c0001t0001g0164 others(6): Show |
9 | HG02132.hp2 HG02135.hp2 NA18981.hp2 others(6): Show |
intron_variant | MODIFIER | c.-45-12152T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15136978 | |||||||
| chr11:15137687 | A | C | 29 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(26): Show |
29 | HG00408.hp1 HG00639.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-45-11443A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15137687 | |||||||
| chr11:15137816 | G | A | 2 | a0001c0001t0002g0009 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-45-11314G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15137816 | |||||||
| chr11:15137854 | A | G | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-11276A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15137854 | |||||||
| chr11:15137867 | C | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0067 a0001c0001t0011g0181 |
3 | HG01256.hp1 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-45-11263C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15137867 | |||||||
| chr11:15138078 | G | A | 1 | a0001c0001t0005g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-45-11052G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15138078 | |||||||
| chr11:15138092 | G | A | 1 | a0001c0001t0004g0001 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-45-11038G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15138092 | |||||||
| chr11:15138196 | G | A | 9 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(6): Show |
9 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45-10934G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15138196 | |||||||
| chr11:15138213 | T | C | 29 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(26): Show |
29 | HG00408.hp1 HG00639.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.-45-10917T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15138213 | |||||||
| chr11:15138374 | T | TA | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-10748dupA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15138374 | ||||||
| chr11:15138381 | A | C | 1 | a0001c0001t0003g0013 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-45-10749A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15138381 | |||||||
| chr11:15138663 | T | C | 3 | a0001c0001t0006g0149 a0001c0001t0016g0042 a0001c0002t0003g0177 |
3 | HG06807.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-45-10467T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15138663 | |||||||
| chr11:15138671 | A | G | 24 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(21): Show |
24 | HG00408.hp1 HG00639.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.-45-10459A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15138671 | |||||||
| chr11:15138678 | T | A | 1 | a0001c0002t0003g0076 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-45-10452T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15138678 | |||||||
| chr11:15138700 | A | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0115 |
2 | NA18949.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-45-10430A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15138700 | |||||||
| chr11:15139111 | G | T | 8 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0250 others(5): Show |
8 | HG00408.hp1 HG02040.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-45-10019G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15139111 | |||||||
| chr11:15139210 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-45-9920T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15139210 | |||||||
| chr11:15139762 | A | C | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-45-9368A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15139762 | |||||||
| chr11:15139961 | C | T | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-9169C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15139961 | |||||||
| chr11:15140219 | G | T | 1 | a0001c0001t0002g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-45-8911G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15140219 | |||||||
| chr11:15140339 | G | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(242): Show |
250 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-45-8791G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15140339 | |||||||
| chr11:15140355 | G | A | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-8775G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15140355 | |||||||
| chr11:15140555 | A | T | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-8575A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15140555 | |||||||
| chr11:15140609 | T | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(143): Show |
150 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.-45-8521T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15140609 | |||||||
| chr11:15140690 | C | G | 3 | a0001c0001t0002g0009 a0001c0001t0006g0008 a0001c0002t0023g0010 |
3 | HG02647.hp2 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-45-8440C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15140690 | |||||||
| chr11:15140719 | C | T | 1 | a0001c0003t0002g0237 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-45-8411C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15140719 | |||||||
| chr11:15140817 | T | G | 1 | a0005c0007t0001g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-45-8313T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15140817 | |||||||
| chr11:15140874 | T | C | 9 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(6): Show |
9 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45-8256T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15140874 | |||||||
| chr11:15141411 | G | A | 2 | a0001c0001t0005g0109 a0001c0001t0005g0110 |
2 | NA18998.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-45-7719G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15141411 | |||||||
| chr11:15141530 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-45-7600T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15141530 | |||||||
| chr11:15141640 | G | T | 20 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0001g0259 others(17): Show |
20 | HG00408.hp1 HG01106.hp2 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.-45-7490G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15141640 | |||||||
| chr11:15141848 | A | G | 12 | a0001c0001t0001g0259 a0001c0001t0003g0255 a0001c0001t0005g0163 others(9): Show |
12 | HG01106.hp2 HG02258.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.-45-7282A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15141848 | |||||||
| chr11:15141879 | T | C | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-7251T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15141879 | |||||||
| chr11:15141903 | G | A | 100 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(97): Show |
101 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.-45-7227G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15141903 | |||||||
| chr11:15141904 | G | T | 100 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(97): Show |
101 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.-45-7226G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15141904 | |||||||
| chr11:15141995 | C | G | 6 | a0001c0001t0008g0195 a0001c0001t0024g0143 a0001c0002t0003g0076 others(3): Show |
6 | HG00639.hp2 HG02145.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45-7135C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15141995 | |||||||
| chr11:15142141 | G | A | 2 | a0001c0001t0006g0088 a0001c0002t0001g0089 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-45-6989G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142141 | |||||||
| chr11:15142263 | A | G | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-45-6867A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142263 | |||||||
| chr11:15142320 | G | A | 5 | a0001c0001t0002g0153 a0001c0001t0005g0167 a0001c0001t0005g0183 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45-6810G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142320 | |||||||
| chr11:15142571 | G | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0036 others(55): Show |
62 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.-45-6559G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142571 | |||||||
| chr11:15142579 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0002g0048 |
2 | NA18956.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-45-6551G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142579 | |||||||
| chr11:15142625 | G | A | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-6505G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142625 | |||||||
| chr11:15142849 | G | A | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-45-6281G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142849 | |||||||
| chr11:15142883 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-45-6247C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142883 | |||||||
| chr11:15142915 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(92): Show |
99 | HG00099.hp1 HG00609.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.-45-6215G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142915 | |||||||
| chr11:15142970 | A | C | 4 | a0001c0001t0006g0149 a0001c0001t0016g0261 a0001c0001t0021g0263 others(1): Show |
4 | HG03471.hp2 HG03486.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45-6160A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142970 | |||||||
| chr11:15142999 | A | C | 1 | a0001c0001t0005g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-45-6131A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15142999 | |||||||
| chr11:15143116 | G | T | 1 | a0001c0002t0003g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-45-6014G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15143116 | |||||||
| chr11:15143288 | A | G | 6 | a0001c0001t0002g0241 a0001c0001t0006g0008 a0001c0002t0003g0239 others(3): Show |
6 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45-5842A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15143288 | |||||||
| chr11:15143348 | C | T | 1 | a0001c0001t0006g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-45-5782C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15143348 | |||||||
| chr11:15143380 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-45-5750G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15143380 | |||||||
| chr11:15143430 | G | A | 100 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(97): Show |
101 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.-45-5700G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15143430 | |||||||
| chr11:15143497 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-45-5633G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15143497 | |||||||
| chr11:15143629 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-45-5501A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15143629 | |||||||
| chr11:15143768 | A | C | 1 | a0001c0001t0024g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-45-5362A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15143768 | |||||||
| chr11:15144078 | CAT | C | 8 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0250 others(5): Show |
8 | HG00408.hp1 HG02040.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-45-5051_-45-5050d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15144078 | |||||||
| chr11:15144210 | G | C | 1 | a0001c0002t0004g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-45-4920G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15144210 | |||||||
| chr11:15144241 | G | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(237): Show |
245 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.-45-4889G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15144241 | |||||||
| chr11:15144524 | C | A | 2 | a0001c0002t0008g0040 a0002c0017t0001g0199 |
2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.-45-4606C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15144524 | |||||||
| chr11:15144562 | G | A | 246 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(243): Show |
251 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-45-4568G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15144562 | |||||||
| chr11:15144597 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-45-4533T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15144597 | |||||||
| chr11:15144655 | C | T | 40 | a0001c0001t0001g0014 a0001c0001t0001g0090 a0001c0001t0001g0099 others(37): Show |
40 | HG00408.hp2 HG00609.hp1 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-45-4475C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15144655 | |||||||
| chr11:15144825 | C | T | 8 | a0001c0001t0001g0246 a0001c0001t0001g0248 a0001c0001t0002g0250 others(5): Show |
8 | HG00408.hp1 HG02040.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.-45-4305C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15144825 | |||||||
| chr11:15144983 | G | A | 3 | a0001c0001t0001g0184 a0001c0001t0001g0189 a0001c0001t0001g0200 |
3 | HG01069.hp1 HG01071.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-45-4147G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15144983 | |||||||
| chr11:15145020 | G | A | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-45-4110G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15145020 | |||||||
| chr11:15145080 | G | T | 1 | a0001c0001t0024g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-45-4050G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15145080 | |||||||
| chr11:15145493 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-45-3637T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15145493 | |||||||
| chr11:15145501 | G | A | 5 | a0001c0001t0002g0241 a0001c0002t0003g0239 a0001c0002t0003g0243 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45-3629G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15145501 | |||||||
| chr11:15145621 | A | C | 9 | a0001c0001t0002g0015 a0001c0001t0002g0018 a0001c0001t0002g0023 others(6): Show |
9 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45-3509A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15145621 | |||||||
| chr11:15145804 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-45-3326G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15145804 | |||||||
| chr11:15145895 | C | T | 2 | a0001c0001t0002g0038 a0001c0001t0014g0213 |
2 | HG00099.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.-45-3235C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15145895 | |||||||
| chr11:15145932 | A | G | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-45-3198A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15145932 | |||||||
| chr11:15146018 | G | T | 1 | a0001c0001t0002g0070 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-45-3112G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146018 | |||||||
| chr11:15146019 | C | T | 1 | a0001c0001t0002g0070 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-45-3111C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146019 | |||||||
| chr11:15146075 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0002g0048 |
2 | NA18956.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-45-3055C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146075 | |||||||
| chr11:15146176 | A | G | 6 | a0001c0001t0002g0130 a0001c0001t0004g0006 a0001c0001t0004g0227 others(3): Show |
7 | HG02280.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45-2954A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146176 | |||||||
| chr11:15146295 | C | T | 1 | a0001c0001t0012g0129 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-45-2835C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146295 | |||||||
| chr11:15146478 | A | G | 17 | a0001c0001t0002g0009 a0001c0001t0002g0023 a0001c0001t0002g0024 others(14): Show |
17 | HG01106.hp2 HG02145.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.-45-2652A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146478 | |||||||
| chr11:15146545 | G | C | 1 | a0001c0002t0006g0252 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-45-2585G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146545 | |||||||
| chr11:15146576 | G | A | 2 | a0001c0001t0002g0119 a0001c0001t0005g0102 |
2 | HG02145.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-45-2554G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146576 | |||||||
| chr11:15146770 | A | G | 4 | a0001c0001t0002g0032 a0001c0001t0002g0173 a0001c0001t0008g0170 others(1): Show |
4 | HG00735.hp1 HG01243.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45-2360A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146770 | |||||||
| chr11:15146827 | A | G | 1 | a0001c0002t0001g0089 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45-2303A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146827 | |||||||
| chr11:15146923 | C | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0028 others(100): Show |
106 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.-45-2207C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15146923 | |||||||
| chr11:15147176 | A | G | 63 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(60): Show |
64 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.-45-1954A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147176 | |||||||
| chr11:15147192 | C | T | 1 | a0004c0006t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-45-1938C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147192 | |||||||
| chr11:15147225 | C | T | 55 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(52): Show |
56 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.-45-1905C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147225 | |||||||
| chr11:15147253 | C | T | 141 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0039 others(138): Show |
145 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(142): Show |
intron_variant | MODIFIER | c.-45-1877C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147253 | |||||||
| chr11:15147317 | T | A | 56 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(53): Show |
57 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(54): Show |
intron_variant | MODIFIER | c.-45-1813T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147317 | |||||||
| chr11:15147443 | G | C | 1 | a0001c0013t0017g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-45-1687G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147443 | |||||||
| chr11:15147485 | C | T | 54 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(51): Show |
57 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.-45-1645C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147485 | |||||||
| chr11:15147511 | A | T | 1 | a0001c0001t0005g0167 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-45-1619A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147511 | |||||||
| chr11:15147705 | C | A | 1 | a0009c0010t0001g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-45-1425C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147705 | |||||||
| chr11:15147833 | G | T | 1 | a0009c0010t0001g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-45-1297G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147833 | |||||||
| chr11:15147874 | C | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0164 a0001c0001t0001g0182 |
3 | NA18982.hp2 NA18989.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-45-1256C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147874 | |||||||
| chr11:15147940 | G | A | 10 | a0001c0001t0007g0030 a0001c0001t0007g0107 a0001c0001t0011g0181 others(7): Show |
10 | HG01192.hp2 HG01257.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.-45-1190G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15147940 | |||||||
| chr11:15148071 | C | T | 2 | a0001c0003t0004g0192 a0003c0005t0001g0216 |
2 | HG01361.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-45-1059C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148071 | |||||||
| chr11:15148093 | G | T | 19 | a0001c0001t0002g0224 a0001c0001t0002g0230 a0001c0001t0007g0030 others(16): Show |
19 | HG01192.hp2 HG01257.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.-45-1037G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148093 | |||||||
| chr11:15148136 | A | G | 2 | a0001c0002t0004g0007 a0005c0007t0001g0215 |
2 | HG01516.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-45-994A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148136 | |||||||
| chr11:15148218 | T | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(59): Show |
66 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.-45-912T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148218 | |||||||
| chr11:15148388 | C | T | 19 | a0001c0001t0002g0224 a0001c0001t0002g0230 a0001c0001t0007g0030 others(16): Show |
19 | HG01192.hp2 HG01257.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.-45-742C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148388 | |||||||
| chr11:15148586 | A | G | 3 | a0001c0001t0006g0008 a0002c0004t0001g0253 a0002c0017t0001g0199 |
3 | HG02615.hp2 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-45-544A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148586 | |||||||
| chr11:15148629 | T | TATGCC | 54 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(51): Show |
57 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.-45-500_-45-496dup others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr11 | 15148629 | ||||||
| chr11:15148671 | A | G | 9 | a0001c0002t0003g0076 a0001c0002t0003g0239 a0001c0002t0003g0243 others(6): Show |
9 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-45-459A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148671 | |||||||
| chr11:15148689 | C | T | 20 | a0001c0001t0001g0131 a0001c0001t0001g0197 a0001c0001t0001g0259 others(17): Show |
20 | HG00621.hp1 HG01261.hp2 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-45-441C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148689 | |||||||
| chr11:15148790 | TA | T | 18 | a0001c0001t0002g0224 a0001c0001t0002g0230 a0001c0001t0007g0030 others(15): Show |
18 | HG01192.hp2 HG01257.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.-45-339delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148790 | |||||||
| chr11:15148929 | G | A | 1 | a0009c0010t0001g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-45-201G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15148929 | |||||||
| chr11:15149098 | T | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0028 others(155): Show |
162 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(159): Show |
intron_variant | MODIFIER | c.-45-32T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15149098 | |||||||
| chr11:15149115 | G | A | 3 | a0001c0001t0003g0144 a0001c0001t0005g0229 a0001c0001t0016g0261 |
3 | HG02895.hp1 HG03041.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-45-15G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 1/12 | chr11 | 15149115 | |||||||
| chr11:15149261 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(59): Show |
66 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.56+31G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15149261 | |||||||
| chr11:15149262 | C | T | 6 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0003g0020 others(3): Show |
6 | HG02895.hp2 HG02897.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.56+32C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15149262 | |||||||
| chr11:15149333 | C | T | 38 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(35): Show |
38 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.56+103C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15149333 | |||||||
| chr11:15149475 | T | C | 9 | a0001c0002t0003g0076 a0001c0002t0003g0239 a0001c0002t0003g0243 others(6): Show |
9 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.56+245T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15149475 | |||||||
| chr11:15149480 | A | G | 8 | a0001c0001t0002g0224 a0001c0001t0002g0230 a0001c0003t0004g0192 others(5): Show |
8 | HG01993.hp2 HG02559.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+250A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15149480 | |||||||
| chr11:15149789 | T | G | 9 | a0001c0002t0003g0076 a0001c0002t0003g0239 a0001c0002t0003g0243 others(6): Show |
9 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.56+559T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15149789 | |||||||
| chr11:15149827 | A | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(59): Show |
66 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.56+597A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15149827 | |||||||
| chr11:15149963 | A | G | 1 | a0001c0001t0003g0188 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.56+733A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15149963 | |||||||
| chr11:15150309 | G | A | 77 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(74): Show |
81 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.56+1079G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15150309 | |||||||
| chr11:15150427 | T | A | 5 | a0001c0001t0002g0018 a0001c0001t0002g0173 a0001c0001t0005g0178 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+1197T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15150427 | |||||||
| chr11:15150543 | A | G | 11 | a0001c0001t0002g0224 a0001c0001t0002g0230 a0001c0001t0005g0163 others(8): Show |
11 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.56+1313A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15150543 | |||||||
| chr11:15150702 | A | G | 11 | a0001c0001t0007g0030 a0001c0001t0007g0107 a0001c0001t0011g0181 others(8): Show |
11 | HG01192.hp2 HG01257.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.56+1472A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15150702 | |||||||
| chr11:15150813 | C | G | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.56+1583C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15150813 | |||||||
| chr11:15150950 | T | A | 1 | a0002c0004t0001g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.56+1720T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15150950 | |||||||
| chr11:15151183 | C | T | 1 | a0001c0001t0008g0170 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.56+1953C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151183 | |||||||
| chr11:15151193 | C | G | 1 | a0001c0002t0003g0260 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.56+1963C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151193 | |||||||
| chr11:15151205 | G | A | 1 | a0002c0004t0002g0218 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.56+1975G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151205 | |||||||
| chr11:15151277 | T | C | 43 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(40): Show |
43 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.56+2047T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151277 | |||||||
| chr11:15151450 | C | T | 1 | a0002c0004t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.56+2220C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151450 | |||||||
| chr11:15151508 | T | C | 78 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(75): Show |
82 | HG00099.hp2 HG00733.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.56+2278T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151508 | |||||||
| chr11:15151566 | T | A | 1 | a0002c0004t0001g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.56+2336T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151566 | |||||||
| chr11:15151606 | CTGA | C | 42 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(39): Show |
42 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.56+2378_56+2380del others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15151606 | ||||||
| chr11:15151609 | ATCT | A | 19 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0002g0224 others(16): Show |
19 | HG01243.hp2 HG02258.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.56+2384_56+2386del others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15151609 | ||||||
| chr11:15151612 | T | A | 42 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(39): Show |
42 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.56+2382T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151612 | |||||||
| chr11:15151823 | C | T | 1 | a0001c0001t0008g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.56+2593C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151823 | |||||||
| chr11:15151857 | C | A | 1 | a0001c0001t0008g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.56+2627C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151857 | |||||||
| chr11:15151911 | C | G | 1 | a0002c0004t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.56+2681C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151911 | |||||||
| chr11:15151917 | G | A | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56+2687G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151917 | |||||||
| chr11:15151919 | A | G | 8 | a0001c0002t0003g0076 a0001c0002t0003g0239 a0001c0002t0003g0243 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+2689A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151919 | |||||||
| chr11:15151996 | T | A | 11 | a0001c0001t0002g0224 a0001c0001t0002g0230 a0001c0001t0005g0163 others(8): Show |
11 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.56+2766T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15151996 | |||||||
| chr11:15152022 | A | C | 154 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0039 others(151): Show |
158 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(155): Show |
intron_variant | MODIFIER | c.56+2792A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15152022 | |||||||
| chr11:15152313 | G | C | 1 | a0002c0004t0001g0142 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.56+3083G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15152313 | |||||||
| chr11:15152326 | G | A | 8 | a0001c0001t0002g0009 a0001c0001t0004g0006 a0001c0001t0004g0227 others(5): Show |
9 | HG01884.hp1 HG01884.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.56+3096G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15152326 | |||||||
| chr11:15152418 | T | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0028 others(77): Show |
82 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.56+3188T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15152418 | |||||||
| chr11:15152750 | G | A | 1 | a0003c0005t0009g0097 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.56+3520G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15152750 | |||||||
| chr11:15152778 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.56+3548A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15152778 | |||||||
| chr11:15152996 | A | G | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.56+3766A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15152996 | |||||||
| chr11:15153116 | A | C | 3 | a0001c0001t0002g0009 a0001c0001t0005g0217 a0001c0002t0023g0010 |
3 | HG01884.hp1 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.56+3886A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153116 | |||||||
| chr11:15153176 | G | C | 166 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0028 others(163): Show |
170 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(167): Show |
intron_variant | MODIFIER | c.56+3946G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153176 | |||||||
| chr11:15153236 | T | C | 1 | a0001c0001t0006g0088 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.56+4006T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153236 | |||||||
| chr11:15153360 | T | C | 82 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(79): Show |
86 | HG00099.hp2 HG00621.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.56+4130T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153360 | |||||||
| chr11:15153424 | C | A | 1 | a0001c0002t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56+4194C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153424 | |||||||
| chr11:15153430 | A | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0085 others(27): Show |
34 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.56+4200A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153430 | |||||||
| chr11:15153594 | A | T | 1 | a0001c0002t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.56+4364A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153594 | |||||||
| chr11:15153615 | T | G | 1 | a0001c0001t0003g0005 | 2 | HG02129.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.56+4385T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153615 | |||||||
| chr11:15153711 | A | G | 81 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(78): Show |
85 | HG00099.hp2 HG00621.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.56+4481A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153711 | |||||||
| chr11:15153733 | C | T | 37 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(34): Show |
37 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.56+4503C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153733 | |||||||
| chr11:15153738 | TC | T | 4 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0021g0263 others(1): Show |
5 | HG01884.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+4509delC | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153738 | |||||||
| chr11:15153832 | G | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0153 |
2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.56+4602G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153832 | |||||||
| chr11:15153959 | C | G | 66 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(63): Show |
66 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.56+4729C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15153959 | |||||||
| chr11:15154013 | A | C | 5 | a0001c0001t0002g0018 a0001c0001t0002g0173 a0001c0001t0005g0178 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+4783A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15154013 | |||||||
| chr11:15154069 | T | TG | 81 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(78): Show |
85 | HG00099.hp2 HG00621.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.56+4843dupG | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15154069 | ||||||
| chr11:15154087 | ATTTATGT others(10): Show |
A | 1 | a0001c0001t0002g0130 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.56+4861_56+4877del others(17): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15154087 | ||||||
| chr11:15154157 | G | C | 1 | a0001c0001t0003g0005 | 2 | HG02129.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.56+4927G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15154157 | |||||||
| chr11:15154158 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.56+4928G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15154158 | |||||||
| chr11:15154197 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0145 |
2 | HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.56+4967G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15154197 | |||||||
| chr11:15154200 | G | T | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.56+4970G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15154200 | |||||||
| chr11:15154439 | C | T | 81 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(78): Show |
85 | HG00099.hp2 HG00621.hp1 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.56+5209C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15154439 | |||||||
| chr11:15154568 | A | C | 1 | a0001c0003t0019g0172 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.56+5338A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15154568 | |||||||
| chr11:15154803 | C | CT | 80 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(77): Show |
84 | HG00099.hp2 HG00621.hp1 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.56+5582dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15154803 | ||||||
| chr11:15154826 | C | G | 1 | a0001c0001t0004g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.56+5596C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15154826 | |||||||
| chr11:15155060 | C | T | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.56+5830C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155060 | |||||||
| chr11:15155091 | G | A | 160 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0028 others(157): Show |
164 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(161): Show |
intron_variant | MODIFIER | c.56+5861G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155091 | |||||||
| chr11:15155104 | T | C | 1 | a0001c0001t0002g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.56+5874T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155104 | |||||||
| chr11:15155123 | A | G | 1 | a0002c0017t0001g0199 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.56+5893A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155123 | |||||||
| chr11:15155432 | T | C | 13 | a0001c0001t0001g0039 a0001c0001t0001g0184 a0001c0001t0001g0189 others(10): Show |
13 | HG01069.hp1 HG01071.hp2 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.56+6202T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155432 | |||||||
| chr11:15155464 | A | C | 1 | a0001c0001t0005g0117 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.56+6234A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155464 | |||||||
| chr11:15155567 | G | A | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.56+6337G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155567 | |||||||
| chr11:15155605 | G | A | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.56+6375G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155605 | |||||||
| chr11:15155631 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.56+6401C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155631 | |||||||
| chr11:15155713 | G | A | 71 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(68): Show |
71 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.56+6483G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155713 | |||||||
| chr11:15155985 | T | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0189 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.56+6755T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15155985 | |||||||
| chr11:15156053 | A | G | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.56+6823A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15156053 | |||||||
| chr11:15156270 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(240): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.56+7040G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15156270 | |||||||
| chr11:15156404 | C | T | 157 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0039 others(154): Show |
161 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(158): Show |
intron_variant | MODIFIER | c.56+7174C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15156404 | |||||||
| chr11:15156650 | C | T | 1 | a0001c0001t0002g0027 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.56+7420C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15156650 | |||||||
| chr11:15156666 | G | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0085 others(27): Show |
34 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.56+7436G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15156666 | |||||||
| chr11:15156781 | A | G | 1 | a0005c0007t0014g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.56+7551A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15156781 | |||||||
| chr11:15156876 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.56+7646T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15156876 | |||||||
| chr11:15157044 | T | C | 83 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(80): Show |
87 | HG00099.hp2 HG00621.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.56+7814T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157044 | |||||||
| chr11:15157095 | A | C | 255 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(252): Show |
261 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(258): Show |
intron_variant | MODIFIER | c.56+7865A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157095 | |||||||
| chr11:15157146 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.56+7916G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157146 | |||||||
| chr11:15157231 | C | T | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.56+8001C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157231 | |||||||
| chr11:15157266 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.56+8036C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157266 | |||||||
| chr11:15157421 | G | A | 1 | a0009c0010t0001g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.56+8191G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157421 | |||||||
| chr11:15157578 | G | T | 1 | a0001c0001t0004g0176 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.56+8348G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157578 | |||||||
| chr11:15157600 | G | A | 1 | a0001c0018t0006g0228 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.56+8370G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157600 | |||||||
| chr11:15157665 | G | T | 3 | a0001c0001t0002g0009 a0001c0001t0005g0217 a0001c0002t0023g0010 |
3 | HG01884.hp1 HG02647.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.56+8435G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157665 | |||||||
| chr11:15157730 | A | C | 1 | a0002c0004t0001g0231 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.56+8500A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157730 | |||||||
| chr11:15157735 | A | G | 82 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0049 others(79): Show |
86 | HG00099.hp2 HG00621.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.56+8505A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157735 | |||||||
| chr11:15157868 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0113 others(1): Show |
5 | HG01257.hp2 HG01258.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+8638T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157868 | |||||||
| chr11:15157876 | A | G | 4 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0021g0263 others(1): Show |
5 | HG01884.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+8646A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15157876 | |||||||
| chr11:15158128 | C | T | 1 | a0009c0010t0001g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.56+8898C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158128 | |||||||
| chr11:15158292 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0061 |
3 | HG01257.hp2 HG01258.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.56+9062G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158292 | |||||||
| chr11:15158443 | A | G | 52 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0131 others(49): Show |
52 | HG00621.hp1 HG01069.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.56+9213A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158443 | |||||||
| chr11:15158538 | A | C | 11 | a0001c0001t0002g0224 a0001c0001t0002g0230 a0001c0001t0005g0163 others(8): Show |
11 | HG02559.hp2 HG02615.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.56+9308A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158538 | |||||||
| chr11:15158642 | G | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0021g0263 others(1): Show |
5 | HG01884.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+9412G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158642 | |||||||
| chr11:15158697 | TCTC | T | 71 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(68): Show |
71 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.56+9471_56+9473del others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158697 | ||||||
| chr11:15158718 | G | T | 2 | a0001c0001t0001g0134 a0001c0001t0003g0152 |
2 | HG00408.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.56+9488G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158718 | |||||||
| chr11:15158748 | G | A | 52 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0131 others(49): Show |
52 | HG00621.hp1 HG01069.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.56+9518G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158748 | |||||||
| chr11:15158801 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.56+9571C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158801 | |||||||
| chr11:15158827 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.56+9597C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158827 | |||||||
| chr11:15158854 | T | G | 1 | a0001c0001t0002g0027 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.56+9624T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158854 | |||||||
| chr11:15158860 | G | GT | 6 | a0001c0001t0001g0090 a0001c0001t0001g0156 a0001c0001t0001g0191 others(3): Show |
6 | HG01952.hp1 HG03579.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.56+9651dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | G | GTAT | 17 | a0001c0001t0001g0197 a0001c0001t0001g0259 a0001c0001t0002g0027 others(14): Show |
17 | HG00621.hp1 HG02071.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+9631_56+9632ins others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | G | GTATT | 32 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0131 others(29): Show |
32 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.56+9631_56+9632ins others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | G | GTT | 7 | a0001c0001t0007g0030 a0001c0001t0007g0107 a0001c0001t0012g0129 others(4): Show |
7 | HG01192.hp2 HG01257.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.56+9650_56+9651dup others(2): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | G | GTTT | 13 | a0001c0001t0001g0235 a0001c0001t0002g0018 a0001c0001t0002g0173 others(10): Show |
13 | HG00735.hp1 HG01433.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.56+9649_56+9651dup others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | G | GTTTT | 32 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0073 others(29): Show |
32 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.56+9648_56+9651dup others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | G | GTTTTT | 17 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0074 others(14): Show |
17 | HG00733.hp2 HG01256.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.56+9647_56+9651dup others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | G | GTTTTTT | 5 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0003t0004g0192 others(2): Show |
6 | HG01884.hp2 HG01993.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.56+9646_56+9651dup others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | G | GTTTTTTT others(1): Show |
6 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0003g0021 others(3): Show |
6 | HG02647.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.56+9644_56+9651dup others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | GTTT | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0085 others(19): Show |
25 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.56+9649_56+9651del others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | GTTTT | G | 8 | a0001c0002t0003g0076 a0001c0002t0003g0239 a0001c0002t0003g0243 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.56+9648_56+9651del others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158860 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0105 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.56+9641_56+9651del others(11): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15158860 | ||||||
| chr11:15158908 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.56+9678A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158908 | |||||||
| chr11:15158914 | G | C | 5 | a0001c0001t0002g0018 a0001c0001t0002g0173 a0001c0001t0005g0178 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+9684G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158914 | |||||||
| chr11:15158947 | C | G | 52 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0131 others(49): Show |
52 | HG00621.hp1 HG01069.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.56+9717C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158947 | |||||||
| chr11:15158987 | G | A | 168 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0028 others(165): Show |
172 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(169): Show |
intron_variant | MODIFIER | c.56+9757G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15158987 | |||||||
| chr11:15159270 | A | G | 11 | a0001c0001t0002g0015 a0001c0001t0002g0032 a0001c0001t0002g0153 others(8): Show |
11 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.56+10040A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15159270 | |||||||
| chr11:15159340 | G | A | 7 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(4): Show |
7 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.56+10110G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15159340 | |||||||
| chr11:15159377 | G | A | 146 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(143): Show |
147 | HG00621.hp1 HG00639.hp1 HG00639.hp2 others(144): Show |
intron_variant | MODIFIER | c.56+10147G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15159377 | |||||||
| chr11:15159385 | A | G | 1 | a0002c0004t0001g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.56+10155A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15159385 | |||||||
| chr11:15159506 | A | G | 1 | a0001c0003t0001g0106 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.56+10276A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15159506 | |||||||
| chr11:15159975 | A | G | 16 | a0001c0001t0002g0018 a0001c0001t0002g0173 a0001c0001t0005g0178 others(13): Show |
16 | HG00735.hp1 HG01192.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.56+10745A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15159975 | |||||||
| chr11:15159985 | A | G | 1 | a0001c0013t0017g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.56+10755A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15159985 | |||||||
| chr11:15159989 | A | G | 8 | a0001c0001t0002g0009 a0001c0001t0004g0006 a0001c0001t0004g0227 others(5): Show |
9 | HG01884.hp1 HG01884.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.56+10759A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15159989 | |||||||
| chr11:15160068 | A | C | 90 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(87): Show |
91 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.56+10838A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160068 | |||||||
| chr11:15160102 | A | AG | 52 | a0001c0001t0001g0039 a0001c0001t0001g0092 a0001c0001t0001g0118 others(49): Show |
52 | HG00621.hp1 HG01069.hp1 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.56+10877dupG | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15160102 | ||||||
| chr11:15160150 | T | G | 127 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0028 others(124): Show |
130 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(127): Show |
intron_variant | MODIFIER | c.56+10920T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160150 | |||||||
| chr11:15160162 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(240): Show |
249 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.56+10932G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160162 | |||||||
| chr11:15160172 | G | A | 54 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(51): Show |
54 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.56+10942G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160172 | |||||||
| chr11:15160245 | C | T | 251 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(248): Show |
257 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.56+11015C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160245 | |||||||
| chr11:15160249 | G | A | 4 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0021g0263 others(1): Show |
5 | HG01884.hp2 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.56+11019G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160249 | |||||||
| chr11:15160402 | C | T | 1 | a0002c0004t0001g0031 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.56+11172C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160402 | |||||||
| chr11:15160419 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.56+11189G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160419 | |||||||
| chr11:15160612 | T | C | 1 | a0001c0001t0003g0152 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.56+11382T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160612 | |||||||
| chr11:15160746 | A | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0115 a0001c0001t0001g0190 others(15): Show |
18 | HG00639.hp2 HG01952.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.56+11516A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15160746 | |||||||
| chr11:15161051 | G | T | 66 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(63): Show |
66 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.56+11821G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161051 | |||||||
| chr11:15161116 | C | G | 18 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0003g0020 others(15): Show |
18 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.56+11886C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161116 | |||||||
| chr11:15161180 | C | T | 1 | a0009c0010t0001g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.56+11950C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161180 | |||||||
| chr11:15161183 | T | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0014 others(204): Show |
213 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.56+11953T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161183 | |||||||
| chr11:15161343 | C | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(21): Show |
27 | HG00099.hp2 HG00733.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.56+12113C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161343 | |||||||
| chr11:15161457 | G | A | 2 | a0001c0003t0002g0137 a0001c0003t0002g0237 |
2 | HG01515.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.56+12227G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161457 | |||||||
| chr11:15161474 | G | A | 2 | a0001c0003t0001g0065 a0005c0007t0014g0155 |
2 | HG02293.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.56+12244G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161474 | |||||||
| chr11:15161488 | C | T | 1 | a0001c0001t0011g0181 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.56+12258C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161488 | |||||||
| chr11:15161517 | T | G | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56+12287T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161517 | |||||||
| chr11:15161733 | G | A | 4 | a0001c0001t0003g0020 a0001c0001t0003g0255 a0001c0002t0001g0089 others(1): Show |
4 | HG02818.hp2 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.56+12503G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15161733 | |||||||
| chr11:15162132 | G | A | 3 | a0001c0002t0023g0010 a0001c0009t0010g0258 a0001c0009t0010g0262 |
3 | HG02647.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.56+12902G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15162132 | |||||||
| chr11:15162352 | C | T | 5 | a0001c0001t0003g0144 a0001c0001t0005g0178 a0001c0001t0005g0217 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+13122C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15162352 | |||||||
| chr11:15162388 | G | C | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.56+13158G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15162388 | |||||||
| chr11:15162539 | C | A | 3 | a0001c0001t0001g0134 a0001c0001t0002g0043 a0001c0001t0002g0070 |
3 | HG00408.hp2 HG01952.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.57-13202C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15162539 | |||||||
| chr11:15162825 | C | T | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-12916C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15162825 | |||||||
| chr11:15163199 | C | A | 1 | a0001c0002t0007g0205 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.57-12542C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163199 | |||||||
| chr11:15163252 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.57-12489G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163252 | |||||||
| chr11:15163263 | G | A | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-12478G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163263 | |||||||
| chr11:15163341 | C | CTTGTGCA others(26): Show |
1 | a0001c0001t0002g0135 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.57-12388_57-12387i others(35): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15163341 | ||||||
| chr11:15163401 | T | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0131 a0001c0001t0001g0184 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.57-12340T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163401 | |||||||
| chr11:15163455 | C | T | 76 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0039 others(73): Show |
77 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.57-12286C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163455 | |||||||
| chr11:15163456 | T | C | 2 | a0001c0003t0001g0066 a0001c0003t0002g0158 |
2 | HG01346.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.57-12285T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163456 | |||||||
| chr11:15163614 | G | A | 17 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0004g0006 others(14): Show |
18 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.57-12127G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163614 | |||||||
| chr11:15163615 | A | G | 17 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0004g0006 others(14): Show |
18 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.57-12126A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163615 | |||||||
| chr11:15163679 | C | T | 19 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0055 others(16): Show |
22 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.57-12062C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163679 | |||||||
| chr11:15163783 | A | G | 1 | a0001c0003t0003g0254 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.57-11958A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163783 | |||||||
| chr11:15163790 | C | T | 1 | a0001c0001t0006g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.57-11951C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163790 | |||||||
| chr11:15163968 | G | T | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 |
3 | HG03209.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.57-11773G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163968 | |||||||
| chr11:15163984 | C | T | 2 | a0001c0001t0004g0006 a0001c0001t0004g0227 |
3 | HG02451.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.57-11757C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15163984 | |||||||
| chr11:15164067 | C | T | 3 | a0001c0001t0016g0042 a0001c0001t0016g0261 a0001c0001t0021g0263 |
3 | HG03471.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.57-11674C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164067 | |||||||
| chr11:15164119 | G | T | 1 | a0001c0002t0003g0260 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.57-11622G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164119 | |||||||
| chr11:15164141 | AT | A | 142 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(139): Show |
144 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.57-11592delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15164141 | ||||||
| chr11:15164149 | T | C | 3 | a0004c0006t0001g0244 a0004c0006t0001g0245 a0008c0015t0001g0093 |
3 | HG02818.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.57-11592T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164149 | |||||||
| chr11:15164155 | A | C | 1 | a0001c0002t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.57-11586A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164155 | |||||||
| chr11:15164183 | C | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(136): Show |
141 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.57-11558C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164183 | |||||||
| chr11:15164220 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.57-11521G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164220 | |||||||
| chr11:15164229 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0003g0013 a0001c0001t0005g0109 others(1): Show |
4 | NA18981.hp2 NA18998.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.57-11512A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164229 | |||||||
| chr11:15164351 | C | T | 3 | a0001c0001t0001g0083 a0001c0001t0001g0105 a0001c0001t0001g0209 |
3 | HG00733.hp2 HG01192.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.57-11390C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164351 | |||||||
| chr11:15164359 | A | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(136): Show |
141 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.57-11382A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164359 | |||||||
| chr11:15164379 | T | C | 5 | a0001c0001t0003g0144 a0001c0001t0005g0178 a0001c0001t0005g0217 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-11362T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164379 | |||||||
| chr11:15164418 | C | T | 2 | a0001c0001t0004g0006 a0001c0001t0004g0227 |
3 | HG02451.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.57-11323C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164418 | |||||||
| chr11:15164705 | C | T | 1 | a0001c0002t0001g0095 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.57-11036C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164705 | |||||||
| chr11:15164734 | G | A | 3 | a0001c0002t0023g0010 a0001c0009t0010g0258 a0001c0009t0010g0262 |
3 | HG02647.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-11007G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164734 | |||||||
| chr11:15164784 | A | G | 1 | a0001c0016t0002g0201 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.57-10957A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164784 | |||||||
| chr11:15164867 | T | A | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.57-10874T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164867 | |||||||
| chr11:15164868 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.57-10873C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164868 | |||||||
| chr11:15164872 | C | T | 223 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(220): Show |
229 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.57-10869C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164872 | |||||||
| chr11:15164979 | C | A | 8 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(5): Show |
8 | HG02486.hp2 HG02818.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-10762C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15164979 | |||||||
| chr11:15165193 | C | A | 1 | a0001c0001t0001g0197 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.57-10548C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15165193 | |||||||
| chr11:15165277 | T | TA | 3 | a0001c0002t0023g0010 a0001c0009t0010g0258 a0001c0009t0010g0262 |
3 | HG02647.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-10458dupA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15165277 | ||||||
| chr11:15165381 | T | C | 5 | a0001c0001t0003g0144 a0001c0001t0005g0178 a0001c0001t0005g0217 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-10360T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15165381 | |||||||
| chr11:15165511 | A | G | 19 | a0001c0001t0001g0196 a0001c0001t0002g0025 a0001c0001t0002g0027 others(16): Show |
19 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-10230A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15165511 | |||||||
| chr11:15165518 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.57-10223G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15165518 | |||||||
| chr11:15165596 | T | C | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-10145T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15165596 | |||||||
| chr11:15165619 | A | T | 19 | a0001c0001t0001g0196 a0001c0001t0002g0025 a0001c0001t0002g0027 others(16): Show |
19 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-10122A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15165619 | |||||||
| chr11:15165695 | T | G | 2 | a0001c0001t0001g0115 a0001c0001t0004g0041 |
2 | NA18969.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.57-10046T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15165695 | |||||||
| chr11:15165696 | G | A | 6 | a0001c0001t0002g0018 a0001c0002t0006g0033 a0001c0002t0006g0179 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.57-10045G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15165696 | |||||||
| chr11:15165959 | G | C | 144 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(141): Show |
146 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.57-9782G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15165959 | |||||||
| chr11:15166156 | T | C | 1 | a0001c0001t0002g0124 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.57-9585T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15166156 | |||||||
| chr11:15166158 | G | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(144): Show |
149 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.57-9583G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15166158 | |||||||
| chr11:15166236 | G | A | 3 | a0001c0001t0002g0224 a0001c0001t0002g0230 a0002c0017t0001g0199 |
3 | HG02615.hp2 HG02818.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.57-9505G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15166236 | |||||||
| chr11:15166298 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0164 |
2 | NA18982.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.57-9443C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15166298 | |||||||
| chr11:15166351 | A | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(190): Show |
196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.57-9390A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15166351 | |||||||
| chr11:15166415 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0189 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.57-9326C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15166415 | |||||||
| chr11:15166443 | A | G | 2 | a0001c0001t0001g0118 a0001c0001t0002g0119 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.57-9298A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15166443 | |||||||
| chr11:15166522 | C | G | 2 | a0001c0001t0016g0261 a0001c0001t0021g0263 |
2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.57-9219C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15166522 | |||||||
| chr11:15167001 | G | A | 8 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(5): Show |
8 | HG02486.hp2 HG02818.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-8740G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167001 | |||||||
| chr11:15167043 | AT | A | 19 | a0001c0001t0001g0196 a0001c0001t0002g0025 a0001c0001t0002g0027 others(16): Show |
19 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-8689delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15167043 | ||||||
| chr11:15167095 | TTCTG | T | 3 | a0001c0001t0003g0144 a0001c0001t0005g0217 a0001c0001t0005g0229 |
3 | HG01884.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.57-8642_57-8639del others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15167095 | ||||||
| chr11:15167103 | A | AT | 11 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0002g0180 others(8): Show |
11 | HG01243.hp2 HG02258.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.57-8627dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15167103 | ||||||
| chr11:15167288 | A | T | 147 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(144): Show |
149 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(146): Show |
intron_variant | MODIFIER | c.57-8453A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167288 | |||||||
| chr11:15167290 | C | T | 1 | a0007c0014t0004g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.57-8451C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167290 | |||||||
| chr11:15167303 | C | T | 1 | a0001c0003t0001g0106 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.57-8438C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167303 | |||||||
| chr11:15167357 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-8384C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167357 | |||||||
| chr11:15167377 | T | C | 1 | a0005c0007t0014g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.57-8364T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167377 | |||||||
| chr11:15167483 | A | G | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57-8258A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167483 | |||||||
| chr11:15167654 | A | T | 4 | a0001c0003t0004g0225 a0001c0003t0004g0240 a0004c0008t0015g0034 others(1): Show |
4 | HG01884.hp2 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.57-8087A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167654 | |||||||
| chr11:15167747 | G | A | 5 | a0001c0001t0003g0144 a0001c0001t0005g0178 a0001c0001t0005g0217 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-7994G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167747 | |||||||
| chr11:15167752 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.57-7989G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167752 | |||||||
| chr11:15167863 | G | A | 228 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(225): Show |
234 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.57-7878G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167863 | |||||||
| chr11:15167902 | T | G | 1 | a0001c0003t0002g0237 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.57-7839T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167902 | |||||||
| chr11:15167964 | G | A | 37 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0061 others(34): Show |
38 | HG00408.hp2 HG01074.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.57-7777G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15167964 | |||||||
| chr11:15168051 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.57-7690C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15168051 | |||||||
| chr11:15168259 | G | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 others(6): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.57-7482G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15168259 | |||||||
| chr11:15168347 | T | TAA | 90 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(87): Show |
91 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.57-7393_57-7392ins others(2): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15168347 | ||||||
| chr11:15168419 | C | T | 4 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(1): Show |
4 | HG00735.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.57-7322C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15168419 | |||||||
| chr11:15168778 | C | G | 6 | a0001c0002t0003g0076 a0001c0002t0003g0177 a0001c0002t0003g0239 others(3): Show |
6 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.57-6963C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15168778 | |||||||
| chr11:15168795 | G | T | 6 | a0001c0002t0003g0076 a0001c0002t0003g0177 a0001c0002t0003g0239 others(3): Show |
6 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.57-6946G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15168795 | |||||||
| chr11:15168857 | G | A | 1 | a0002c0004t0001g0253 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57-6884G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15168857 | |||||||
| chr11:15169020 | C | A | 8 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.57-6721C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169020 | |||||||
| chr11:15169115 | C | G | 1 | a0001c0001t0005g0080 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.57-6626C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169115 | |||||||
| chr11:15169200 | T | TC | 212 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(209): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.57-6538dupC | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15169200 | ||||||
| chr11:15169273 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(229): Show |
238 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(235): Show |
intron_variant | MODIFIER | c.57-6468A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169273 | |||||||
| chr11:15169276 | G | T | 19 | a0001c0001t0001g0196 a0001c0001t0002g0025 a0001c0001t0002g0027 others(16): Show |
19 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.57-6465G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169276 | |||||||
| chr11:15169417 | C | A | 3 | a0001c0002t0023g0010 a0001c0009t0010g0258 a0001c0009t0010g0262 |
3 | HG02647.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-6324C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169417 | |||||||
| chr11:15169530 | GTTGTTTG others(1): Show |
G | 2 | a0001c0001t0004g0006 a0001c0001t0004g0227 |
3 | HG02451.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.57-6192_57-6185del others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15169530 | ||||||
| chr11:15169537 | G | GTTTC | 3 | a0001c0001t0005g0022 a0001c0001t0005g0167 a0001c0001t0005g0183 |
3 | HG02965.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.57-6201_57-6200ins others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15169537 | ||||||
| chr11:15169545 | G | C | 3 | a0001c0001t0005g0022 a0001c0001t0005g0167 a0001c0001t0005g0183 |
3 | HG02965.hp2 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.57-6196G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169545 | |||||||
| chr11:15169545 | G | GTTTC | 98 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(95): Show |
99 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.57-6193_57-6192ins others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15169545 | ||||||
| chr11:15169589 | TG | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(157): Show |
162 | HG00099.hp1 HG00408.hp2 HG00609.hp1 others(159): Show |
intron_variant | MODIFIER | c.57-6150delG | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15169589 | ||||||
| chr11:15169618 | T | C | 1 | a0003c0005t0009g0171 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.57-6123T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169618 | |||||||
| chr11:15169642 | A | G | 3 | a0001c0001t0001g0057 a0001c0001t0001g0067 a0001c0001t0004g0133 |
3 | HG00735.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.57-6099A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169642 | |||||||
| chr11:15169708 | A | AT | 17 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0004g0006 others(14): Show |
18 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.57-6021dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15169708 | ||||||
| chr11:15169810 | G | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(188): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.57-5931G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169810 | |||||||
| chr11:15169866 | T | C | 90 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(87): Show |
91 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.57-5875T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169866 | |||||||
| chr11:15169984 | C | T | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57-5757C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15169984 | |||||||
| chr11:15170029 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(197): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.57-5712A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170029 | |||||||
| chr11:15170047 | C | T | 8 | a0001c0001t0002g0018 a0001c0002t0003g0016 a0001c0002t0003g0222 others(5): Show |
8 | HG02257.hp2 HG02572.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.57-5694C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170047 | |||||||
| chr11:15170415 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(197): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.57-5326A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170415 | |||||||
| chr11:15170435 | T | A | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(197): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.57-5306T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170435 | |||||||
| chr11:15170467 | C | T | 2 | a0001c0003t0002g0114 a0001c0018t0006g0228 |
2 | HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.57-5274C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170467 | |||||||
| chr11:15170503 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(197): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.57-5238A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170503 | |||||||
| chr11:15170557 | A | T | 8 | a0002c0004t0001g0031 a0002c0004t0001g0142 a0002c0004t0001g0219 others(5): Show |
8 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-5184A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170557 | |||||||
| chr11:15170729 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.57-5012T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170729 | |||||||
| chr11:15170940 | C | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(176): Show |
181 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.57-4801C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170940 | |||||||
| chr11:15170945 | T | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0055 others(18): Show |
24 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.57-4796T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15170945 | |||||||
| chr11:15171195 | G | GA | 8 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(5): Show |
8 | HG02486.hp2 HG02818.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-4545dupA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15171195 | ||||||
| chr11:15171562 | C | T | 1 | a0001c0016t0002g0201 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.57-4179C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15171562 | |||||||
| chr11:15171578 | C | G | 179 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(176): Show |
181 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.57-4163C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15171578 | |||||||
| chr11:15171608 | C | T | 3 | a0001c0001t0002g0032 a0001c0001t0002g0130 a0001c0001t0002g0153 |
3 | HG01243.hp1 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.57-4133C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15171608 | |||||||
| chr11:15171639 | C | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(176): Show |
181 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.57-4102C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15171639 | |||||||
| chr11:15171830 | C | A | 1 | a0001c0001t0014g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.57-3911C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15171830 | |||||||
| chr11:15171851 | A | C | 220 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(217): Show |
226 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.57-3890A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15171851 | |||||||
| chr11:15171919 | C | T | 3 | a0001c0002t0023g0010 a0001c0009t0010g0258 a0001c0009t0010g0262 |
3 | HG02647.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-3822C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15171919 | |||||||
| chr11:15172159 | A | C | 5 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-3582A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15172159 | |||||||
| chr11:15172277 | C | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 others(6): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.57-3464C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15172277 | |||||||
| chr11:15172294 | C | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 others(6): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.57-3447C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15172294 | |||||||
| chr11:15172337 | T | G | 5 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-3404T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15172337 | |||||||
| chr11:15172344 | G | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 others(6): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.57-3397G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15172344 | |||||||
| chr11:15172734 | C | T | 3 | a0001c0002t0023g0010 a0001c0009t0010g0258 a0001c0009t0010g0262 |
3 | HG02647.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-3007C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15172734 | |||||||
| chr11:15172851 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.57-2890C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15172851 | |||||||
| chr11:15172863 | CATCTT | C | 9 | a0001c0001t0002g0018 a0001c0002t0003g0016 a0001c0002t0003g0222 others(6): Show |
9 | HG02257.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.57-2876_57-2872del others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr11 | 15172863 | ||||||
| chr11:15172945 | A | G | 5 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.57-2796A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15172945 | |||||||
| chr11:15173158 | C | T | 1 | a0001c0003t0002g0194 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.57-2583C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15173158 | |||||||
| chr11:15173169 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0164 a0001c0001t0018g0098 |
3 | NA18954.hp1 NA18982.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.57-2572A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15173169 | |||||||
| chr11:15173213 | G | T | 179 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(176): Show |
181 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.57-2528G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15173213 | |||||||
| chr11:15173486 | C | T | 3 | a0001c0002t0023g0010 a0001c0009t0010g0258 a0001c0009t0010g0262 |
3 | HG02647.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-2255C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15173486 | |||||||
| chr11:15173594 | C | G | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.57-2147C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15173594 | |||||||
| chr11:15173613 | T | A | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.57-2128T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15173613 | |||||||
| chr11:15173645 | T | C | 9 | a0001c0001t0002g0018 a0001c0002t0003g0016 a0001c0002t0003g0222 others(6): Show |
9 | HG02257.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.57-2096T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15173645 | |||||||
| chr11:15173911 | C | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(179): Show |
184 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.57-1830C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15173911 | |||||||
| chr11:15174102 | T | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(238): Show |
247 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.57-1639T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174102 | |||||||
| chr11:15174112 | A | C | 190 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(187): Show |
192 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.57-1629A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174112 | |||||||
| chr11:15174247 | G | C | 1 | a0001c0001t0003g0255 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.57-1494G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174247 | |||||||
| chr11:15174270 | G | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0057 others(48): Show |
52 | HG00408.hp2 HG00735.hp2 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.57-1471G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174270 | |||||||
| chr11:15174326 | C | T | 1 | a0001c0003t0002g0221 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.57-1415C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174326 | |||||||
| chr11:15174410 | C | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(177): Show |
182 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.57-1331C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174410 | |||||||
| chr11:15174564 | G | A | 1 | a0001c0001t0005g0102 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.57-1177G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174564 | |||||||
| chr11:15174638 | A | G | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57-1103A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174638 | |||||||
| chr11:15174686 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.57-1055G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174686 | |||||||
| chr11:15174895 | G | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 others(6): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.57-846G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174895 | |||||||
| chr11:15174960 | A | G | 1 | a0003c0005t0001g0216 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.57-781A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15174960 | |||||||
| chr11:15175006 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(179): Show |
184 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.57-735A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15175006 | |||||||
| chr11:15175008 | G | A | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.57-733G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15175008 | |||||||
| chr11:15175206 | A | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(179): Show |
184 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.57-535A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15175206 | |||||||
| chr11:15175304 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(179): Show |
184 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.57-437G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15175304 | |||||||
| chr11:15175345 | A | G | 1 | a0001c0001t0001g0004 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.57-396A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15175345 | |||||||
| chr11:15175347 | C | A | 2 | a0001c0001t0007g0030 a0001c0001t0012g0129 |
2 | HG01192.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.57-394C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15175347 | |||||||
| chr11:15175407 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.57-334G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15175407 | |||||||
| chr11:15175495 | A | C | 1 | a0001c0001t0002g0208 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.57-246A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15175495 | |||||||
| chr11:15175640 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(179): Show |
184 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.57-101A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 2/12 | chr11 | 15175640 | |||||||
| chr11:15176372 | A | T | 1 | a0001c0001t0005g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.402+286A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 3/12 | chr11 | 15176372 | |||||||
| chr11:15176572 | T | C | 6 | a0001c0002t0003g0076 a0001c0002t0003g0177 a0001c0002t0003g0239 others(3): Show |
6 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.402+486T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 3/12 | chr11 | 15176572 | |||||||
| chr11:15176653 | C | G | 5 | a0001c0001t0003g0144 a0001c0001t0005g0178 a0001c0001t0005g0217 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.403-458C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 3/12 | chr11 | 15176653 | |||||||
| chr11:15176924 | A | G | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.403-187A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 3/12 | chr11 | 15176924 | |||||||
| chr11:15177037 | C | T | 8 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.403-74C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 3/12 | chr11 | 15177037 | |||||||
| chr11:15177038 | G | A | 4 | a0001c0001t0004g0001 a0001c0001t0004g0234 a0001c0001t0004g0236 others(1): Show |
5 | HG00733.hp1 HG00741.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.403-73G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 3/12 | chr11 | 15177038 | |||||||
| chr11:15177226 | G | T | 180 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(177): Show |
182 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.455+63G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 4/12 | chr11 | 15177226 | |||||||
| chr11:15177262 | C | T | 8 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.455+99C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 4/12 | chr11 | 15177262 | |||||||
| chr11:15177263 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.455+100G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 4/12 | chr11 | 15177263 | |||||||
| chr11:15177266 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.455+103G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 4/12 | chr11 | 15177266 | |||||||
| chr11:15177417 | G | A | 5 | a0001c0003t0001g0106 a0001c0003t0004g0225 a0001c0003t0004g0240 others(2): Show |
5 | HG00738.hp1 HG01884.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.455+254G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 4/12 | chr11 | 15177417 | |||||||
| chr11:15177615 | C | A | 1 | a0001c0001t0002g0048 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.455+452C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 4/12 | chr11 | 15177615 | |||||||
| chr11:15177739 | C | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0055 others(16): Show |
22 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.455+576C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 4/12 | chr11 | 15177739 | |||||||
| chr11:15177855 | G | A | 1 | a0001c0001t0018g0098 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.456-469G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 4/12 | chr11 | 15177855 | |||||||
| chr11:15178232 | G | T | 8 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(5): Show |
8 | HG02486.hp2 HG02818.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.456-92G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 4/12 | chr11 | 15178232 | |||||||
| chr11:15178596 | AT | A | 24 | a0001c0001t0001g0196 a0001c0001t0002g0025 a0001c0001t0002g0027 others(21): Show |
24 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.579+152delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15178596 | ||||||
| chr11:15178669 | G | A | 1 | a0001c0001t0005g0178 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.579+222G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15178669 | |||||||
| chr11:15178753 | A | G | 4 | a0001c0001t0004g0001 a0001c0001t0004g0234 a0001c0001t0004g0236 others(1): Show |
5 | HG00733.hp1 HG00741.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+306A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15178753 | |||||||
| chr11:15178784 | C | A | 9 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 others(6): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.579+337C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15178784 | |||||||
| chr11:15178845 | T | C | 2 | a0001c0002t0003g0045 a0001c0002t0003g0046 |
2 | NA18944.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.579+398T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15178845 | |||||||
| chr11:15178866 | T | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(178): Show |
183 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.579+419T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15178866 | |||||||
| chr11:15178916 | G | A | 9 | a0002c0004t0001g0031 a0002c0004t0001g0142 a0002c0004t0001g0219 others(6): Show |
9 | HG02559.hp2 HG02615.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+469G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15178916 | |||||||
| chr11:15178946 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(177): Show |
182 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.579+499G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15178946 | |||||||
| chr11:15179465 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.579+1018G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15179465 | |||||||
| chr11:15179614 | C | T | 27 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(24): Show |
31 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.579+1167C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15179614 | |||||||
| chr11:15179638 | C | T | 52 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0115 others(49): Show |
52 | HG00408.hp2 HG00639.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.579+1191C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15179638 | |||||||
| chr11:15179985 | A | G | 217 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.579+1538A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15179985 | |||||||
| chr11:15180002 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.579+1555A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180002 | |||||||
| chr11:15180071 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.579+1624G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180071 | |||||||
| chr11:15180072 | T | C | 1 | a0001c0001t0004g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.579+1625T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180072 | |||||||
| chr11:15180073 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.579+1626G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180073 | |||||||
| chr11:15180099 | G | A | 192 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(189): Show |
193 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.579+1652G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180099 | |||||||
| chr11:15180114 | C | T | 176 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(173): Show |
177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.579+1667C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180114 | |||||||
| chr11:15180119 | A | G | 11 | a0001c0002t0023g0010 a0002c0004t0001g0031 a0002c0004t0001g0142 others(8): Show |
11 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.579+1672A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180119 | |||||||
| chr11:15180127 | G | A | 52 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0115 others(49): Show |
52 | HG00408.hp2 HG00639.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.579+1680G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180127 | |||||||
| chr11:15180128 | A | G | 193 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.579+1681A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180128 | |||||||
| chr11:15180182 | T | C | 22 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0003g0020 others(19): Show |
22 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.579+1735T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180182 | |||||||
| chr11:15180214 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0002g0044 |
2 | HG02074.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.579+1767C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180214 | |||||||
| chr11:15180217 | C | T | 2 | a0001c0001t0016g0042 a0001c0001t0016g0261 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.579+1770C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180217 | |||||||
| chr11:15180276 | A | AAAAC | 3 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 |
4 | HG02451.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.579+1849_579+1852d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15180276 | ||||||
| chr11:15180280 | C | CA | 3 | a0004c0006t0001g0244 a0004c0006t0001g0245 a0008c0015t0001g0093 |
3 | HG02818.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.579+1836dupA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15180280 | ||||||
| chr11:15180348 | T | C | 26 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0002g0173 others(23): Show |
26 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.579+1901T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180348 | |||||||
| chr11:15180381 | C | T | 6 | a0001c0002t0003g0076 a0001c0002t0003g0177 a0001c0002t0003g0239 others(3): Show |
6 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+1934C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180381 | |||||||
| chr11:15180484 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(239): Show |
248 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(245): Show |
intron_variant | MODIFIER | c.579+2037A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180484 | |||||||
| chr11:15180553 | C | T | 1 | a0007c0014t0004g0026 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.579+2106C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180553 | |||||||
| chr11:15180692 | G | GC | 7 | a0001c0001t0016g0261 a0001c0002t0001g0089 a0001c0003t0019g0172 others(4): Show |
7 | HG02486.hp2 HG03471.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+2245_579+2246i others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180692 | |||||||
| chr11:15180692 | G | GGGC | 24 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0001c0001t0001g0115 others(21): Show |
24 | HG00609.hp2 HG00735.hp2 HG01346.hp1 others(21): Show |
intron_variant | MODIFIER | c.579+2246_579+2247i others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15180692 | ||||||
| chr11:15180693 | G | C | 13 | a0001c0001t0002g0151 a0001c0001t0003g0020 a0001c0001t0003g0021 others(10): Show |
13 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.579+2246G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180693 | |||||||
| chr11:15180693 | G | GGC | 19 | a0001c0001t0001g0112 a0001c0001t0001g0131 a0001c0001t0001g0160 others(16): Show |
19 | HG00099.hp2 HG01516.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.579+2246_579+2247i others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180693 | |||||||
| chr11:15180694 | C | CG | 66 | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0001g0036 others(63): Show |
67 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.579+2256dupG | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15180694 | ||||||
| chr11:15180694 | C | CGG | 54 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0057 others(51): Show |
54 | HG00609.hp1 HG00733.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.579+2255_579+2256d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15180694 | ||||||
| chr11:15180694 | C | G | 84 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0058 others(81): Show |
85 | HG00099.hp2 HG00408.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.579+2247C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180694 | |||||||
| chr11:15180695 | G | C | 2 | a0001c0001t0016g0042 a0001c0002t0023g0010 |
2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.579+2248G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180695 | |||||||
| chr11:15180701 | G | C | 5 | a0001c0002t0003g0076 a0001c0002t0003g0177 a0001c0002t0003g0239 others(2): Show |
5 | HG01106.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+2254G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180701 | |||||||
| chr11:15180936 | G | A | 1 | a0001c0001t0001g0211 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.579+2489G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15180936 | |||||||
| chr11:15181206 | C | T | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+2759C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181206 | |||||||
| chr11:15181209 | G | A | 2 | a0001c0001t0001g0138 a0001c0001t0001g0156 |
2 | NA18944.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.579+2762G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181209 | |||||||
| chr11:15181222 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(194): Show |
203 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.579+2775G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181222 | |||||||
| chr11:15181252 | T | C | 1 | a0001c0003t0001g0106 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.579+2805T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181252 | |||||||
| chr11:15181282 | C | T | 16 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0003g0020 others(13): Show |
16 | HG01243.hp2 HG02258.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.579+2835C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181282 | |||||||
| chr11:15181307 | C | T | 30 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0051 others(27): Show |
31 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.579+2860C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181307 | |||||||
| chr11:15181382 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0006g0175 |
3 | HG01081.hp2 HG04204.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.579+2935G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181382 | |||||||
| chr11:15181408 | A | C | 5 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+2961A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181408 | |||||||
| chr11:15181431 | G | T | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.579+2984G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181431 | |||||||
| chr11:15181455 | T | A | 8 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(5): Show |
8 | HG02486.hp2 HG02818.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+3008T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181455 | |||||||
| chr11:15181474 | A | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(202): Show |
211 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.579+3027A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181474 | |||||||
| chr11:15181522 | C | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+3075C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181522 | |||||||
| chr11:15181805 | G | A | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.579+3358G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181805 | |||||||
| chr11:15181998 | C | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+3551C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15181998 | |||||||
| chr11:15182075 | G | A | 1 | a0001c0001t0005g0178 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.579+3628G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182075 | |||||||
| chr11:15182163 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.579+3716C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182163 | |||||||
| chr11:15182171 | A | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+3724A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182171 | |||||||
| chr11:15182262 | G | A | 1 | a0001c0012t0001g0204 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.579+3815G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182262 | |||||||
| chr11:15182280 | A | G | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.579+3833A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182280 | |||||||
| chr11:15182307 | A | T | 1 | a0001c0001t0002g0166 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.579+3860A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182307 | |||||||
| chr11:15182350 | G | C | 1 | a0001c0003t0003g0254 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.579+3903G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182350 | |||||||
| chr11:15182498 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.579+4051G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182498 | |||||||
| chr11:15182556 | G | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+4109G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182556 | |||||||
| chr11:15182629 | T | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+4182T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182629 | |||||||
| chr11:15182724 | T | G | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.579+4277T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182724 | |||||||
| chr11:15182811 | T | C | 1 | a0002c0004t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.579+4364T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15182811 | |||||||
| chr11:15182877 | C | CA | 10 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(7): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.579+4431dupA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15182877 | ||||||
| chr11:15183078 | C | T | 1 | a0003c0005t0004g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.579+4631C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183078 | |||||||
| chr11:15183086 | G | A | 18 | a0001c0001t0003g0144 a0001c0001t0005g0094 a0001c0001t0005g0178 others(15): Show |
18 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.579+4639G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183086 | |||||||
| chr11:15183114 | G | A | 8 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(5): Show |
8 | HG02486.hp2 HG02818.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+4667G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183114 | |||||||
| chr11:15183145 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+4698C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183145 | |||||||
| chr11:15183192 | A | T | 4 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(1): Show |
4 | HG00735.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+4745A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183192 | |||||||
| chr11:15183244 | G | A | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.579+4797G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183244 | |||||||
| chr11:15183325 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.579+4878T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183325 | |||||||
| chr11:15183351 | C | CA | 19 | a0001c0001t0001g0079 a0001c0001t0001g0197 a0001c0001t0002g0145 others(16): Show |
19 | HG02055.hp2 HG02074.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.579+4923dupA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15183351 | ||||||
| chr11:15183351 | CA | C | 64 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0029 others(61): Show |
68 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.579+4923delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15183351 | ||||||
| chr11:15183430 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.579+4983T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183430 | |||||||
| chr11:15183443 | A | ATG | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+5010_579+5011d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15183443 | ||||||
| chr11:15183534 | T | A | 169 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(166): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.579+5087T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183534 | |||||||
| chr11:15183682 | G | A | 2 | a0001c0001t0016g0042 a0001c0001t0016g0261 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.579+5235G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183682 | |||||||
| chr11:15183780 | C | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+5333C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183780 | |||||||
| chr11:15183795 | T | C | 221 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(218): Show |
227 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.579+5348T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183795 | |||||||
| chr11:15183864 | C | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+5417C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15183864 | |||||||
| chr11:15184019 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+5572C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184019 | |||||||
| chr11:15184083 | G | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+5636G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184083 | |||||||
| chr11:15184204 | C | T | 5 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+5757C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184204 | |||||||
| chr11:15184215 | AT | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+5771delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15184215 | ||||||
| chr11:15184248 | T | C | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.579+5801T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184248 | |||||||
| chr11:15184474 | C | T | 54 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0115 others(51): Show |
54 | HG00408.hp2 HG00639.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.579+6027C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184474 | |||||||
| chr11:15184500 | A | C | 5 | a0001c0001t0003g0144 a0001c0001t0005g0178 a0001c0001t0005g0217 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+6053A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184500 | |||||||
| chr11:15184585 | G | A | 1 | a0001c0001t0004g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.580-6116G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184585 | |||||||
| chr11:15184608 | G | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0141 |
2 | HG00609.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.580-6093G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184608 | |||||||
| chr11:15184633 | A | T | 10 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(7): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-6068A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184633 | |||||||
| chr11:15184684 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(232): Show |
241 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.580-6017A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15184684 | |||||||
| chr11:15185231 | G | C | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.580-5470G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15185231 | |||||||
| chr11:15185231 | G | T | 8 | a0002c0004t0001g0031 a0002c0004t0001g0142 a0002c0004t0001g0219 others(5): Show |
8 | HG02109.hp2 HG02559.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-5470G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15185231 | |||||||
| chr11:15185290 | T | C | 10 | a0002c0004t0001g0031 a0002c0004t0001g0142 a0002c0004t0001g0219 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-5411T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15185290 | |||||||
| chr11:15185644 | A | C | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.580-5057A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15185644 | |||||||
| chr11:15185902 | G | C | 10 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(7): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-4799G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15185902 | |||||||
| chr11:15185997 | CT | C | 54 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0115 others(51): Show |
54 | HG00408.hp2 HG00639.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.580-4703delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15185997 | |||||||
| chr11:15186047 | C | T | 222 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(219): Show |
228 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.580-4654C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186047 | |||||||
| chr11:15186248 | C | CT | 232 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(229): Show |
236 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.580-4442dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15186248 | ||||||
| chr11:15186352 | C | T | 10 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(7): Show |
10 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.580-4349C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186352 | |||||||
| chr11:15186384 | T | C | 13 | a0001c0001t0005g0094 a0001c0001t0011g0186 a0001c0002t0001g0095 others(10): Show |
13 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-4317T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186384 | |||||||
| chr11:15186392 | A | G | 1 | a0001c0002t0013g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.580-4309A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186392 | |||||||
| chr11:15186423 | C | T | 2 | a0001c0001t0016g0042 a0001c0001t0016g0261 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.580-4278C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186423 | |||||||
| chr11:15186557 | A | C | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-4144A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186557 | |||||||
| chr11:15186623 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(195): Show |
204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.580-4078G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186623 | |||||||
| chr11:15186689 | C | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(195): Show |
204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.580-4012C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186689 | |||||||
| chr11:15186717 | T | C | 41 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0115 others(38): Show |
41 | HG00408.hp2 HG01074.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.580-3984T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186717 | |||||||
| chr11:15186851 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.580-3850C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186851 | |||||||
| chr11:15186877 | A | T | 3 | a0001c0001t0001g0248 a0001c0001t0002g0145 a0001c0001t0004g0001 |
4 | HG01515.hp1 HG01517.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-3824A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15186877 | |||||||
| chr11:15187027 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.580-3674G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187027 | |||||||
| chr11:15187109 | G | A | 1 | a0001c0001t0002g0120 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.580-3592G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187109 | |||||||
| chr11:15187277 | T | C | 3 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 |
4 | HG02451.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-3424T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187277 | |||||||
| chr11:15187397 | T | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0112 a0001c0001t0001g0138 others(3): Show |
6 | HG00099.hp1 HG02135.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-3304T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187397 | |||||||
| chr11:15187445 | G | T | 5 | a0001c0001t0003g0144 a0001c0001t0005g0178 a0001c0001t0005g0217 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.580-3256G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187445 | |||||||
| chr11:15187586 | G | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.580-3115G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187586 | |||||||
| chr11:15187737 | A | G | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.580-2964A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187737 | |||||||
| chr11:15187751 | A | G | 13 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(10): Show |
13 | HG01243.hp2 HG02258.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.580-2950A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187751 | |||||||
| chr11:15187845 | C | T | 54 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0115 others(51): Show |
54 | HG00408.hp2 HG00639.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.580-2856C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187845 | |||||||
| chr11:15187846 | G | T | 23 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(20): Show |
23 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.580-2855G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187846 | |||||||
| chr11:15187916 | C | T | 195 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(192): Show |
201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.580-2785C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187916 | |||||||
| chr11:15187960 | A | C | 91 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.580-2741A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15187960 | |||||||
| chr11:15188167 | G | T | 1 | a0001c0001t0002g0009 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.580-2534G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15188167 | |||||||
| chr11:15188170 | G | A | 1 | a0002c0017t0001g0199 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.580-2531G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15188170 | |||||||
| chr11:15188387 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.580-2314G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15188387 | |||||||
| chr11:15188513 | C | T | 3 | a0001c0001t0003g0144 a0001c0001t0005g0217 a0001c0001t0005g0229 |
3 | HG01884.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.580-2188C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15188513 | |||||||
| chr11:15188525 | A | G | 15 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(12): Show |
15 | HG00735.hp1 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.580-2176A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15188525 | |||||||
| chr11:15188709 | A | C | 3 | a0001c0003t0013g0104 a0001c0003t0019g0172 a0001c0003t0020g0101 |
3 | HG02056.hp2 HG02129.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.580-1992A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15188709 | |||||||
| chr11:15188710 | A | G | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.580-1991A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15188710 | |||||||
| chr11:15189288 | A | T | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.580-1413A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15189288 | |||||||
| chr11:15189367 | GTTTA | G | 25 | a0001c0001t0002g0023 a0001c0001t0002g0024 a0001c0001t0002g0025 others(22): Show |
25 | HG00738.hp1 HG01261.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.580-1290_580-1287d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15189367 | ||||||
| chr11:15189367 | GTTTATTT others(1): Show |
G | 17 | a0001c0001t0002g0151 a0001c0001t0005g0150 a0001c0001t0005g0187 others(14): Show |
17 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.580-1294_580-1287d others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15189367 | ||||||
| chr11:15189367 | GTTTATTT others(5): Show |
G | 2 | a0001c0001t0001g0235 a0008c0015t0001g0093 |
2 | HG02818.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.580-1298_580-1287d others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15189367 | ||||||
| chr11:15189367 | GTTTATTT others(9): Show |
G | 15 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(12): Show |
15 | HG00735.hp1 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.580-1302_580-1287d others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15189367 | ||||||
| chr11:15189367 | GTTTATTT others(13): Show |
G | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.580-1306_580-1287d others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15189367 | ||||||
| chr11:15189367 | GTTTATTT others(17): Show |
G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(190): Show |
199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.580-1310_580-1287d others(26): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15189367 | ||||||
| chr11:15189377 | TTATTTAT others(15): Show |
T | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 |
3 | HG03209.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.580-1322_580-1301d others(24): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr11 | 15189377 | ||||||
| chr11:15189425 | T | A | 10 | a0002c0004t0001g0031 a0002c0004t0001g0142 a0002c0004t0001g0219 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-1276T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15189425 | |||||||
| chr11:15189451 | T | C | 1 | a0001c0002t0004g0063 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.580-1250T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15189451 | |||||||
| chr11:15189690 | T | C | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.580-1011T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15189690 | |||||||
| chr11:15189803 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.580-898A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15189803 | |||||||
| chr11:15189920 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.580-781C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15189920 | |||||||
| chr11:15190105 | G | A | 22 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0115 others(19): Show |
22 | HG00408.hp2 HG01433.hp2 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.580-596G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15190105 | |||||||
| chr11:15190123 | A | G | 11 | a0001c0002t0023g0010 a0002c0004t0001g0031 a0002c0004t0001g0142 others(8): Show |
11 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.580-578A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15190123 | |||||||
| chr11:15190241 | C | A | 1 | a0001c0001t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.580-460C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15190241 | |||||||
| chr11:15190338 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.580-363G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15190338 | |||||||
| chr11:15190355 | G | A | 25 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0003g0144 others(22): Show |
25 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.580-346G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15190355 | |||||||
| chr11:15190374 | A | T | 1 | a0001c0002t0004g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.580-327A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15190374 | |||||||
| chr11:15190524 | T | C | 13 | a0001c0001t0001g0036 a0001c0001t0001g0052 a0001c0001t0001g0058 others(10): Show |
13 | HG00609.hp1 HG01952.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.580-177T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15190524 | |||||||
| chr11:15190565 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.580-136C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 5/12 | chr11 | 15190565 | |||||||
| chr11:15190908 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.693+94C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15190908 | |||||||
| chr11:15190978 | A | AT | 13 | a0001c0001t0001g0053 a0001c0001t0001g0074 a0001c0001t0001g0115 others(10): Show |
13 | HG00609.hp1 HG02145.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.693+184dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15190978 | ||||||
| chr11:15190978 | A | ATTT | 7 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(4): Show |
7 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+182_693+184dup others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15190978 | ||||||
| chr11:15190978 | AT | A | 18 | a0001c0001t0001g0061 a0001c0001t0001g0164 a0001c0001t0001g0202 others(15): Show |
18 | HG01261.hp1 HG01515.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+184delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15190978 | ||||||
| chr11:15191003 | C | T | 1 | a0001c0003t0013g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.693+189C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191003 | |||||||
| chr11:15191015 | CTG | C | 6 | a0001c0001t0002g0018 a0001c0002t0006g0033 a0001c0002t0006g0179 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+203_693+204del others(2): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15191015 | ||||||
| chr11:15191043 | C | T | 12 | a0001c0001t0006g0008 a0001c0002t0023g0010 a0002c0004t0001g0031 others(9): Show |
12 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.693+229C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191043 | |||||||
| chr11:15191073 | C | T | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.693+259C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191073 | |||||||
| chr11:15191125 | C | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(55): Show |
62 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.693+311C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191125 | |||||||
| chr11:15191133 | A | T | 2 | a0002c0004t0002g0218 a0002c0011t0002g0017 |
2 | HG02109.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.693+319A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191133 | |||||||
| chr11:15191172 | G | T | 2 | a0001c0001t0003g0020 a0001c0001t0003g0255 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.693+358G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191172 | |||||||
| chr11:15191180 | C | G | 18 | a0001c0001t0003g0144 a0001c0001t0005g0094 a0001c0001t0005g0178 others(15): Show |
18 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+366C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191180 | |||||||
| chr11:15191181 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.693+367G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191181 | |||||||
| chr11:15191221 | C | T | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.693+407C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191221 | |||||||
| chr11:15191236 | C | A | 149 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(146): Show |
151 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.693+422C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191236 | |||||||
| chr11:15191268 | C | T | 6 | a0001c0001t0002g0018 a0001c0002t0006g0033 a0001c0002t0006g0179 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+454C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191268 | |||||||
| chr11:15191358 | C | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(55): Show |
62 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.693+544C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191358 | |||||||
| chr11:15191496 | T | A | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.693+682T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191496 | |||||||
| chr11:15191549 | T | C | 1 | a0001c0003t0002g0237 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.693+735T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191549 | |||||||
| chr11:15191568 | G | A | 55 | a0001c0001t0001g0012 a0001c0001t0001g0079 a0001c0001t0001g0115 others(52): Show |
55 | HG00408.hp2 HG00639.hp1 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.693+754G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191568 | |||||||
| chr11:15191606 | T | G | 7 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(4): Show |
7 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+792T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191606 | |||||||
| chr11:15191859 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.693+1045G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191859 | |||||||
| chr11:15191861 | G | T | 11 | a0001c0001t0002g0018 a0001c0002t0001g0089 a0001c0002t0006g0033 others(8): Show |
11 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.693+1047G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15191861 | |||||||
| chr11:15192210 | G | A | 18 | a0001c0001t0001g0057 a0001c0001t0001g0067 a0001c0001t0001g0072 others(15): Show |
18 | HG00639.hp1 HG00735.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.693+1396G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15192210 | |||||||
| chr11:15192218 | A | C | 5 | a0002c0004t0001g0031 a0002c0004t0001g0219 a0002c0004t0001g0231 others(2): Show |
5 | HG02109.hp2 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.693+1404A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15192218 | |||||||
| chr11:15192342 | T | C | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.693+1528T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15192342 | |||||||
| chr11:15192417 | G | C | 77 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(74): Show |
81 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.693+1603G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15192417 | |||||||
| chr11:15192746 | G | C | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.693+1932G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15192746 | |||||||
| chr11:15192851 | C | A | 1 | a0001c0003t0001g0106 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.693+2037C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15192851 | |||||||
| chr11:15192915 | C | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(17): Show |
24 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.693+2101C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15192915 | |||||||
| chr11:15193023 | G | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(17): Show |
24 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.693+2209G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193023 | |||||||
| chr11:15193093 | G | C | 18 | a0001c0001t0003g0144 a0001c0001t0005g0094 a0001c0001t0005g0178 others(15): Show |
18 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+2279G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193093 | |||||||
| chr11:15193282 | T | C | 16 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0024 others(13): Show |
16 | HG02257.hp2 HG02486.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.693+2468T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193282 | |||||||
| chr11:15193386 | T | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0078 |
2 | HG01361.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.693+2572T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193386 | |||||||
| chr11:15193450 | C | A | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.693+2636C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193450 | |||||||
| chr11:15193489 | T | C | 4 | a0001c0002t0004g0007 a0001c0002t0004g0063 a0001c0002t0004g0103 others(1): Show |
4 | HG00639.hp1 HG01081.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+2675T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193489 | |||||||
| chr11:15193513 | T | A | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(62): Show |
69 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.693+2699T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193513 | |||||||
| chr11:15193539 | C | T | 6 | a0001c0001t0001g0191 a0001c0001t0002g0075 a0001c0001t0003g0013 others(3): Show |
6 | HG01074.hp1 NA18960.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+2725C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193539 | |||||||
| chr11:15193746 | A | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.693+2932A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193746 | |||||||
| chr11:15193935 | C | T | 1 | a0001c0003t0004g0192 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.693+3121C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15193935 | |||||||
| chr11:15193936 | A | AACC | 91 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.693+3125_693+3127d others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15193936 | ||||||
| chr11:15194290 | G | A | 10 | a0002c0004t0001g0031 a0002c0004t0001g0142 a0002c0004t0001g0219 others(7): Show |
10 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.693+3476G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15194290 | |||||||
| chr11:15194359 | G | C | 18 | a0001c0001t0003g0144 a0001c0001t0005g0094 a0001c0001t0005g0178 others(15): Show |
18 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+3545G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15194359 | |||||||
| chr11:15194418 | G | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(44): Show |
51 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.693+3604G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15194418 | |||||||
| chr11:15194681 | A | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(69): Show |
76 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.693+3867A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15194681 | |||||||
| chr11:15194706 | T | C | 18 | a0001c0001t0003g0144 a0001c0001t0005g0094 a0001c0001t0005g0178 others(15): Show |
18 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+3892T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15194706 | |||||||
| chr11:15194710 | G | A | 7 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(4): Show |
7 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+3896G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15194710 | |||||||
| chr11:15194789 | T | C | 3 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 |
4 | HG02451.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+3975T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15194789 | |||||||
| chr11:15194883 | G | T | 1 | a0001c0002t0006g0179 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.693+4069G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15194883 | |||||||
| chr11:15194907 | G | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.693+4093G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15194907 | |||||||
| chr11:15195010 | G | A | 18 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(15): Show |
18 | HG01243.hp2 HG02109.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.693+4196G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195010 | |||||||
| chr11:15195027 | A | G | 11 | a0001c0002t0023g0010 a0002c0004t0001g0031 a0002c0004t0001g0142 others(8): Show |
11 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.693+4213A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195027 | |||||||
| chr11:15195060 | C | A | 3 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 |
4 | HG02451.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.693+4246C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195060 | |||||||
| chr11:15195146 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(44): Show |
51 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.693+4332C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195146 | |||||||
| chr11:15195239 | T | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(72): Show |
79 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.693+4425T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195239 | |||||||
| chr11:15195293 | A | G | 1 | a0001c0002t0003g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.693+4479A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195293 | |||||||
| chr11:15195298 | T | A | 2 | a0001c0001t0002g0023 a0001c0001t0002g0024 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.693+4484T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195298 | |||||||
| chr11:15195340 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(234): Show |
243 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.693+4526A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195340 | |||||||
| chr11:15195403 | T | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(232): Show |
241 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(238): Show |
intron_variant | MODIFIER | c.693+4589T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195403 | |||||||
| chr11:15195728 | G | A | 11 | a0001c0002t0023g0010 a0002c0004t0001g0031 a0002c0004t0001g0142 others(8): Show |
11 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.693+4914G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195728 | |||||||
| chr11:15195911 | G | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-4913G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195911 | |||||||
| chr11:15195937 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(69): Show |
76 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.694-4887C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15195937 | |||||||
| chr11:15196119 | G | T | 11 | a0001c0002t0023g0010 a0002c0004t0001g0031 a0002c0004t0001g0142 others(8): Show |
11 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.694-4705G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196119 | |||||||
| chr11:15196210 | C | A | 11 | a0001c0002t0023g0010 a0002c0004t0001g0031 a0002c0004t0001g0142 others(8): Show |
11 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.694-4614C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196210 | |||||||
| chr11:15196210 | C | T | 19 | a0001c0001t0003g0144 a0001c0001t0005g0094 a0001c0001t0005g0178 others(16): Show |
19 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.694-4614C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196210 | |||||||
| chr11:15196216 | T | C | 3 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 |
4 | HG02451.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-4608T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196216 | |||||||
| chr11:15196411 | A | G | 19 | a0001c0001t0001g0235 a0001c0001t0002g0018 a0001c0001t0002g0151 others(16): Show |
19 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.694-4413A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196411 | |||||||
| chr11:15196423 | C | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(17): Show |
24 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.694-4401C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196423 | |||||||
| chr11:15196466 | C | T | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 |
3 | HG03209.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.694-4358C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196466 | |||||||
| chr11:15196482 | TA | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(51): Show |
58 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.694-4340delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15196482 | ||||||
| chr11:15196559 | C | T | 1 | a0001c0002t0003g0251 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.694-4265C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196559 | |||||||
| chr11:15196635 | G | A | 54 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(51): Show |
58 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.694-4189G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196635 | |||||||
| chr11:15196665 | C | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(53): Show |
60 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.694-4159C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196665 | |||||||
| chr11:15196702 | T | C | 1 | a0001c0001t0004g0001 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.694-4122T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196702 | |||||||
| chr11:15196756 | T | C | 1 | a0001c0002t0005g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.694-4068T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196756 | |||||||
| chr11:15196860 | TAAGGGAC others(3): Show |
T | 1 | a0001c0001t0001g0058 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.694-3962_694-3953d others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15196860 | ||||||
| chr11:15196944 | G | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0131 a0001c0001t0001g0184 others(5): Show |
8 | HG01069.hp1 HG01071.hp2 HG01993.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-3880G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15196944 | |||||||
| chr11:15197000 | C | T | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 |
3 | HG03209.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.694-3824C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197000 | |||||||
| chr11:15197122 | A | G | 6 | a0001c0001t0001g0090 a0001c0001t0001g0140 a0001c0001t0001g0154 others(3): Show |
6 | HG03831.hp1 NA18948.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.694-3702A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197122 | |||||||
| chr11:15197268 | T | C | 5 | a0001c0002t0001g0089 a0004c0006t0001g0136 a0004c0006t0001g0244 others(2): Show |
5 | HG02486.hp2 HG02818.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-3556T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197268 | |||||||
| chr11:15197332 | C | T | 1 | a0009c0010t0001g0111 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.694-3492C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197332 | |||||||
| chr11:15197454 | C | T | 4 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(1): Show |
4 | HG00735.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-3370C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197454 | |||||||
| chr11:15197549 | T | C | 1 | a0001c0003t0002g0194 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.694-3275T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197549 | |||||||
| chr11:15197686 | C | T | 1 | a0001c0002t0013g0159 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.694-3138C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197686 | |||||||
| chr11:15197712 | C | A | 17 | a0001c0001t0003g0144 a0001c0001t0005g0094 a0001c0001t0005g0178 others(14): Show |
17 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.694-3112C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197712 | |||||||
| chr11:15197785 | A | G | 1 | a0001c0001t0001g0053 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.694-3039A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197785 | |||||||
| chr11:15197916 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.694-2908G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15197916 | |||||||
| chr11:15198008 | G | GGTTCT | 18 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(15): Show |
22 | HG00733.hp1 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.694-2815_694-2811d others(7): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15198008 | ||||||
| chr11:15198008 | G | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0168 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.694-2816G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198008 | |||||||
| chr11:15198072 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.694-2752T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198072 | |||||||
| chr11:15198152 | G | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 |
3 | HG03209.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.694-2672G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198152 | |||||||
| chr11:15198262 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.694-2562C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198262 | |||||||
| chr11:15198373 | G | A | 2 | a0001c0001t0016g0042 a0001c0001t0016g0261 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.694-2451G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198373 | |||||||
| chr11:15198515 | G | A | 17 | a0001c0001t0002g0018 a0001c0002t0006g0033 a0001c0002t0006g0179 others(14): Show |
17 | HG02109.hp2 HG02257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.694-2309G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198515 | |||||||
| chr11:15198519 | G | A | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.694-2305G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198519 | |||||||
| chr11:15198527 | T | G | 151 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(148): Show |
153 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.694-2297T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198527 | |||||||
| chr11:15198765 | A | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0131 a0001c0001t0001g0184 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.694-2059A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198765 | |||||||
| chr11:15198858 | G | A | 10 | a0001c0001t0007g0030 a0001c0001t0007g0107 a0001c0001t0012g0129 others(7): Show |
10 | HG00639.hp1 HG01081.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.694-1966G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198858 | |||||||
| chr11:15198945 | C | T | 2 | a0001c0001t0001g0174 a0001c0003t0003g0254 |
2 | HG02074.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.694-1879C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198945 | |||||||
| chr11:15198994 | C | G | 91 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.694-1830C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15198994 | |||||||
| chr11:15199136 | C | T | 5 | a0001c0002t0001g0089 a0004c0006t0001g0136 a0004c0006t0001g0244 others(2): Show |
5 | HG02486.hp2 HG02818.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.694-1688C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15199136 | |||||||
| chr11:15199471 | A | G | 20 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0049 others(17): Show |
24 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.694-1353A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15199471 | |||||||
| chr11:15199546 | T | C | 83 | a0001c0001t0001g0012 a0001c0001t0001g0057 a0001c0001t0001g0067 others(80): Show |
83 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.694-1278T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15199546 | |||||||
| chr11:15199677 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.694-1147G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15199677 | |||||||
| chr11:15199757 | C | T | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-1067C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15199757 | |||||||
| chr11:15200153 | T | TCA | 74 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(71): Show |
75 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.694-634_694-633dup others(2): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200153 | ||||||
| chr11:15200153 | T | TCACA | 8 | a0001c0001t0001g0058 a0001c0001t0001g0090 a0001c0001t0005g0117 others(5): Show |
8 | HG00639.hp2 HG02056.hp2 HG06807.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-636_694-633dup others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200153 | ||||||
| chr11:15200153 | TCA | T | 44 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0055 others(41): Show |
48 | HG00099.hp2 HG00408.hp1 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.694-634_694-633del others(2): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200153 | ||||||
| chr11:15200153 | TCACA | T | 64 | a0001c0001t0001g0012 a0001c0001t0001g0072 a0001c0001t0001g0074 others(61): Show |
64 | HG00408.hp2 HG00639.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.694-636_694-633del others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200153 | ||||||
| chr11:15200153 | TCACACA | T | 14 | a0001c0001t0005g0080 a0001c0001t0005g0094 a0001c0002t0003g0045 others(11): Show |
14 | HG02109.hp2 HG02615.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.694-638_694-633del others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200153 | ||||||
| chr11:15200153 | TCACACAC others(1): Show |
T | 4 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(1): Show |
4 | HG00735.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-640_694-633del others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200153 | ||||||
| chr11:15200153 | TCACACAC others(3): Show |
T | 2 | a0001c0001t0021g0263 a0001c0003t0020g0101 |
2 | HG02129.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.694-642_694-633del others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200153 | ||||||
| chr11:15200153 | TCACACAC others(19): Show |
T | 3 | a0001c0001t0004g0006 a0001c0001t0004g0227 a0001c0001t0005g0019 |
4 | HG02451.hp1 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.694-658_694-633del others(26): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200153 | ||||||
| chr11:15200189 | A | ACG | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-634_694-633ins others(2): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200189 | ||||||
| chr11:15200315 | T | A | 1 | a0001c0001t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.694-509T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15200315 | |||||||
| chr11:15200475 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(113): Show |
120 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.694-349A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15200475 | |||||||
| chr11:15200531 | G | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.694-293G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15200531 | |||||||
| chr11:15200572 | G | A | 88 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(85): Show |
90 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.694-252G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15200572 | |||||||
| chr11:15200622 | G | A | 1 | a0001c0001t0004g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.694-202G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15200622 | |||||||
| chr11:15200674 | GAGTGTGT others(3): Show |
G | 1 | a0001c0001t0005g0080 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.694-140_694-131del others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr11 | 15200674 | ||||||
| chr11:15200698 | C | T | 1 | a0001c0001t0016g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.694-126C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15200698 | |||||||
| chr11:15200726 | G | A | 5 | a0001c0001t0003g0144 a0001c0001t0005g0178 a0001c0001t0005g0217 others(2): Show |
5 | HG01884.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-98G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 6/12 | chr11 | 15200726 | |||||||
| chr11:15201081 | G | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 |
3 | HG03209.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.819+132G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201081 | |||||||
| chr11:15201183 | A | G | 4 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(1): Show |
4 | HG02486.hp1 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+234A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201183 | |||||||
| chr11:15201215 | A | G | 1 | a0001c0001t0005g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.819+266A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201215 | |||||||
| chr11:15201243 | CAGGCAAG others(5): Show |
C | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.819+295_819+306del others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201243 | |||||||
| chr11:15201264 | C | T | 5 | a0001c0002t0001g0089 a0004c0006t0001g0136 a0004c0006t0001g0244 others(2): Show |
5 | HG02486.hp2 HG02818.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+315C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201264 | |||||||
| chr11:15201476 | G | T | 3 | a0001c0001t0003g0144 a0001c0001t0005g0217 a0001c0001t0005g0229 |
3 | HG01884.hp1 HG02895.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.819+527G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201476 | |||||||
| chr11:15201495 | G | T | 1 | a0001c0003t0006g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.819+546G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201495 | |||||||
| chr11:15201564 | C | T | 1 | a0001c0002t0004g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.819+615C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201564 | |||||||
| chr11:15201638 | C | T | 1 | a0003c0005t0001g0216 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.819+689C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201638 | |||||||
| chr11:15201645 | G | A | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.819+696G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201645 | |||||||
| chr11:15201742 | G | C | 2 | a0001c0001t0007g0030 a0001c0001t0012g0129 |
2 | HG01192.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.819+793G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201742 | |||||||
| chr11:15201770 | C | G | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.819+821C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201770 | |||||||
| chr11:15201904 | C | G | 90 | a0001c0001t0001g0004 a0001c0001t0001g0049 a0001c0001t0001g0079 others(87): Show |
93 | HG00408.hp2 HG00609.hp2 HG00733.hp1 others(90): Show |
intron_variant | MODIFIER | c.819+955C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201904 | |||||||
| chr11:15201923 | C | G | 169 | a0001c0001t0001g0004 a0001c0001t0001g0014 a0001c0001t0001g0028 others(166): Show |
172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.819+974C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201923 | |||||||
| chr11:15201935 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.819+986A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15201935 | |||||||
| chr11:15202085 | T | A | 12 | a0001c0001t0001g0036 a0001c0001t0001g0052 a0001c0001t0001g0058 others(9): Show |
12 | HG00609.hp1 HG01952.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.819+1136T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202085 | |||||||
| chr11:15202092 | A | G | 1 | a0001c0002t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+1143A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202092 | |||||||
| chr11:15202189 | G | A | 107 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(104): Show |
108 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.819+1240G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202189 | |||||||
| chr11:15202212 | T | G | 81 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(78): Show |
82 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.819+1263T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202212 | |||||||
| chr11:15202284 | T | C | 19 | a0001c0001t0002g0173 a0001c0001t0005g0094 a0001c0001t0008g0147 others(16): Show |
19 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.819+1335T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202284 | |||||||
| chr11:15202293 | G | A | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.819+1344G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202293 | |||||||
| chr11:15202489 | TGA | T | 8 | a0001c0002t0004g0007 a0001c0002t0004g0063 a0001c0002t0004g0103 others(5): Show |
8 | HG00639.hp1 HG01081.hp1 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.819+1550_819+1551d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15202489 | ||||||
| chr11:15202517 | G | A | 1 | a0001c0013t0017g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.819+1568G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202517 | |||||||
| chr11:15202548 | C | G | 1 | a0001c0002t0001g0089 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.819+1599C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202548 | |||||||
| chr11:15202598 | T | A | 16 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0039 others(13): Show |
16 | HG01069.hp1 HG01071.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.819+1649T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202598 | |||||||
| chr11:15202604 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.819+1655G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202604 | |||||||
| chr11:15202723 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.819+1774A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202723 | |||||||
| chr11:15202900 | G | A | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.819+1951G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15202900 | |||||||
| chr11:15203078 | A | T | 103 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(100): Show |
104 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.819+2129A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15203078 | |||||||
| chr11:15203169 | C | T | 20 | a0001c0001t0005g0094 a0001c0002t0001g0095 a0001c0002t0001g0116 others(17): Show |
20 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.819+2220C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15203169 | |||||||
| chr11:15203621 | T | C | 5 | a0001c0001t0001g0235 a0001c0001t0002g0151 a0001c0001t0005g0150 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.819+2672T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15203621 | |||||||
| chr11:15203640 | A | T | 20 | a0001c0001t0005g0094 a0001c0002t0001g0095 a0001c0002t0001g0116 others(17): Show |
20 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.819+2691A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15203640 | |||||||
| chr11:15203749 | A | G | 94 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(91): Show |
95 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.819+2800A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15203749 | |||||||
| chr11:15203762 | T | C | 7 | a0001c0001t0002g0018 a0001c0002t0006g0033 a0001c0002t0006g0179 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+2813T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15203762 | |||||||
| chr11:15203821 | A | AT | 23 | a0001c0001t0001g0057 a0001c0001t0001g0067 a0001c0001t0001g0072 others(20): Show |
23 | HG00735.hp2 HG01081.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.819+2883dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15203821 | ||||||
| chr11:15203821 | AT | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.819+2883delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15203821 | ||||||
| chr11:15203849 | GA | G | 110 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(107): Show |
111 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.819+2909delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15203849 | ||||||
| chr11:15204110 | C | T | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.819+3161C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204110 | |||||||
| chr11:15204112 | G | A | 232 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.819+3163G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204112 | |||||||
| chr11:15204139 | C | T | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.819+3190C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204139 | |||||||
| chr11:15204316 | T | C | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.819+3367T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204316 | |||||||
| chr11:15204317 | C | T | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.819+3368C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204317 | |||||||
| chr11:15204419 | T | C | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.819+3470T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204419 | |||||||
| chr11:15204450 | G | C | 17 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0080 others(14): Show |
17 | HG01192.hp2 HG01257.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.819+3501G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204450 | |||||||
| chr11:15204641 | A | G | 6 | a0003c0005t0001g0216 a0003c0005t0004g0064 a0003c0005t0004g0082 others(3): Show |
6 | HG00099.hp2 HG01361.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.819+3692A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204641 | |||||||
| chr11:15204730 | A | T | 215 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(212): Show |
218 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.819+3781A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204730 | |||||||
| chr11:15204754 | G | C | 1 | a0001c0001t0016g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.819+3805G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204754 | |||||||
| chr11:15204861 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.819+3912T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204861 | |||||||
| chr11:15204882 | C | T | 2 | a0001c0001t0006g0086 a0001c0001t0006g0087 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.819+3933C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204882 | |||||||
| chr11:15204926 | T | C | 100 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0029 others(97): Show |
101 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.819+3977T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15204926 | |||||||
| chr11:15205043 | C | T | 1 | a0001c0013t0017g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.819+4094C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15205043 | |||||||
| chr11:15205559 | C | T | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.819+4610C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15205559 | |||||||
| chr11:15205597 | G | C | 1 | a0001c0001t0005g0080 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.819+4648G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15205597 | |||||||
| chr11:15205640 | G | T | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.819+4691G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15205640 | |||||||
| chr11:15206089 | G | C | 1 | a0001c0001t0008g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.819+5140G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15206089 | |||||||
| chr11:15206384 | ACAGCAGG others(9): Show |
A | 1 | a0001c0001t0005g0080 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.819+5452_819+5467d others(18): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15206384 | ||||||
| chr11:15206443 | C | T | 131 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0036 others(128): Show |
132 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.819+5494C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15206443 | |||||||
| chr11:15206508 | C | T | 42 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0029 others(39): Show |
45 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.819+5559C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15206508 | |||||||
| chr11:15206597 | G | A | 1 | a0001c0001t0004g0133 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.819+5648G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15206597 | |||||||
| chr11:15206642 | G | C | 89 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(86): Show |
90 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.819+5693G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15206642 | |||||||
| chr11:15206829 | A | G | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.819+5880A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15206829 | |||||||
| chr11:15206833 | A | G | 26 | a0001c0001t0001g0235 a0001c0001t0002g0015 a0001c0001t0002g0151 others(23): Show |
26 | HG00735.hp1 HG01106.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.819+5884A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15206833 | |||||||
| chr11:15206904 | T | C | 232 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(229): Show |
235 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.819+5955T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15206904 | |||||||
| chr11:15206990 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.819+6041G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15206990 | |||||||
| chr11:15207228 | G | T | 1 | a0001c0001t0002g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.819+6279G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15207228 | |||||||
| chr11:15207372 | G | A | 1 | a0001c0001t0024g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.819+6423G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15207372 | |||||||
| chr11:15207394 | G | T | 58 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(55): Show |
59 | HG00408.hp2 HG00639.hp2 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.819+6445G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15207394 | |||||||
| chr11:15207448 | C | G | 91 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.819+6499C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15207448 | |||||||
| chr11:15207646 | C | T | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.819+6697C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15207646 | |||||||
| chr11:15207836 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.819+6887C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15207836 | |||||||
| chr11:15207876 | C | T | 1 | a0001c0003t0002g0194 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.819+6927C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15207876 | |||||||
| chr11:15207989 | G | A | 11 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(8): Show |
11 | HG02258.hp2 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+7040G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15207989 | |||||||
| chr11:15208277 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.819+7328C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15208277 | |||||||
| chr11:15208278 | C | T | 1 | a0001c0001t0003g0005 | 2 | HG02129.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.819+7329C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15208278 | |||||||
| chr11:15208358 | ACT | A | 17 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0080 others(14): Show |
17 | HG01192.hp2 HG01257.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.819+7412_819+7413d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15208358 | ||||||
| chr11:15208392 | G | C | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.819+7443G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15208392 | |||||||
| chr11:15208442 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+7493T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15208442 | |||||||
| chr11:15208463 | G | C | 11 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(8): Show |
11 | HG02258.hp2 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+7514G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15208463 | |||||||
| chr11:15208717 | G | A | 11 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(8): Show |
11 | HG02258.hp2 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.819+7768G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15208717 | |||||||
| chr11:15208724 | A | G | 107 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(104): Show |
108 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.819+7775A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15208724 | |||||||
| chr11:15208735 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.819+7786T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15208735 | |||||||
| chr11:15209059 | CAG | C | 17 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0080 others(14): Show |
17 | HG01192.hp2 HG01257.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.819+8115_819+8116d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15209059 | ||||||
| chr11:15209267 | G | C | 1 | a0001c0001t0003g0255 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.819+8318G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15209267 | |||||||
| chr11:15209349 | A | G | 1 | a0001c0002t0002g0121 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819+8400A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15209349 | |||||||
| chr11:15209398 | G | C | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.819+8449G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15209398 | |||||||
| chr11:15209766 | A | T | 1 | a0001c0001t0011g0181 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.819+8817A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15209766 | |||||||
| chr11:15209801 | G | A | 1 | a0001c0001t0001g0002 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.819+8852G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15209801 | |||||||
| chr11:15210307 | A | G | 20 | a0001c0002t0001g0089 a0001c0002t0001g0095 a0001c0002t0001g0116 others(17): Show |
20 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.819+9358A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15210307 | |||||||
| chr11:15210371 | A | AGCCTGTT others(17): Show |
99 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.819+9437_819+9460d others(26): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210371 | ||||||
| chr11:15210371 | A | AGCCTGTT others(41): Show |
1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.819+9460_819+9461i others(50): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210371 | ||||||
| chr11:15210400 | G | GTTCTGTG others(17): Show |
15 | a0001c0001t0001g0235 a0001c0001t0002g0173 a0001c0001t0005g0150 others(12): Show |
15 | HG00735.hp1 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.819+9460_819+9461i others(26): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210400 | ||||||
| chr11:15210502 | A | G | 7 | a0001c0002t0003g0016 a0001c0002t0003g0177 a0001c0002t0003g0222 others(4): Show |
7 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+9553A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15210502 | |||||||
| chr11:15210504 | T | G | 1 | a0001c0002t0003g0076 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.819+9555T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15210504 | |||||||
| chr11:15210505 | T | TGTGTGTG others(4): Show |
2 | a0001c0001t0002g0135 a0001c0002t0003g0157 |
2 | HG03704.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.819+9556_819+9557i others(13): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15210505 | |||||||
| chr11:15210505 | T | TTG | 22 | a0001c0001t0001g0004 a0001c0001t0001g0055 a0001c0001t0001g0146 others(19): Show |
22 | HG01069.hp2 HG01192.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.819+9597_819+9598d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210505 | ||||||
| chr11:15210505 | T | TTGTG | 14 | a0001c0001t0001g0090 a0001c0001t0001g0235 a0001c0001t0002g0120 others(11): Show |
14 | HG00639.hp2 HG01074.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.819+9595_819+9598d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210505 | ||||||
| chr11:15210505 | T | TTGTGTG | 25 | a0001c0001t0002g0015 a0001c0001t0002g0025 a0001c0001t0002g0091 others(22): Show |
25 | HG00639.hp1 HG01081.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.819+9593_819+9598d others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210505 | ||||||
| chr11:15210505 | T | TTGTGTGT others(1): Show |
35 | a0001c0001t0001g0115 a0001c0001t0001g0118 a0001c0001t0002g0003 others(32): Show |
36 | HG01070.hp2 HG01071.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.819+9591_819+9598d others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210505 | ||||||
| chr11:15210505 | T | TTGTGTGT others(3): Show |
14 | a0001c0001t0001g0134 a0001c0001t0002g0027 a0001c0001t0002g0124 others(11): Show |
14 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.819+9589_819+9598d others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210505 | ||||||
| chr11:15210505 | T | TTGTGTGT others(5): Show |
5 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0006g0008 others(2): Show |
5 | HG00621.hp1 HG03098.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.819+9587_819+9598d others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210505 | ||||||
| chr11:15210505 | T | TTGTGTGT others(7): Show |
1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.819+9585_819+9598d others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210505 | ||||||
| chr11:15210505 | TTG | T | 16 | a0001c0001t0001g0028 a0001c0001t0001g0036 a0001c0001t0001g0052 others(13): Show |
17 | HG00609.hp1 HG01074.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.819+9597_819+9598d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210505 | ||||||
| chr11:15210505 | TTGTG | T | 71 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0029 others(68): Show |
71 | HG00099.hp2 HG00609.hp2 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.819+9595_819+9598d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15210505 | ||||||
| chr11:15210753 | C | G | 26 | a0001c0002t0001g0089 a0001c0002t0001g0095 a0001c0002t0001g0116 others(23): Show |
26 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.819+9804C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15210753 | |||||||
| chr11:15210817 | T | G | 2 | a0001c0003t0004g0225 a0001c0003t0004g0240 |
2 | HG01884.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.819+9868T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15210817 | |||||||
| chr11:15210828 | G | A | 1 | a0001c0001t0016g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.819+9879G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15210828 | |||||||
| chr11:15211000 | G | A | 2 | a0001c0001t0002g0241 a0001c0001t0008g0195 |
2 | HG02976.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.819+10051G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211000 | |||||||
| chr11:15211032 | A | T | 4 | a0001c0001t0002g0009 a0001c0001t0002g0032 a0001c0001t0002g0130 others(1): Show |
4 | HG01243.hp1 HG02630.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+10083A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211032 | |||||||
| chr11:15211113 | G | A | 1 | a0001c0003t0002g0137 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.819+10164G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211113 | |||||||
| chr11:15211120 | TA | T | 90 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.819+10173delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15211120 | ||||||
| chr11:15211133 | A | G | 1 | a0001c0003t0001g0065 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.819+10184A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211133 | |||||||
| chr11:15211146 | T | C | 1 | a0001c0001t0005g0022 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.819+10197T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211146 | |||||||
| chr11:15211152 | G | A | 101 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.819+10203G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211152 | |||||||
| chr11:15211176 | A | T | 4 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(1): Show |
4 | HG00735.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.819+10227A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211176 | |||||||
| chr11:15211236 | C | T | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.820-10241C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211236 | |||||||
| chr11:15211490 | T | A | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-9987T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211490 | |||||||
| chr11:15211543 | T | A | 9 | a0001c0002t0001g0089 a0001c0002t0004g0007 a0001c0002t0004g0063 others(6): Show |
9 | HG00639.hp1 HG01081.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.820-9934T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211543 | |||||||
| chr11:15211573 | G | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.820-9904G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211573 | |||||||
| chr11:15211778 | G | A | 101 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.820-9699G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211778 | |||||||
| chr11:15211808 | T | G | 1 | a0002c0017t0001g0199 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.820-9669T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15211808 | |||||||
| chr11:15211856 | A | AT | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.820-9611dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15211856 | ||||||
| chr11:15211969 | CTTCT | C | 2 | a0001c0001t0001g0112 a0001c0001t0018g0098 |
2 | HG02135.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.820-9505_820-9502d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15211969 | ||||||
| chr11:15212187 | C | T | 57 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(54): Show |
58 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.820-9290C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212187 | |||||||
| chr11:15212324 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-9153T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212324 | |||||||
| chr11:15212450 | G | A | 90 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(87): Show |
91 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.820-9027G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212450 | |||||||
| chr11:15212584 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.820-8893T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212584 | |||||||
| chr11:15212609 | T | C | 5 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0005g0150 others(2): Show |
5 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-8868T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212609 | |||||||
| chr11:15212649 | C | G | 1 | a0001c0001t0012g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.820-8828C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212649 | |||||||
| chr11:15212705 | T | A | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-8772T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212705 | |||||||
| chr11:15212781 | C | A | 96 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.820-8696C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212781 | |||||||
| chr11:15212830 | A | T | 5 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0005g0150 others(2): Show |
5 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-8647A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212830 | |||||||
| chr11:15212893 | C | T | 5 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0005g0150 others(2): Show |
5 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-8584C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15212893 | |||||||
| chr11:15213140 | G | GT | 91 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.820-8325dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr11 | 15213140 | ||||||
| chr11:15213142 | T | TG | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-8335_820-8334i others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15213142 | |||||||
| chr11:15213205 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.820-8272C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15213205 | |||||||
| chr11:15213466 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-8011T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15213466 | |||||||
| chr11:15213506 | T | C | 26 | a0001c0002t0001g0089 a0001c0002t0001g0095 a0001c0002t0001g0116 others(23): Show |
26 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.820-7971T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15213506 | |||||||
| chr11:15213619 | C | G | 100 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(97): Show |
101 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.820-7858C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15213619 | |||||||
| chr11:15213718 | G | A | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-7759G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15213718 | |||||||
| chr11:15213934 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-7543C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15213934 | |||||||
| chr11:15213947 | C | G | 106 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(103): Show |
107 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.820-7530C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15213947 | |||||||
| chr11:15214351 | G | T | 96 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.820-7126G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15214351 | |||||||
| chr11:15214367 | C | T | 1 | a0001c0001t0014g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.820-7110C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15214367 | |||||||
| chr11:15214368 | G | A | 4 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0141 others(1): Show |
4 | HG00609.hp2 NA18952.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-7109G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15214368 | |||||||
| chr11:15214437 | A | G | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.820-7040A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15214437 | |||||||
| chr11:15214924 | G | A | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.820-6553G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15214924 | |||||||
| chr11:15215042 | A | G | 1 | a0005c0007t0001g0215 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.820-6435A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215042 | |||||||
| chr11:15215239 | A | G | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-6238A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215239 | |||||||
| chr11:15215356 | C | G | 1 | a0001c0001t0012g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.820-6121C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215356 | |||||||
| chr11:15215398 | G | C | 1 | a0001c0001t0007g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.820-6079G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215398 | |||||||
| chr11:15215441 | C | G | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-6036C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215441 | |||||||
| chr11:15215497 | G | A | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.820-5980G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215497 | |||||||
| chr11:15215533 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-5944C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215533 | |||||||
| chr11:15215560 | G | T | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-5917G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215560 | |||||||
| chr11:15215583 | T | G | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-5894T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215583 | |||||||
| chr11:15215606 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.820-5871C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215606 | |||||||
| chr11:15215641 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-5836T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215641 | |||||||
| chr11:15215658 | C | A | 101 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.820-5819C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215658 | |||||||
| chr11:15215693 | G | C | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.820-5784G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215693 | |||||||
| chr11:15215695 | A | G | 114 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.820-5782A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215695 | |||||||
| chr11:15215816 | A | T | 96 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(93): Show |
97 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.820-5661A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215816 | |||||||
| chr11:15215917 | C | A | 1 | a0005c0007t0014g0155 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.820-5560C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215917 | |||||||
| chr11:15215947 | G | A | 101 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.820-5530G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15215947 | |||||||
| chr11:15216003 | T | C | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-5474T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216003 | |||||||
| chr11:15216142 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.820-5335A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216142 | |||||||
| chr11:15216201 | T | C | 1 | a0001c0001t0002g0241 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.820-5276T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216201 | |||||||
| chr11:15216205 | C | A | 5 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(2): Show |
5 | HG03209.hp1 NA18906.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.820-5272C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216205 | |||||||
| chr11:15216208 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.820-5269G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216208 | |||||||
| chr11:15216459 | T | G | 1 | a0001c0001t0002g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.820-5018T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216459 | |||||||
| chr11:15216629 | G | T | 1 | a0001c0001t0005g0117 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.820-4848G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216629 | |||||||
| chr11:15216663 | C | A | 12 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0024 others(9): Show |
12 | HG02109.hp2 HG02559.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.820-4814C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216663 | |||||||
| chr11:15216870 | G | T | 91 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.820-4607G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216870 | |||||||
| chr11:15216960 | G | A | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-4517G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216960 | |||||||
| chr11:15216971 | G | A | 1 | a0002c0004t0001g0253 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.820-4506G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15216971 | |||||||
| chr11:15217169 | A | G | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.820-4308A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15217169 | |||||||
| chr11:15217276 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.820-4201G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15217276 | |||||||
| chr11:15217352 | T | C | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.820-4125T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15217352 | |||||||
| chr11:15217574 | G | C | 1 | a0001c0001t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.820-3903G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15217574 | |||||||
| chr11:15217808 | G | A | 60 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(57): Show |
61 | HG00408.hp2 HG00639.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.820-3669G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15217808 | |||||||
| chr11:15217878 | C | A | 4 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(1): Show |
4 | HG00735.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.820-3599C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15217878 | |||||||
| chr11:15217950 | C | T | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.820-3527C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15217950 | |||||||
| chr11:15217953 | T | C | 1 | a0001c0003t0020g0101 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.820-3524T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15217953 | |||||||
| chr11:15217981 | A | G | 4 | a0001c0001t0005g0080 a0001c0001t0005g0193 a0001c0001t0007g0030 others(1): Show |
4 | HG01192.hp2 HG01257.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-3496A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15217981 | |||||||
| chr11:15218023 | C | T | 2 | a0001c0001t0002g0207 a0001c0003t0002g0194 |
2 | NA18959.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.820-3454C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218023 | |||||||
| chr11:15218054 | A | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(95): Show |
100 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.820-3423A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218054 | |||||||
| chr11:15218334 | A | G | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 |
3 | HG03209.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.820-3143A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218334 | |||||||
| chr11:15218345 | T | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(95): Show |
100 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.820-3132T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218345 | |||||||
| chr11:15218431 | G | A | 1 | a0001c0001t0012g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.820-3046G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218431 | |||||||
| chr11:15218448 | T | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(95): Show |
100 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.820-3029T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218448 | |||||||
| chr11:15218454 | T | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(95): Show |
100 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.820-3023T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218454 | |||||||
| chr11:15218560 | C | A | 2 | a0001c0001t0001g0202 a0001c0001t0002g0075 |
2 | HG01074.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.820-2917C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218560 | |||||||
| chr11:15218562 | C | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0028 others(56): Show |
61 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.820-2915C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218562 | |||||||
| chr11:15218564 | A | C | 50 | a0001c0001t0002g0119 a0001c0001t0002g0207 a0001c0001t0002g0224 others(47): Show |
50 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.820-2913A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218564 | |||||||
| chr11:15218566 | A | C | 17 | a0001c0001t0016g0042 a0001c0002t0001g0095 a0001c0002t0001g0116 others(14): Show |
17 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.820-2911A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218566 | |||||||
| chr11:15218604 | G | A | 13 | a0001c0001t0001g0036 a0001c0001t0001g0052 a0001c0001t0001g0058 others(10): Show |
13 | HG00609.hp1 HG01952.hp1 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.820-2873G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218604 | |||||||
| chr11:15218643 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.820-2834A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218643 | |||||||
| chr11:15218668 | G | A | 91 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(88): Show |
92 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.820-2809G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218668 | |||||||
| chr11:15218863 | G | T | 24 | a0001c0001t0001g0235 a0001c0001t0002g0173 a0001c0001t0005g0150 others(21): Show |
24 | HG00735.hp1 HG01106.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.820-2614G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218863 | |||||||
| chr11:15218865 | C | T | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.820-2612C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15218865 | |||||||
| chr11:15219083 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.820-2394T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15219083 | |||||||
| chr11:15219329 | C | T | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.820-2148C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15219329 | |||||||
| chr11:15219706 | G | A | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.820-1771G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15219706 | |||||||
| chr11:15219722 | C | T | 1 | a0002c0004t0001g0242 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.820-1755C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15219722 | |||||||
| chr11:15219765 | C | G | 1 | a0001c0013t0017g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.820-1712C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15219765 | |||||||
| chr11:15219774 | G | C | 60 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(57): Show |
61 | HG00408.hp2 HG00639.hp2 HG01070.hp2 others(58): Show |
intron_variant | MODIFIER | c.820-1703G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15219774 | |||||||
| chr11:15219880 | T | C | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.820-1597T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15219880 | |||||||
| chr11:15219948 | G | A | 1 | a0001c0002t0007g0068 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.820-1529G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15219948 | |||||||
| chr11:15219988 | A | G | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.820-1489A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15219988 | |||||||
| chr11:15220008 | T | C | 1 | a0001c0001t0002g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.820-1469T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15220008 | |||||||
| chr11:15220013 | T | C | 1 | a0001c0003t0001g0106 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.820-1464T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15220013 | |||||||
| chr11:15220278 | G | A | 1 | a0003c0005t0004g0082 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.820-1199G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15220278 | |||||||
| chr11:15220290 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.820-1187C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15220290 | |||||||
| chr11:15220305 | C | T | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.820-1172C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15220305 | |||||||
| chr11:15220497 | G | A | 1 | a0001c0001t0004g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.820-980G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15220497 | |||||||
| chr11:15220512 | C | T | 58 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(55): Show |
59 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.820-965C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15220512 | |||||||
| chr11:15220551 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.820-926T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15220551 | |||||||
| chr11:15220943 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.820-534C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15220943 | |||||||
| chr11:15221014 | C | T | 5 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0126 others(2): Show |
5 | HG01256.hp2 HG03239.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-463C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15221014 | |||||||
| chr11:15221051 | C | G | 231 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.820-426C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15221051 | |||||||
| chr11:15221071 | A | T | 7 | a0001c0002t0001g0095 a0001c0002t0001g0116 a0001c0002t0003g0045 others(4): Show |
7 | HG00408.hp1 HG00621.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.820-406A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15221071 | |||||||
| chr11:15221197 | A | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0259 |
2 | HG03831.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.820-280A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15221197 | |||||||
| chr11:15221204 | A | C | 5 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-273A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15221204 | |||||||
| chr11:15221220 | C | T | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.820-257C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15221220 | |||||||
| chr11:15221222 | G | A | 5 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-255G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 7/12 | chr11 | 15221222 | |||||||
| chr11:15221821 | T | C | 41 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0005g0150 others(38): Show |
41 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.991+173T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15221821 | |||||||
| chr11:15221846 | A | G | 46 | a0001c0001t0001g0235 a0001c0001t0002g0173 a0001c0001t0002g0232 others(43): Show |
46 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.991+198A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15221846 | |||||||
| chr11:15221966 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.991+318G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15221966 | |||||||
| chr11:15222047 | T | C | 46 | a0001c0001t0001g0235 a0001c0001t0002g0173 a0001c0001t0002g0232 others(43): Show |
46 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.991+399T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222047 | |||||||
| chr11:15222133 | C | T | 8 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.991+485C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222133 | |||||||
| chr11:15222204 | C | T | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.991+556C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222204 | |||||||
| chr11:15222260 | A | G | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.991+612A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222260 | |||||||
| chr11:15222262 | C | T | 95 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(92): Show |
96 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.991+614C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222262 | |||||||
| chr11:15222269 | C | G | 97 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(94): Show |
98 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.991+621C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222269 | |||||||
| chr11:15222397 | T | C | 231 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(228): Show |
234 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.991+749T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222397 | |||||||
| chr11:15222422 | T | C | 212 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.991+774T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222422 | |||||||
| chr11:15222480 | A | G | 1 | a0001c0002t0001g0123 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.991+832A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222480 | |||||||
| chr11:15222523 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.991+875C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222523 | |||||||
| chr11:15222634 | T | C | 41 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0005g0150 others(38): Show |
41 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.991+986T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222634 | |||||||
| chr11:15222669 | C | T | 1 | a0004c0006t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.991+1021C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222669 | |||||||
| chr11:15222692 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.991+1044A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222692 | |||||||
| chr11:15222929 | G | T | 1 | a0001c0001t0002g0078 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.991+1281G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222929 | |||||||
| chr11:15222975 | T | G | 106 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(103): Show |
107 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.991+1327T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15222975 | |||||||
| chr11:15223159 | A | G | 1 | a0001c0001t0002g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.991+1511A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15223159 | |||||||
| chr11:15223229 | A | G | 65 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(62): Show |
66 | HG00408.hp2 HG00639.hp2 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.991+1581A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15223229 | |||||||
| chr11:15223572 | C | T | 104 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(101): Show |
105 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.991+1924C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15223572 | |||||||
| chr11:15223779 | T | C | 6 | a0004c0006t0001g0136 a0004c0006t0001g0244 a0004c0006t0001g0245 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-1871T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15223779 | |||||||
| chr11:15224000 | T | C | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.992-1650T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15224000 | |||||||
| chr11:15224317 | G | C | 1 | a0001c0001t0001g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.992-1333G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15224317 | |||||||
| chr11:15224367 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0146 a0001c0001t0001g0168 |
3 | HG00738.hp2 HG00741.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.992-1283A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15224367 | |||||||
| chr11:15224493 | C | T | 1 | a0001c0002t0008g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.992-1157C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15224493 | |||||||
| chr11:15224602 | C | T | 1 | a0001c0003t0002g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.992-1048C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15224602 | |||||||
| chr11:15224836 | G | A | 41 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0005g0150 others(38): Show |
41 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.992-814G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15224836 | |||||||
| chr11:15224839 | T | C | 26 | a0001c0002t0001g0089 a0001c0002t0001g0095 a0001c0002t0001g0116 others(23): Show |
26 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.992-811T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15224839 | |||||||
| chr11:15224973 | GTC | G | 5 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(2): Show |
5 | HG03209.hp1 NA18906.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.992-671_992-670del others(2): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr11 | 15224973 | ||||||
| chr11:15225020 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.992-630C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15225020 | |||||||
| chr11:15225039 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.992-611G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15225039 | |||||||
| chr11:15225154 | C | T | 6 | a0004c0006t0001g0136 a0004c0006t0001g0244 a0004c0006t0001g0245 others(3): Show |
6 | HG02486.hp2 HG02818.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.992-496C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15225154 | |||||||
| chr11:15225192 | C | T | 1 | a0001c0012t0001g0204 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.992-458C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15225192 | |||||||
| chr11:15225197 | T | C | 1 | a0001c0003t0002g0158 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.992-453T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15225197 | |||||||
| chr11:15225321 | T | C | 1 | a0001c0001t0002g0070 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.992-329T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15225321 | |||||||
| chr11:15225340 | A | G | 106 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(103): Show |
107 | HG00408.hp1 HG00408.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.992-310A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15225340 | |||||||
| chr11:15225446 | G | A | 41 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0005g0150 others(38): Show |
41 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.992-204G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15225446 | |||||||
| chr11:15225618 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.992-32C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 8/12 | chr11 | 15225618 | |||||||
| chr11:15225854 | A | C | 41 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0005g0150 others(38): Show |
41 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.1170+26A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15225854 | |||||||
| chr11:15225921 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1170+93G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15225921 | |||||||
| chr11:15226102 | C | T | 193 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(190): Show |
196 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.1170+274C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226102 | |||||||
| chr11:15226187 | C | T | 1 | a0001c0001t0006g0175 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1170+359C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226187 | |||||||
| chr11:15226199 | T | C | 37 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0003g0020 others(34): Show |
37 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1170+371T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226199 | |||||||
| chr11:15226253 | G | A | 1 | a0001c0001t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1170+425G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226253 | |||||||
| chr11:15226293 | T | C | 195 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(192): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.1170+465T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226293 | |||||||
| chr11:15226306 | C | T | 9 | a0001c0002t0003g0016 a0001c0002t0003g0076 a0001c0002t0003g0177 others(6): Show |
9 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+478C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226306 | |||||||
| chr11:15226333 | A | G | 196 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(193): Show |
199 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1170+505A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226333 | |||||||
| chr11:15226441 | A | C | 37 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0003g0020 others(34): Show |
37 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1170+613A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226441 | |||||||
| chr11:15226685 | C | T | 1 | a0001c0002t0004g0103 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1170+857C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226685 | |||||||
| chr11:15226815 | A | AC | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1170+987_1170+988i others(3): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226815 | |||||||
| chr11:15226817 | G | T | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1170+989G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226817 | |||||||
| chr11:15226983 | C | T | 162 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(159): Show |
165 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1170+1155C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226983 | |||||||
| chr11:15226984 | C | T | 1 | a0001c0001t0005g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1170+1156C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226984 | |||||||
| chr11:15226985 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1170+1157G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15226985 | |||||||
| chr11:15227037 | A | G | 58 | a0001c0001t0001g0079 a0001c0001t0001g0090 a0001c0001t0001g0115 others(55): Show |
59 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.1170+1209A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227037 | |||||||
| chr11:15227115 | C | T | 156 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1170+1287C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227115 | |||||||
| chr11:15227133 | G | A | 26 | a0001c0001t0001g0235 a0001c0001t0002g0232 a0001c0001t0003g0020 others(23): Show |
26 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1170+1305G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227133 | |||||||
| chr11:15227332 | T | C | 1 | a0001c0001t0007g0030 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1170+1504T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227332 | |||||||
| chr11:15227549 | G | A | 4 | a0004c0006t0001g0136 a0004c0006t0001g0244 a0004c0006t0001g0245 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+1721G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227549 | |||||||
| chr11:15227622 | G | T | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1170+1794G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227622 | |||||||
| chr11:15227648 | A | G | 205 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(202): Show |
208 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1170+1820A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227648 | |||||||
| chr11:15227673 | T | C | 9 | a0001c0002t0001g0089 a0001c0002t0004g0007 a0001c0002t0004g0063 others(6): Show |
9 | HG00639.hp1 HG01081.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+1845T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227673 | |||||||
| chr11:15227696 | C | T | 1 | a0001c0001t0016g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1170+1868C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227696 | |||||||
| chr11:15227762 | C | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0126 others(3): Show |
6 | HG01256.hp2 HG02735.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+1934C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15227762 | |||||||
| chr11:15228171 | T | C | 2 | a0001c0002t0001g0139 a0001c0002t0001g0247 |
2 | HG00621.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1170+2343T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228171 | |||||||
| chr11:15228303 | C | G | 4 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(1): Show |
4 | HG00735.hp1 HG02109.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+2475C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228303 | |||||||
| chr11:15228342 | G | T | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1170+2514G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228342 | |||||||
| chr11:15228389 | C | T | 5 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(2): Show |
5 | HG03209.hp1 NA18906.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+2561C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228389 | |||||||
| chr11:15228419 | C | T | 189 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(186): Show |
192 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(189): Show |
intron_variant | MODIFIER | c.1170+2591C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228419 | |||||||
| chr11:15228472 | C | A | 156 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(153): Show |
159 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1170+2644C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228472 | |||||||
| chr11:15228763 | C | T | 9 | a0001c0002t0001g0089 a0001c0002t0004g0007 a0001c0002t0004g0063 others(6): Show |
9 | HG00639.hp1 HG01081.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+2935C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228763 | |||||||
| chr11:15228785 | G | C | 1 | a0001c0003t0002g0114 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1170+2957G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228785 | |||||||
| chr11:15228829 | TC | T | 5 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(2): Show |
5 | HG03209.hp1 NA18906.hp2 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+3003delC | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15228829 | ||||||
| chr11:15228848 | G | T | 15 | a0001c0002t0001g0089 a0001c0002t0004g0007 a0001c0002t0004g0063 others(12): Show |
15 | HG00639.hp1 HG01081.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1170+3020G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228848 | |||||||
| chr11:15228856 | G | A | 155 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(152): Show |
157 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1170+3028G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228856 | |||||||
| chr11:15228922 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.1170+3094C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228922 | |||||||
| chr11:15228981 | A | G | 1 | a0001c0001t0011g0181 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1170+3153A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15228981 | |||||||
| chr11:15229105 | C | A | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1170+3277C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229105 | |||||||
| chr11:15229105 | C | T | 167 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(164): Show |
170 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.1170+3277C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229105 | |||||||
| chr11:15229136 | A | C | 1 | a0001c0002t0003g0076 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1170+3308A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229136 | |||||||
| chr11:15229380 | T | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(96): Show |
101 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(98): Show |
intron_variant | MODIFIER | c.1170+3552T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229380 | |||||||
| chr11:15229395 | A | G | 16 | a0001c0002t0001g0089 a0001c0002t0004g0007 a0001c0002t0004g0063 others(13): Show |
16 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1170+3567A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229395 | |||||||
| chr11:15229420 | G | A | 207 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(204): Show |
210 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.1170+3592G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229420 | |||||||
| chr11:15229615 | G | A | 1 | a0001c0002t0001g0139 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1170+3787G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229615 | |||||||
| chr11:15229632 | G | A | 1 | a0001c0001t0012g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1170+3804G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229632 | |||||||
| chr11:15229689 | C | T | 4 | a0004c0006t0001g0136 a0004c0006t0001g0244 a0004c0006t0001g0245 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+3861C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229689 | |||||||
| chr11:15229704 | T | C | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 |
3 | HG03209.hp1 NA18906.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1170+3876T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229704 | |||||||
| chr11:15229861 | CAGCCTGG others(142): Show |
C | 2 | a0004c0008t0015g0034 a0004c0008t0015g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1170+4035_1170+418 others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229861 | ||||||
| chr11:15229873 | C | T | 2 | a0001c0003t0001g0066 a0001c0003t0002g0158 |
2 | HG01346.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.1170+4045C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229873 | |||||||
| chr11:15229919 | A | T | 6 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(3): Show |
6 | HG00735.hp1 HG02109.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+4091A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229919 | |||||||
| chr11:15229920 | A | T | 166 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(163): Show |
169 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.1170+4092A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229920 | |||||||
| chr11:15229925 | T | G | 16 | a0001c0002t0001g0089 a0001c0002t0004g0007 a0001c0002t0004g0063 others(13): Show |
16 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.1170+4097T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229925 | |||||||
| chr11:15229928 | T | TATATTAT others(9): Show |
2 | a0001c0001t0003g0144 a0001c0001t0005g0217 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1170+4116_1170+413 others(20): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229928 | ||||||
| chr11:15229928 | T | TATATTTT others(9): Show |
1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1170+4105_1170+410 others(20): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229928 | ||||||
| chr11:15229944 | AATATTAT others(49): Show |
A | 30 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0092 others(27): Show |
30 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1170+4121_1170+417 others(60): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229944 | ||||||
| chr11:15229944 | AATATTAT others(51): Show |
A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0105 |
2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1170+4121_1170+417 others(62): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229944 | ||||||
| chr11:15229945 | ATAT | A | 66 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(63): Show |
68 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1170+4121_1170+412 others(7): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229945 | ||||||
| chr11:15229948 | TTATATAT others(11): Show |
T | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1170+4132_1170+414 others(22): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229948 | ||||||
| chr11:15229948 | TTATATAT others(42): Show |
T | 1 | a0002c0017t0001g0199 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1170+4132_1170+418 others(53): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229948 | ||||||
| chr11:15229948 | TTATATAT others(46): Show |
T | 1 | a0001c0003t0002g0237 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1170+4132_1170+418 others(57): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229948 | ||||||
| chr11:15229950 | A | T | 7 | a0001c0002t0006g0033 a0001c0002t0006g0179 a0001c0002t0006g0252 others(4): Show |
7 | HG00639.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1170+4122A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229950 | |||||||
| chr11:15229950 | ATATATAT others(3): Show |
A | 2 | a0001c0003t0019g0172 a0001c0003t0020g0101 |
2 | HG02129.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1170+4132_1170+414 others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229950 | ||||||
| chr11:15229957 | TA | T | 66 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(63): Show |
68 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1170+4130delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229957 | |||||||
| chr11:15229958 | AT | A | 5 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+4133delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229958 | ||||||
| chr11:15229958 | ATTTATAT others(4): Show |
A | 1 | a0001c0003t0002g0137 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1170+4131_1170+414 others(15): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229958 | |||||||
| chr11:15229959 | T | TAA | 3 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0002t0023g0010 |
3 | HG02647.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1170+4131_1170+413 others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229959 | |||||||
| chr11:15229959 | T | TAATA | 26 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0080 others(23): Show |
26 | HG01106.hp2 HG01192.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.1170+4131_1170+413 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229959 | |||||||
| chr11:15229959 | TTTATATA | T | 4 | a0001c0001t0001g0118 a0001c0001t0002g0027 a0001c0001t0005g0019 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4133_1170+413 others(11): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229959 | ||||||
| chr11:15229959 | TTTATATA others(2): Show |
T | 47 | a0001c0001t0001g0115 a0001c0001t0001g0134 a0001c0001t0002g0003 others(44): Show |
48 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1170+4133_1170+414 others(13): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229959 | ||||||
| chr11:15229959 | TTTATATA others(8): Show |
T | 11 | a0001c0002t0001g0095 a0001c0002t0001g0116 a0001c0002t0001g0123 others(8): Show |
11 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+4133_1170+414 others(19): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229959 | ||||||
| chr11:15229959 | TTTATATA others(33): Show |
T | 2 | a0001c0001t0001g0079 a0001c0001t0002g0044 |
2 | HG02074.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1170+4133_1170+417 others(44): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229959 | ||||||
| chr11:15229959 | TTTATATA others(37): Show |
T | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1170+4133_1170+417 others(48): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229959 | ||||||
| chr11:15229960 | T | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0055 others(48): Show |
54 | HG00639.hp1 HG00639.hp2 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.1170+4132T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229960 | |||||||
| chr11:15229961 | T | A | 8 | a0001c0001t0002g0173 a0001c0001t0003g0020 a0001c0001t0003g0021 others(5): Show |
8 | HG00735.hp1 HG02109.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170+4133T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229961 | |||||||
| chr11:15229962 | A | AT | 17 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0146 others(14): Show |
19 | HG00733.hp1 HG00738.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.1170+4135dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229962 | ||||||
| chr11:15229962 | A | T | 5 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0002t0023g0010 others(2): Show |
5 | HG02647.hp2 HG03209.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1170+4134A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229962 | |||||||
| chr11:15229963 | TA | T | 6 | a0001c0001t0001g0073 a0001c0001t0003g0255 a0001c0001t0004g0006 others(3): Show |
7 | HG01884.hp2 HG02451.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1170+4136delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229963 | |||||||
| chr11:15229963 | TATATATA others(25): Show |
T | 4 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(1): Show |
4 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4136_1170+416 others(36): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229963 | |||||||
| chr11:15229963 | TATATATA others(29): Show |
T | 1 | a0001c0001t0001g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1170+4136_1170+417 others(40): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229963 | |||||||
| chr11:15229963 | TATATATA others(43): Show |
T | 49 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(46): Show |
51 | HG00099.hp1 HG01081.hp2 HG01256.hp1 others(48): Show |
intron_variant | MODIFIER | c.1170+4152_1170+420 others(54): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229963 | ||||||
| chr11:15229964 | A | ATATATAA others(19): Show |
2 | a0001c0001t0003g0144 a0001c0001t0005g0217 |
2 | HG01884.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1170+4142_1170+414 others(30): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229964 | ||||||
| chr11:15229964 | A | ATATATAT others(31): Show |
1 | a0001c0002t0003g0243 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1170+4144_1170+414 others(42): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229964 | ||||||
| chr11:15229964 | A | ATATATAT others(35): Show |
14 | a0001c0001t0005g0022 a0001c0001t0005g0102 a0001c0001t0005g0163 others(11): Show |
14 | HG01106.hp2 HG02055.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1170+4144_1170+414 others(46): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229964 | ||||||
| chr11:15229964 | A | ATATATAT others(76): Show |
4 | a0001c0001t0005g0080 a0001c0001t0005g0178 a0001c0001t0007g0030 others(1): Show |
4 | HG01192.hp2 HG01257.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4144_1170+414 others(87): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229964 | ||||||
| chr11:15229964 | A | ATATATAT others(21): Show |
1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1170+4144_1170+414 others(32): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229964 | ||||||
| chr11:15229965 | TATATATA others(23): Show |
T | 2 | a0001c0001t0016g0261 a0008c0015t0001g0093 |
2 | HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1170+4138_1170+416 others(34): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229965 | |||||||
| chr11:15229965 | TATATATA others(27): Show |
T | 2 | a0004c0006t0001g0244 a0004c0006t0001g0245 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1170+4138_1170+417 others(38): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229965 | |||||||
| chr11:15229965 | TATATATA others(29): Show |
T | 1 | a0004c0006t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1170+4138_1170+417 others(40): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229965 | |||||||
| chr11:15229965 | TATATATA others(41): Show |
T | 12 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0125 others(9): Show |
12 | HG00099.hp2 HG00609.hp1 HG02698.hp2 others(9): Show |
intron_variant | MODIFIER | c.1170+4152_1170+419 others(52): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229965 | ||||||
| chr11:15229965 | TATATATA others(44): Show |
T | 15 | a0001c0002t0001g0089 a0001c0002t0004g0007 a0001c0002t0004g0063 others(12): Show |
15 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1170+4138_1170+418 others(55): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229965 | |||||||
| chr11:15229966 | A | ATATATAA others(72): Show |
1 | a0001c0001t0012g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1170+4144_1170+414 others(83): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229966 | ||||||
| chr11:15229967 | T | A | 4 | a0001c0001t0001g0118 a0001c0001t0002g0027 a0001c0001t0005g0019 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4139T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229967 | |||||||
| chr11:15229967 | TATATATA others(39): Show |
T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0141 a0001c0001t0004g0133 |
3 | HG00609.hp2 HG00735.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1170+4152_1170+419 others(50): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229967 | ||||||
| chr11:15229968 | A | ATATAATA others(61): Show |
1 | a0001c0001t0005g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1170+4144_1170+414 others(72): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229968 | ||||||
| chr11:15229969 | T | A | 47 | a0001c0001t0001g0115 a0001c0001t0001g0134 a0001c0001t0002g0003 others(44): Show |
48 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.1170+4141T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229969 | |||||||
| chr11:15229969 | TATATATA others(37): Show |
T | 1 | a0001c0001t0001g0164 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1170+4152_1170+419 others(48): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229969 | ||||||
| chr11:15229970 | A | ATAATATT others(45): Show |
2 | a0001c0001t0005g0198 a0001c0001t0006g0088 |
2 | HG02280.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1170+4144_1170+414 others(56): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229970 | ||||||
| chr11:15229970 | ATATATAT others(46): Show |
A | 1 | a0001c0001t0001g0196 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1170+4143_1170+419 others(57): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229970 | |||||||
| chr11:15229971 | TATATATA others(35): Show |
T | 1 | a0001c0001t0005g0094 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1170+4152_1170+419 others(46): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229971 | ||||||
| chr11:15229971 | TATATATA others(40): Show |
T | 5 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(2): Show |
5 | HG00735.hp1 HG02109.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+4144_1170+419 others(51): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229971 | |||||||
| chr11:15229974 | AT | A | 4 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(1): Show |
4 | HG02647.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4147delT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229974 | |||||||
| chr11:15229975 | T | A | 11 | a0001c0002t0001g0095 a0001c0002t0001g0116 a0001c0002t0001g0123 others(8): Show |
11 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+4147T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229975 | |||||||
| chr11:15229975 | T | TA | 18 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0102 others(15): Show |
18 | HG01106.hp2 HG01884.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1170+4148dupA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229975 | ||||||
| chr11:15229978 | A | T | 4 | a0001c0001t0001g0118 a0001c0001t0002g0027 a0001c0001t0005g0019 others(1): Show |
4 | HG02622.hp1 HG02809.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4150A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229978 | |||||||
| chr11:15229979 | TTATA | T | 6 | a0001c0001t0001g0002 a0001c0001t0001g0146 a0001c0001t0001g0168 others(3): Show |
8 | HG00738.hp2 HG01069.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1170+4182_1170+418 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229979 | ||||||
| chr11:15229979 | TTATATA | T | 3 | a0001c0001t0001g0202 a0001c0001t0002g0062 a0001c0001t0002g0078 |
3 | HG01361.hp1 HG02293.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1170+4180_1170+418 others(10): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229979 | ||||||
| chr11:15229979 | TTATATAT others(1): Show |
T | 6 | a0001c0001t0001g0049 a0001c0001t0002g0075 a0001c0001t0004g0071 others(3): Show |
6 | HG00738.hp1 HG01074.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+4178_1170+418 others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229979 | ||||||
| chr11:15229979 | TTATATAT others(3): Show |
T | 4 | a0001c0001t0001g0190 a0001c0001t0004g0234 a0001c0001t0007g0107 others(1): Show |
4 | HG00741.hp1 HG01433.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170+4176_1170+418 others(14): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229979 | ||||||
| chr11:15229980 | T | A | 3 | a0001c0001t0001g0073 a0001c0001t0005g0198 a0001c0001t0006g0088 |
3 | HG02280.hp2 HG03209.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1170+4152T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229980 | |||||||
| chr11:15229981 | A | T | 52 | a0001c0001t0001g0073 a0001c0001t0001g0115 a0001c0001t0001g0134 others(49): Show |
53 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.1170+4153A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229981 | |||||||
| chr11:15229984 | TATATATA others(22): Show |
T | 1 | a0001c0001t0005g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1170+4184_1170+421 others(33): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229984 | ||||||
| chr11:15229985 | A | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0168 |
2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1170+4157A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229985 | |||||||
| chr11:15229989 | A | AATAT | 17 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0102 others(14): Show |
17 | HG01106.hp2 HG01884.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.1170+4161_1170+416 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229989 | |||||||
| chr11:15229990 | TATATATA others(16): Show |
T | 1 | a0001c0001t0006g0008 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1170+4186_1170+420 others(27): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229990 | ||||||
| chr11:15229991 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0004g0236 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1170+4164_1170+417 others(15): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229991 | |||||||
| chr11:15229992 | TATA | T | 4 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(1): Show |
4 | HG02647.hp2 HG03209.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4165_1170+416 others(7): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229992 | |||||||
| chr11:15229992 | TATATA | T | 11 | a0001c0002t0001g0095 a0001c0002t0001g0116 a0001c0002t0001g0123 others(8): Show |
11 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+4165_1170+416 others(9): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229992 | |||||||
| chr11:15229992 | TATATATA others(14): Show |
T | 1 | a0001c0001t0001g0118 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1170+4186_1170+420 others(25): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229992 | ||||||
| chr11:15229996 | TATATATA others(10): Show |
T | 5 | a0001c0001t0002g0009 a0001c0001t0002g0120 a0001c0001t0002g0207 others(2): Show |
5 | HG01074.hp2 HG03017.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1170+4186_1170+420 others(21): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229996 | ||||||
| chr11:15229997 | A | T | 10 | a0001c0001t0001g0235 a0001c0001t0003g0020 a0001c0001t0003g0021 others(7): Show |
10 | HG02258.hp2 HG02647.hp2 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+4169A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229997 | |||||||
| chr11:15229998 | TA | T | 4 | a0001c0001t0005g0080 a0001c0001t0005g0178 a0001c0001t0005g0193 others(1): Show |
4 | HG02258.hp1 HG02280.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4171delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229998 | |||||||
| chr11:15229998 | TATATATA others(8): Show |
T | 6 | a0001c0001t0002g0091 a0001c0001t0002g0135 a0001c0001t0002g0206 others(3): Show |
6 | HG02056.hp2 HG02071.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170+4186_1170+420 others(19): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229998 | ||||||
| chr11:15229999 | A | AT | 13 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0102 others(10): Show |
13 | HG01884.hp1 HG02055.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1170+4172dupT | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15229999 | ||||||
| chr11:15229999 | A | T | 11 | a0001c0002t0001g0095 a0001c0002t0001g0116 a0001c0002t0001g0123 others(8): Show |
11 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.1170+4171A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15229999 | |||||||
| chr11:15230000 | T | A | 2 | a0001c0001t0001g0079 a0001c0001t0002g0044 |
2 | HG02074.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1170+4172T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230000 | |||||||
| chr11:15230000 | TA | T | 4 | a0001c0002t0003g0076 a0001c0002t0003g0177 a0001c0002t0003g0260 others(1): Show |
4 | HG01106.hp2 HG02145.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1170+4173delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230000 | |||||||
| chr11:15230000 | TATATATA others(6): Show |
T | 8 | a0001c0001t0002g0119 a0001c0001t0002g0145 a0001c0001t0002g0224 others(5): Show |
8 | HG01346.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1170+4186_1170+419 others(17): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15230000 | ||||||
| chr11:15230001 | A | T | 2 | a0004c0006t0001g0244 a0004c0006t0001g0245 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1170+4173A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230001 | |||||||
| chr11:15230002 | TATATATA others(4): Show |
T | 4 | a0001c0001t0001g0115 a0001c0001t0002g0250 a0001c0001t0011g0181 others(1): Show |
4 | HG01433.hp2 HG01993.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4186_1170+419 others(15): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15230002 | ||||||
| chr11:15230003 | A | T | 1 | a0004c0006t0001g0136 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1170+4175A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230003 | |||||||
| chr11:15230004 | T | A | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1170+4176T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230004 | |||||||
| chr11:15230004 | TATATATA others(2): Show |
T | 10 | a0001c0001t0002g0070 a0001c0001t0002g0130 a0001c0001t0002g0151 others(7): Show |
10 | HG01243.hp2 HG01516.hp2 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1170+4186_1170+419 others(13): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15230004 | ||||||
| chr11:15230005 | A | G | 1 | a0001c0009t0010g0262 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1170+4177A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230005 | |||||||
| chr11:15230006 | TATATATA | T | 8 | a0001c0001t0001g0134 a0001c0001t0002g0003 a0001c0001t0002g0025 others(5): Show |
9 | HG00408.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170+4186_1170+419 others(11): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15230006 | ||||||
| chr11:15230007 | A | G | 1 | a0001c0009t0010g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1170+4179A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230007 | |||||||
| chr11:15230008 | TATATA | T | 3 | a0001c0001t0002g0153 a0001c0001t0002g0180 a0001c0001t0002g0208 |
3 | NA19009.hp2 NA19030.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1170+4186_1170+419 others(9): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15230008 | ||||||
| chr11:15230010 | TATA | T | 4 | a0001c0001t0002g0060 a0001c0001t0002g0132 a0001c0001t0002g0166 others(1): Show |
4 | NA18967.hp2 NA18973.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.1170+4186_1170+418 others(7): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15230010 | ||||||
| chr11:15230011 | A | G | 1 | a0001c0009t0010g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1170+4183A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230011 | |||||||
| chr11:15230011 | A | T | 33 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0079 others(30): Show |
33 | HG01069.hp1 HG01070.hp1 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.1170+4183A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230011 | |||||||
| chr11:15230012 | T | A | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1170+4184T>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230012 | |||||||
| chr11:15230012 | TA | T | 12 | a0001c0001t0001g0055 a0001c0001t0002g0015 a0001c0001t0002g0027 others(9): Show |
13 | HG01515.hp1 HG01517.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1170+4186delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15230012 | ||||||
| chr11:15230012 | TAATA | T | 5 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(2): Show |
5 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1170+4185_1170+418 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230012 | |||||||
| chr11:15230013 | A | ATATATAT others(20): Show |
1 | a0001c0009t0010g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1170+4185_1170+418 others(31): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230013 | |||||||
| chr11:15230013 | A | ATATATAT others(18): Show |
1 | a0001c0009t0010g0262 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1170+4185_1170+418 others(29): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230013 | |||||||
| chr11:15230013 | A | ATTAT | 6 | a0001c0001t0005g0022 a0001c0001t0005g0102 a0001c0001t0005g0163 others(3): Show |
6 | HG02717.hp1 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1170+4185_1170+418 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230013 | |||||||
| chr11:15230013 | A | G | 2 | a0004c0008t0015g0034 a0004c0008t0015g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1170+4185A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230013 | |||||||
| chr11:15230013 | A | T | 35 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0079 others(32): Show |
35 | HG00733.hp2 HG01069.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1170+4185A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230013 | |||||||
| chr11:15230014 | A | T | 37 | a0001c0001t0001g0061 a0001c0001t0001g0083 a0001c0001t0001g0105 others(34): Show |
37 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1170+4186A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230014 | |||||||
| chr11:15230016 | A | T | 2 | a0001c0001t0021g0263 a0002c0017t0001g0199 |
2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1170+4188A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230016 | |||||||
| chr11:15230017 | T | C | 2 | a0004c0008t0015g0034 a0004c0008t0015g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1170+4189T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230017 | |||||||
| chr11:15230018 | A | T | 17 | a0001c0002t0001g0089 a0001c0002t0004g0007 a0001c0002t0004g0063 others(14): Show |
17 | HG00639.hp1 HG00639.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.1170+4190A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230018 | |||||||
| chr11:15230019 | TATA | T | 15 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0255 others(12): Show |
15 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1170+4192_1170+419 others(7): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230019 | |||||||
| chr11:15230020 | A | T | 7 | a0001c0001t0002g0173 a0001c0001t0008g0147 a0001c0001t0008g0148 others(4): Show |
7 | HG00735.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1170+4192A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230020 | |||||||
| chr11:15230024 | A | T | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1170+4196A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230024 | |||||||
| chr11:15230026 | A | T | 1 | a0001c0003t0002g0237 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1170+4198A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230026 | |||||||
| chr11:15230041 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1170+4213A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230041 | |||||||
| chr11:15230063 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1170+4235A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230063 | |||||||
| chr11:15230115 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1170+4287G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230115 | |||||||
| chr11:15230145 | G | A | 28 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0080 others(25): Show |
28 | HG01106.hp2 HG01192.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1170+4317G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230145 | |||||||
| chr11:15230504 | C | A | 1 | a0001c0001t0001g0259 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1170+4676C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230504 | |||||||
| chr11:15230601 | G | T | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1170+4773G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230601 | |||||||
| chr11:15230607 | T | C | 162 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(159): Show |
165 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1170+4779T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230607 | |||||||
| chr11:15230758 | C | T | 4 | a0004c0006t0001g0136 a0004c0006t0001g0244 a0004c0006t0001g0245 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1171-4844C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230758 | |||||||
| chr11:15230886 | A | T | 224 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(221): Show |
227 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.1171-4716A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230886 | |||||||
| chr11:15230898 | A | G | 162 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(159): Show |
165 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1171-4704A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230898 | |||||||
| chr11:15230962 | C | T | 1 | a0001c0016t0002g0201 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1171-4640C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15230962 | |||||||
| chr11:15231020 | G | A | 2 | a0004c0006t0001g0244 a0004c0006t0001g0245 |
2 | HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1171-4582G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15231020 | |||||||
| chr11:15231349 | C | A | 6 | a0001c0001t0005g0080 a0001c0001t0005g0178 a0001c0001t0005g0193 others(3): Show |
6 | HG01192.hp2 HG01257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-4253C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15231349 | |||||||
| chr11:15231412 | G | A | 209 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1171-4190G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15231412 | |||||||
| chr11:15231502 | G | T | 6 | a0001c0002t0006g0033 a0001c0002t0006g0179 a0001c0002t0006g0252 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-4100G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15231502 | |||||||
| chr11:15231659 | C | T | 1 | a0001c0001t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1171-3943C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15231659 | |||||||
| chr11:15231746 | T | G | 1 | a0001c0001t0016g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1171-3856T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15231746 | |||||||
| chr11:15231857 | C | T | 1 | a0001c0001t0005g0019 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1171-3745C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15231857 | |||||||
| chr11:15231936 | A | G | 45 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0144 others(42): Show |
45 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1171-3666A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15231936 | |||||||
| chr11:15231990 | G | A | 2 | a0003c0005t0009g0171 a0003c0005t0009g0249 |
2 | HG00099.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1171-3612G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15231990 | |||||||
| chr11:15232027 | C | T | 231 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0028 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.1171-3575C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232027 | |||||||
| chr11:15232166 | G | C | 6 | a0001c0001t0001g0235 a0001c0001t0005g0150 a0001c0001t0005g0187 others(3): Show |
6 | HG02258.hp2 HG03139.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1171-3436G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232166 | |||||||
| chr11:15232174 | G | A | 43 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0144 others(40): Show |
43 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(40): Show |
intron_variant | MODIFIER | c.1171-3428G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232174 | |||||||
| chr11:15232291 | T | G | 1 | a0003c0005t0009g0249 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1171-3311T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232291 | |||||||
| chr11:15232296 | C | T | 6 | a0001c0002t0006g0033 a0001c0002t0006g0179 a0001c0002t0006g0252 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-3306C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232296 | |||||||
| chr11:15232324 | G | T | 11 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0102 others(8): Show |
11 | HG01884.hp1 HG02280.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171-3278G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232324 | |||||||
| chr11:15232338 | A | G | 6 | a0001c0002t0006g0033 a0001c0002t0006g0179 a0001c0002t0006g0252 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-3264A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232338 | |||||||
| chr11:15232341 | G | A | 4 | a0004c0006t0001g0136 a0004c0006t0001g0244 a0004c0006t0001g0245 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1171-3261G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232341 | |||||||
| chr11:15232404 | A | T | 223 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(220): Show |
226 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.1171-3198A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232404 | |||||||
| chr11:15232448 | G | A | 28 | a0001c0001t0003g0144 a0001c0001t0005g0022 a0001c0001t0005g0080 others(25): Show |
28 | HG01106.hp2 HG01192.hp2 HG01257.hp1 others(25): Show |
intron_variant | MODIFIER | c.1171-3154G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232448 | |||||||
| chr11:15232512 | G | T | 1 | a0001c0001t0002g0206 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1171-3090G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232512 | |||||||
| chr11:15232516 | G | C | 259 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(256): Show |
265 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.1171-3086G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232516 | |||||||
| chr11:15232537 | G | A | 4 | a0004c0006t0001g0136 a0004c0006t0001g0244 a0004c0006t0001g0245 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1171-3065G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232537 | |||||||
| chr11:15232592 | G | A | 208 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(205): Show |
211 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1171-3010G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232592 | |||||||
| chr11:15232650 | G | A | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1171-2952G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232650 | |||||||
| chr11:15232652 | G | T | 2 | a0001c0009t0010g0258 a0001c0009t0010g0262 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1171-2950G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232652 | |||||||
| chr11:15232780 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1171-2822C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232780 | |||||||
| chr11:15232850 | C | G | 100 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0014 others(97): Show |
102 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.1171-2752C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232850 | |||||||
| chr11:15232858 | T | C | 1 | a0001c0013t0017g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1171-2744T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15232858 | |||||||
| chr11:15233113 | T | C | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1171-2489T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15233113 | |||||||
| chr11:15233529 | G | A | 1 | a0001c0001t0022g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1171-2073G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15233529 | |||||||
| chr11:15233530 | A | G | 1 | a0001c0001t0022g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1171-2072A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15233530 | |||||||
| chr11:15233583 | ATCTAAAT others(5): Show |
A | 1 | a0001c0001t0022g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1171-2017_1171-200 others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15233583 | ||||||
| chr11:15233694 | G | GTCCT | 65 | a0001c0001t0001g0002 a0001c0001t0001g0061 a0001c0001t0001g0073 others(62): Show |
67 | HG00621.hp2 HG00733.hp2 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.1171-1894_1171-189 others(8): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15233694 | ||||||
| chr11:15233694 | G | GTCCTTCC others(1): Show |
42 | a0001c0001t0001g0055 a0001c0001t0001g0099 a0001c0001t0002g0015 others(39): Show |
42 | HG00621.hp1 HG00639.hp2 HG02040.hp2 others(39): Show |
intron_variant | MODIFIER | c.1171-1898_1171-189 others(12): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15233694 | ||||||
| chr11:15233694 | G | GTCCTTCC others(5): Show |
1 | a0001c0001t0003g0144 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1171-1902_1171-189 others(16): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr11 | 15233694 | ||||||
| chr11:15233878 | A | T | 2 | a0001c0002t0023g0010 a0001c0013t0017g0081 |
2 | HG00639.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1171-1724A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15233878 | |||||||
| chr11:15233960 | C | G | 3 | a0001c0001t0016g0261 a0001c0002t0023g0010 a0001c0013t0017g0081 |
3 | HG00639.hp2 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1171-1642C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15233960 | |||||||
| chr11:15234004 | C | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0090 others(8): Show |
11 | HG02040.hp1 HG02040.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.1171-1598C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15234004 | |||||||
| chr11:15234161 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0056 a0001c0001t0001g0090 others(8): Show |
11 | HG02040.hp1 HG02056.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1171-1441G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15234161 | |||||||
| chr11:15234547 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1171-1055G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15234547 | |||||||
| chr11:15234640 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1171-962T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15234640 | |||||||
| chr11:15234721 | T | G | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1171-881T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15234721 | |||||||
| chr11:15234996 | G | A | 2 | a0001c0002t0003g0016 a0001c0002t0003g0222 |
2 | HG02922.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1171-606G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15234996 | |||||||
| chr11:15235165 | C | T | 2 | a0001c0001t0001g0099 a0001c0001t0001g0246 |
2 | NA18953.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.1171-437C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15235165 | |||||||
| chr11:15235421 | A | T | 6 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0105 others(3): Show |
6 | HG01192.hp1 HG01256.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.1171-181A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15235421 | |||||||
| chr11:15235462 | C | T | 1 | a0001c0001t0008g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1171-140C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15235462 | |||||||
| chr11:15235470 | G | A | 2 | a0001c0001t0002g0207 a0001c0003t0002g0194 |
2 | NA18959.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1171-132G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15235470 | |||||||
| chr11:15235500 | G | A | 29 | a0001c0001t0003g0013 a0001c0001t0003g0020 a0001c0001t0003g0021 others(26): Show |
29 | HG00408.hp1 HG00621.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1171-102G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 9/12 | chr11 | 15235500 | |||||||
| chr11:15235696 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1237+28A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15235696 | |||||||
| chr11:15235871 | C | T | 1 | a0001c0002t0001g0089 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1237+203C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15235871 | |||||||
| chr11:15235872 | A | T | 1 | a0001c0001t0002g0075 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1237+204A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15235872 | |||||||
| chr11:15235882 | C | G | 1 | a0001c0001t0005g0178 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1237+214C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15235882 | |||||||
| chr11:15236055 | CAA | C | 19 | a0001c0001t0001g0053 a0001c0001t0001g0197 a0001c0001t0003g0020 others(16): Show |
19 | HG00621.hp2 HG01516.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.1237+409_1237+410d others(4): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 15236055 | ||||||
| chr11:15236055 | CAAA | C | 146 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(143): Show |
151 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1237+408_1237+410d others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 15236055 | ||||||
| chr11:15236055 | CAAAA | C | 34 | a0001c0001t0001g0061 a0001c0001t0001g0090 a0001c0001t0001g0235 others(31): Show |
34 | HG00639.hp2 HG00735.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.1237+407_1237+410d others(6): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 15236055 | ||||||
| chr11:15236088 | G | A | 1 | a0001c0003t0006g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1237+420G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236088 | |||||||
| chr11:15236112 | A | G | 1 | a0001c0001t0006g0149 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1237+444A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236112 | |||||||
| chr11:15236252 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1237+584C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236252 | |||||||
| chr11:15236253 | G | A | 23 | a0001c0001t0003g0013 a0001c0001t0003g0054 a0001c0001t0003g0069 others(20): Show |
23 | HG00408.hp1 HG00621.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.1237+585G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236253 | |||||||
| chr11:15236297 | G | T | 10 | a0001c0001t0001g0036 a0001c0001t0001g0052 a0001c0001t0001g0125 others(7): Show |
11 | HG00609.hp1 HG02071.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1237+629G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236297 | |||||||
| chr11:15236365 | TA | T | 20 | a0001c0001t0002g0173 a0001c0001t0005g0022 a0001c0001t0005g0080 others(17): Show |
20 | HG00735.hp1 HG01192.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1237+705delA | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr11 | 15236365 | ||||||
| chr11:15236371 | A | T | 20 | a0001c0001t0002g0173 a0001c0001t0005g0022 a0001c0001t0005g0080 others(17): Show |
20 | HG00735.hp1 HG01192.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.1237+703A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236371 | |||||||
| chr11:15236422 | A | G | 1 | a0001c0013t0017g0081 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1237+754A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236422 | |||||||
| chr11:15236455 | G | C | 1 | a0001c0001t0008g0195 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1237+787G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236455 | |||||||
| chr11:15236485 | C | T | 65 | a0001c0001t0002g0173 a0001c0001t0003g0013 a0001c0001t0003g0020 others(62): Show |
65 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1237+817C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236485 | |||||||
| chr11:15236535 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1237+867C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236535 | |||||||
| chr11:15236588 | G | A | 29 | a0001c0001t0003g0013 a0001c0001t0003g0020 a0001c0001t0003g0021 others(26): Show |
29 | HG00408.hp1 HG00621.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1237+920G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236588 | |||||||
| chr11:15236700 | G | A | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1237+1032G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236700 | |||||||
| chr11:15236743 | G | A | 29 | a0001c0001t0003g0013 a0001c0001t0003g0020 a0001c0001t0003g0021 others(26): Show |
29 | HG00408.hp1 HG00621.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1237+1075G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236743 | |||||||
| chr11:15236964 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1237+1296G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236964 | |||||||
| chr11:15236986 | C | T | 1 | a0001c0001t0002g0180 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1237+1318C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15236986 | |||||||
| chr11:15237087 | A | G | 18 | a0001c0001t0005g0022 a0001c0001t0005g0080 a0001c0001t0005g0102 others(15): Show |
18 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1237+1419A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15237087 | |||||||
| chr11:15237440 | C | T | 196 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(193): Show |
201 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.1238-1479C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15237440 | |||||||
| chr11:15237510 | G | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0144 a0001c0001t0003g0255 |
3 | HG02895.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1238-1409G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15237510 | |||||||
| chr11:15237629 | A | T | 1 | a0001c0001t0001g0122 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1238-1290A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15237629 | |||||||
| chr11:15237691 | A | G | 1 | a0001c0001t0011g0186 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1238-1228A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15237691 | |||||||
| chr11:15237790 | C | A | 16 | a0001c0001t0006g0008 a0001c0001t0006g0086 a0001c0001t0006g0087 others(13): Show |
16 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.1238-1129C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15237790 | |||||||
| chr11:15237927 | G | C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0138 a0001c0001t0001g0156 |
3 | NA18944.hp2 NA18948.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1238-992G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15237927 | |||||||
| chr11:15238174 | G | C | 1 | a0001c0001t0004g0041 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1238-745G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15238174 | |||||||
| chr11:15238178 | G | A | 1 | a0001c0001t0002g0173 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1238-741G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15238178 | |||||||
| chr11:15238269 | A | T | 260 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(257): Show |
266 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(263): Show |
intron_variant | MODIFIER | c.1238-650A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15238269 | |||||||
| chr11:15238554 | T | C | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(198): Show |
206 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.1238-365T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15238554 | |||||||
| chr11:15238578 | A | C | 147 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(144): Show |
152 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.1238-341A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15238578 | |||||||
| chr11:15238767 | G | A | 1 | a0001c0001t0004g0001 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1238-152G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15238767 | |||||||
| chr11:15238821 | C | G | 16 | a0001c0001t0006g0008 a0001c0001t0006g0086 a0001c0001t0006g0087 others(13): Show |
16 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.1238-98C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 10/12 | chr11 | 15238821 | |||||||
| chr11:15239210 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0024 |
3 | HG02717.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1393+136G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239210 | |||||||
| chr11:15239295 | T | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(127): Show |
135 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.1393+221T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239295 | |||||||
| chr11:15239336 | C | T | 4 | a0001c0001t0001g0061 a0001c0001t0001g0073 a0001c0001t0001g0202 others(1): Show |
4 | HG01261.hp1 HG02273.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1393+262C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239336 | |||||||
| chr11:15239432 | T | C | 1 | a0001c0001t0002g0232 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1393+358T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239432 | |||||||
| chr11:15239515 | A | G | 16 | a0001c0001t0006g0008 a0001c0001t0006g0086 a0001c0001t0006g0087 others(13): Show |
16 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.1393+441A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239515 | |||||||
| chr11:15239687 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1393+613A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239687 | |||||||
| chr11:15239761 | G | A | 2 | a0004c0008t0015g0034 a0004c0008t0015g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1394-686G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239761 | |||||||
| chr11:15239783 | A | T | 5 | a0001c0001t0008g0147 a0001c0001t0008g0148 a0001c0001t0008g0170 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394-664A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239783 | |||||||
| chr11:15239826 | T | G | 1 | a0001c0002t0003g0016 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1394-621T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239826 | |||||||
| chr11:15239837 | G | A | 4 | a0001c0001t0008g0147 a0001c0001t0008g0148 a0001c0001t0008g0170 others(1): Show |
4 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394-610G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239837 | |||||||
| chr11:15239954 | T | C | 1 | a0001c0002t0001g0089 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1394-493T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15239954 | |||||||
| chr11:15240003 | C | G | 18 | a0001c0001t0006g0008 a0001c0001t0006g0086 a0001c0001t0006g0087 others(15): Show |
18 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.1394-444C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240003 | |||||||
| chr11:15240039 | A | G | 5 | a0001c0001t0008g0147 a0001c0001t0008g0148 a0001c0001t0008g0170 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394-408A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240039 | |||||||
| chr11:15240087 | C | T | 6 | a0001c0001t0002g0003 a0001c0001t0002g0037 a0001c0001t0002g0038 others(3): Show |
7 | HG00099.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1394-360C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240087 | |||||||
| chr11:15240122 | T | C | 133 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(130): Show |
137 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.1394-325T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240122 | |||||||
| chr11:15240145 | A | G | 135 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(132): Show |
139 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.1394-302A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240145 | |||||||
| chr11:15240151 | T | C | 4 | a0001c0001t0001g0090 a0001c0002t0007g0050 a0001c0002t0007g0165 others(1): Show |
4 | NA18949.hp1 NA18969.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1394-296T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240151 | |||||||
| chr11:15240177 | A | G | 1 | a0001c0001t0016g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1394-270A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240177 | |||||||
| chr11:15240203 | T | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(197): Show |
205 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.1394-244T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240203 | |||||||
| chr11:15240279 | C | T | 2 | a0004c0008t0015g0034 a0004c0008t0015g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1394-168C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240279 | |||||||
| chr11:15240280 | G | A | 19 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0041 others(16): Show |
21 | HG00639.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1394-167G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240280 | |||||||
| chr11:15240329 | G | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(202): Show |
210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1394-118G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 11/12 | chr11 | 15240329 | |||||||
| chr11:15240701 | A | G | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1470+178A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15240701 | |||||||
| chr11:15240715 | A | G | 19 | a0001c0001t0004g0001 a0001c0001t0004g0006 a0001c0001t0004g0041 others(16): Show |
21 | HG00639.hp1 HG00733.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1470+192A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15240715 | |||||||
| chr11:15240775 | C | G | 150 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(147): Show |
154 | HG00099.hp2 HG00408.hp2 HG00609.hp1 others(151): Show |
intron_variant | MODIFIER | c.1470+252C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15240775 | |||||||
| chr11:15240802 | G | A | 1 | a0001c0001t0021g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1470+279G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15240802 | |||||||
| chr11:15240809 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0196 a0001c0001t0001g0259 |
3 | HG02135.hp1 NA18948.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1470+286C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15240809 | |||||||
| chr11:15240863 | C | A | 6 | a0001c0001t0002g0009 a0001c0001t0002g0032 a0001c0001t0002g0130 others(3): Show |
6 | HG00735.hp1 HG01243.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470+340C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15240863 | |||||||
| chr11:15240913 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(197): Show |
205 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.1470+390A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15240913 | |||||||
| chr11:15241006 | G | A | 20 | a0001c0001t0005g0022 a0001c0001t0005g0080 a0001c0001t0005g0102 others(17): Show |
20 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1470+483G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15241006 | |||||||
| chr11:15241010 | A | G | 4 | a0004c0006t0001g0136 a0004c0006t0001g0244 a0004c0006t0001g0245 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1470+487A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15241010 | |||||||
| chr11:15241147 | T | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(202): Show |
210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1470+624T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15241147 | |||||||
| chr11:15241148 | G | A | 1 | a0001c0001t0005g0193 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1470+625G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15241148 | |||||||
| chr11:15241157 | A | G | 18 | a0001c0001t0005g0022 a0001c0001t0005g0080 a0001c0001t0005g0102 others(15): Show |
18 | HG01192.hp2 HG01884.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.1470+634A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15241157 | |||||||
| chr11:15241193 | A | G | 23 | a0001c0001t0003g0005 a0001c0001t0003g0013 a0001c0001t0003g0054 others(20): Show |
24 | HG00408.hp1 HG00621.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1470+670A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15241193 | |||||||
| chr11:15241548 | G | A | 2 | a0001c0001t0016g0042 a0001c0001t0016g0261 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1470+1025G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15241548 | |||||||
| chr11:15242106 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1470+1583C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15242106 | |||||||
| chr11:15242442 | T | C | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(140): Show |
147 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(144): Show |
intron_variant | MODIFIER | c.1470+1919T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15242442 | |||||||
| chr11:15242620 | A | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(202): Show |
210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.1470+2097A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15242620 | |||||||
| chr11:15243014 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1470+2491C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15243014 | |||||||
| chr11:15243100 | A | G | 2 | a0001c0001t0003g0203 a0001c0002t0003g0251 |
2 | HG00408.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.1470+2577A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15243100 | |||||||
| chr11:15243285 | G | C | 25 | a0001c0001t0006g0008 a0001c0001t0006g0086 a0001c0001t0006g0087 others(22): Show |
25 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(22): Show |
intron_variant | MODIFIER | c.1471-2627G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15243285 | |||||||
| chr11:15243302 | G | C | 1 | a0001c0001t0016g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1471-2610G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15243302 | |||||||
| chr11:15243322 | G | A | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1471-2590G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15243322 | |||||||
| chr11:15243344 | C | A | 16 | a0001c0001t0006g0008 a0001c0001t0006g0086 a0001c0001t0006g0087 others(13): Show |
16 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(13): Show |
intron_variant | MODIFIER | c.1471-2568C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15243344 | |||||||
| chr11:15243852 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1471-2060C>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15243852 | |||||||
| chr11:15243901 | T | TC | 5 | a0001c0001t0008g0147 a0001c0001t0008g0148 a0001c0001t0008g0170 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1471-2011_1471-201 others(5): Show |
INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15243901 | |||||||
| chr11:15243902 | TC | T | 44 | a0001c0001t0003g0005 a0001c0001t0003g0013 a0001c0001t0003g0020 others(41): Show |
45 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.1471-2008delC | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr11 | 15243902 | ||||||
| chr11:15243903 | C | T | 1 | a0001c0002t0003g0260 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1471-2009C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15243903 | |||||||
| chr11:15244038 | T | C | 1 | a0001c0001t0012g0169 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1471-1874T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15244038 | |||||||
| chr11:15244138 | T | G | 50 | a0001c0001t0003g0005 a0001c0001t0003g0013 a0001c0001t0003g0020 others(47): Show |
51 | HG00099.hp2 HG00408.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1471-1774T>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15244138 | |||||||
| chr11:15244264 | T | C | 5 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0144 others(2): Show |
5 | HG02647.hp2 HG02895.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1471-1648T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15244264 | |||||||
| chr11:15244316 | G | A | 29 | a0001c0001t0003g0005 a0001c0001t0003g0013 a0001c0001t0003g0020 others(26): Show |
30 | HG00408.hp1 HG00621.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1471-1596G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15244316 | |||||||
| chr11:15244325 | A | T | 29 | a0001c0001t0003g0005 a0001c0001t0003g0013 a0001c0001t0003g0020 others(26): Show |
30 | HG00408.hp1 HG00621.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.1471-1587A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15244325 | |||||||
| chr11:15244526 | C | T | 1 | a0001c0001t0016g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1471-1386C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15244526 | |||||||
| chr11:15244723 | T | C | 4 | a0004c0006t0001g0136 a0004c0006t0001g0244 a0004c0006t0001g0245 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1471-1189T>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15244723 | |||||||
| chr11:15244726 | G | A | 2 | a0004c0008t0015g0034 a0004c0008t0015g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1471-1186G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15244726 | |||||||
| chr11:15245092 | G | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0013 a0001c0001t0003g0020 others(28): Show |
32 | HG00408.hp1 HG00621.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1471-820G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245092 | |||||||
| chr11:15245172 | G | A | 5 | a0001c0001t0008g0147 a0001c0001t0008g0148 a0001c0001t0008g0170 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1471-740G>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245172 | |||||||
| chr11:15245276 | C | T | 9 | a0001c0001t0006g0008 a0001c0001t0006g0086 a0001c0001t0006g0087 others(6): Show |
9 | HG00099.hp2 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1471-636C>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245276 | |||||||
| chr11:15245344 | A | C | 207 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0012 others(204): Show |
212 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1471-568A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245344 | |||||||
| chr11:15245401 | G | T | 2 | a0004c0008t0015g0034 a0004c0008t0015g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1471-511G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245401 | |||||||
| chr11:15245415 | G | C | 1 | a0001c0002t0023g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1471-497G>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245415 | |||||||
| chr11:15245463 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1471-449C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245463 | |||||||
| chr11:15245643 | C | A | 2 | a0001c0001t0016g0042 a0001c0001t0016g0261 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1471-269C>A | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245643 | |||||||
| chr11:15245709 | A | C | 2 | a0004c0006t0001g0136 a0008c0015t0001g0093 |
2 | HG02486.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1471-203A>C | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245709 | |||||||
| chr11:15245751 | A | G | 2 | a0001c0001t0016g0042 a0001c0001t0016g0261 |
2 | HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1471-161A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245751 | |||||||
| chr11:15245759 | A | T | 1 | a0001c0001t0022g0128 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1471-153A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245759 | |||||||
| chr11:15245770 | A | G | 1 | a0001c0001t0016g0042 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1471-142A>G | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245770 | |||||||
| chr11:15245787 | A | T | 1 | a0001c0001t0002g0070 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1471-125A>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245787 | |||||||
| chr11:15245859 | G | T | 1 | a0002c0017t0001g0199 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1471-53G>T | INSC | ENSG00000188487.12 | transcript | ENST00000379556.8 | protein_coding | 12/12 | chr11 | 15245859 |