Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 54970 |
| ensemblid | ENSG00000149292.17 |
| hgncid | 23700 |
| symbol | TTC12 |
| name | tetratricopeptide repeat domain 12 |
| refseq_nuc | NM_017868.4 |
| refseq_prot | NP_060338.3 |
| ensembl_nuc | ENST00000529221.6 |
| ensembl_prot | ENSP00000433757.1 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 113314583 |
| end | 113366387 |
| strand | + |
| ver | v1.2 |
| region | chr11:113314583-113366387 |
| region5000 | chr11:113309583-113371387 |
| regionname0 | TTC12_chr11_113314583_113366387 |
| regionname5000 | TTC12_chr11_113309583_113371387 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 705 | 227 | 69 | 32 | 90 | 8 | 26 | 70 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0002 | 0/0 | 705 | 102 | 9 | 25 | 46 | 4 | 18 | 33 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0003 | 0/0 | 705 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0004 | 0/0 | 705 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0005 | 0/0 | 705 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0006 | 0/0 | 705 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0007 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0008 | 0/0 | 705 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0009 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0010 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0011 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| a0012 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | MDADK others(700): Show |
chr11 | 113309583 | 113371387 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2115 | 212 | 60 | 30 | 90 | 6 | 24 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0001c0003 | 0/0 | 2115 | 11 | 6 | 1 | 0 | 2 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0001c0006 | 0/0 | 2115 | 3 | 2 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0001c0011 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0002c0002 | 0/0 | 2115 | 93 | 5 | 25 | 44 | 4 | 15 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0002c0004 | 0/0 | 2115 | 4 | 4 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0002c0007 | 0/0 | 2115 | 2 | 0 | 0 | 0 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0002c0018 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0002c0019 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0002c0020 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0003c0008 | 0/0 | 2115 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0003c0016 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0004c0005 | 0/0 | 2115 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0005c0009 | 0/0 | 2115 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0006c0017 | 0/0 | 2115 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0007c0013 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0008c0021 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0009c0015 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0010c0010 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0011c0012 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 | ||
| a0012c0014 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ATGGA others(2110): Show |
chr11 | 113309583 | 113371387 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2256 | 208 | 59 | 28 | 89 | 6 | 24 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0001c0001t0002 | 0/0 | 2256 | 3 | 1 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0001c0001t0004 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0001c0003t0001 | 0/0 | 2256 | 11 | 6 | 1 | 0 | 2 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0001c0006t0001 | 0/0 | 2256 | 3 | 2 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0001c0011t0001 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0002c0002t0001 | 0/0 | 2256 | 93 | 5 | 25 | 44 | 4 | 15 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0002c0004t0001 | 0/0 | 2256 | 4 | 4 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0002c0007t0001 | 0/0 | 2256 | 2 | 0 | 0 | 0 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0002c0018t0001 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0002c0019t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0002c0020t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0003c0008t0001 | 0/0 | 2256 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0003c0016t0001 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0004c0005t0001 | 0/0 | 2256 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0005c0009t0003 | 0/0 | 2256 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0006c0017t0001 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0007c0013t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0008c0021t0001 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0009c0015t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0010c0010t0001 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0011c0012t0001 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| a0012c0014t0001 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | ACTGC others(2251): Show |
chr11 | 113309583 | 113371387 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0007 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0242 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0002g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0006t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0006t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0001c0011t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0001 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0034 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0037 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0004t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0007t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0007t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0018t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0019t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0002c0020t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0003c0008t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0003c0016t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0004c0005t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0004c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0005c0009t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0005c0009t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0006c0017t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0007c0013t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0008c0021t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0009c0015t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0010c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0011c0012t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| a0012c0014t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | GBR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | FIN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0110 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | CHS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00733 | hp1 | a0002 | c0002 | t0001 | g0167 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0166 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0165 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01243 | hp2 | a0001 | c0006 | t0001 | g0022 | AMR | PUR | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01255 | hp1 | a0003 | c0008 | t0001 | g0023 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0157 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01346 | hp1 | a0003 | c0008 | t0001 | g0023 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0159 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01516 | hp1 | a0001 | c0003 | t0001 | g0087 | EUR | IBS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0086 | EUR | IBS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0037 | EUR | IBS | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0202 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02004 | hp2 | a0006 | c0017 | t0001 | g0006 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02027 | hp2 | a0007 | c0013 | t0001 | g0123 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02080 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0162 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02451 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02451 | hp2 | a0002 | c0004 | t0001 | g0173 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02572 | hp1 | a0005 | c0009 | t0003 | g0074 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02572 | hp2 | a0001 | c0011 | t0001 | g0058 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0195 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02647 | hp2 | a0001 | c0003 | t0001 | g0108 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0168 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0151 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0193 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0219 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0196 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02738 | hp2 | a0001 | c0003 | t0001 | g0059 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02818 | hp2 | a0002 | c0004 | t0001 | g0176 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02896 | hp2 | a0005 | c0009 | t0003 | g0075 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03130 | hp1 | a0002 | c0004 | t0001 | g0172 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03139 | hp2 | a0001 | c0006 | t0001 | g0200 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03239 | hp2 | a0003 | c0016 | t0001 | g0077 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03486 | hp2 | a0002 | c0004 | t0001 | g0174 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03491 | hp1 | a0002 | c0018 | t0001 | g0035 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0216 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03710 | hp2 | a0002 | c0007 | t0001 | g0163 | SAS | PJL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0150 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04184 | hp2 | a0002 | c0007 | t0001 | g0164 | SAS | BEB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04199 | hp2 | a0002 | c0002 | t0001 | g0187 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04204 | hp2 | a0002 | c0002 | t0001 | g0035 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04228 | hp1 | a0008 | c0021 | t0001 | g0184 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG04228 | hp2 | a0002 | c0002 | t0001 | g0185 | SAS | STU | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18963 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0191 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18972 | hp1 | a0002 | c0020 | t0001 | g0183 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18981 | hp1 | a0009 | c0015 | t0001 | g0061 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18995 | hp1 | a0010 | c0010 | t0001 | g0145 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19009 | hp2 | a0004 | c0005 | t0001 | g0040 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19030 | hp1 | a0001 | c0006 | t0001 | g0022 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19057 | hp1 | a0004 | c0005 | t0001 | g0040 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19064 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19082 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19086 | hp2 | a0004 | c0005 | t0001 | g0179 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19087 | hp1 | a0002 | c0019 | t0001 | g0247 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19240 | hp1 | a0011 | c0012 | t0001 | g0057 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | YRI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | ASW | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0158 | EUR | TSI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0016 | EUR | TSI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0069 | EUR | TSI | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0188 | SAS | GIH | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02486 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0204 | AFR | USA | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA20300 | hp2 | a0001 | c0003 | t0001 | g0109 | AFR | USA | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| NA21309 | hp2 | a0012 | c0014 | t0001 | g0114 | AFR | LWK | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0242 | REF | REF | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0116 | REF | REF | TTC12_chr11_113309583_113371387 | TTC12 | chr11 | 113309583 | 113371387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:113323347 | G | C | 1 | a0004 | 3 | NA19009.hp2 NA19057.hp1 NA19086.hp2 |
missense_variant | MODERATE | c.118G>C | p.Glu40Gln | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/22 | 169/2256 | 118/2118 | 40/705 | chr11 | 113323347 | |||
| chr11:113323446 | A | C | 5 | a0002 a0004 a0005 others(2): Show |
109 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(106): Show |
missense_variant | MODERATE | c.217A>C | p.Met73Leu | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/22 | 268/2256 | 217/2118 | 73/705 | chr11 | 113323446 | |||
| chr11:113325530 | A | G | 1 | a0005 | 2 | HG02572.hp1 HG02896.hp2 |
missense_variant | MODERATE | c.329A>G | p.Lys110Arg | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/22 | 380/2256 | 329/2118 | 110/705 | chr11 | 113325530 | |||
| chr11:113325570 | A | C | 1 | a0008 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.369A>C | p.Glu123Asp | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/22 | 420/2256 | 369/2118 | 123/705 | chr11 | 113325570 | |||
| chr11:113325584 | G | A | 1 | a0010 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.383G>A | p.Arg128His | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/22 | 434/2256 | 383/2118 | 128/705 | chr11 | 113325584 | |||
| chr11:113352155 | G | A | 1 | a0006 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.1394G>A | p.Arg465Gln | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/22 | 1445/2256 | 1394/2118 | 465/705 | chr11 | 113352155 | |||
| chr11:113352163 | A | T | 1 | a0003 | 3 | HG01255.hp1 HG01346.hp1 HG03239.hp2 |
missense_variant | MODERATE | c.1402A>T | p.Met468Leu | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/22 | 1453/2256 | 1402/2118 | 468/705 | chr11 | 113352163 | |||
| chr11:113359426 | A | G | 1 | a0009 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.1510A>G | p.Met504Val | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/22 | 1561/2256 | 1510/2118 | 504/705 | chr11 | 113359426 | |||
| chr11:113362474 | T | C | 1 | a0011 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1688T>C | p.Val563Ala | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/22 | 1739/2256 | 1688/2118 | 563/705 | chr11 | 113362474 | |||
| chr11:113363853 | A | G | 1 | a0012 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1742A>G | p.Tyr581Cys | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/22 | 1793/2256 | 1742/2118 | 581/705 | chr11 | 113363853 | |||
| chr11:113366253 | G | A | 1 | a0007 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.2071G>A | p.Gly691Ser | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 22/22 | 2122/2256 | 2071/2118 | 691/705 | chr11 | 113366253 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:113323346 | G | A | 1 | a0002c0007 | 2 | HG03710.hp2 HG04184.hp2 |
synonymous_variant | LOW | c.117G>A | p.Leu39Leu | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/22 | 168/2256 | 117/2118 | 39/705 | chr11 | 113323346 | |||
| chr11:113325630 | C | T | 1 | a0002c0020 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.429C>T | p.Tyr143Tyr | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/22 | 480/2256 | 429/2118 | 143/705 | chr11 | 113325630 | |||
| chr11:113339374 | C | T | 1 | a0001c0006 | 3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.726C>T | p.Ala242Ala | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/22 | 777/2256 | 726/2118 | 242/705 | chr11 | 113339374 | |||
| chr11:113344402 | C | T | 3 | a0001c0003 a0001c0006 a0002c0019 |
15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
synonymous_variant | LOW | c.1116C>T | p.Ser372Ser | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/22 | 1167/2256 | 1116/2118 | 372/705 | chr11 | 113344402 | |||
| chr11:113352099 | G | A | 2 | a0001c0011 a0002c0004 |
5 | HG02451.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
synonymous_variant | LOW | c.1338G>A | p.Ser446Ser | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/22 | 1389/2256 | 1338/2118 | 446/705 | chr11 | 113352099 | |||
| chr11:113363881 | G | A | 1 | a0003c0016 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.1770G>A | p.Thr590Thr | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/22 | 1821/2256 | 1770/2118 | 590/705 | chr11 | 113363881 | |||
| chr11:113364953 | G | A | 1 | a0002c0018 | 1 | HG03491.hp1 | synonymous_variant | LOW | c.1935G>A | p.Thr645Thr | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/22 | 1986/2256 | 1935/2118 | 645/705 | chr11 | 113364953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:113314607 | T | A | 1 | a0001c0001t0002 | 3 | HG00738.hp1 HG01099.hp2 HG02559.hp2 |
5_prime_UTR_variant | MODIFIER | c.-27T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/22 | 1651 | chr11 | 113314607 | ||||||
| chr11:113314611 | C | T | 1 | a0001c0001t0004 | 1 | NA18974.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/22 | 1647 | chr11 | 113314611 | ||||||
| chr11:113316254 | C | T | 1 | a0005c0009t0003 | 2 | HG02572.hp1 HG02896.hp2 |
5_prime_UTR_variant | MODIFIER | c.-4C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/22 | 4 | chr11 | 113316254 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:113314683 | G | T | 1 | a0001c0001t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-16+65G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314683 | |||||||
| chr11:113314745 | C | T | 6 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
10 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+127C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314745 | |||||||
| chr11:113314764 | T | A | 1 | a0002c0002t0001g0054 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-16+146T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314764 | |||||||
| chr11:113314842 | C | T | 1 | a0002c0019t0001g0247 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-16+224C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314842 | |||||||
| chr11:113314857 | T | TGGGGCAG others(17): Show |
17 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0046 others(14): Show |
22 | HG00738.hp1 HG01099.hp2 HG01358.hp1 others(19): Show |
intron_variant | MODIFIER | c.-16+242_-16+265dup others(24): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113314857 | ||||||
| chr11:113314857 | T | TGGGGCAG others(41): Show |
8 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0217 others(5): Show |
11 | HG01099.hp1 HG02280.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+265_-16+266ins others(48): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113314857 | ||||||
| chr11:113314857 | T | TGGGGCAG others(17): Show |
1 | a0001c0001t0001g0246 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-16+249_-16+250ins others(24): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113314857 | ||||||
| chr11:113314869 | C | CGCGCGGG others(17): Show |
27 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0049 others(24): Show |
34 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-16+265_-16+266ins others(24): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113314869 | ||||||
| chr11:113314869 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-16+251C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314869 | |||||||
| chr11:113314873 | C | T | 1 | a0001c0001t0001g0051 | 2 | NA18991.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-16+255C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113314873 | |||||||
| chr11:113315080 | C | T | 5 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0003t0001g0202 others(2): Show |
5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+462C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315080 | |||||||
| chr11:113315153 | C | CT | 102 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(99): Show |
140 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.-16+536dupT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113315153 | ||||||
| chr11:113315223 | ACTCGTCG others(11): Show |
A | 23 | a0002c0002t0001g0005 a0002c0002t0001g0011 a0002c0002t0001g0012 others(20): Show |
34 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.-16+608_-16+625del others(18): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr11 | 113315223 | ||||||
| chr11:113315423 | G | C | 2 | a0001c0001t0002g0043 a0001c0001t0002g0205 |
3 | HG00738.hp1 HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-16+805G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315423 | |||||||
| chr11:113315594 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-15-649A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315594 | |||||||
| chr11:113315650 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0003t0001g0216 |
3 | HG03017.hp1 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-15-593A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315650 | |||||||
| chr11:113315708 | G | A | 1 | a0001c0001t0001g0048 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-15-535G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315708 | |||||||
| chr11:113315741 | G | A | 6 | a0002c0002t0001g0036 a0002c0002t0001g0037 a0002c0002t0001g0165 others(3): Show |
8 | HG00733.hp1 HG01081.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-502G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315741 | |||||||
| chr11:113315750 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-15-493C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113315750 | |||||||
| chr11:113316054 | G | A | 160 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(157): Show |
216 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(213): Show |
intron_variant | MODIFIER | c.-15-189G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113316054 | |||||||
| chr11:113316073 | C | T | 2 | a0005c0009t0003g0074 a0005c0009t0003g0075 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-15-170C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113316073 | |||||||
| chr11:113316157 | C | T | 49 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0014 others(46): Show |
72 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.-15-86C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 1/21 | chr11 | 113316157 | |||||||
| chr11:113316455 | G | C | 1 | a0002c0002t0001g0169 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.58+140G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113316455 | |||||||
| chr11:113316961 | A | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
10 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+646A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113316961 | |||||||
| chr11:113317104 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+789C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317104 | |||||||
| chr11:113317120 | C | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.58+805C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317120 | |||||||
| chr11:113317227 | A | G | 49 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(46): Show |
64 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.58+912A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317227 | |||||||
| chr11:113317475 | G | A | 138 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(135): Show |
191 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.58+1160G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317475 | |||||||
| chr11:113317536 | C | T | 1 | a0002c0002t0001g0199 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.58+1221C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317536 | |||||||
| chr11:113317718 | A | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0244 a0001c0001t0001g0245 |
4 | HG01243.hp1 HG02258.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+1403A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317718 | |||||||
| chr11:113317749 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.58+1434C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317749 | |||||||
| chr11:113317800 | CT | C | 50 | a0001c0001t0001g0207 a0002c0002t0001g0001 a0002c0002t0001g0006 others(47): Show |
73 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.58+1494delT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113317800 | ||||||
| chr11:113317810 | A | C | 49 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0014 others(46): Show |
72 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.58+1495A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113317810 | |||||||
| chr11:113318003 | T | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG03017.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.58+1688T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318003 | |||||||
| chr11:113318166 | T | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0055 others(3): Show |
8 | HG01109.hp1 HG01123.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+1851T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318166 | |||||||
| chr11:113318201 | T | G | 23 | a0002c0002t0001g0005 a0002c0002t0001g0011 a0002c0002t0001g0012 others(20): Show |
34 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.58+1886T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318201 | |||||||
| chr11:113318235 | CAG | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0055 others(3): Show |
8 | HG01109.hp1 HG01123.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.58+1924_58+1925del others(2): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113318235 | ||||||
| chr11:113318411 | T | C | 3 | a0001c0001t0001g0076 a0003c0008t0001g0023 a0003c0016t0001g0077 |
4 | HG01255.hp1 HG01346.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+2096T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318411 | |||||||
| chr11:113318515 | C | T | 23 | a0002c0002t0001g0005 a0002c0002t0001g0011 a0002c0002t0001g0012 others(20): Show |
34 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.58+2200C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318515 | |||||||
| chr11:113318570 | C | T | 1 | a0002c0002t0001g0198 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.58+2255C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318570 | |||||||
| chr11:113318609 | T | TG | 53 | a0001c0001t0002g0043 a0001c0001t0002g0205 a0001c0003t0001g0216 others(50): Show |
77 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.58+2301dupG | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113318609 | ||||||
| chr11:113318919 | C | T | 2 | a0002c0007t0001g0163 a0002c0007t0001g0164 |
2 | HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.58+2604C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113318919 | |||||||
| chr11:113319025 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.58+2710A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319025 | |||||||
| chr11:113319317 | T | C | 2 | a0001c0001t0002g0043 a0001c0001t0002g0205 |
3 | HG00738.hp1 HG01099.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.58+3002T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319317 | |||||||
| chr11:113319322 | G | A | 3 | a0002c0002t0001g0038 a0002c0002t0001g0170 a0002c0002t0001g0171 |
4 | HG02071.hp1 NA18981.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+3007G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319322 | |||||||
| chr11:113319482 | A | G | 1 | a0002c0002t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.58+3167A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319482 | |||||||
| chr11:113319503 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.58+3188G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319503 | |||||||
| chr11:113319560 | G | A | 57 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0053 others(54): Show |
84 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.58+3245G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319560 | |||||||
| chr11:113319678 | GA | G | 35 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0214 others(32): Show |
47 | HG00609.hp1 HG00738.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.58+3376delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113319678 | ||||||
| chr11:113319763 | C | T | 1 | a0002c0002t0001g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.58+3448C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319763 | |||||||
| chr11:113319802 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0055 others(3): Show |
8 | HG01109.hp1 HG01123.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3486C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113319802 | |||||||
| chr11:113320153 | C | T | 76 | a0001c0001t0001g0243 a0002c0002t0001g0001 a0002c0002t0001g0005 others(73): Show |
110 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.59-3135C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320153 | |||||||
| chr11:113320232 | C | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0055 others(3): Show |
8 | HG01109.hp1 HG01123.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-3056C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320232 | |||||||
| chr11:113320233 | G | A | 2 | a0005c0009t0003g0074 a0005c0009t0003g0075 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.59-3055G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320233 | |||||||
| chr11:113320246 | A | G | 2 | a0005c0009t0003g0074 a0005c0009t0003g0075 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.59-3042A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320246 | |||||||
| chr11:113320248 | G | C | 5 | a0002c0002t0001g0175 a0002c0004t0001g0172 a0002c0004t0001g0173 others(2): Show |
5 | HG02451.hp2 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-3040G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320248 | |||||||
| chr11:113320248 | G | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0003t0001g0216 |
3 | HG03017.hp1 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.59-3040G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320248 | |||||||
| chr11:113320330 | A | C | 1 | a0001c0001t0001g0004 | 6 | HG00408.hp2 HG02129.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-2958A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320330 | |||||||
| chr11:113320421 | C | T | 5 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0003t0001g0202 others(2): Show |
5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-2867C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320421 | |||||||
| chr11:113320424 | C | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | HG02886.hp2 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.59-2864C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320424 | |||||||
| chr11:113320537 | A | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
10 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.59-2751A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320537 | |||||||
| chr11:113320631 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | NA18970.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.59-2657G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320631 | |||||||
| chr11:113320706 | C | T | 48 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(45): Show |
63 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.59-2582C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320706 | |||||||
| chr11:113320836 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.59-2452C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320836 | |||||||
| chr11:113320858 | A | T | 1 | a0002c0002t0001g0196 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.59-2430A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320858 | |||||||
| chr11:113320875 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.59-2413C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113320875 | |||||||
| chr11:113321365 | G | T | 1 | a0010c0010t0001g0145 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.59-1923G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321365 | |||||||
| chr11:113321570 | G | T | 10 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0214 others(7): Show |
10 | HG01891.hp2 HG02572.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.59-1718G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321570 | |||||||
| chr11:113321590 | A | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0003t0001g0216 |
3 | HG03017.hp1 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.59-1698A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321590 | |||||||
| chr11:113321648 | G | A | 1 | a0001c0001t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.59-1640G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321648 | |||||||
| chr11:113321684 | G | A | 49 | a0002c0002t0001g0001 a0002c0002t0001g0006 a0002c0002t0001g0014 others(46): Show |
72 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.59-1604G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321684 | |||||||
| chr11:113321702 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0249 a0001c0001t0001g0250 |
5 | HG02258.hp1 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-1586A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321702 | |||||||
| chr11:113321797 | T | C | 1 | a0002c0002t0001g0150 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.59-1491T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321797 | |||||||
| chr11:113321799 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0241 |
5 | HG00642.hp2 HG01070.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-1489C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321799 | |||||||
| chr11:113321802 | G | T | 138 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(135): Show |
191 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.59-1486G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321802 | |||||||
| chr11:113321859 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.59-1429A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113321859 | |||||||
| chr11:113322075 | C | T | 47 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(44): Show |
61 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.59-1213C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322075 | |||||||
| chr11:113322340 | C | G | 132 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(129): Show |
181 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.59-948C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322340 | |||||||
| chr11:113322340 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.59-948C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322340 | |||||||
| chr11:113322484 | C | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0208 |
3 | HG01358.hp1 NA18956.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.59-804C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322484 | |||||||
| chr11:113322484 | C | G | 45 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(42): Show |
58 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.59-804C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322484 | |||||||
| chr11:113322595 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-693C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322595 | |||||||
| chr11:113322657 | C | T | 1 | a0002c0002t0001g0168 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.59-631C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322657 | |||||||
| chr11:113322683 | A | C | 1 | a0001c0003t0001g0204 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.59-605A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322683 | |||||||
| chr11:113322879 | C | T | 132 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(129): Show |
181 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.59-409C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322879 | |||||||
| chr11:113322888 | G | A | 1 | a0001c0001t0001g0024 | 2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.59-400G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322888 | |||||||
| chr11:113322890 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.59-398T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322890 | |||||||
| chr11:113322951 | G | T | 1 | a0002c0002t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.59-337G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113322951 | |||||||
| chr11:113323102 | C | CA | 48 | a0001c0001t0001g0055 a0001c0001t0001g0081 a0001c0001t0001g0082 others(45): Show |
63 | HG00609.hp1 HG01069.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.59-167dupA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr11 | 113323102 | ||||||
| chr11:113323111 | A | C | 1 | a0002c0002t0001g0162 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.59-177A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323111 | |||||||
| chr11:113323114 | A | C | 1 | a0002c0002t0001g0199 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.59-174A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323114 | |||||||
| chr11:113323189 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.59-99T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323189 | |||||||
| chr11:113323241 | C | G | 21 | a0001c0001t0001g0017 a0001c0001t0001g0044 a0001c0001t0001g0045 others(18): Show |
29 | HG00738.hp1 HG01099.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-47C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323241 | |||||||
| chr11:113323254 | T | C | 1 | a0001c0001t0001g0008 | 3 | HG01074.hp2 HG03942.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.59-34T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 2/21 | chr11 | 113323254 | |||||||
| chr11:113323499 | C | A | 1 | a0002c0007t0001g0163 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.222+48C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323499 | |||||||
| chr11:113323510 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0251 |
2 | HG02723.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.222+59G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323510 | |||||||
| chr11:113323597 | AT | A | 23 | a0002c0002t0001g0005 a0002c0002t0001g0011 a0002c0002t0001g0012 others(20): Show |
34 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.222+156delT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr11 | 113323597 | ||||||
| chr11:113323640 | C | T | 5 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0003t0001g0202 others(2): Show |
5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.222+189C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323640 | |||||||
| chr11:113323723 | G | A | 2 | a0002c0002t0001g0015 a0002c0002t0001g0177 |
4 | HG02015.hp1 HG02027.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.223-271G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323723 | |||||||
| chr11:113323726 | T | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0025 others(11): Show |
18 | HG00140.hp2 HG01074.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.223-268T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323726 | |||||||
| chr11:113323739 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.223-255C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323739 | |||||||
| chr11:113323775 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.223-219G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323775 | |||||||
| chr11:113323828 | C | A | 5 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0003t0001g0202 others(2): Show |
5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-166C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323828 | |||||||
| chr11:113323932 | A | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0003t0001g0202 others(2): Show |
5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.223-62A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 3/21 | chr11 | 113323932 | |||||||
| chr11:113324206 | C | T | 8 | a0001c0001t0001g0050 a0001c0001t0001g0227 a0001c0001t0001g0238 others(5): Show |
9 | HG01243.hp1 HG02258.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.244+191C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 4/21 | chr11 | 113324206 | |||||||
| chr11:113324319 | C | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
10 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.245-286C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 4/21 | chr11 | 113324319 | |||||||
| chr11:113324467 | G | A | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0003t0001g0216 |
3 | HG03017.hp1 HG03654.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.245-138G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 4/21 | chr11 | 113324467 | |||||||
| chr11:113324482 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18984.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.245-123G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 4/21 | chr11 | 113324482 | |||||||
| chr11:113324687 | T | G | 5 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0003t0001g0202 others(2): Show |
5 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.322+5T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324687 | |||||||
| chr11:113324830 | A | T | 1 | a0002c0002t0001g0195 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.322+148A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324830 | |||||||
| chr11:113324873 | A | G | 152 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0010 others(149): Show |
215 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.322+191A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324873 | |||||||
| chr11:113324889 | A | G | 75 | a0002c0002t0001g0001 a0002c0002t0001g0005 a0002c0002t0001g0006 others(72): Show |
109 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.322+207A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324889 | |||||||
| chr11:113324974 | G | A | 3 | a0002c0002t0001g0178 a0002c0002t0001g0180 a0002c0002t0001g0181 |
3 | HG00423.hp2 HG00673.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.322+292G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113324974 | |||||||
| chr11:113325202 | A | T | 2 | a0001c0001t0001g0070 a0001c0006t0001g0022 |
3 | HG01243.hp2 NA18906.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.323-322A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113325202 | |||||||
| chr11:113325371 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.323-153T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113325371 | |||||||
| chr11:113325435 | G | A | 1 | a0003c0008t0001g0023 | 2 | HG01255.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.323-89G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113325435 | |||||||
| chr11:113325509 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.323-15C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 5/21 | chr11 | 113325509 | |||||||
| chr11:113325792 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.444+147A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113325792 | |||||||
| chr11:113325811 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.444+166C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113325811 | |||||||
| chr11:113326026 | C | T | 1 | a0002c0002t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444+381C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113326026 | |||||||
| chr11:113326029 | C | CT | 4 | a0001c0001t0001g0240 a0001c0011t0001g0058 a0002c0002t0001g0175 others(1): Show |
4 | HG02572.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.444+390dupT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 113326029 | ||||||
| chr11:113326113 | C | T | 13 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(10): Show |
16 | HG00558.hp2 HG00673.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.444+468C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113326113 | |||||||
| chr11:113326136 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.444+491A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113326136 | |||||||
| chr11:113326521 | T | A | 169 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(166): Show |
235 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.444+876T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113326521 | |||||||
| chr11:113326550 | GGAAGAGG others(11): Show |
G | 1 | a0002c0002t0001g0206 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.444+909_444+926del others(18): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 113326550 | ||||||
| chr11:113326598 | TG | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(2): Show |
5 | NA18945.hp2 NA18957.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.444+957delG | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 113326598 | ||||||
| chr11:113327350 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.444+1705C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327350 | |||||||
| chr11:113327421 | AC | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(77): Show |
104 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.444+1779delC | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr11 | 113327421 | ||||||
| chr11:113327540 | T | C | 1 | a0001c0001t0001g0029 | 2 | NA18960.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.444+1895T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327540 | |||||||
| chr11:113327792 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.445-2128C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327792 | |||||||
| chr11:113327913 | G | A | 1 | a0001c0006t0001g0022 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.445-2007G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327913 | |||||||
| chr11:113327963 | C | G | 15 | a0001c0001t0001g0010 a0001c0001t0001g0062 a0001c0001t0001g0063 others(12): Show |
17 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.445-1957C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113327963 | |||||||
| chr11:113328177 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.445-1743G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328177 | |||||||
| chr11:113328203 | G | A | 2 | a0001c0003t0001g0059 a0002c0019t0001g0247 |
2 | HG02738.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.445-1717G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328203 | |||||||
| chr11:113328210 | G | A | 7 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(4): Show |
8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.445-1710G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328210 | |||||||
| chr11:113328293 | A | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0221 others(1): Show |
6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-1627A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328293 | |||||||
| chr11:113328302 | A | C | 16 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0203 others(13): Show |
16 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.445-1618A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328302 | |||||||
| chr11:113328424 | C | T | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0024 others(30): Show |
54 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.445-1496C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328424 | |||||||
| chr11:113328504 | A | G | 2 | a0004c0005t0001g0040 a0004c0005t0001g0179 |
3 | NA19009.hp2 NA19057.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.445-1416A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328504 | |||||||
| chr11:113328551 | C | G | 6 | a0001c0001t0001g0203 a0001c0011t0001g0058 a0002c0004t0001g0172 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.445-1369C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328551 | |||||||
| chr11:113328618 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.445-1302C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328618 | |||||||
| chr11:113328669 | C | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG00733.hp2 HG00738.hp2 |
intron_variant | MODIFIER | c.445-1251C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328669 | |||||||
| chr11:113328983 | G | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0221 others(1): Show |
6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-937G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113328983 | |||||||
| chr11:113329142 | T | A | 1 | a0002c0002t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.445-778T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329142 | |||||||
| chr11:113329281 | C | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(112): Show |
146 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.445-639C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329281 | |||||||
| chr11:113329386 | C | G | 1 | a0011c0012t0001g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.445-534C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329386 | |||||||
| chr11:113329532 | C | T | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.445-388C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329532 | |||||||
| chr11:113329535 | G | T | 1 | a0002c0002t0001g0171 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.445-385G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329535 | |||||||
| chr11:113329540 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0107 a0001c0001t0002g0043 |
6 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.445-380C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329540 | |||||||
| chr11:113329542 | G | A | 7 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(4): Show |
7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.445-378G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329542 | |||||||
| chr11:113329582 | C | T | 1 | a0001c0006t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.445-338C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329582 | |||||||
| chr11:113329725 | G | C | 1 | a0002c0002t0001g0005 | 5 | NA18960.hp2 NA19000.hp2 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.445-195G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329725 | |||||||
| chr11:113329836 | A | G | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(96): Show |
129 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.445-84A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329836 | |||||||
| chr11:113329893 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.445-27G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 6/21 | chr11 | 113329893 | |||||||
| chr11:113329987 | G | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(159): Show |
221 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
splice_region_variant&intron_variant | LOW | c.504+8G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113329987 | |||||||
| chr11:113330009 | A | G | 16 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(13): Show |
17 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.504+30A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330009 | |||||||
| chr11:113330063 | G | T | 4 | a0001c0011t0001g0058 a0002c0004t0001g0172 a0002c0004t0001g0173 others(1): Show |
4 | HG02451.hp2 HG02572.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.504+84G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330063 | |||||||
| chr11:113330148 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.504+169C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330148 | |||||||
| chr11:113330185 | C | G | 2 | a0005c0009t0003g0074 a0005c0009t0003g0075 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.504+206C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330185 | |||||||
| chr11:113330558 | C | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(31): Show |
56 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.504+579C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330558 | |||||||
| chr11:113330615 | C | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0139 |
2 | NA18967.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.504+636C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330615 | |||||||
| chr11:113330647 | C | T | 7 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(4): Show |
7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.504+668C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330647 | |||||||
| chr11:113330801 | T | A | 1 | a0001c0001t0001g0248 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.504+822T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330801 | |||||||
| chr11:113330968 | G | A | 1 | a0002c0002t0001g0193 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.504+989G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113330968 | |||||||
| chr11:113331119 | C | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(92): Show |
123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.504+1140C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331119 | |||||||
| chr11:113331137 | T | C | 1 | a0001c0003t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.504+1158T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331137 | |||||||
| chr11:113331230 | G | A | 11 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0221 others(8): Show |
14 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.504+1251G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331230 | |||||||
| chr11:113331570 | C | A | 1 | a0002c0002t0001g0034 | 2 | HG01261.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.504+1591C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331570 | |||||||
| chr11:113331689 | A | G | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+1710A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331689 | |||||||
| chr11:113331708 | G | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(215): Show |
300 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(297): Show |
intron_variant | MODIFIER | c.504+1729G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331708 | |||||||
| chr11:113331966 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0049 a0001c0001t0001g0107 others(1): Show |
8 | HG00738.hp1 HG01099.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.504+1987T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113331966 | |||||||
| chr11:113332033 | A | ATGCCAAT others(6056): Show |
1 | a0002c0002t0001g0170 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.504+2072_504+2073i others(6065): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr11 | 113332033 | ||||||
| chr11:113332301 | C | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(110): Show |
144 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.504+2322C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332301 | |||||||
| chr11:113332421 | C | T | 7 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(4): Show |
8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.504+2442C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332421 | |||||||
| chr11:113332447 | G | A | 1 | a0002c0002t0001g0165 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.504+2468G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332447 | |||||||
| chr11:113332526 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0197 |
4 | HG01069.hp2 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-2440C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332526 | |||||||
| chr11:113332592 | G | A | 1 | a0005c0009t0003g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.505-2374G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332592 | |||||||
| chr11:113332717 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0079 |
3 | NA18970.hp1 NA19002.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.505-2249A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332717 | |||||||
| chr11:113332755 | G | C | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-2211G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332755 | |||||||
| chr11:113332796 | A | G | 1 | a0001c0003t0001g0059 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.505-2170A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113332796 | |||||||
| chr11:113333273 | A | G | 2 | a0001c0003t0001g0059 a0002c0019t0001g0247 |
2 | HG02738.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.505-1693A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333273 | |||||||
| chr11:113333315 | C | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-1651C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333315 | |||||||
| chr11:113333352 | C | A | 1 | a0009c0015t0001g0061 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.505-1614C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333352 | |||||||
| chr11:113333435 | T | A | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(40): Show |
62 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.505-1531T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333435 | |||||||
| chr11:113333488 | G | A | 8 | a0001c0001t0001g0203 a0001c0011t0001g0058 a0002c0004t0001g0172 others(5): Show |
8 | HG02451.hp2 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.505-1478G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333488 | |||||||
| chr11:113333544 | C | T | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(31): Show |
56 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.505-1422C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333544 | |||||||
| chr11:113333552 | A | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.505-1414A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333552 | |||||||
| chr11:113333558 | G | A | 7 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(4): Show |
8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-1408G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333558 | |||||||
| chr11:113333649 | G | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.505-1317G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333649 | |||||||
| chr11:113333703 | G | A | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-1263G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333703 | |||||||
| chr11:113333759 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(110): Show |
144 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.505-1207A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333759 | |||||||
| chr11:113333807 | A | T | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-1159A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333807 | |||||||
| chr11:113333840 | C | A | 1 | a0001c0001t0001g0218 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.505-1126C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113333840 | |||||||
| chr11:113334028 | G | A | 1 | a0002c0002t0001g0155 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.505-938G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334028 | |||||||
| chr11:113334074 | A | T | 1 | a0002c0002t0001g0192 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.505-892A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334074 | |||||||
| chr11:113334130 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.505-836C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334130 | |||||||
| chr11:113334154 | A | G | 1 | a0002c0002t0001g0196 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.505-812A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334154 | |||||||
| chr11:113334190 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.505-776A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334190 | |||||||
| chr11:113334296 | G | A | 2 | a0001c0001t0001g0062 a0002c0002t0001g0182 |
2 | NA18945.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.505-670G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334296 | |||||||
| chr11:113334313 | C | A | 1 | a0001c0001t0001g0063 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.505-653C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334313 | |||||||
| chr11:113334452 | G | T | 8 | a0001c0001t0001g0055 a0001c0001t0001g0093 a0001c0001t0001g0233 others(5): Show |
8 | HG00323.hp1 HG02698.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.505-514G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334452 | |||||||
| chr11:113334456 | ACT | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0024 others(30): Show |
54 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.505-509_505-508del others(2): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334456 | |||||||
| chr11:113334873 | T | C | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.505-93T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 7/21 | chr11 | 113334873 | |||||||
| chr11:113335313 | G | C | 2 | a0001c0001t0001g0078 a0002c0020t0001g0183 |
2 | NA18972.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.576+276G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335313 | |||||||
| chr11:113335313 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.576+276G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335313 | |||||||
| chr11:113335355 | A | G | 4 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(1): Show |
4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+318A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335355 | |||||||
| chr11:113335363 | A | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0024 others(30): Show |
54 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.576+326A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335363 | |||||||
| chr11:113335415 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.576+378T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335415 | |||||||
| chr11:113335467 | T | C | 1 | a0001c0003t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.576+430T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335467 | |||||||
| chr11:113335553 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(155): Show |
213 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.576+516G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335553 | |||||||
| chr11:113335631 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.576+594C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335631 | |||||||
| chr11:113335742 | A | C | 106 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(103): Show |
136 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.576+705A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113335742 | |||||||
| chr11:113336002 | T | G | 7 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(4): Show |
8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.576+965T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336002 | |||||||
| chr11:113336077 | A | C | 33 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0024 others(30): Show |
54 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.576+1040A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336077 | |||||||
| chr11:113336141 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0025 |
5 | HG01074.hp2 HG02004.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1104G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336141 | |||||||
| chr11:113336145 | T | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(92): Show |
123 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.576+1108T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336145 | |||||||
| chr11:113336357 | T | G | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.576+1320T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336357 | |||||||
| chr11:113336362 | G | A | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.576+1325G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336362 | |||||||
| chr11:113336392 | T | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 |
5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1355T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336392 | |||||||
| chr11:113336458 | C | T | 1 | a0002c0002t0001g0191 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.576+1421C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336458 | |||||||
| chr11:113336854 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.576+1817C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336854 | |||||||
| chr11:113336867 | G | A | 5 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(2): Show |
5 | NA18945.hp2 NA18957.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1830G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336867 | |||||||
| chr11:113336871 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.576+1834C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113336871 | |||||||
| chr11:113337224 | A | C | 6 | a0001c0001t0001g0203 a0001c0011t0001g0058 a0002c0004t0001g0172 others(3): Show |
6 | HG02451.hp2 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.577-1550A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337224 | |||||||
| chr11:113337376 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(151): Show |
207 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.577-1398C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337376 | |||||||
| chr11:113337404 | A | T | 1 | a0001c0001t0001g0055 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.577-1370A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337404 | |||||||
| chr11:113337421 | T | C | 1 | a0002c0002t0001g0175 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.577-1353T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337421 | |||||||
| chr11:113337464 | C | A | 162 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(159): Show |
221 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.577-1310C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337464 | |||||||
| chr11:113337525 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.577-1249C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337525 | |||||||
| chr11:113337660 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(155): Show |
213 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.577-1114A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337660 | |||||||
| chr11:113337767 | G | A | 7 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(4): Show |
7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.577-1007G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337767 | |||||||
| chr11:113337811 | G | A | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(77): Show |
104 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.577-963G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113337811 | |||||||
| chr11:113337813 | G | GGACCAGG others(14): Show |
2 | a0001c0003t0001g0202 a0001c0003t0001g0204 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.577-959_577-939dup others(21): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 113337813 | ||||||
| chr11:113338038 | C | T | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.577-736C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338038 | |||||||
| chr11:113338069 | T | TTTG | 4 | a0002c0002t0001g0035 a0002c0002t0001g0185 a0002c0018t0001g0035 others(1): Show |
4 | HG03491.hp1 HG04204.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-678_577-676dup others(3): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 113338069 | ||||||
| chr11:113338069 | TTTG | T | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(147): Show |
205 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.577-678_577-676del others(3): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr11 | 113338069 | ||||||
| chr11:113338137 | T | G | 1 | a0001c0001t0001g0249 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.577-637T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338137 | |||||||
| chr11:113338226 | A | G | 1 | a0005c0009t0003g0074 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.577-548A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338226 | |||||||
| chr11:113338465 | G | A | 1 | a0001c0003t0001g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.577-309G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338465 | |||||||
| chr11:113338474 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0222 |
4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-300A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338474 | |||||||
| chr11:113338486 | A | G | 2 | a0001c0003t0001g0109 a0001c0003t0001g0110 |
2 | HG00642.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.577-288A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338486 | |||||||
| chr11:113338706 | C | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(31): Show |
56 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.577-68C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 8/21 | chr11 | 113338706 | |||||||
| chr11:113338998 | T | C | 1 | a0001c0001t0001g0020 | 2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.637+164T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 9/21 | chr11 | 113338998 | |||||||
| chr11:113339209 | GA | G | 14 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(11): Show |
15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.638-68delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr11 | 113339209 | ||||||
| chr11:113339639 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.826+165G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339639 | |||||||
| chr11:113339712 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0221 others(1): Show |
6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+238C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339712 | |||||||
| chr11:113339736 | T | A | 1 | a0001c0003t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.826+262T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339736 | |||||||
| chr11:113339868 | C | T | 1 | a0001c0001t0001g0232 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.826+394C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339868 | |||||||
| chr11:113339872 | C | T | 2 | a0001c0003t0001g0086 a0001c0003t0001g0087 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.826+398C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339872 | |||||||
| chr11:113339964 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.826+490G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339964 | |||||||
| chr11:113339973 | C | T | 14 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(11): Show |
15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.826+499C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113339973 | |||||||
| chr11:113340039 | G | A | 1 | a0001c0003t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.826+565G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340039 | |||||||
| chr11:113340068 | T | A | 2 | a0002c0002t0001g0035 a0002c0018t0001g0035 |
2 | HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.826+594T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340068 | |||||||
| chr11:113340268 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.827-396G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340268 | |||||||
| chr11:113340390 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0238 |
2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.827-274G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340390 | |||||||
| chr11:113340414 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.827-250G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340414 | |||||||
| chr11:113340465 | G | A | 2 | a0005c0009t0003g0074 a0005c0009t0003g0075 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.827-199G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340465 | |||||||
| chr11:113340607 | G | T | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(116): Show |
150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.827-57G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340607 | |||||||
| chr11:113340648 | T | G | 34 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(31): Show |
56 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.827-16T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 10/21 | chr11 | 113340648 | |||||||
| chr11:113340956 | G | C | 1 | a0001c0001t0001g0020 | 2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.896+223G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113340956 | |||||||
| chr11:113341091 | A | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(102): Show |
135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.896+358A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341091 | |||||||
| chr11:113341251 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.896+518A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341251 | |||||||
| chr11:113341396 | GATATAA | G | 1 | a0002c0002t0001g0014 | 3 | HG01069.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.897-432_897-427del others(6): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr11 | 113341396 | ||||||
| chr11:113341425 | T | G | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.897-412T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341425 | |||||||
| chr11:113341452 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.897-385A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341452 | |||||||
| chr11:113341452 | A | T | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.897-385A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341452 | |||||||
| chr11:113341453 | T | C | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.897-384T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341453 | |||||||
| chr11:113341805 | C | T | 2 | a0005c0009t0003g0074 a0005c0009t0003g0075 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.897-32C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341805 | |||||||
| chr11:113341831 | T | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(98): Show |
129 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
splice_region_variant&intron_variant | LOW | c.897-6T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 11/21 | chr11 | 113341831 | |||||||
| chr11:113341975 | A | C | 1 | a0001c0001t0001g0049 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.985+50A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113341975 | |||||||
| chr11:113341980 | C | T | 4 | a0001c0001t0001g0220 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02280.hp2 HG03041.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.985+55C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113341980 | |||||||
| chr11:113342042 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA18991.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.985+117G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342042 | |||||||
| chr11:113342050 | C | T | 1 | a0001c0006t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.985+125C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342050 | |||||||
| chr11:113342181 | C | T | 1 | a0001c0001t0001g0047 | 2 | NA19054.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.985+256C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342181 | |||||||
| chr11:113342239 | C | A | 7 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(4): Show |
7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.985+314C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342239 | |||||||
| chr11:113342347 | C | G | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(102): Show |
135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.985+422C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342347 | |||||||
| chr11:113342455 | T | G | 7 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(4): Show |
8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.985+530T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342455 | |||||||
| chr11:113342511 | G | T | 14 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(11): Show |
15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.985+586G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342511 | |||||||
| chr11:113342576 | T | C | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(83): Show |
110 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.985+651T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342576 | |||||||
| chr11:113342588 | G | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0232 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.985+663G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342588 | |||||||
| chr11:113342809 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.985+884G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342809 | |||||||
| chr11:113342822 | G | C | 2 | a0005c0009t0003g0074 a0005c0009t0003g0075 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.985+897G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342822 | |||||||
| chr11:113342880 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.985+955G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113342880 | |||||||
| chr11:113343068 | A | G | 1 | a0001c0001t0004g0129 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.985+1143A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343068 | |||||||
| chr11:113343089 | G | A | 2 | a0002c0002t0001g0036 a0002c0002t0001g0167 |
3 | HG00733.hp1 HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.985+1164G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343089 | |||||||
| chr11:113343134 | A | G | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.986-1138A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343134 | |||||||
| chr11:113343217 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0217 a0001c0001t0001g0241 others(2): Show |
8 | HG00642.hp2 HG01070.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.986-1055A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343217 | |||||||
| chr11:113343218 | TGAG | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0221 others(1): Show |
6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.986-1052_986-1050d others(5): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr11 | 113343218 | ||||||
| chr11:113343256 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0128 a0001c0001t0001g0138 |
9 | NA18956.hp1 NA18963.hp2 NA18978.hp2 others(6): Show |
intron_variant | MODIFIER | c.986-1016C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343256 | |||||||
| chr11:113343363 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.986-909A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343363 | |||||||
| chr11:113343713 | G | T | 5 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(2): Show |
5 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.986-559G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343713 | |||||||
| chr11:113343871 | C | T | 1 | a0001c0003t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.986-401C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113343871 | |||||||
| chr11:113344098 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.986-174C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113344098 | |||||||
| chr11:113344110 | C | T | 2 | a0005c0009t0003g0074 a0005c0009t0003g0075 |
2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.986-162C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 12/21 | chr11 | 113344110 | |||||||
| chr11:113344658 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0222 |
4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+218G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113344658 | |||||||
| chr11:113344696 | G | A | 1 | a0001c0001t0001g0004 | 6 | HG00408.hp2 HG02129.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154+256G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113344696 | |||||||
| chr11:113344798 | A | T | 1 | a0001c0001t0001g0021 | 2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1154+358A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113344798 | |||||||
| chr11:113344832 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1154+392T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113344832 | |||||||
| chr11:113345007 | T | C | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+567T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345007 | |||||||
| chr11:113345201 | G | A | 59 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(56): Show |
80 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1154+761G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345201 | |||||||
| chr11:113345239 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0002g0043 |
4 | HG00738.hp1 HG01099.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1154+799C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345239 | |||||||
| chr11:113345317 | G | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0107 |
6 | HG01109.hp1 HG01123.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154+877G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345317 | |||||||
| chr11:113345444 | CTG | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(98): Show |
129 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.1154+1008_1154+100 others(6): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113345444 | ||||||
| chr11:113345487 | C | T | 1 | a0001c0006t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1154+1047C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345487 | |||||||
| chr11:113345582 | A | T | 1 | a0002c0002t0001g0190 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1154+1142A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345582 | |||||||
| chr11:113345864 | A | G | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0221 others(1): Show |
6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154+1424A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345864 | |||||||
| chr11:113345907 | ACCTCGGG others(8): Show |
A | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1154+1471_1154+148 others(19): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113345907 | ||||||
| chr11:113345996 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1154+1556C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113345996 | |||||||
| chr11:113346066 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1154+1626G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346066 | |||||||
| chr11:113346084 | G | A | 1 | a0002c0002t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1154+1644G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346084 | |||||||
| chr11:113346171 | C | A | 1 | a0002c0002t0001g0034 | 2 | HG01261.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1154+1731C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346171 | |||||||
| chr11:113346265 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1154+1825T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346265 | |||||||
| chr11:113346302 | C | G | 1 | a0001c0003t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1154+1862C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346302 | |||||||
| chr11:113346318 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1154+1878C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346318 | |||||||
| chr11:113346458 | A | T | 1 | a0001c0003t0001g0219 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1154+2018A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346458 | |||||||
| chr11:113346463 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1154+2023C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346463 | |||||||
| chr11:113346601 | C | G | 12 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0220 others(9): Show |
12 | HG02280.hp2 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1154+2161C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346601 | |||||||
| chr11:113346642 | A | G | 86 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(83): Show |
110 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1154+2202A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346642 | |||||||
| chr11:113346652 | G | GA | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0221 others(1): Show |
6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1154+2220dupA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113346652 | ||||||
| chr11:113346747 | T | A | 4 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(1): Show |
4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1154+2307T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346747 | |||||||
| chr11:113346751 | G | GA | 8 | a0001c0001t0001g0065 a0001c0001t0001g0097 a0001c0001t0001g0101 others(5): Show |
8 | HG01192.hp1 HG01192.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1154+2328dupA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113346751 | ||||||
| chr11:113346751 | GA | G | 10 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0053 others(7): Show |
13 | HG00741.hp1 HG02622.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1154+2328delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr11 | 113346751 | ||||||
| chr11:113346752 | A | G | 1 | a0002c0002t0001g0001 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1154+2312A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346752 | |||||||
| chr11:113346918 | G | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1154+2478G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346918 | |||||||
| chr11:113346978 | G | T | 1 | a0001c0001t0001g0100 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1154+2538G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113346978 | |||||||
| chr11:113347018 | G | C | 1 | a0002c0004t0001g0173 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1154+2578G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113347018 | |||||||
| chr11:113347328 | C | T | 35 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(32): Show |
59 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1155-2745C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113347328 | |||||||
| chr11:113347867 | C | T | 1 | a0002c0002t0001g0175 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1155-2206C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113347867 | |||||||
| chr11:113348082 | G | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0233 a0001c0001t0001g0234 others(4): Show |
7 | HG00323.hp1 HG02698.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-1991G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348082 | |||||||
| chr11:113348171 | A | T | 1 | a0002c0020t0001g0183 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1155-1902A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348171 | |||||||
| chr11:113348180 | C | T | 3 | a0001c0001t0001g0201 a0005c0009t0003g0074 a0005c0009t0003g0075 |
3 | HG02572.hp1 HG02896.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1155-1893C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348180 | |||||||
| chr11:113348248 | G | A | 1 | a0001c0003t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1155-1825G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348248 | |||||||
| chr11:113348288 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1155-1785A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348288 | |||||||
| chr11:113348603 | A | G | 7 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(4): Show |
8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155-1470A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348603 | |||||||
| chr11:113348680 | G | A | 14 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(11): Show |
15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1155-1393G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348680 | |||||||
| chr11:113348700 | A | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0139 |
2 | NA18967.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1155-1373A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348700 | |||||||
| chr11:113348786 | G | A | 1 | a0001c0006t0001g0022 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1155-1287G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348786 | |||||||
| chr11:113348836 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1155-1237G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348836 | |||||||
| chr11:113348860 | A | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0143 a0001c0001t0001g0226 others(3): Show |
8 | HG02145.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1155-1213A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113348860 | |||||||
| chr11:113349011 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1155-1062C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349011 | |||||||
| chr11:113349185 | A | G | 2 | a0001c0001t0001g0049 a0001c0001t0002g0043 |
4 | HG00738.hp1 HG01099.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1155-888A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349185 | |||||||
| chr11:113349205 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 |
5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1155-868C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349205 | |||||||
| chr11:113349308 | C | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0227 a0001c0001t0001g0239 others(3): Show |
7 | HG01243.hp1 HG02258.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1155-765C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349308 | |||||||
| chr11:113349323 | A | T | 1 | a0001c0001t0001g0049 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1155-750A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349323 | |||||||
| chr11:113349449 | C | T | 1 | a0002c0002t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1155-624C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349449 | |||||||
| chr11:113349524 | C | A | 2 | a0001c0003t0001g0202 a0001c0003t0001g0204 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1155-549C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349524 | |||||||
| chr11:113349877 | G | A | 2 | a0001c0003t0001g0202 a0001c0003t0001g0204 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1155-196G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 13/21 | chr11 | 113349877 | |||||||
| chr11:113350189 | T | C | 2 | a0001c0001t0001g0092 a0002c0002t0001g0012 |
4 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1247+24T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350189 | |||||||
| chr11:113350475 | T | A | 4 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0221 others(1): Show |
6 | HG02622.hp1 HG02630.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1247+310T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350475 | |||||||
| chr11:113350518 | C | A | 2 | a0002c0002t0001g0039 a0002c0002t0001g0192 |
3 | NA18962.hp2 NA18967.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1247+353C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350518 | |||||||
| chr11:113350620 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1247+455G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350620 | |||||||
| chr11:113350847 | G | A | 1 | a0002c0002t0001g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1248-392G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350847 | |||||||
| chr11:113350884 | A | T | 1 | a0001c0001t0001g0070 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1248-355A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350884 | |||||||
| chr11:113350918 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0238 |
2 | HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1248-321A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113350918 | |||||||
| chr11:113351064 | A | G | 1 | a0002c0002t0001g0153 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1248-175A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113351064 | |||||||
| chr11:113351072 | A | G | 2 | a0001c0001t0001g0135 a0002c0002t0001g0198 |
2 | HG00558.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.1248-167A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 14/21 | chr11 | 113351072 | |||||||
| chr11:113351504 | C | T | 1 | a0001c0001t0001g0025 | 2 | HG02004.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.1308+205C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 15/21 | chr11 | 113351504 | |||||||
| chr11:113351685 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0128 others(2): Show |
12 | NA18956.hp1 NA18963.hp2 NA18972.hp2 others(9): Show |
intron_variant | MODIFIER | c.1309-385G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 15/21 | chr11 | 113351685 | |||||||
| chr11:113352209 | T | C | 3 | a0001c0001t0001g0115 a0002c0002t0001g0011 a0002c0002t0001g0154 |
5 | HG00609.hp1 HG01496.hp1 HG01978.hp2 others(2): Show |
splice_donor_variant&intron_variant | HIGH | c.1446+2T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352209 | |||||||
| chr11:113352262 | G | T | 14 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(11): Show |
15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1446+55G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352262 | |||||||
| chr11:113352354 | A | AT | 7 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(4): Show |
8 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1446+148dupT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr11 | 113352354 | ||||||
| chr11:113352365 | G | T | 1 | a0001c0001t0001g0141 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1446+158G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352365 | |||||||
| chr11:113352389 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1446+182G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352389 | |||||||
| chr11:113352412 | T | A | 7 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(4): Show |
7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1446+205T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352412 | |||||||
| chr11:113352520 | G | A | 7 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(4): Show |
7 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1446+313G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352520 | |||||||
| chr11:113352735 | A | G | 1 | a0001c0001t0001g0099 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1446+528A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352735 | |||||||
| chr11:113352785 | T | A | 14 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(11): Show |
15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1446+578T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352785 | |||||||
| chr11:113352906 | G | A | 2 | a0001c0001t0001g0049 a0001c0001t0002g0043 |
4 | HG00738.hp1 HG01099.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1446+699G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113352906 | |||||||
| chr11:113353256 | T | C | 1 | a0002c0002t0001g0181 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1446+1049T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353256 | |||||||
| chr11:113353295 | C | T | 32 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0024 others(29): Show |
53 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1446+1088C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353295 | |||||||
| chr11:113353298 | A | C | 1 | a0001c0003t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1446+1091A>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353298 | |||||||
| chr11:113353328 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1446+1121T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353328 | |||||||
| chr11:113353398 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1446+1191T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353398 | |||||||
| chr11:113353538 | G | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1446+1331G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353538 | |||||||
| chr11:113353682 | A | G | 37 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(34): Show |
61 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1446+1475A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353682 | |||||||
| chr11:113353754 | T | C | 4 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(1): Show |
4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1446+1547T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113353754 | |||||||
| chr11:113354022 | A | T | 1 | a0001c0001t0001g0049 | 2 | HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1446+1815A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354022 | |||||||
| chr11:113354194 | C | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(116): Show |
150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1446+1987C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354194 | |||||||
| chr11:113354393 | C | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1446+2186C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354393 | |||||||
| chr11:113354422 | C | T | 32 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0024 others(29): Show |
53 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.1446+2215C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354422 | |||||||
| chr11:113354495 | A | G | 7 | a0001c0001t0001g0093 a0001c0001t0001g0233 a0001c0001t0001g0234 others(4): Show |
7 | HG00323.hp1 HG02698.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1446+2288A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354495 | |||||||
| chr11:113354877 | A | T | 14 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(11): Show |
15 | HG00642.hp1 HG01243.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1446+2670A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354877 | |||||||
| chr11:113354958 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1446+2751G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113354958 | |||||||
| chr11:113354991 | TC | T | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1446+2787delC | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr11 | 113354991 | ||||||
| chr11:113355032 | G | A | 1 | a0001c0001t0001g0026 | 2 | NA18993.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1446+2825G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355032 | |||||||
| chr11:113355096 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1446+2889T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355096 | |||||||
| chr11:113355139 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1446+2932A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355139 | |||||||
| chr11:113355276 | T | G | 3 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 |
5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1446+3069T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355276 | |||||||
| chr11:113355484 | G | A | 105 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(102): Show |
135 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1446+3277G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355484 | |||||||
| chr11:113355568 | C | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0224 a0001c0001t0001g0238 |
3 | HG02280.hp2 HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1446+3361C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355568 | |||||||
| chr11:113355682 | G | A | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1446+3475G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355682 | |||||||
| chr11:113355953 | A | T | 2 | a0001c0003t0001g0202 a0001c0003t0001g0204 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1447-3410A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113355953 | |||||||
| chr11:113356509 | A | G | 1 | a0002c0002t0001g0154 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1447-2854A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356509 | |||||||
| chr11:113356562 | G | C | 4 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(1): Show |
4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1447-2801G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356562 | |||||||
| chr11:113356647 | ATTTCCTC others(5): Show |
A | 10 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0220 others(7): Show |
10 | HG02280.hp2 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1447-2713_1447-270 others(16): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr11 | 113356647 | ||||||
| chr11:113356657 | C | T | 1 | a0001c0001t0001g0064 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1447-2706C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356657 | |||||||
| chr11:113356888 | T | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0029 others(14): Show |
32 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1447-2475T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356888 | |||||||
| chr11:113356941 | C | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0107 |
4 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-2422C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113356941 | |||||||
| chr11:113357001 | G | C | 37 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(34): Show |
61 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.1447-2362G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357001 | |||||||
| chr11:113357068 | T | A | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(116): Show |
150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1447-2295T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357068 | |||||||
| chr11:113357195 | A | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1447-2168A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357195 | |||||||
| chr11:113357626 | G | A | 2 | a0001c0006t0001g0022 a0001c0006t0001g0200 |
3 | HG01243.hp2 HG03139.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1447-1737G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357626 | |||||||
| chr11:113357657 | G | C | 5 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(2): Show |
5 | NA18945.hp2 NA18957.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1447-1706G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357657 | |||||||
| chr11:113357779 | T | C | 119 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(116): Show |
150 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1447-1584T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357779 | |||||||
| chr11:113357824 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0232 others(1): Show |
4 | HG02630.hp1 HG03130.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-1539C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113357824 | |||||||
| chr11:113358136 | A | G | 1 | a0002c0002t0001g0036 | 2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1447-1227A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358136 | |||||||
| chr11:113358174 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1447-1189C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358174 | |||||||
| chr11:113358458 | A | G | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1447-905A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358458 | |||||||
| chr11:113358576 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1447-787T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358576 | |||||||
| chr11:113358612 | A | G | 1 | a0002c0002t0001g0185 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1447-751A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358612 | |||||||
| chr11:113358943 | T | C | 47 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(44): Show |
71 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1447-420T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113358943 | |||||||
| chr11:113359200 | C | CT | 10 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 others(7): Show |
13 | HG01243.hp2 HG01516.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.1447-162dupT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr11 | 113359200 | ||||||
| chr11:113359207 | A | G | 1 | a0002c0002t0001g0198 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1447-156A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113359207 | |||||||
| chr11:113359213 | C | T | 4 | a0001c0001t0001g0148 a0002c0002t0001g0150 a0002c0002t0001g0158 others(1): Show |
4 | HG00741.hp2 HG04115.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1447-150C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113359213 | |||||||
| chr11:113359283 | G | A | 1 | a0002c0002t0001g0154 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1447-80G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 16/21 | chr11 | 113359283 | |||||||
| chr11:113359605 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1545+144C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359605 | |||||||
| chr11:113359694 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1545+233G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359694 | |||||||
| chr11:113359736 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 |
5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-204G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359736 | |||||||
| chr11:113359737 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1546-203C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359737 | |||||||
| chr11:113359838 | G | A | 2 | a0001c0003t0001g0086 a0001c0003t0001g0087 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1546-102G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359838 | |||||||
| chr11:113359878 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(95): Show |
125 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1546-62C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 17/21 | chr11 | 113359878 | |||||||
| chr11:113360020 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0245 a0001c0001t0001g0249 |
5 | HG02258.hp2 HG02280.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+12C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360020 | |||||||
| chr11:113360051 | C | CTTGTTTT others(3): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 others(2): Show |
8 | HG01243.hp2 HG02809.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1614+61_1614+70dup others(10): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360051 | ||||||
| chr11:113360051 | C | CTTGTTTT others(8): Show |
8 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(5): Show |
14 | HG01516.hp1 HG01517.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1614+56_1614+70dup others(15): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360051 | ||||||
| chr11:113360051 | C | CTTGTTTT others(13): Show |
34 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0024 others(31): Show |
50 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.1614+51_1614+70dup others(20): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360051 | ||||||
| chr11:113360051 | C | CTTGTTTT others(18): Show |
2 | a0001c0001t0001g0018 a0001c0001t0001g0107 |
4 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614+46_1614+70dup others(25): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360051 | ||||||
| chr11:113360206 | A | G | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(216): Show |
302 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.1614+198A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360206 | |||||||
| chr11:113360208 | A | G | 1 | a0001c0001t0001g0222 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1614+200A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360208 | |||||||
| chr11:113360409 | GA | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0049 others(6): Show |
14 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1614+412delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113360409 | ||||||
| chr11:113360454 | G | T | 8 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(5): Show |
12 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1614+446G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360454 | |||||||
| chr11:113360485 | T | C | 1 | a0001c0001t0004g0129 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1614+477T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360485 | |||||||
| chr11:113360569 | A | T | 1 | a0002c0002t0001g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1614+561A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360569 | |||||||
| chr11:113360625 | G | C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(5): Show |
12 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1614+617G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360625 | |||||||
| chr11:113360628 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1614+620C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360628 | |||||||
| chr11:113360668 | CCT | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0208 |
3 | HG01358.hp1 NA18956.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1614+661_1614+662d others(4): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360668 | |||||||
| chr11:113360723 | G | A | 8 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(5): Show |
12 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1614+715G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360723 | |||||||
| chr11:113360761 | G | A | 1 | a0001c0001t0001g0052 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1614+753G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360761 | |||||||
| chr11:113360869 | G | T | 1 | a0001c0003t0001g0216 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1614+861G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360869 | |||||||
| chr11:113360879 | G | A | 5 | a0001c0003t0001g0108 a0001c0003t0001g0109 a0001c0003t0001g0110 others(2): Show |
5 | HG00642.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+871G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360879 | |||||||
| chr11:113360892 | C | T | 43 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0018 others(40): Show |
66 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.1614+884C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360892 | |||||||
| chr11:113360896 | C | T | 11 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0220 others(8): Show |
12 | HG01243.hp2 HG02280.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.1614+888C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360896 | |||||||
| chr11:113360969 | G | A | 30 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0065 others(27): Show |
48 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1614+961G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360969 | |||||||
| chr11:113360987 | G | T | 1 | a0001c0001t0001g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1614+979G>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113360987 | |||||||
| chr11:113361021 | G | C | 3 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 |
5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1614+1013G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361021 | |||||||
| chr11:113361168 | G | A | 1 | a0001c0006t0001g0022 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1614+1160G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361168 | |||||||
| chr11:113361198 | C | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1614+1190C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361198 | |||||||
| chr11:113361208 | C | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 others(1): Show |
6 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-1193C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361208 | |||||||
| chr11:113361244 | A | T | 11 | a0001c0001t0001g0083 a0001c0001t0001g0120 a0001c0001t0001g0124 others(8): Show |
11 | HG00639.hp1 HG01256.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.1615-1157A>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361244 | |||||||
| chr11:113361348 | A | G | 8 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0220 others(5): Show |
8 | HG02280.hp2 HG02630.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1615-1053A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361348 | |||||||
| chr11:113361367 | A | G | 4 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 others(1): Show |
6 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1615-1034A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361367 | |||||||
| chr11:113361374 | C | T | 2 | a0001c0003t0001g0202 a0001c0003t0001g0204 |
2 | HG01891.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1615-1027C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361374 | |||||||
| chr11:113361490 | T | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0079 |
3 | NA18970.hp1 NA19002.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1615-911T>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361490 | |||||||
| chr11:113361576 | ATC | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(94): Show |
124 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1615-823_1615-822d others(4): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113361576 | ||||||
| chr11:113361700 | T | G | 39 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0020 others(36): Show |
60 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1615-701T>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361700 | |||||||
| chr11:113361951 | AT | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0222 a0001c0001t0001g0230 |
5 | HG02809.hp1 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1615-447delT | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113361951 | ||||||
| chr11:113361954 | T | TA | 38 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0020 others(35): Show |
58 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1615-432dupA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113361954 | ||||||
| chr11:113361954 | TA | T | 6 | a0001c0001t0001g0052 a0001c0001t0001g0120 a0001c0001t0001g0125 others(3): Show |
7 | HG01256.hp2 HG02258.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1615-432delA | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113361954 | ||||||
| chr11:113361981 | C | T | 155 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(152): Show |
209 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1615-420C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113361981 | |||||||
| chr11:113362109 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0209 |
3 | NA18987.hp2 NA19065.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1615-292T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113362109 | |||||||
| chr11:113362337 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(154): Show |
213 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.1615-64G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | chr11 | 113362337 | |||||||
| chr11:113362342 | T | TAA | 2 | a0001c0001t0001g0018 a0001c0001t0001g0107 |
4 | HG02055.hp1 HG02486.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1615-57_1615-56dup others(2): Show |
TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr11 | 113362342 | ||||||
| chr11:113362653 | G | A | 6 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1716+151G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362653 | |||||||
| chr11:113362724 | A | G | 6 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1716+222A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362724 | |||||||
| chr11:113362783 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1716+281C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362783 | |||||||
| chr11:113362822 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1716+320T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362822 | |||||||
| chr11:113362842 | A | G | 7 | a0001c0001t0001g0093 a0001c0001t0001g0233 a0001c0001t0001g0234 others(4): Show |
7 | HG00323.hp1 HG02698.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1716+340A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362842 | |||||||
| chr11:113362898 | C | T | 4 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(1): Show |
4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+396C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113362898 | |||||||
| chr11:113363004 | T | C | 2 | a0002c0002t0001g0015 a0002c0002t0001g0177 |
4 | HG02015.hp1 HG02027.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.1716+502T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363004 | |||||||
| chr11:113363171 | C | T | 4 | a0001c0003t0001g0059 a0001c0003t0001g0086 a0001c0003t0001g0087 others(1): Show |
4 | HG01516.hp1 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1717-657C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363171 | |||||||
| chr11:113363572 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1717-256C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363572 | |||||||
| chr11:113363744 | G | A | 116 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(113): Show |
147 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1717-84G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363744 | |||||||
| chr11:113363749 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(94): Show |
124 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1717-79A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 19/21 | chr11 | 113363749 | |||||||
| chr11:113363957 | T | C | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(122): Show |
170 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(167): Show |
intron_variant | MODIFIER | c.1816+30T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113363957 | |||||||
| chr11:113363997 | C | T | 8 | a0001c0001t0001g0113 a0001c0001t0001g0136 a0001c0001t0001g0220 others(5): Show |
8 | HG02280.hp2 HG02630.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1816+70C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113363997 | |||||||
| chr11:113364001 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1816+74G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364001 | |||||||
| chr11:113364053 | A | G | 42 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(39): Show |
49 | HG00140.hp1 HG00423.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.1816+126A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364053 | |||||||
| chr11:113364273 | A | G | 1 | a0002c0002t0001g0151 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1816+346A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364273 | |||||||
| chr11:113364309 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0091 |
2 | HG01346.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1816+382C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364309 | |||||||
| chr11:113364384 | C | A | 1 | a0002c0002t0001g0169 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1817-451C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364384 | |||||||
| chr11:113364697 | A | G | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0007 others(146): Show |
203 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1817-138A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364697 | |||||||
| chr11:113364743 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0107 others(2): Show |
9 | HG02055.hp1 HG02486.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1817-92G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364743 | |||||||
| chr11:113364807 | T | C | 1 | a0001c0006t0001g0200 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1817-28T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 20/21 | chr11 | 113364807 | |||||||
| chr11:113365142 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(110): Show |
144 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.2042+82A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365142 | |||||||
| chr11:113365189 | C | T | 6 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2042+129C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365189 | |||||||
| chr11:113365276 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG01109.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.2042+216G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365276 | |||||||
| chr11:113365294 | G | A | 1 | a0002c0002t0001g0182 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2042+234G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365294 | |||||||
| chr11:113365365 | C | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0112 a0001c0001t0001g0146 |
3 | HG03453.hp1 NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2042+305C>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365365 | |||||||
| chr11:113365477 | A | G | 45 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(42): Show |
69 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.2042+417A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365477 | |||||||
| chr11:113365498 | G | A | 1 | a0001c0006t0001g0022 | 2 | HG01243.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2042+438G>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365498 | |||||||
| chr11:113365594 | T | C | 1 | a0002c0002t0001g0167 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2042+534T>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365594 | |||||||
| chr11:113365613 | C | A | 1 | a0001c0001t0001g0048 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.2042+553C>A | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365613 | |||||||
| chr11:113365770 | G | C | 41 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0020 others(38): Show |
65 | HG00140.hp2 HG00639.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.2043-455G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113365770 | |||||||
| chr11:113366040 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2043-185C>T | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113366040 | |||||||
| chr11:113366109 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2043-116A>G | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113366109 | |||||||
| chr11:113366201 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2043-24G>C | TTC12 | ENSG00000149292.17 | transcript | ENST00000529221.6 | protein_coding | 21/21 | chr11 | 113366201 |