Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 134526 |
| ensemblid | ENSG00000172497.9 |
| hgncid | 24436 |
| symbol | ACOT12 |
| name | acyl-CoA thioesterase 12 |
| refseq_nuc | NM_130767.3 |
| refseq_prot | NP_570123.1 |
| ensembl_nuc | ENST00000307624.8 |
| ensembl_prot | ENSP00000303246.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 81329996 |
| end | 81394134 |
| strand | - |
| ver | v1.2 |
| region | chr5:81329996-81394134 |
| region5000 | chr5:81324996-81399134 |
| regionname0 | ACOT12_chr5_81329996_81394134 |
| regionname5000 | ACOT12_chr5_81324996_81399134 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 555 | 240 | 72 | 51 | 78 | 11 | 26 | 48 | ACOT12_chr5_81324996_81399134 | ACOT12 | MERPA others(550): Show |
chr5 | 81324996 | 81399134 |
| a0002 | 0/0 | 555 | 30 | 15 | 10 | 0 | 1 | 4 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | MERPA others(550): Show |
chr5 | 81324996 | 81399134 |
| a0003 | 0/0 | 555 | 5 | 2 | 1 | 0 | 0 | 2 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | MERPA others(550): Show |
chr5 | 81324996 | 81399134 |
| a0004 | 0/0 | 555 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | MERPA others(550): Show |
chr5 | 81324996 | 81399134 |
| a0005 | 0/0 | 555 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | MERPA others(550): Show |
chr5 | 81324996 | 81399134 |
| a0006 | 0/0 | 555 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | MERPA others(550): Show |
chr5 | 81324996 | 81399134 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1665 | 238 | 70 | 51 | 78 | 11 | 26 | ACOT12_chr5_81324996_81399134 | ACOT12 | ATGGA others(1660): Show |
chr5 | 81324996 | 81399134 | ||
| a0001c0005 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | ATGGA others(1660): Show |
chr5 | 81324996 | 81399134 | ||
| a0001c0007 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | ATGGA others(1660): Show |
chr5 | 81324996 | 81399134 | ||
| a0002c0002 | 0/0 | 1665 | 29 | 15 | 10 | 0 | 0 | 4 | ACOT12_chr5_81324996_81399134 | ACOT12 | ATGGA others(1660): Show |
chr5 | 81324996 | 81399134 | ||
| a0002c0009 | 0/0 | 1665 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | ATGGA others(1660): Show |
chr5 | 81324996 | 81399134 | ||
| a0003c0003 | 0/0 | 1665 | 5 | 2 | 1 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | ATGGA others(1660): Show |
chr5 | 81324996 | 81399134 | ||
| a0004c0008 | 0/0 | 1665 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | ATGGA others(1660): Show |
chr5 | 81324996 | 81399134 | ||
| a0005c0004 | 0/0 | 1665 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | ATGGA others(1660): Show |
chr5 | 81324996 | 81399134 | ||
| a0006c0006 | 0/0 | 1665 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | ATGGA others(1660): Show |
chr5 | 81324996 | 81399134 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2086 | 74 | 5 | 11 | 43 | 3 | 11 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0001c0001t0002 | 0/1 | 2086 | 61 | 9 | 23 | 17 | 4 | 7 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0001c0001t0003 | 0/0 | 2086 | 55 | 29 | 12 | 7 | 3 | 4 | ACOT12_chr5_81324996_81399134 | ACOT12 | TTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0001c0001t0004 | 0/0 | 2086 | 43 | 23 | 4 | 11 | 1 | 4 | ACOT12_chr5_81324996_81399134 | ACOT12 | TTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0001c0001t0005 | 0/0 | 2086 | 4 | 4 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | TTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0001c0001t0006 | 0/0 | 2086 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0001c0005t0003 | 0/0 | 2086 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | TTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0001c0007t0004 | 0/0 | 2086 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | TTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0002c0002t0001 | 0/0 | 2086 | 6 | 4 | 2 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0002c0002t0002 | 0/0 | 2086 | 14 | 6 | 6 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0002c0002t0003 | 0/0 | 2086 | 5 | 2 | 1 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | TTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0002c0002t0004 | 0/0 | 2086 | 3 | 2 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | TTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0002c0002t0007 | 0/0 | 2086 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0002c0009t0001 | 0/0 | 2086 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0003c0003t0001 | 0/0 | 2086 | 2 | 0 | 0 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0003c0003t0004 | 0/0 | 2086 | 3 | 2 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | TTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0004c0008t0002 | 0/0 | 2086 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0005c0004t0002 | 0/0 | 2086 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| a0006c0006t0002 | 0/0 | 2086 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | GTAGC others(2081): Show |
chr5 | 81324996 | 81399134 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0007 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0005g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0005t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0001c0007t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0008 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0009 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0004g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0002t0007g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0002c0009t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0003c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0003c0003t0004g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0003c0003t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0004c0008t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0005c0004t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| a0006c0006t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0029 | EUR | GBR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0222 | EUR | GBR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0078 | EUR | GBR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | GBR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0196 | EUR | FIN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0159 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | CHS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0065 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0227 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01106 | hp2 | a0002 | c0002 | t0004 | g0239 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0118 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0005 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0008 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01243 | hp1 | a0003 | c0003 | t0004 | g0015 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01243 | hp2 | a0004 | c0008 | t0002 | g0135 | AMR | PUR | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01361 | hp2 | a0005 | c0004 | t0002 | g0214 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0113 | EUR | IBS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0228 | EUR | IBS | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0237 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0100 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0062 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02004 | hp1 | a0001 | c0001 | t0006 | g0102 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02004 | hp2 | a0002 | c0002 | t0003 | g0238 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0171 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02145 | hp1 | a0003 | c0003 | t0004 | g0195 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0240 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | CDX | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0111 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0250 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0211 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0073 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0229 | EAS | KHV | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02572 | hp1 | a0002 | c0002 | t0004 | g0025 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0151 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0230 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0249 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0243 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0143 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0169 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0061 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0167 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0226 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02886 | hp1 | a0006 | c0006 | t0002 | g0184 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0204 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0206 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0024 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0022 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0027 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0248 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0148 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0247 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03225 | hp2 | a0001 | c0005 | t0003 | g0199 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ESN | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0164 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0235 | SAS | PJL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0012 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03831 | hp1 | a0001 | c0001 | t0004 | g0245 | SAS | BEB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | BEB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04115 | hp1 | a0002 | c0002 | t0003 | g0198 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0241 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0009 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0012 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0173 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | STU | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0242 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18522 | hp2 | a0001 | c0007 | t0004 | g0039 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | CHB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18950 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0142 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0009 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19043 | hp2 | a0002 | c0002 | t0003 | g0035 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | YRI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | ASW | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0063 | AFR | ASW | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0075 | EUR | TSI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20805 | hp1 | a0002 | c0009 | t0001 | g0256 | EUR | TSI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0007 | EUR | TSI | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0042 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0232 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0036 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03471 | hp1 | a0003 | c0003 | t0004 | g0015 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | USA | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | USA | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | USA | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA20300 | hp2 | a0002 | c0002 | t0007 | g0208 | AFR | USA | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0161 | AFR | LWK | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0076 | REF | REF | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | ACOT12_chr5_81324996_81399134 | ACOT12 | chr5 | 81324996 | 81399134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:81330515 | C | G | 1 | a0003 | 5 | HG01243.hp1 HG02145.hp1 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.1547G>C | p.Ser516Thr | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 15/15 | 1567/2086 | 1547/1668 | 516/555 | chr5 | 81330515 | |||
| chr5:81335823 | C | T | 1 | a0002 | 30 | HG01070.hp2 HG01099.hp2 HG01106.hp2 others(27): Show |
missense_variant | MODERATE | c.1207G>A | p.Ala403Thr | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/15 | 1227/2086 | 1207/1668 | 403/555 | chr5 | 81335823 | |||
| chr5:81343841 | T | C | 1 | a0006 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1021A>G | p.Ile341Val | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/15 | 1041/2086 | 1021/1668 | 341/555 | chr5 | 81343841 | |||
| chr5:81345970 | C | T | 1 | a0005 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.688G>A | p.Val230Ile | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/15 | 708/2086 | 688/1668 | 230/555 | chr5 | 81345970 | |||
| chr5:81363805 | G | A | 1 | a0004 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.343C>T | p.Pro115Ser | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/15 | 363/2086 | 343/1668 | 115/555 | chr5 | 81363805 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:81335845 | G | A | 1 | a0001c0005 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1185C>T | p.His395His | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/15 | 1205/2086 | 1185/1668 | 395/555 | chr5 | 81335845 | |||
| chr5:81344993 | G | A | 1 | a0001c0007 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.822C>T | p.Ala274Ala | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/15 | 842/2086 | 822/1668 | 274/555 | chr5 | 81344993 | |||
| chr5:81394034 | G | A | 1 | a0002c0009 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.81C>T | p.Ser27Ser | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/15 | 101/2086 | 81/1668 | 27/555 | chr5 | 81394034 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:81330127 | C | T | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(8): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*267G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 15/15 | 267 | chr5 | 81330127 | ||||||
| chr5:81330266 | C | T | 2 | a0001c0001t0005 a0002c0002t0007 |
5 | HG02572.hp2 HG03098.hp1 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*128G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 15/15 | 128 | chr5 | 81330266 | ||||||
| chr5:81330340 | G | T | 1 | a0001c0001t0006 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*54C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 15/15 | 54 | chr5 | 81330340 | ||||||
| chr5:81394134 | C | A | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(5): Show |
115 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(112): Show |
5_prime_UTR_variant | MODIFIER | c.-20G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/15 | 20 | chr5 | 81394134 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:81330678 | G | C | 2 | a0001c0001t0002g0226 a0002c0002t0002g0061 |
2 | HG02683.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1519-135C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 14/14 | chr5 | 81330678 | |||||||
| chr5:81331169 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0077 others(2): Show |
6 | NA18965.hp2 NA18971.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.1392-229T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331169 | |||||||
| chr5:81331259 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1392-319G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331259 | |||||||
| chr5:81331266 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1392-326T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331266 | |||||||
| chr5:81331277 | C | T | 1 | a0001c0001t0003g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1392-337G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331277 | |||||||
| chr5:81331298 | G | A | 2 | a0001c0001t0004g0165 a0001c0001t0004g0176 |
2 | HG00673.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1392-358C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331298 | |||||||
| chr5:81331335 | C | G | 2 | a0001c0001t0002g0060 a0001c0001t0002g0228 |
2 | HG01516.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1392-395G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331335 | |||||||
| chr5:81331341 | T | C | 108 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0052 others(105): Show |
115 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1392-401A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331341 | |||||||
| chr5:81331354 | A | G | 93 | a0001c0001t0001g0047 a0001c0001t0001g0052 a0001c0001t0001g0058 others(90): Show |
100 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1392-414T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331354 | |||||||
| chr5:81331403 | G | T | 11 | a0001c0001t0001g0128 a0001c0001t0001g0193 a0001c0001t0002g0194 others(8): Show |
11 | HG02258.hp1 HG02559.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1392-463C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331403 | |||||||
| chr5:81331406 | G | A | 1 | a0002c0002t0001g0186 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1392-466C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331406 | |||||||
| chr5:81331632 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1392-692C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331632 | |||||||
| chr5:81331635 | C | T | 2 | a0001c0001t0003g0157 a0001c0001t0003g0162 |
2 | HG01346.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.1392-695G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331635 | |||||||
| chr5:81331658 | G | T | 1 | a0002c0002t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1392-718C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331658 | |||||||
| chr5:81331848 | T | C | 6 | a0001c0001t0002g0207 a0001c0001t0003g0152 a0001c0001t0003g0191 others(3): Show |
6 | HG02486.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391+629A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331848 | |||||||
| chr5:81331919 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1391+558A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81331919 | |||||||
| chr5:81332065 | A | G | 6 | a0001c0001t0002g0207 a0001c0001t0003g0152 a0001c0001t0003g0191 others(3): Show |
6 | HG02486.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391+412T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332065 | |||||||
| chr5:81332113 | T | C | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+364A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332113 | |||||||
| chr5:81332120 | T | C | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+357A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332120 | |||||||
| chr5:81332228 | C | G | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+249G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332228 | |||||||
| chr5:81332298 | T | A | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0001c0001t0004g0155 |
3 | HG02486.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+179A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332298 | |||||||
| chr5:81332385 | A | G | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0001c0001t0004g0155 |
3 | HG02486.hp1 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1391+92T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 13/14 | chr5 | 81332385 | |||||||
| chr5:81332836 | G | A | 31 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0133 others(28): Show |
33 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1263-231C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81332836 | |||||||
| chr5:81332908 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1263-303A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81332908 | |||||||
| chr5:81333063 | TA | T | 55 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0047 others(52): Show |
57 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.1263-459delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333063 | |||||||
| chr5:81333082 | ACAAC | A | 32 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0047 others(29): Show |
32 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263-481_1263-478d others(6): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333082 | |||||||
| chr5:81333083 | C | T | 26 | a0001c0001t0001g0192 a0001c0001t0002g0125 a0001c0001t0003g0145 others(23): Show |
28 | HG00642.hp2 HG01070.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1263-478G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333083 | |||||||
| chr5:81333087 | A | T | 32 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0047 others(29): Show |
32 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263-482T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333087 | |||||||
| chr5:81333100 | A | C | 2 | a0001c0001t0002g0083 a0001c0001t0003g0200 |
2 | HG00741.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1263-495T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333100 | |||||||
| chr5:81333119 | A | G | 5 | a0001c0001t0001g0192 a0001c0001t0003g0145 a0001c0001t0003g0147 others(2): Show |
5 | HG02055.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1263-514T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333119 | |||||||
| chr5:81333128 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1263-523T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333128 | |||||||
| chr5:81333156 | C | T | 4 | a0001c0001t0001g0086 a0001c0001t0002g0079 a0001c0001t0003g0235 others(1): Show |
4 | HG01192.hp2 HG02148.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263-551G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333156 | |||||||
| chr5:81333220 | A | C | 60 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0047 others(57): Show |
62 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1263-615T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333220 | |||||||
| chr5:81333447 | C | T | 32 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0047 others(29): Show |
32 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263-842G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333447 | |||||||
| chr5:81333514 | G | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0114 |
2 | NA18982.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1263-909C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333514 | |||||||
| chr5:81333553 | A | C | 60 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0047 others(57): Show |
62 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.1263-948T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333553 | |||||||
| chr5:81333626 | A | T | 32 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0047 others(29): Show |
32 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.1263-1021T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333626 | |||||||
| chr5:81333680 | C | T | 1 | a0001c0001t0002g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1263-1075G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333680 | |||||||
| chr5:81333747 | A | G | 33 | a0001c0001t0001g0040 a0001c0001t0001g0044 a0001c0001t0001g0047 others(30): Show |
33 | HG00438.hp2 HG00558.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.1263-1142T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81333747 | |||||||
| chr5:81334110 | A | G | 6 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(3): Show |
6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263-1505T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334110 | |||||||
| chr5:81334123 | C | T | 6 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(3): Show |
6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263-1518G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334123 | |||||||
| chr5:81334163 | T | TA | 6 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(3): Show |
6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263-1559dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334163 | |||||||
| chr5:81334245 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0002g0228 a0001c0001t0003g0028 others(4): Show |
7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1262+1523G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334245 | |||||||
| chr5:81334345 | C | T | 6 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(3): Show |
6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+1423G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334345 | |||||||
| chr5:81334469 | G | C | 36 | a0001c0001t0001g0054 a0001c0001t0001g0113 a0001c0001t0001g0133 others(33): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.1262+1299C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334469 | |||||||
| chr5:81334734 | G | A | 95 | a0001c0001t0001g0044 a0001c0001t0001g0054 a0001c0001t0001g0113 others(92): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1262+1034C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334734 | |||||||
| chr5:81334854 | G | A | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0001c0007t0004g0039 |
3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1262+914C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334854 | |||||||
| chr5:81334866 | G | C | 2 | a0001c0001t0004g0146 a0001c0001t0005g0248 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1262+902C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81334866 | |||||||
| chr5:81335013 | G | A | 6 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(3): Show |
6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+755C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335013 | |||||||
| chr5:81335128 | T | C | 7 | a0002c0002t0002g0009 a0002c0002t0002g0059 a0002c0002t0002g0062 others(4): Show |
8 | HG01099.hp2 HG01109.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1262+640A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335128 | |||||||
| chr5:81335160 | G | A | 1 | a0001c0001t0004g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1262+608C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335160 | |||||||
| chr5:81335325 | T | A | 1 | a0002c0002t0003g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1262+443A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335325 | |||||||
| chr5:81335333 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1262+435A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335333 | |||||||
| chr5:81335440 | C | T | 6 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(3): Show |
6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+328G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335440 | |||||||
| chr5:81335445 | G | A | 9 | a0001c0001t0001g0193 a0001c0001t0002g0083 a0001c0001t0002g0194 others(6): Show |
9 | HG00741.hp2 HG02615.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1262+323C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335445 | |||||||
| chr5:81335502 | T | C | 98 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0133 others(95): Show |
102 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1262+266A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335502 | |||||||
| chr5:81335656 | A | G | 1 | a0001c0001t0004g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1262+112T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335656 | |||||||
| chr5:81335692 | G | A | 85 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0133 others(82): Show |
89 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1262+76C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335692 | |||||||
| chr5:81335700 | T | G | 6 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(3): Show |
6 | HG01516.hp2 HG01934.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1262+68A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335700 | |||||||
| chr5:81335728 | G | T | 1 | a0001c0001t0003g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1262+40C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 12/14 | chr5 | 81335728 | |||||||
| chr5:81335962 | A | G | 2 | a0001c0001t0002g0211 a0001c0001t0005g0037 |
2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1129-61T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81335962 | |||||||
| chr5:81335987 | C | A | 5 | a0001c0001t0002g0211 a0001c0001t0003g0191 a0001c0001t0003g0232 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-86G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81335987 | |||||||
| chr5:81336036 | CAT | C | 85 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0133 others(82): Show |
89 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1129-137_1129-136d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336036 | |||||||
| chr5:81336058 | C | T | 7 | a0001c0001t0001g0192 a0001c0001t0003g0145 a0001c0001t0003g0147 others(4): Show |
8 | HG01167.hp2 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1129-157G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336058 | |||||||
| chr5:81336096 | C | T | 1 | a0001c0001t0003g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1129-195G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336096 | |||||||
| chr5:81336097 | G | A | 1 | a0001c0001t0004g0024 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1129-196C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336097 | |||||||
| chr5:81336152 | G | GT | 6 | a0001c0001t0001g0097 a0001c0001t0001g0116 a0001c0001t0002g0002 others(3): Show |
8 | HG00408.hp2 HG02027.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.1129-252dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336152 | |||||||
| chr5:81336163 | T | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0050 a0001c0001t0002g0084 others(1): Show |
4 | HG00438.hp2 NA18612.hp2 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1129-262A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336163 | |||||||
| chr5:81336244 | A | G | 1 | a0001c0001t0002g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1129-343T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336244 | |||||||
| chr5:81336258 | C | T | 4 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(1): Show |
4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-357G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336258 | |||||||
| chr5:81336360 | G | C | 1 | a0001c0001t0002g0120 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1129-459C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336360 | |||||||
| chr5:81336394 | C | G | 2 | a0002c0002t0001g0008 a0002c0002t0003g0035 |
3 | HG01167.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1129-493G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336394 | |||||||
| chr5:81336430 | T | C | 1 | a0001c0001t0002g0194 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1129-529A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336430 | |||||||
| chr5:81336444 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0004g0146 a0001c0001t0004g0154 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-543C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336444 | |||||||
| chr5:81336474 | G | A | 1 | a0001c0001t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1129-573C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336474 | |||||||
| chr5:81336586 | A | G | 1 | a0001c0001t0004g0022 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1129-685T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336586 | |||||||
| chr5:81336714 | T | C | 1 | a0001c0001t0003g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1129-813A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336714 | |||||||
| chr5:81336731 | A | G | 5 | a0001c0001t0001g0044 a0001c0001t0004g0146 a0001c0001t0004g0154 others(2): Show |
5 | HG01496.hp1 HG02055.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-830T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336731 | |||||||
| chr5:81336849 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1129-948G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336849 | |||||||
| chr5:81336903 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1129-1002G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336903 | |||||||
| chr5:81336936 | A | G | 1 | a0001c0001t0003g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1129-1035T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81336936 | |||||||
| chr5:81337042 | G | C | 4 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(1): Show |
4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-1141C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337042 | |||||||
| chr5:81337053 | C | A | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1129-1152G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337053 | |||||||
| chr5:81337082 | A | G | 7 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(4): Show |
7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-1181T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337082 | |||||||
| chr5:81337154 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0133 |
2 | HG01516.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1129-1253C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337154 | |||||||
| chr5:81337181 | C | T | 60 | a0001c0001t0001g0113 a0001c0001t0001g0133 a0001c0001t0001g0192 others(57): Show |
64 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1129-1280G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337181 | |||||||
| chr5:81337218 | T | G | 7 | a0002c0002t0001g0074 a0002c0002t0002g0061 a0002c0002t0002g0073 others(4): Show |
7 | HG01106.hp2 HG01346.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1129-1317A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337218 | |||||||
| chr5:81337255 | G | A | 7 | a0001c0001t0002g0083 a0001c0001t0003g0152 a0001c0001t0003g0200 others(4): Show |
7 | HG00741.hp2 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1129-1354C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337255 | |||||||
| chr5:81337322 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1129-1421T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337322 | |||||||
| chr5:81337350 | C | T | 1 | a0001c0001t0004g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1129-1449G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337350 | |||||||
| chr5:81337354 | G | A | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1129-1453C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337354 | |||||||
| chr5:81337377 | T | G | 4 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(1): Show |
4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-1476A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337377 | |||||||
| chr5:81337619 | A | G | 5 | a0001c0001t0002g0211 a0001c0001t0003g0191 a0001c0001t0003g0232 others(2): Show |
5 | HG02258.hp1 HG02486.hp1 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1129-1718T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337619 | |||||||
| chr5:81337848 | T | G | 4 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(1): Show |
4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-1947A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337848 | |||||||
| chr5:81337962 | T | C | 7 | a0001c0001t0002g0083 a0001c0001t0003g0152 a0001c0001t0003g0200 others(4): Show |
7 | HG00741.hp2 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1129-2061A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337962 | |||||||
| chr5:81337977 | A | G | 4 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(1): Show |
4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-2076T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81337977 | |||||||
| chr5:81338043 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0004g0146 a0001c0001t0005g0248 |
3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1129-2142G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338043 | |||||||
| chr5:81338150 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1129-2249A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338150 | |||||||
| chr5:81338161 | A | G | 4 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(1): Show |
4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1129-2260T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338161 | |||||||
| chr5:81338293 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1129-2392G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338293 | |||||||
| chr5:81338496 | G | A | 20 | a0002c0002t0001g0074 a0002c0002t0001g0186 a0002c0002t0002g0009 others(17): Show |
21 | HG01070.hp2 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.1129-2595C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338496 | |||||||
| chr5:81338644 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1129-2743G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338644 | |||||||
| chr5:81338893 | A | C | 7 | a0001c0001t0001g0044 a0001c0001t0002g0228 a0001c0001t0003g0028 others(4): Show |
7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-2992T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338893 | |||||||
| chr5:81338946 | T | C | 3 | a0001c0001t0001g0054 a0001c0001t0002g0053 a0001c0001t0002g0055 |
3 | HG02735.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1129-3045A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81338946 | |||||||
| chr5:81339201 | T | C | 7 | a0001c0001t0001g0044 a0001c0001t0002g0228 a0001c0001t0003g0028 others(4): Show |
7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-3300A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339201 | |||||||
| chr5:81339221 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0002g0228 a0001c0001t0003g0028 others(4): Show |
7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1129-3320G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339221 | |||||||
| chr5:81339240 | A | C | 60 | a0001c0001t0001g0113 a0001c0001t0001g0133 a0001c0001t0001g0192 others(57): Show |
64 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1129-3339T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339240 | |||||||
| chr5:81339300 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1128+3372G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339300 | |||||||
| chr5:81339683 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1128+2989G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339683 | |||||||
| chr5:81339716 | A | G | 7 | a0001c0001t0001g0044 a0001c0001t0002g0228 a0001c0001t0003g0028 others(4): Show |
7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+2956T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339716 | |||||||
| chr5:81339800 | C | T | 98 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0133 others(95): Show |
102 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1128+2872G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339800 | |||||||
| chr5:81339896 | AT | A | 61 | a0001c0001t0001g0113 a0001c0001t0001g0133 a0001c0001t0001g0213 others(58): Show |
64 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.1128+2775delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339896 | |||||||
| chr5:81339970 | C | T | 1 | a0001c0001t0003g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1128+2702G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81339970 | |||||||
| chr5:81340042 | C | CT | 9 | a0001c0001t0001g0044 a0001c0001t0002g0087 a0001c0001t0002g0228 others(6): Show |
9 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1128+2629dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340042 | |||||||
| chr5:81340042 | C | CTT | 6 | a0001c0001t0002g0083 a0001c0001t0003g0152 a0001c0001t0003g0200 others(3): Show |
6 | HG00741.hp2 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1128+2628_1128+262 others(6): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340042 | |||||||
| chr5:81340060 | T | A | 1 | a0001c0001t0004g0167 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1128+2612A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340060 | |||||||
| chr5:81340183 | G | A | 16 | a0001c0001t0001g0193 a0001c0001t0002g0043 a0001c0001t0002g0194 others(13): Show |
16 | HG02055.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.1128+2489C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340183 | |||||||
| chr5:81340435 | C | T | 4 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1128+2237G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340435 | |||||||
| chr5:81340450 | C | T | 7 | a0001c0001t0001g0044 a0001c0001t0002g0228 a0001c0001t0003g0028 others(4): Show |
7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+2222G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340450 | |||||||
| chr5:81340507 | G | A | 4 | a0002c0002t0001g0186 a0002c0002t0002g0042 a0002c0002t0002g0206 others(1): Show |
4 | HG01891.hp1 HG02109.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+2165C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340507 | |||||||
| chr5:81340508 | C | T | 1 | a0001c0001t0004g0245 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1128+2164G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340508 | |||||||
| chr5:81340653 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1128+2019G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340653 | |||||||
| chr5:81340717 | G | A | 98 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0133 others(95): Show |
102 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1128+1955C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340717 | |||||||
| chr5:81340733 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1128+1939C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340733 | |||||||
| chr5:81340900 | T | G | 1 | a0001c0001t0005g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1128+1772A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81340900 | |||||||
| chr5:81341141 | T | C | 4 | a0001c0001t0002g0211 a0001c0001t0004g0154 a0001c0001t0004g0155 others(1): Show |
4 | HG01496.hp1 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+1531A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341141 | |||||||
| chr5:81341203 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1128+1469A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341203 | |||||||
| chr5:81341616 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0002g0228 a0001c0001t0003g0028 others(4): Show |
7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+1056C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341616 | |||||||
| chr5:81341617 | C | A | 2 | a0001c0001t0001g0077 a0001c0001t0002g0095 |
2 | NA19081.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1128+1055G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341617 | |||||||
| chr5:81341652 | T | C | 6 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0141 others(3): Show |
7 | HG01167.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+1020A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341652 | |||||||
| chr5:81341653 | G | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1128+1019C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341653 | |||||||
| chr5:81341710 | G | A | 53 | a0001c0001t0001g0113 a0001c0001t0001g0133 a0001c0001t0001g0213 others(50): Show |
56 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1128+962C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341710 | |||||||
| chr5:81341712 | T | C | 9 | a0001c0001t0002g0043 a0001c0001t0003g0026 a0001c0001t0003g0143 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1128+960A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341712 | |||||||
| chr5:81341894 | T | C | 4 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(1): Show |
4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+778A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341894 | |||||||
| chr5:81341999 | A | AT | 7 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(4): Show |
7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+672dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341999 | |||||||
| chr5:81341999 | A | T | 2 | a0001c0001t0002g0083 a0001c0001t0003g0200 |
2 | HG00741.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1128+673T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81341999 | |||||||
| chr5:81342002 | T | TATTA | 7 | a0001c0001t0001g0044 a0001c0001t0002g0228 a0001c0001t0003g0028 others(4): Show |
7 | HG01516.hp2 HG01934.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1128+669_1128+670i others(6): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342002 | |||||||
| chr5:81342037 | C | A | 4 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(1): Show |
4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+635G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342037 | |||||||
| chr5:81342286 | C | T | 1 | a0001c0001t0004g0177 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1128+386G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342286 | |||||||
| chr5:81342439 | C | T | 4 | a0001c0001t0002g0228 a0001c0001t0003g0028 a0001c0001t0003g0034 others(1): Show |
4 | HG01516.hp2 HG01934.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128+233G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342439 | |||||||
| chr5:81342474 | T | C | 1 | a0001c0007t0004g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1128+198A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 11/14 | chr5 | 81342474 | |||||||
| chr5:81342772 | A | G | 1 | a0001c0001t0003g0235 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1045-17T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81342772 | |||||||
| chr5:81342790 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1045-35C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81342790 | |||||||
| chr5:81342934 | C | T | 1 | a0001c0001t0003g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1045-179G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81342934 | |||||||
| chr5:81343143 | C | T | 1 | a0006c0006t0002g0184 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1045-388G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343143 | |||||||
| chr5:81343144 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG00609.hp2 NA18957.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-389C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343144 | |||||||
| chr5:81343197 | C | CA | 6 | a0001c0001t0001g0071 a0001c0001t0001g0110 a0001c0001t0003g0143 others(3): Show |
6 | HG00621.hp2 HG01175.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1045-443dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343197 | |||||||
| chr5:81343207 | C | A | 1 | a0001c0001t0003g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1045-452G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343207 | |||||||
| chr5:81343209 | C | T | 1 | a0001c0001t0004g0177 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1045-454G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343209 | |||||||
| chr5:81343246 | A | C | 3 | a0001c0001t0001g0044 a0001c0001t0004g0146 a0001c0001t0005g0248 |
3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1045-491T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343246 | |||||||
| chr5:81343533 | G | A | 6 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0141 others(3): Show |
7 | HG01167.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1044+285C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343533 | |||||||
| chr5:81343682 | T | C | 54 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0080 others(51): Show |
60 | HG00099.hp1 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1044+136A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343682 | |||||||
| chr5:81343687 | A | G | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1044+131T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343687 | |||||||
| chr5:81343691 | C | T | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0001c0007t0004g0039 |
3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1044+127G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 10/14 | chr5 | 81343691 | |||||||
| chr5:81344314 | G | A | 2 | a0001c0001t0003g0021 a0001c0001t0004g0024 |
2 | HG02895.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.925-99C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344314 | |||||||
| chr5:81344406 | G | A | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.925-191C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344406 | |||||||
| chr5:81344580 | C | T | 8 | a0001c0001t0002g0043 a0001c0001t0003g0026 a0001c0001t0003g0145 others(5): Show |
8 | HG02055.hp2 HG02451.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.924+311G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344580 | |||||||
| chr5:81344727 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0004g0146 a0001c0001t0005g0248 |
3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.924+164G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344727 | |||||||
| chr5:81344803 | A | C | 7 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(4): Show |
7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.924+88T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344803 | |||||||
| chr5:81344817 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.924+74G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 8/14 | chr5 | 81344817 | |||||||
| chr5:81345064 | G | T | 29 | a0001c0001t0001g0044 a0001c0001t0001g0193 a0001c0001t0002g0043 others(26): Show |
30 | HG01167.hp2 HG01884.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.774-23C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345064 | |||||||
| chr5:81345093 | CCCTCCTT others(14): Show |
C | 1 | a0001c0007t0004g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.774-73_774-53delTG others(19): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345093 | |||||||
| chr5:81345100 | TGCACACC others(14): Show |
T | 95 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0133 others(92): Show |
99 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.774-80_774-60delGA others(19): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345100 | |||||||
| chr5:81345103 | ACACCGCT others(14): Show |
A | 1 | a0001c0001t0003g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.774-83_774-63delGG others(19): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345103 | |||||||
| chr5:81345111 | GCCACCTC others(5): Show |
G | 2 | a0001c0001t0003g0246 a0001c0001t0004g0249 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.774-82_774-71delGC others(10): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345111 | |||||||
| chr5:81345128 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0002g0211 a0001c0001t0004g0146 others(2): Show |
5 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.774-87G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345128 | |||||||
| chr5:81345129 | G | A | 3 | a0001c0001t0003g0144 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG01496.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.774-88C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345129 | |||||||
| chr5:81345153 | G | T | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0001c0007t0004g0039 |
3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.774-112C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345153 | |||||||
| chr5:81345347 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0141 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.774-306C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345347 | |||||||
| chr5:81345362 | A | T | 9 | a0001c0001t0003g0143 a0001c0001t0003g0152 a0001c0001t0003g0191 others(6): Show |
9 | HG02486.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.774-321T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345362 | |||||||
| chr5:81345526 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.773+359A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345526 | |||||||
| chr5:81345652 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0106 a0001c0001t0001g0140 |
4 | NA18965.hp2 NA18971.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.773+233T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345652 | |||||||
| chr5:81345663 | C | T | 3 | a0001c0001t0002g0211 a0001c0001t0005g0037 a0001c0005t0003g0199 |
3 | HG02258.hp1 HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.773+222G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345663 | |||||||
| chr5:81345790 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0004g0146 a0001c0001t0005g0248 |
3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.773+95G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 7/14 | chr5 | 81345790 | |||||||
| chr5:81346039 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.654-35C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346039 | |||||||
| chr5:81346101 | T | G | 5 | a0001c0001t0001g0192 a0001c0001t0003g0021 a0001c0001t0003g0147 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-97A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346101 | |||||||
| chr5:81346396 | T | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0192 a0001c0001t0003g0021 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-392A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346396 | |||||||
| chr5:81346424 | C | T | 1 | a0001c0001t0002g0078 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.654-420G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346424 | |||||||
| chr5:81346438 | G | A | 1 | a0001c0001t0004g0159 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.654-434C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346438 | |||||||
| chr5:81346475 | A | G | 2 | a0001c0001t0002g0085 a0001c0001t0002g0096 |
2 | NA18968.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.654-471T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346475 | |||||||
| chr5:81346506 | A | G | 8 | a0001c0001t0001g0044 a0001c0001t0001g0192 a0001c0001t0003g0021 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-502T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346506 | |||||||
| chr5:81346694 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.654-690G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346694 | |||||||
| chr5:81346785 | CTA | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0192 a0001c0001t0003g0021 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.654-783_654-782del others(2): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346785 | |||||||
| chr5:81346874 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.654-870A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346874 | |||||||
| chr5:81346903 | A | G | 7 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(4): Show |
7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.653+871T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346903 | |||||||
| chr5:81346917 | G | C | 3 | a0001c0001t0001g0064 a0001c0001t0004g0165 a0001c0001t0004g0176 |
3 | HG00673.hp2 NA18950.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.653+857C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81346917 | |||||||
| chr5:81347019 | C | T | 5 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.653+755G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347019 | |||||||
| chr5:81347020 | T | C | 1 | a0001c0001t0004g0247 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.653+754A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347020 | |||||||
| chr5:81347401 | C | A | 97 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0133 others(94): Show |
101 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.653+373G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347401 | |||||||
| chr5:81347510 | C | G | 20 | a0001c0001t0002g0228 a0002c0002t0001g0074 a0002c0002t0001g0186 others(17): Show |
21 | HG01070.hp2 HG01099.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.653+264G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347510 | |||||||
| chr5:81347729 | C | G | 1 | a0001c0001t0001g0045 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.653+45G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 6/14 | chr5 | 81347729 | |||||||
| chr5:81348003 | G | A | 9 | a0001c0001t0001g0072 a0001c0001t0001g0126 a0001c0001t0001g0129 others(6): Show |
9 | HG00597.hp2 HG01346.hp2 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-73C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348003 | |||||||
| chr5:81348019 | C | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0192 a0001c0001t0003g0021 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-89G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348019 | |||||||
| chr5:81348288 | A | T | 1 | a0002c0002t0003g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.497-358T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348288 | |||||||
| chr5:81348355 | A | G | 100 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0133 others(97): Show |
104 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.497-425T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348355 | |||||||
| chr5:81348403 | A | G | 2 | a0001c0001t0002g0211 a0001c0001t0005g0037 |
2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.497-473T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348403 | |||||||
| chr5:81348456 | A | C | 8 | a0001c0001t0001g0044 a0001c0001t0001g0192 a0001c0001t0003g0021 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-526T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348456 | |||||||
| chr5:81348629 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0004g0146 a0001c0001t0005g0248 |
3 | HG02055.hp1 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.497-699T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348629 | |||||||
| chr5:81348689 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-759G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348689 | |||||||
| chr5:81348746 | G | T | 1 | a0001c0001t0004g0033 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.497-816C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348746 | |||||||
| chr5:81348764 | A | G | 9 | a0001c0001t0002g0043 a0001c0001t0003g0026 a0001c0001t0003g0145 others(6): Show |
9 | HG02055.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-834T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348764 | |||||||
| chr5:81348775 | G | T | 7 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(4): Show |
7 | HG02615.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-845C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348775 | |||||||
| chr5:81348815 | C | T | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-885G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348815 | |||||||
| chr5:81348842 | G | A | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0001c0007t0004g0039 |
3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.497-912C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348842 | |||||||
| chr5:81348889 | C | T | 8 | a0001c0001t0001g0044 a0001c0001t0001g0192 a0001c0001t0003g0021 others(5): Show |
8 | HG02055.hp1 HG02451.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-959G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348889 | |||||||
| chr5:81348900 | A | C | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.497-970T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81348900 | |||||||
| chr5:81349005 | C | T | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-1075G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349005 | |||||||
| chr5:81349273 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-1343C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349273 | |||||||
| chr5:81349317 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0002g0094 |
2 | NA18612.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.497-1387G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349317 | |||||||
| chr5:81349319 | C | T | 6 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0003g0241 others(3): Show |
6 | HG01361.hp2 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-1389G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349319 | |||||||
| chr5:81349405 | C | T | 9 | a0001c0001t0001g0192 a0001c0001t0003g0021 a0001c0001t0003g0147 others(6): Show |
9 | HG01361.hp2 HG02572.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-1475G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349405 | |||||||
| chr5:81349486 | T | A | 3 | a0001c0001t0004g0146 a0001c0001t0005g0248 a0001c0005t0003g0199 |
3 | HG02451.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.497-1556A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349486 | |||||||
| chr5:81349528 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.497-1598G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349528 | |||||||
| chr5:81349537 | C | T | 8 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0001g0186 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-1607G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349537 | |||||||
| chr5:81349541 | C | A | 2 | a0001c0001t0002g0211 a0001c0001t0005g0037 |
2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.497-1611G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349541 | |||||||
| chr5:81349642 | T | C | 3 | a0001c0001t0002g0083 a0001c0001t0003g0028 a0001c0001t0003g0034 |
3 | HG00741.hp2 HG03139.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.497-1712A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349642 | |||||||
| chr5:81349745 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.497-1815C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349745 | |||||||
| chr5:81349828 | C | T | 5 | a0001c0001t0003g0021 a0001c0001t0003g0243 a0001c0001t0003g0244 others(2): Show |
6 | HG01167.hp2 HG02630.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-1898G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81349828 | |||||||
| chr5:81350005 | G | A | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-2075C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350005 | |||||||
| chr5:81350127 | C | T | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-2197G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350127 | |||||||
| chr5:81350192 | G | T | 11 | a0001c0001t0001g0058 a0001c0001t0001g0086 a0001c0001t0002g0079 others(8): Show |
13 | HG00099.hp1 HG01123.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.497-2262C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350192 | |||||||
| chr5:81350257 | A | G | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0001c0007t0004g0039 |
3 | HG02486.hp1 NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.497-2327T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350257 | |||||||
| chr5:81350291 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.497-2361A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350291 | |||||||
| chr5:81350306 | T | C | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-2376A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350306 | |||||||
| chr5:81350567 | G | A | 25 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0170 others(22): Show |
27 | HG00408.hp1 HG00673.hp1 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.497-2637C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350567 | |||||||
| chr5:81350699 | G | C | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-2769C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350699 | |||||||
| chr5:81350736 | A | G | 2 | a0001c0001t0003g0034 a0002c0002t0007g0208 |
2 | HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.497-2806T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350736 | |||||||
| chr5:81350839 | G | A | 6 | a0001c0001t0002g0043 a0001c0001t0003g0026 a0001c0001t0003g0028 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.497-2909C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350839 | |||||||
| chr5:81350846 | C | A | 1 | a0001c0001t0003g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.497-2916G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350846 | |||||||
| chr5:81350957 | G | C | 4 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-3027C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81350957 | |||||||
| chr5:81351062 | T | G | 1 | a0001c0001t0003g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.497-3132A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351062 | |||||||
| chr5:81351305 | C | T | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-3375G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351305 | |||||||
| chr5:81351326 | A | G | 6 | a0001c0001t0004g0005 a0001c0001t0004g0006 a0001c0001t0004g0020 others(3): Show |
8 | HG01109.hp2 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.497-3396T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351326 | |||||||
| chr5:81351365 | T | C | 89 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(86): Show |
97 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.497-3435A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351365 | |||||||
| chr5:81351678 | C | T | 75 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(72): Show |
82 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.497-3748G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351678 | |||||||
| chr5:81351864 | C | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0066 a0001c0001t0001g0105 others(3): Show |
6 | HG01074.hp1 HG01106.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-3934G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351864 | |||||||
| chr5:81351994 | C | T | 1 | a0001c0001t0002g0083 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.497-4064G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81351994 | |||||||
| chr5:81352009 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.497-4079G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352009 | |||||||
| chr5:81352022 | C | A | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-4092G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352022 | |||||||
| chr5:81352080 | C | T | 2 | a0001c0001t0002g0211 a0001c0001t0005g0037 |
2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.497-4150G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352080 | |||||||
| chr5:81352295 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.497-4365A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352295 | |||||||
| chr5:81352297 | T | C | 1 | a0001c0001t0004g0030 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.497-4367A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352297 | |||||||
| chr5:81352696 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.497-4766C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352696 | |||||||
| chr5:81352795 | A | G | 1 | a0001c0001t0002g0096 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.497-4865T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352795 | |||||||
| chr5:81352844 | C | T | 53 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(50): Show |
57 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.497-4914G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352844 | |||||||
| chr5:81352876 | G | A | 111 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(108): Show |
119 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.497-4946C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352876 | |||||||
| chr5:81352961 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-5031A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81352961 | |||||||
| chr5:81353054 | T | C | 21 | a0001c0001t0002g0075 a0001c0001t0002g0112 a0001c0001t0002g0203 others(18): Show |
24 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.497-5124A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353054 | |||||||
| chr5:81353091 | C | T | 17 | a0001c0001t0001g0193 a0001c0001t0002g0083 a0001c0001t0002g0194 others(14): Show |
17 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.497-5161G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353091 | |||||||
| chr5:81353186 | G | A | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-5256C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353186 | |||||||
| chr5:81353255 | G | A | 22 | a0001c0001t0001g0193 a0001c0001t0002g0083 a0001c0001t0002g0194 others(19): Show |
22 | HG00741.hp2 HG01884.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.497-5325C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353255 | |||||||
| chr5:81353293 | GA | G | 3 | a0001c0001t0003g0034 a0002c0002t0007g0208 a0005c0004t0002g0214 |
3 | HG01361.hp2 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.497-5364delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353293 | |||||||
| chr5:81353306 | T | A | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-5376A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353306 | |||||||
| chr5:81353307 | T | A | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-5377A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353307 | |||||||
| chr5:81353308 | T | A | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-5378A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353308 | |||||||
| chr5:81353309 | T | A | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.497-5379A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353309 | |||||||
| chr5:81353444 | C | T | 38 | a0001c0001t0001g0058 a0001c0001t0001g0086 a0001c0001t0001g0119 others(35): Show |
42 | HG00099.hp1 HG01123.hp2 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.497-5514G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353444 | |||||||
| chr5:81353579 | T | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.497-5649A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353579 | |||||||
| chr5:81353625 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0132 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.497-5695G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353625 | |||||||
| chr5:81353677 | C | T | 8 | a0001c0001t0003g0021 a0001c0001t0003g0144 a0001c0001t0003g0243 others(5): Show |
9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.497-5747G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353677 | |||||||
| chr5:81353802 | A | G | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.497-5872T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353802 | |||||||
| chr5:81353996 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496+5907G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81353996 | |||||||
| chr5:81354047 | T | A | 26 | a0001c0001t0001g0113 a0001c0001t0001g0213 a0001c0001t0001g0215 others(23): Show |
29 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+5856A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354047 | |||||||
| chr5:81354062 | C | A | 8 | a0001c0001t0003g0021 a0001c0001t0003g0144 a0001c0001t0003g0243 others(5): Show |
9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+5841G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354062 | |||||||
| chr5:81354099 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.496+5804G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354099 | |||||||
| chr5:81354198 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.496+5705A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354198 | |||||||
| chr5:81354229 | T | A | 88 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(85): Show |
96 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.496+5674A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354229 | |||||||
| chr5:81354283 | A | C | 1 | a0001c0001t0003g0235 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.496+5620T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354283 | |||||||
| chr5:81354328 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.496+5575C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354328 | |||||||
| chr5:81354367 | T | C | 112 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(109): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.496+5536A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354367 | |||||||
| chr5:81354378 | G | A | 87 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(84): Show |
95 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.496+5525C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354378 | |||||||
| chr5:81354595 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.496+5308T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354595 | |||||||
| chr5:81354643 | C | T | 90 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(87): Show |
98 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.496+5260G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354643 | |||||||
| chr5:81354704 | C | CT | 72 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0192 others(69): Show |
79 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.496+5198dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354704 | |||||||
| chr5:81354825 | T | A | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+5078A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354825 | |||||||
| chr5:81354912 | G | A | 2 | a0001c0001t0004g0146 a0001c0001t0005g0248 |
2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.496+4991C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354912 | |||||||
| chr5:81354943 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496+4960G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81354943 | |||||||
| chr5:81355071 | G | T | 112 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(109): Show |
120 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.496+4832C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355071 | |||||||
| chr5:81355183 | T | C | 8 | a0001c0001t0003g0021 a0001c0001t0003g0144 a0001c0001t0003g0243 others(5): Show |
9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+4720A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355183 | |||||||
| chr5:81355264 | C | T | 5 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+4639G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355264 | |||||||
| chr5:81355368 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.496+4535C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355368 | |||||||
| chr5:81355490 | A | G | 82 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(79): Show |
90 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.496+4413T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355490 | |||||||
| chr5:81355515 | A | G | 19 | a0001c0001t0001g0193 a0001c0001t0002g0083 a0001c0001t0002g0194 others(16): Show |
19 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+4388T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355515 | |||||||
| chr5:81355556 | C | A | 19 | a0001c0001t0001g0193 a0001c0001t0002g0083 a0001c0001t0002g0194 others(16): Show |
19 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+4347G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355556 | |||||||
| chr5:81355751 | T | G | 26 | a0001c0001t0001g0193 a0001c0001t0002g0083 a0001c0001t0002g0194 others(23): Show |
26 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.496+4152A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355751 | |||||||
| chr5:81355896 | A | C | 19 | a0001c0001t0001g0193 a0001c0001t0002g0083 a0001c0001t0002g0194 others(16): Show |
19 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.496+4007T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81355896 | |||||||
| chr5:81356010 | C | T | 53 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(50): Show |
57 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.496+3893G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356010 | |||||||
| chr5:81356034 | G | A | 20 | a0001c0001t0001g0193 a0001c0001t0002g0083 a0001c0001t0002g0194 others(17): Show |
20 | HG00741.hp2 HG02258.hp1 HG02559.hp2 others(17): Show |
intron_variant | MODIFIER | c.496+3869C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356034 | |||||||
| chr5:81356124 | A | G | 5 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+3779T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356124 | |||||||
| chr5:81356225 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.496+3678G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356225 | |||||||
| chr5:81356272 | A | G | 28 | a0001c0001t0001g0193 a0001c0001t0002g0083 a0001c0001t0002g0194 others(25): Show |
29 | HG00741.hp2 HG01167.hp2 HG01496.hp1 others(26): Show |
intron_variant | MODIFIER | c.496+3631T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356272 | |||||||
| chr5:81356331 | C | T | 26 | a0001c0001t0001g0192 a0001c0001t0002g0075 a0001c0001t0002g0083 others(23): Show |
29 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+3572G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356331 | |||||||
| chr5:81356336 | C | T | 52 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(49): Show |
56 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.496+3567G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356336 | |||||||
| chr5:81356511 | C | T | 49 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0083 others(46): Show |
53 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.496+3392G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356511 | |||||||
| chr5:81356512 | A | G | 49 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0083 others(46): Show |
53 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.496+3391T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356512 | |||||||
| chr5:81356596 | C | G | 2 | a0001c0001t0002g0211 a0001c0001t0005g0037 |
2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.496+3307G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356596 | |||||||
| chr5:81356628 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.496+3275C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356628 | |||||||
| chr5:81356644 | A | T | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+3259T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356644 | |||||||
| chr5:81356645 | T | C | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.496+3258A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356645 | |||||||
| chr5:81356648 | A | G | 1 | a0001c0001t0004g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.496+3255T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356648 | |||||||
| chr5:81356661 | A | G | 5 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+3242T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356661 | |||||||
| chr5:81356749 | C | T | 5 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0141 others(2): Show |
5 | HG01361.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+3154G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356749 | |||||||
| chr5:81356854 | C | T | 1 | a0001c0001t0003g0049 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.496+3049G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356854 | |||||||
| chr5:81356937 | C | T | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.496+2966G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356937 | |||||||
| chr5:81356973 | A | G | 49 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0083 others(46): Show |
53 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.496+2930T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81356973 | |||||||
| chr5:81357137 | C | T | 5 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0141 others(2): Show |
5 | HG01361.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.496+2766G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357137 | |||||||
| chr5:81357195 | A | G | 8 | a0001c0001t0003g0021 a0001c0001t0003g0144 a0001c0001t0003g0243 others(5): Show |
9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+2708T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357195 | |||||||
| chr5:81357380 | G | A | 1 | a0001c0001t0002g0083 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.496+2523C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357380 | |||||||
| chr5:81357413 | T | A | 1 | a0001c0001t0002g0212 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.496+2490A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357413 | |||||||
| chr5:81357503 | C | T | 51 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0083 others(48): Show |
55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+2400G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357503 | |||||||
| chr5:81357522 | C | T | 1 | a0001c0001t0004g0019 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.496+2381G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357522 | |||||||
| chr5:81357641 | C | T | 51 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0083 others(48): Show |
55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+2262G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357641 | |||||||
| chr5:81357734 | G | A | 40 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0112 others(37): Show |
44 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.496+2169C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357734 | |||||||
| chr5:81357775 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0141 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.496+2128C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357775 | |||||||
| chr5:81357780 | C | A | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.496+2123G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357780 | |||||||
| chr5:81357781 | G | A | 39 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0112 others(36): Show |
43 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.496+2122C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357781 | |||||||
| chr5:81357827 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.496+2076C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357827 | |||||||
| chr5:81357839 | C | A | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.496+2064G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357839 | |||||||
| chr5:81357971 | A | C | 1 | a0001c0001t0003g0200 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.496+1932T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81357971 | |||||||
| chr5:81358007 | C | CA | 25 | a0001c0001t0001g0052 a0001c0001t0001g0080 a0001c0001t0001g0082 others(22): Show |
25 | HG00140.hp2 HG00438.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.496+1895dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358007 | |||||||
| chr5:81358007 | CA | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0067 a0001c0001t0001g0137 others(3): Show |
6 | HG01069.hp2 HG01167.hp1 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.496+1895delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358007 | |||||||
| chr5:81358007 | CAAAAA | C | 46 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0083 others(43): Show |
50 | HG00741.hp2 HG01070.hp2 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.496+1891_496+1895d others(7): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358007 | |||||||
| chr5:81358043 | A | G | 51 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0083 others(48): Show |
55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+1860T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358043 | |||||||
| chr5:81358046 | C | G | 51 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0083 others(48): Show |
55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+1857G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358046 | |||||||
| chr5:81358049 | C | G | 51 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0083 others(48): Show |
55 | HG00741.hp1 HG00741.hp2 HG01070.hp2 others(52): Show |
intron_variant | MODIFIER | c.496+1854G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358049 | |||||||
| chr5:81358050 | T | C | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+1853A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358050 | |||||||
| chr5:81358136 | T | A | 40 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0112 others(37): Show |
44 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.496+1767A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358136 | |||||||
| chr5:81358357 | G | C | 8 | a0001c0001t0003g0021 a0001c0001t0003g0144 a0001c0001t0003g0243 others(5): Show |
9 | HG01167.hp2 HG01496.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+1546C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358357 | |||||||
| chr5:81358388 | T | C | 1 | a0001c0001t0003g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.496+1515A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358388 | |||||||
| chr5:81358453 | C | A | 40 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0112 others(37): Show |
44 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(41): Show |
intron_variant | MODIFIER | c.496+1450G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358453 | |||||||
| chr5:81358693 | T | C | 5 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+1210A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358693 | |||||||
| chr5:81358709 | C | T | 5 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(2): Show |
5 | HG01884.hp1 HG02572.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.496+1194G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358709 | |||||||
| chr5:81358782 | T | C | 15 | a0001c0001t0001g0192 a0001c0001t0002g0083 a0001c0001t0002g0207 others(12): Show |
15 | HG00741.hp2 HG02451.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.496+1121A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358782 | |||||||
| chr5:81358798 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.496+1105C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358798 | |||||||
| chr5:81358838 | A | G | 1 | a0001c0001t0004g0171 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.496+1065T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358838 | |||||||
| chr5:81358853 | G | GA | 18 | a0001c0001t0001g0192 a0001c0001t0002g0083 a0001c0001t0002g0207 others(15): Show |
18 | HG00741.hp2 HG02451.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.496+1049dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358853 | |||||||
| chr5:81358853 | GA | G | 7 | a0001c0001t0001g0080 a0001c0001t0001g0103 a0001c0001t0001g0104 others(4): Show |
7 | HG01943.hp2 HG01975.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.496+1049delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358853 | |||||||
| chr5:81358853 | GAA | G | 41 | a0001c0001t0001g0193 a0001c0001t0002g0075 a0001c0001t0002g0112 others(38): Show |
45 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(42): Show |
intron_variant | MODIFIER | c.496+1048_496+1049d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81358853 | |||||||
| chr5:81359051 | A | C | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.496+852T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359051 | |||||||
| chr5:81359147 | T | G | 212 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0041 others(209): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.496+756A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359147 | |||||||
| chr5:81359242 | C | T | 1 | a0001c0001t0004g0006 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.496+661G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359242 | |||||||
| chr5:81359304 | C | T | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.496+599G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359304 | |||||||
| chr5:81359317 | T | C | 4 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(1): Show |
4 | HG01884.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+586A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359317 | |||||||
| chr5:81359325 | C | A | 8 | a0001c0001t0003g0021 a0001c0001t0003g0187 a0001c0001t0003g0188 others(5): Show |
9 | HG01167.hp2 HG01168.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.496+578G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359325 | |||||||
| chr5:81359369 | C | T | 1 | a0002c0002t0003g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496+534G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359369 | |||||||
| chr5:81359443 | T | C | 1 | a0001c0001t0004g0006 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.496+460A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359443 | |||||||
| chr5:81359447 | T | C | 114 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(111): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.496+456A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359447 | |||||||
| chr5:81359687 | T | G | 1 | a0001c0001t0002g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.496+216A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359687 | |||||||
| chr5:81359798 | A | G | 1 | a0002c0002t0002g0111 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.496+105T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359798 | |||||||
| chr5:81359890 | T | C | 26 | a0001c0001t0001g0113 a0001c0001t0001g0213 a0001c0001t0001g0215 others(23): Show |
29 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.496+13A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 5/14 | chr5 | 81359890 | |||||||
| chr5:81360147 | T | C | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.361-109A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360147 | |||||||
| chr5:81360225 | A | T | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-187T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360225 | |||||||
| chr5:81360345 | G | T | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-307C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360345 | |||||||
| chr5:81360393 | C | CTTTGCAA others(29): Show |
1 | a0001c0001t0003g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.361-391_361-356dup others(36): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360393 | |||||||
| chr5:81360393 | CTTTGCAA others(29): Show |
C | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-391_361-356del others(36): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360393 | |||||||
| chr5:81360525 | G | C | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.361-487C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360525 | |||||||
| chr5:81360550 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.361-512T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360550 | |||||||
| chr5:81360595 | A | C | 1 | a0002c0002t0003g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.361-557T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360595 | |||||||
| chr5:81360827 | G | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0243 a0001c0001t0003g0244 others(1): Show |
5 | HG01167.hp2 HG02630.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-789C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360827 | |||||||
| chr5:81360911 | G | C | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-873C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360911 | |||||||
| chr5:81360934 | C | T | 3 | a0002c0002t0001g0186 a0002c0002t0002g0042 a0002c0002t0004g0242 |
3 | HG01891.hp1 HG02109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.361-896G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360934 | |||||||
| chr5:81360949 | AC | A | 7 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(4): Show |
7 | HG02486.hp1 HG02717.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-912delG | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360949 | |||||||
| chr5:81360992 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0141 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-954G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360992 | |||||||
| chr5:81360993 | G | T | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-955C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81360993 | |||||||
| chr5:81361077 | C | CA | 80 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(77): Show |
89 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.361-1040dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361077 | |||||||
| chr5:81361077 | C | CAAAAAAA others(6): Show |
1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-1052_361-1040d others(15): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361077 | |||||||
| chr5:81361077 | CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0092 a0001c0001t0002g0094 others(1): Show |
4 | NA18612.hp1 NA18944.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-1053_361-1040d others(16): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361077 | |||||||
| chr5:81361103 | A | G | 4 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.361-1065T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361103 | |||||||
| chr5:81361124 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.361-1086A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361124 | |||||||
| chr5:81361218 | C | CTT | 21 | a0001c0001t0002g0075 a0001c0001t0002g0112 a0001c0001t0002g0203 others(18): Show |
24 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.361-1182_361-1181d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361218 | |||||||
| chr5:81361258 | G | C | 4 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(1): Show |
4 | HG01884.hp1 HG02886.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.361-1220C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361258 | |||||||
| chr5:81361315 | G | T | 27 | a0001c0001t0002g0075 a0001c0001t0002g0112 a0001c0001t0002g0203 others(24): Show |
30 | HG00741.hp1 HG01070.hp2 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.361-1277C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361315 | |||||||
| chr5:81361343 | C | T | 1 | a0001c0001t0003g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.361-1305G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361343 | |||||||
| chr5:81361366 | T | C | 2 | a0001c0001t0002g0211 a0001c0001t0005g0037 |
2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.361-1328A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361366 | |||||||
| chr5:81361417 | T | G | 1 | a0001c0001t0004g0229 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.361-1379A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361417 | |||||||
| chr5:81361481 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.361-1443C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361481 | |||||||
| chr5:81361497 | A | G | 1 | a0005c0004t0002g0214 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.361-1459T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361497 | |||||||
| chr5:81361511 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0004g0019 a0002c0002t0007g0208 |
3 | HG02055.hp1 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.361-1473T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361511 | |||||||
| chr5:81361573 | G | C | 1 | a0002c0002t0003g0035 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.361-1535C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361573 | |||||||
| chr5:81361580 | G | C | 1 | a0001c0001t0004g0233 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.361-1542C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361580 | |||||||
| chr5:81361650 | T | G | 3 | a0001c0001t0004g0146 a0001c0001t0005g0248 a0005c0004t0002g0214 |
3 | HG01361.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.361-1612A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361650 | |||||||
| chr5:81361740 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.361-1702A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361740 | |||||||
| chr5:81361761 | A | C | 6 | a0001c0001t0002g0043 a0001c0001t0003g0026 a0001c0001t0003g0028 others(3): Show |
6 | HG02055.hp2 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.361-1723T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361761 | |||||||
| chr5:81361870 | G | C | 127 | a0001c0001t0001g0044 a0001c0001t0001g0067 a0001c0001t0001g0068 others(124): Show |
137 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.361-1832C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361870 | |||||||
| chr5:81361910 | T | C | 29 | a0001c0001t0001g0086 a0001c0001t0001g0113 a0001c0001t0001g0213 others(26): Show |
32 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.361-1872A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81361910 | |||||||
| chr5:81362163 | CT | C | 40 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0086 others(37): Show |
42 | HG00408.hp1 HG00673.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.360+1624delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362163 | |||||||
| chr5:81362163 | CTT | C | 64 | a0001c0001t0001g0044 a0001c0001t0001g0113 a0001c0001t0001g0119 others(61): Show |
70 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.360+1623_360+1624d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362163 | |||||||
| chr5:81362166 | T | C | 13 | a0001c0001t0001g0041 a0001c0001t0001g0058 a0001c0001t0001g0114 others(10): Show |
15 | HG00099.hp1 HG01069.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.360+1622A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362166 | |||||||
| chr5:81362172 | T | C | 1 | a0001c0001t0004g0019 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.360+1616A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362172 | |||||||
| chr5:81362187 | C | T | 1 | a0001c0001t0002g0093 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.360+1601G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362187 | |||||||
| chr5:81362293 | G | A | 1 | a0001c0001t0004g0019 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.360+1495C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362293 | |||||||
| chr5:81362306 | T | C | 3 | a0001c0001t0002g0083 a0001c0001t0003g0152 a0001c0001t0004g0247 |
3 | HG00741.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.360+1482A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362306 | |||||||
| chr5:81362354 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.360+1434C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362354 | |||||||
| chr5:81362376 | G | A | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.360+1412C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362376 | |||||||
| chr5:81362525 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.360+1263C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362525 | |||||||
| chr5:81362529 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0141 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.360+1259C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362529 | |||||||
| chr5:81362850 | G | A | 2 | a0001c0001t0002g0207 a0001c0001t0003g0143 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.360+938C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362850 | |||||||
| chr5:81362958 | C | T | 6 | a0001c0001t0003g0017 a0001c0001t0003g0252 a0001c0001t0004g0250 others(3): Show |
7 | HG02257.hp2 HG02258.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.360+830G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81362958 | |||||||
| chr5:81363020 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.360+768T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363020 | |||||||
| chr5:81363078 | T | G | 1 | a0001c0001t0002g0115 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.360+710A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363078 | |||||||
| chr5:81363247 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.360+541G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363247 | |||||||
| chr5:81363413 | T | C | 1 | a0002c0002t0003g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.360+375A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363413 | |||||||
| chr5:81363429 | G | T | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.360+359C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363429 | |||||||
| chr5:81363757 | T | C | 5 | a0001c0001t0003g0150 a0001c0001t0003g0230 a0001c0001t0004g0154 others(2): Show |
5 | HG01496.hp1 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.360+31A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 4/14 | chr5 | 81363757 | |||||||
| chr5:81363919 | C | T | 1 | a0001c0001t0002g0121 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.259-30G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81363919 | |||||||
| chr5:81364158 | C | T | 1 | a0001c0001t0004g0245 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.259-269G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364158 | |||||||
| chr5:81364199 | G | C | 1 | a0001c0001t0002g0142 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.259-310C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364199 | |||||||
| chr5:81364239 | A | C | 2 | a0001c0001t0004g0146 a0001c0005t0003g0199 |
2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.259-350T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364239 | |||||||
| chr5:81364287 | C | T | 58 | a0001c0001t0001g0044 a0001c0001t0001g0072 a0001c0001t0001g0193 others(55): Show |
63 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.259-398G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364287 | |||||||
| chr5:81364581 | C | T | 2 | a0001c0001t0003g0152 a0001c0001t0004g0153 |
2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.259-692G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364581 | |||||||
| chr5:81364621 | A | C | 1 | a0001c0001t0003g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.259-732T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364621 | |||||||
| chr5:81364852 | CT | C | 65 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0072 others(62): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.259-964delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364852 | |||||||
| chr5:81364870 | C | A | 14 | a0001c0001t0003g0004 a0001c0001t0003g0235 a0001c0001t0003g0236 others(11): Show |
16 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.259-981G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364870 | |||||||
| chr5:81364872 | C | G | 19 | a0001c0001t0001g0170 a0001c0001t0003g0166 a0001c0001t0003g0172 others(16): Show |
20 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.259-983G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81364872 | |||||||
| chr5:81365126 | T | C | 87 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(84): Show |
95 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.259-1237A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365126 | |||||||
| chr5:81365149 | A | G | 7 | a0001c0001t0003g0150 a0001c0001t0003g0230 a0001c0001t0004g0146 others(4): Show |
7 | HG01496.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-1260T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365149 | |||||||
| chr5:81365215 | A | G | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259-1326T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365215 | |||||||
| chr5:81365231 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG03098.hp2 NA18957.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.259-1342T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365231 | |||||||
| chr5:81365299 | T | A | 7 | a0001c0001t0003g0150 a0001c0001t0003g0230 a0001c0001t0004g0146 others(4): Show |
7 | HG01496.hp1 HG02451.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.259-1410A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365299 | |||||||
| chr5:81365518 | A | G | 1 | a0001c0001t0001g0092 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.259-1629T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365518 | |||||||
| chr5:81365721 | C | T | 5 | a0001c0001t0003g0150 a0001c0001t0003g0230 a0001c0001t0004g0154 others(2): Show |
5 | HG01496.hp1 HG02615.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-1832G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365721 | |||||||
| chr5:81365742 | G | A | 1 | a0001c0001t0003g0161 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.259-1853C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365742 | |||||||
| chr5:81365877 | A | G | 159 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(156): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.259-1988T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365877 | |||||||
| chr5:81365927 | T | A | 1 | a0001c0001t0003g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.259-2038A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81365927 | |||||||
| chr5:81366205 | A | C | 1 | a0001c0001t0002g0091 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.259-2316T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366205 | |||||||
| chr5:81366265 | T | C | 1 | a0001c0001t0004g0019 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.259-2376A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366265 | |||||||
| chr5:81366324 | A | C | 20 | a0001c0001t0001g0192 a0001c0001t0002g0142 a0001c0001t0003g0004 others(17): Show |
22 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.259-2435T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366324 | |||||||
| chr5:81366435 | A | G | 21 | a0001c0001t0001g0170 a0001c0001t0003g0166 a0001c0001t0003g0172 others(18): Show |
22 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.259-2546T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366435 | |||||||
| chr5:81366582 | C | A | 2 | a0001c0001t0003g0246 a0001c0001t0004g0247 |
2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.259-2693G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366582 | |||||||
| chr5:81366609 | A | C | 2 | a0001c0001t0003g0034 a0001c0001t0005g0037 |
2 | HG03139.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.259-2720T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366609 | |||||||
| chr5:81366673 | T | A | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.259-2784A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366673 | |||||||
| chr5:81366742 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.259-2853T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366742 | |||||||
| chr5:81366770 | A | T | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259-2881T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366770 | |||||||
| chr5:81366827 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.259-2938T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366827 | |||||||
| chr5:81366869 | G | A | 12 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0156 others(9): Show |
13 | HG00609.hp1 HG01074.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.259-2980C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366869 | |||||||
| chr5:81366882 | C | A | 5 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0004g0019 others(2): Show |
5 | HG02572.hp2 HG02809.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.259-2993G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366882 | |||||||
| chr5:81366895 | T | G | 1 | a0001c0001t0003g0162 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.259-3006A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81366895 | |||||||
| chr5:81367291 | T | A | 8 | a0001c0001t0001g0041 a0001c0001t0001g0132 a0001c0001t0002g0075 others(5): Show |
8 | HG00642.hp2 HG00741.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.259-3402A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367291 | |||||||
| chr5:81367490 | A | G | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.259-3601T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367490 | |||||||
| chr5:81367551 | T | C | 3 | a0001c0001t0003g0230 a0001c0001t0004g0154 a0001c0001t0004g0155 |
3 | HG01496.hp1 HG02615.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.259-3662A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367551 | |||||||
| chr5:81367648 | G | A | 27 | a0001c0001t0001g0170 a0001c0001t0003g0166 a0001c0001t0003g0168 others(24): Show |
28 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.259-3759C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367648 | |||||||
| chr5:81367691 | A | G | 61 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0072 others(58): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.259-3802T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367691 | |||||||
| chr5:81367711 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.259-3822G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367711 | |||||||
| chr5:81367724 | T | C | 4 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.259-3835A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367724 | |||||||
| chr5:81367736 | T | C | 2 | a0001c0001t0003g0018 a0001c0001t0003g0200 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.259-3847A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367736 | |||||||
| chr5:81367828 | A | T | 3 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0151 |
3 | HG02572.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.258+3922T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367828 | |||||||
| chr5:81367919 | A | G | 23 | a0001c0001t0001g0170 a0001c0001t0003g0166 a0001c0001t0003g0168 others(20): Show |
24 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.258+3831T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367919 | |||||||
| chr5:81367948 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.258+3802C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81367948 | |||||||
| chr5:81368016 | G | T | 6 | a0001c0001t0003g0150 a0001c0001t0003g0230 a0001c0001t0004g0154 others(3): Show |
6 | HG01496.hp1 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+3734C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368016 | |||||||
| chr5:81368044 | C | A | 1 | a0001c0001t0001g0117 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.258+3706G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368044 | |||||||
| chr5:81368247 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.258+3503C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368247 | |||||||
| chr5:81368583 | A | G | 3 | a0001c0001t0003g0150 a0001c0001t0004g0190 a0001c0001t0005g0141 |
3 | HG06807.hp2 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.258+3167T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368583 | |||||||
| chr5:81368745 | A | G | 1 | a0001c0001t0003g0144 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.258+3005T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368745 | |||||||
| chr5:81368781 | TAGAATG | T | 4 | a0001c0001t0003g0034 a0001c0001t0005g0037 a0002c0002t0002g0206 others(1): Show |
4 | HG02896.hp2 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+2963_258+2968d others(8): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81368781 | |||||||
| chr5:81369002 | G | A | 68 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0072 others(65): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.258+2748C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369002 | |||||||
| chr5:81369047 | T | C | 1 | a0001c0001t0003g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.258+2703A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369047 | |||||||
| chr5:81369154 | C | CA | 14 | a0001c0001t0001g0119 a0001c0001t0003g0034 a0001c0001t0003g0243 others(11): Show |
14 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.258+2595dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369154 | |||||||
| chr5:81369154 | CA | C | 12 | a0001c0001t0001g0072 a0001c0001t0002g0078 a0001c0001t0002g0079 others(9): Show |
12 | HG00140.hp1 HG01192.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.258+2595delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369154 | |||||||
| chr5:81369311 | G | C | 86 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(83): Show |
94 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(91): Show |
intron_variant | MODIFIER | c.258+2439C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369311 | |||||||
| chr5:81369312 | A | G | 1 | a0001c0001t0002g0088 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.258+2438T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369312 | |||||||
| chr5:81369378 | C | T | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.258+2372G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369378 | |||||||
| chr5:81369439 | T | A | 4 | a0001c0001t0001g0193 a0001c0001t0002g0194 a0001c0001t0002g0201 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+2311A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369439 | |||||||
| chr5:81369549 | C | T | 23 | a0001c0001t0001g0170 a0001c0001t0003g0166 a0001c0001t0003g0168 others(20): Show |
24 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.258+2201G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369549 | |||||||
| chr5:81369552 | C | A | 2 | a0001c0001t0003g0152 a0001c0001t0004g0153 |
2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.258+2198G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369552 | |||||||
| chr5:81369552 | C | T | 19 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0086 others(16): Show |
21 | HG01106.hp1 HG01243.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.258+2198G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369552 | |||||||
| chr5:81369559 | A | G | 1 | a0001c0001t0002g0085 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.258+2191T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369559 | |||||||
| chr5:81369597 | G | A | 3 | a0001c0001t0003g0150 a0001c0001t0004g0146 a0001c0005t0003g0199 |
3 | HG02451.hp1 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.258+2153C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369597 | |||||||
| chr5:81369730 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.258+2020G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369730 | |||||||
| chr5:81369773 | T | A | 13 | a0001c0001t0003g0004 a0001c0001t0003g0235 a0001c0001t0003g0236 others(10): Show |
15 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.258+1977A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369773 | |||||||
| chr5:81369881 | C | T | 67 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0128 others(64): Show |
72 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.258+1869G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369881 | |||||||
| chr5:81369953 | T | C | 3 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 |
3 | HG01884.hp1 HG02886.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.258+1797A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81369953 | |||||||
| chr5:81370010 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.258+1740T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370010 | |||||||
| chr5:81370016 | C | T | 72 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0072 others(69): Show |
79 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.258+1734G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370016 | |||||||
| chr5:81370032 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.258+1718A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370032 | |||||||
| chr5:81370144 | T | C | 4 | a0001c0001t0003g0180 a0001c0001t0003g0230 a0001c0001t0004g0154 others(1): Show |
4 | HG01496.hp1 HG02615.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+1606A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370144 | |||||||
| chr5:81370144 | T | G | 13 | a0001c0001t0002g0083 a0001c0001t0003g0004 a0001c0001t0003g0235 others(10): Show |
15 | HG00741.hp2 HG01106.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.258+1606A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370144 | |||||||
| chr5:81370395 | A | G | 1 | a0001c0001t0002g0228 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.258+1355T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370395 | |||||||
| chr5:81370564 | G | A | 1 | a0001c0001t0003g0180 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.258+1186C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370564 | |||||||
| chr5:81370649 | A | G | 155 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(152): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.258+1101T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370649 | |||||||
| chr5:81370698 | T | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0209 a0001c0001t0001g0210 |
4 | NA18957.hp1 NA18961.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.258+1052A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370698 | |||||||
| chr5:81370775 | C | A | 1 | a0001c0001t0002g0120 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.258+975G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370775 | |||||||
| chr5:81370820 | C | G | 1 | a0001c0001t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.258+930G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370820 | |||||||
| chr5:81370840 | G | C | 1 | a0001c0001t0004g0173 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.258+910C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370840 | |||||||
| chr5:81370846 | G | A | 1 | a0001c0001t0004g0249 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258+904C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370846 | |||||||
| chr5:81370914 | G | A | 121 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(118): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.258+836C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370914 | |||||||
| chr5:81370919 | T | A | 1 | a0002c0002t0001g0185 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.258+831A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81370919 | |||||||
| chr5:81371059 | T | C | 2 | a0001c0001t0001g0041 a0001c0001t0001g0132 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.258+691A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371059 | |||||||
| chr5:81371097 | G | A | 7 | a0001c0001t0003g0032 a0001c0001t0004g0007 a0001c0001t0004g0023 others(4): Show |
8 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.258+653C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371097 | |||||||
| chr5:81371361 | G | A | 9 | a0001c0001t0001g0192 a0001c0001t0002g0142 a0001c0001t0002g0207 others(6): Show |
9 | HG02451.hp1 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.258+389C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371361 | |||||||
| chr5:81371418 | A | AT | 5 | a0001c0001t0001g0016 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG03098.hp2 NA18957.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.258+331dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371418 | |||||||
| chr5:81371418 | AT | A | 25 | a0001c0001t0002g0211 a0001c0001t0003g0021 a0001c0001t0003g0026 others(22): Show |
28 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.258+331delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371418 | |||||||
| chr5:81371515 | A | G | 1 | a0001c0001t0001g0010 | 2 | NA18971.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.258+235T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371515 | |||||||
| chr5:81371551 | C | T | 3 | a0001c0001t0003g0156 a0001c0001t0003g0157 a0001c0001t0003g0162 |
3 | HG01346.hp2 HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.258+199G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371551 | |||||||
| chr5:81371688 | C | T | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.258+62G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 3/14 | chr5 | 81371688 | |||||||
| chr5:81371853 | T | C | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.198-43A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81371853 | |||||||
| chr5:81371873 | A | G | 4 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-63T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81371873 | |||||||
| chr5:81371919 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0082 |
2 | HG02135.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.198-109G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81371919 | |||||||
| chr5:81371938 | C | G | 123 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0128 others(120): Show |
132 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.198-128G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81371938 | |||||||
| chr5:81372085 | G | A | 1 | a0001c0001t0004g0153 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.198-275C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372085 | |||||||
| chr5:81372096 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.198-286G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372096 | |||||||
| chr5:81372306 | C | T | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0002c0002t0007g0208 |
3 | HG02486.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.198-496G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372306 | |||||||
| chr5:81372329 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.198-519G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372329 | |||||||
| chr5:81372402 | A | G | 30 | a0001c0001t0001g0170 a0001c0001t0001g0192 a0001c0001t0002g0142 others(27): Show |
30 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.198-592T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372402 | |||||||
| chr5:81372426 | C | T | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.198-616G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372426 | |||||||
| chr5:81372589 | T | C | 31 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(28): Show |
34 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.198-779A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372589 | |||||||
| chr5:81372662 | C | T | 30 | a0001c0001t0001g0170 a0001c0001t0001g0192 a0001c0001t0002g0142 others(27): Show |
30 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.198-852G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372662 | |||||||
| chr5:81372748 | T | C | 1 | a0003c0003t0001g0012 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.198-938A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372748 | |||||||
| chr5:81372903 | T | C | 1 | a0001c0001t0002g0121 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.198-1093A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372903 | |||||||
| chr5:81372913 | C | T | 22 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0128 others(19): Show |
25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.198-1103G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81372913 | |||||||
| chr5:81373082 | G | A | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.198-1272C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373082 | |||||||
| chr5:81373085 | C | T | 35 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(32): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-1275G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373085 | |||||||
| chr5:81373156 | A | C | 35 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(32): Show |
38 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.198-1346T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373156 | |||||||
| chr5:81373193 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.198-1383G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373193 | |||||||
| chr5:81373432 | C | G | 25 | a0001c0001t0002g0211 a0001c0001t0003g0021 a0001c0001t0003g0026 others(22): Show |
28 | HG00099.hp1 HG01070.hp2 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.198-1622G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373432 | |||||||
| chr5:81373438 | G | A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0122 |
3 | HG00642.hp1 HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.198-1628C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373438 | |||||||
| chr5:81373540 | G | A | 3 | a0001c0001t0003g0152 a0001c0001t0003g0230 a0001c0001t0004g0153 |
3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.198-1730C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373540 | |||||||
| chr5:81373560 | G | A | 1 | a0002c0002t0002g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.198-1750C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373560 | |||||||
| chr5:81373586 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.198-1776C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373586 | |||||||
| chr5:81373741 | C | A | 11 | a0001c0001t0003g0014 a0001c0001t0003g0156 a0001c0001t0003g0157 others(8): Show |
12 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.198-1931G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373741 | |||||||
| chr5:81373748 | A | C | 1 | a0001c0001t0001g0077 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.198-1938T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373748 | |||||||
| chr5:81373904 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(15): Show |
19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-2094G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373904 | |||||||
| chr5:81373922 | A | T | 6 | a0001c0001t0003g0034 a0001c0001t0003g0152 a0001c0001t0003g0230 others(3): Show |
6 | HG02615.hp1 HG02970.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.198-2112T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81373922 | |||||||
| chr5:81374240 | A | T | 1 | a0001c0001t0001g0080 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.198-2430T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374240 | |||||||
| chr5:81374245 | G | A | 1 | a0001c0001t0003g0145 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.198-2435C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374245 | |||||||
| chr5:81374392 | G | A | 30 | a0001c0001t0001g0170 a0001c0001t0001g0192 a0001c0001t0002g0142 others(27): Show |
30 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.198-2582C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374392 | |||||||
| chr5:81374499 | T | C | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0002c0002t0007g0208 |
3 | HG02486.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.198-2689A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374499 | |||||||
| chr5:81374686 | A | T | 22 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0128 others(19): Show |
25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.198-2876T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374686 | |||||||
| chr5:81374838 | A | T | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.198-3028T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374838 | |||||||
| chr5:81374922 | A | T | 1 | a0001c0001t0002g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.198-3112T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81374922 | |||||||
| chr5:81375080 | G | A | 156 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(153): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.198-3270C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375080 | |||||||
| chr5:81375135 | C | T | 13 | a0001c0001t0003g0014 a0001c0001t0003g0156 a0001c0001t0003g0157 others(10): Show |
14 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.198-3325G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375135 | |||||||
| chr5:81375176 | C | G | 156 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(153): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.198-3366G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375176 | |||||||
| chr5:81375205 | G | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(15): Show |
19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-3395C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375205 | |||||||
| chr5:81375468 | C | G | 7 | a0001c0001t0003g0032 a0001c0001t0004g0007 a0001c0001t0004g0023 others(4): Show |
8 | HG01891.hp2 HG02572.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.198-3658G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375468 | |||||||
| chr5:81375566 | T | C | 90 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(87): Show |
98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.198-3756A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375566 | |||||||
| chr5:81375601 | T | C | 3 | a0001c0001t0003g0034 a0001c0001t0005g0037 a0002c0002t0003g0035 |
3 | HG03139.hp2 HG03579.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.198-3791A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375601 | |||||||
| chr5:81375674 | A | G | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.198-3864T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81375674 | |||||||
| chr5:81376036 | ATTC | A | 4 | a0002c0002t0001g0138 a0002c0002t0001g0185 a0002c0002t0002g0204 others(1): Show |
4 | HG01884.hp1 HG02886.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.198-4229_198-4227d others(5): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376036 | |||||||
| chr5:81376147 | C | T | 14 | a0001c0001t0003g0004 a0001c0001t0003g0235 a0001c0001t0003g0236 others(11): Show |
16 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.198-4337G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376147 | |||||||
| chr5:81376460 | G | A | 2 | a0001c0001t0003g0032 a0001c0001t0004g0033 |
2 | HG02965.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.198-4650C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376460 | |||||||
| chr5:81376478 | ATAAC | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(15): Show |
19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-4672_198-4669d others(6): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376478 | |||||||
| chr5:81376623 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(15): Show |
19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-4813G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376623 | |||||||
| chr5:81376701 | C | A | 17 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(14): Show |
18 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(15): Show |
intron_variant | MODIFIER | c.198-4891G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376701 | |||||||
| chr5:81376746 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.198-4936C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376746 | |||||||
| chr5:81376894 | G | A | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.198-5084C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81376894 | |||||||
| chr5:81377107 | C | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(15): Show |
19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.198-5297G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377107 | |||||||
| chr5:81377107 | C | T | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | HG00140.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.198-5297G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377107 | |||||||
| chr5:81377289 | A | G | 155 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(152): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.198-5479T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377289 | |||||||
| chr5:81377497 | C | T | 14 | a0001c0001t0003g0004 a0001c0001t0003g0235 a0001c0001t0003g0236 others(11): Show |
16 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.198-5687G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377497 | |||||||
| chr5:81377647 | A | G | 22 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0128 others(19): Show |
25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.198-5837T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377647 | |||||||
| chr5:81377677 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.198-5867C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377677 | |||||||
| chr5:81377835 | C | T | 125 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(122): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.198-6025G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377835 | |||||||
| chr5:81377860 | T | A | 1 | a0001c0001t0003g0162 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.198-6050A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377860 | |||||||
| chr5:81377874 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.198-6064T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377874 | |||||||
| chr5:81377955 | T | A | 72 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0128 others(69): Show |
79 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.198-6145A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81377955 | |||||||
| chr5:81378049 | T | C | 90 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(87): Show |
98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.198-6239A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378049 | |||||||
| chr5:81378246 | T | C | 1 | a0001c0001t0003g0163 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.198-6436A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378246 | |||||||
| chr5:81378261 | G | A | 14 | a0001c0001t0003g0004 a0001c0001t0003g0235 a0001c0001t0003g0236 others(11): Show |
16 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.198-6451C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378261 | |||||||
| chr5:81378320 | T | C | 1 | a0001c0001t0003g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.198-6510A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378320 | |||||||
| chr5:81378658 | A | C | 1 | a0001c0001t0001g0216 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.198-6848T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378658 | |||||||
| chr5:81378668 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.198-6858G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378668 | |||||||
| chr5:81378750 | T | G | 7 | a0001c0001t0003g0178 a0001c0001t0003g0179 a0001c0001t0004g0165 others(4): Show |
7 | HG00408.hp1 HG00621.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.198-6940A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81378750 | |||||||
| chr5:81379130 | C | T | 20 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(17): Show |
22 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.197+6627G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379130 | |||||||
| chr5:81379178 | C | T | 1 | a0002c0002t0003g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.197+6579G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379178 | |||||||
| chr5:81379184 | C | T | 1 | a0001c0001t0004g0020 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.197+6573G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379184 | |||||||
| chr5:81379317 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(15): Show |
19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.197+6440G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379317 | |||||||
| chr5:81379332 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.197+6425C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379332 | |||||||
| chr5:81379339 | G | A | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.197+6418C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379339 | |||||||
| chr5:81379499 | C | T | 1 | a0002c0002t0003g0198 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.197+6258G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379499 | |||||||
| chr5:81379534 | C | T | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.197+6223G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379534 | |||||||
| chr5:81379555 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.197+6202G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379555 | |||||||
| chr5:81379578 | C | T | 1 | a0006c0006t0002g0184 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.197+6179G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379578 | |||||||
| chr5:81379622 | T | G | 1 | a0001c0001t0002g0125 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.197+6135A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379622 | |||||||
| chr5:81379677 | G | A | 125 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(122): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.197+6080C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379677 | |||||||
| chr5:81379880 | G | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(15): Show |
19 | HG02559.hp2 HG02615.hp1 HG02717.hp2 others(16): Show |
intron_variant | MODIFIER | c.197+5877C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81379880 | |||||||
| chr5:81380061 | T | G | 2 | a0001c0001t0003g0246 a0001c0001t0004g0247 |
2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.197+5696A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380061 | |||||||
| chr5:81380272 | A | G | 1 | a0001c0001t0003g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.197+5485T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380272 | |||||||
| chr5:81380446 | C | G | 1 | a0001c0001t0003g0143 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.197+5311G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380446 | |||||||
| chr5:81380519 | G | C | 1 | a0001c0001t0002g0202 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.197+5238C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380519 | |||||||
| chr5:81380527 | G | GCACTT | 90 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(87): Show |
98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.197+5225_197+5229d others(7): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380527 | |||||||
| chr5:81380574 | AAAAAAAG | A | 21 | a0001c0001t0001g0170 a0001c0001t0003g0166 a0001c0001t0003g0168 others(18): Show |
21 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.197+5176_197+5182d others(9): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380574 | |||||||
| chr5:81380578 | A | G | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.197+5179T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380578 | |||||||
| chr5:81380579 | A | G | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0002c0002t0007g0208 |
3 | HG02486.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.197+5178T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380579 | |||||||
| chr5:81380580 | AG | A | 61 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0058 others(58): Show |
65 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.197+5176delC | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380580 | |||||||
| chr5:81380581 | G | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0040 others(169): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.197+5176C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380581 | |||||||
| chr5:81380587 | A | G | 2 | a0001c0001t0003g0191 a0001c0001t0003g0232 |
2 | HG02486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.197+5170T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380587 | |||||||
| chr5:81380610 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.197+5147C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380610 | |||||||
| chr5:81380721 | A | T | 90 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(87): Show |
98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.197+5036T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380721 | |||||||
| chr5:81380726 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.197+5031A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380726 | |||||||
| chr5:81380732 | G | A | 2 | a0001c0001t0002g0002 a0002c0002t0002g0227 |
4 | HG01099.hp2 NA18972.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.197+5025C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380732 | |||||||
| chr5:81380741 | A | G | 1 | a0001c0001t0005g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.197+5016T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81380741 | |||||||
| chr5:81381003 | A | C | 1 | a0002c0002t0002g0065 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.197+4754T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381003 | |||||||
| chr5:81381067 | C | T | 154 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(151): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.197+4690G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381067 | |||||||
| chr5:81381068 | C | T | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.197+4689G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381068 | |||||||
| chr5:81381201 | G | A | 1 | a0001c0001t0003g0180 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.197+4556C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381201 | |||||||
| chr5:81381442 | G | A | 1 | a0001c0001t0004g0181 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.197+4315C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381442 | |||||||
| chr5:81381487 | T | C | 90 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(87): Show |
98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.197+4270A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381487 | |||||||
| chr5:81381494 | T | C | 90 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(87): Show |
98 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.197+4263A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381494 | |||||||
| chr5:81381533 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.197+4224C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381533 | |||||||
| chr5:81381989 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.197+3768C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81381989 | |||||||
| chr5:81382103 | ACT | A | 3 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0005g0151 |
3 | HG02572.hp2 HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.197+3652_197+3653d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382103 | |||||||
| chr5:81382283 | C | G | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.197+3474G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382283 | |||||||
| chr5:81382477 | G | T | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.197+3280C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382477 | |||||||
| chr5:81382512 | A | G | 37 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(34): Show |
41 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.197+3245T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382512 | |||||||
| chr5:81382579 | C | T | 22 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0128 others(19): Show |
25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.197+3178G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382579 | |||||||
| chr5:81382604 | C | A | 6 | a0001c0001t0001g0192 a0001c0001t0003g0147 a0001c0001t0004g0019 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.197+3153G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382604 | |||||||
| chr5:81382617 | T | C | 3 | a0001c0001t0003g0191 a0001c0001t0003g0232 a0002c0002t0007g0208 |
3 | HG02486.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.197+3140A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382617 | |||||||
| chr5:81382632 | A | G | 37 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(34): Show |
41 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.197+3125T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382632 | |||||||
| chr5:81382694 | C | T | 6 | a0001c0001t0003g0021 a0001c0001t0004g0005 a0001c0001t0004g0006 others(3): Show |
8 | HG01109.hp2 HG01884.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.197+3063G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382694 | |||||||
| chr5:81382831 | G | T | 37 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(34): Show |
41 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.197+2926C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81382831 | |||||||
| chr5:81383045 | A | C | 2 | a0001c0001t0001g0067 a0001c0001t0001g0068 |
2 | NA18965.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.197+2712T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383045 | |||||||
| chr5:81383159 | C | T | 2 | a0003c0003t0004g0015 a0003c0003t0004g0195 |
3 | HG01243.hp1 HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.197+2598G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383159 | |||||||
| chr5:81383188 | G | T | 1 | a0001c0007t0004g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.197+2569C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383188 | |||||||
| chr5:81383331 | C | A | 99 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(96): Show |
108 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.197+2426G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383331 | |||||||
| chr5:81383381 | A | C | 1 | a0002c0002t0002g0065 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.197+2376T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383381 | |||||||
| chr5:81383382 | A | C | 1 | a0001c0001t0001g0254 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.197+2375T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383382 | |||||||
| chr5:81383395 | A | G | 7 | a0001c0001t0001g0041 a0001c0001t0001g0132 a0001c0001t0002g0075 others(4): Show |
7 | HG00741.hp1 HG01074.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+2362T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383395 | |||||||
| chr5:81383526 | A | G | 113 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(110): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.197+2231T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383526 | |||||||
| chr5:81383530 | T | C | 113 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(110): Show |
124 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.197+2227A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383530 | |||||||
| chr5:81383671 | C | G | 1 | a0001c0001t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.197+2086G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383671 | |||||||
| chr5:81383808 | TTTTTAAA others(3): Show |
T | 1 | a0001c0001t0001g0215 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.197+1939_197+1948d others(12): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383808 | |||||||
| chr5:81383819 | C | G | 1 | a0001c0001t0001g0215 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.197+1938G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383819 | |||||||
| chr5:81383886 | T | G | 22 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0128 others(19): Show |
25 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.197+1871A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383886 | |||||||
| chr5:81383974 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.197+1783C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81383974 | |||||||
| chr5:81384107 | C | T | 9 | a0001c0001t0001g0192 a0001c0001t0002g0142 a0001c0001t0002g0207 others(6): Show |
9 | HG02451.hp1 HG02572.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.197+1650G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384107 | |||||||
| chr5:81384117 | C | CT | 68 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0058 others(65): Show |
74 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.197+1639dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384117 | |||||||
| chr5:81384117 | C | CTT | 21 | a0001c0001t0001g0170 a0001c0001t0003g0168 a0001c0001t0003g0172 others(18): Show |
21 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.197+1638_197+1639d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384117 | |||||||
| chr5:81384270 | G | A | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.197+1487C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384270 | |||||||
| chr5:81384273 | C | T | 12 | a0001c0001t0003g0004 a0001c0001t0003g0235 a0001c0001t0003g0236 others(9): Show |
14 | HG01106.hp2 HG01123.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.197+1484G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384273 | |||||||
| chr5:81384329 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.197+1428G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384329 | |||||||
| chr5:81384330 | G | A | 19 | a0001c0001t0001g0170 a0001c0001t0003g0166 a0001c0001t0003g0172 others(16): Show |
19 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.197+1427C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384330 | |||||||
| chr5:81384430 | G | A | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.197+1327C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384430 | |||||||
| chr5:81384610 | T | G | 11 | a0001c0001t0001g0016 a0001c0001t0001g0193 a0001c0001t0001g0209 others(8): Show |
12 | HG02559.hp2 HG02717.hp2 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.197+1147A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384610 | |||||||
| chr5:81384682 | G | A | 29 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0001g0128 others(26): Show |
32 | HG00323.hp1 HG01106.hp1 HG01175.hp2 others(29): Show |
intron_variant | MODIFIER | c.197+1075C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384682 | |||||||
| chr5:81384741 | T | G | 21 | a0001c0001t0001g0170 a0001c0001t0003g0166 a0001c0001t0003g0168 others(18): Show |
21 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.197+1016A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384741 | |||||||
| chr5:81384840 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.197+917C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384840 | |||||||
| chr5:81384906 | G | A | 1 | a0001c0001t0004g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.197+851C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81384906 | |||||||
| chr5:81385001 | T | C | 1 | a0001c0001t0002g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.197+756A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385001 | |||||||
| chr5:81385006 | A | G | 3 | a0001c0001t0003g0152 a0001c0001t0003g0230 a0001c0001t0004g0153 |
3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.197+751T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385006 | |||||||
| chr5:81385072 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.197+685G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385072 | |||||||
| chr5:81385247 | G | A | 85 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(82): Show |
91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.197+510C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385247 | |||||||
| chr5:81385480 | G | A | 1 | a0001c0001t0004g0245 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.197+277C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385480 | |||||||
| chr5:81385483 | A | G | 1 | a0001c0001t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.197+274T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385483 | |||||||
| chr5:81385485 | T | C | 1 | a0001c0001t0003g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.197+272A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385485 | |||||||
| chr5:81385731 | A | G | 3 | a0001c0001t0003g0152 a0001c0001t0003g0230 a0001c0001t0004g0153 |
3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.197+26T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 2/14 | chr5 | 81385731 | |||||||
| chr5:81386372 | T | C | 3 | a0001c0001t0003g0152 a0001c0001t0003g0230 a0001c0001t0004g0153 |
3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.128-546A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386372 | |||||||
| chr5:81386482 | T | G | 1 | a0001c0001t0003g0183 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.128-656A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386482 | |||||||
| chr5:81386499 | G | A | 3 | a0001c0001t0003g0152 a0001c0001t0003g0230 a0001c0001t0004g0153 |
3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.128-673C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386499 | |||||||
| chr5:81386502 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.128-676A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386502 | |||||||
| chr5:81386896 | C | T | 64 | a0001c0001t0001g0058 a0001c0001t0001g0066 a0001c0001t0002g0060 others(61): Show |
69 | HG00099.hp1 HG00323.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.128-1070G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386896 | |||||||
| chr5:81386947 | A | G | 2 | a0001c0001t0003g0018 a0001c0001t0003g0200 |
2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.128-1121T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386947 | |||||||
| chr5:81386991 | T | C | 2 | a0001c0001t0002g0207 a0001c0001t0003g0143 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.128-1165A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386991 | |||||||
| chr5:81386994 | C | CT | 23 | a0001c0001t0001g0058 a0001c0001t0001g0192 a0001c0001t0001g0193 others(20): Show |
24 | HG00609.hp1 HG01070.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.128-1169_128-1168i others(3): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | |||||||
| chr5:81386994 | CA | C | 44 | a0001c0001t0002g0142 a0001c0001t0002g0211 a0001c0001t0003g0018 others(41): Show |
47 | HG00099.hp1 HG01109.hp2 HG01243.hp2 others(44): Show |
intron_variant | MODIFIER | c.128-1169delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | |||||||
| chr5:81386994 | CAT | C | 18 | a0001c0001t0001g0170 a0001c0001t0003g0168 a0001c0001t0003g0172 others(15): Show |
18 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.128-1170_128-1169d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | |||||||
| chr5:81386994 | CATTTTTT others(4): Show |
C | 3 | a0001c0001t0003g0152 a0001c0001t0003g0230 a0001c0001t0004g0153 |
3 | HG02615.hp1 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.128-1179_128-1169d others(13): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | |||||||
| chr5:81386994 | CATTTTTT others(8): Show |
C | 22 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(19): Show |
24 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.128-1183_128-1169d others(17): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386994 | |||||||
| chr5:81386995 | A | AT | 12 | a0001c0001t0001g0010 a0001c0001t0001g0064 a0001c0001t0001g0071 others(9): Show |
12 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-1170dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386995 | |||||||
| chr5:81386995 | A | T | 62 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0066 others(59): Show |
69 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.128-1169T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386995 | |||||||
| chr5:81386995 | AT | A | 12 | a0001c0001t0001g0067 a0001c0001t0001g0080 a0001c0001t0001g0092 others(9): Show |
12 | HG00140.hp1 HG00597.hp1 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.128-1170delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81386995 | |||||||
| chr5:81387019 | C | T | 25 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(22): Show |
27 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.128-1193G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387019 | |||||||
| chr5:81387048 | C | T | 74 | a0001c0001t0001g0170 a0001c0001t0001g0192 a0001c0001t0001g0193 others(71): Show |
78 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.128-1222G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387048 | |||||||
| chr5:81387532 | C | CT | 45 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0064 others(42): Show |
51 | HG00323.hp1 HG01106.hp2 HG01123.hp2 others(48): Show |
intron_variant | MODIFIER | c.128-1707dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387532 | |||||||
| chr5:81387532 | CT | C | 33 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0133 others(30): Show |
33 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.128-1707delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387532 | |||||||
| chr5:81387604 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.128-1778G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387604 | |||||||
| chr5:81387615 | G | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02559.hp2 HG03139.hp1 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.128-1789C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387615 | |||||||
| chr5:81387675 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.128-1849T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387675 | |||||||
| chr5:81387927 | G | T | 4 | a0001c0001t0001g0054 a0001c0001t0002g0053 a0001c0001t0002g0055 others(1): Show |
4 | HG00609.hp2 HG02735.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.128-2101C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81387927 | |||||||
| chr5:81388055 | C | T | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.128-2229G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388055 | |||||||
| chr5:81388094 | T | C | 1 | a0001c0007t0004g0039 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.128-2268A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388094 | |||||||
| chr5:81388447 | G | A | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.128-2621C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388447 | |||||||
| chr5:81388483 | G | A | 22 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(19): Show |
24 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.128-2657C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388483 | |||||||
| chr5:81388509 | G | T | 1 | a0001c0001t0001g0052 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.128-2683C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388509 | |||||||
| chr5:81388624 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0002g0051 |
2 | HG00597.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.128-2798G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388624 | |||||||
| chr5:81388776 | T | C | 2 | a0001c0001t0003g0246 a0001c0001t0004g0247 |
2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.128-2950A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388776 | |||||||
| chr5:81388803 | T | C | 3 | a0002c0002t0001g0185 a0002c0002t0001g0186 a0006c0006t0002g0184 |
3 | HG01884.hp1 HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.128-2977A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388803 | |||||||
| chr5:81388811 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.128-2985A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388811 | |||||||
| chr5:81388860 | C | T | 2 | a0001c0001t0002g0048 a0001c0001t0003g0049 |
2 | HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.128-3034G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388860 | |||||||
| chr5:81388881 | G | C | 2 | a0001c0001t0003g0187 a0001c0001t0003g0188 |
2 | HG01168.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.128-3055C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388881 | |||||||
| chr5:81388909 | T | G | 2 | a0001c0001t0003g0144 a0001c0001t0003g0231 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.128-3083A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388909 | |||||||
| chr5:81388996 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.128-3170G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388996 | |||||||
| chr5:81388997 | G | A | 104 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0170 others(101): Show |
111 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.128-3171C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81388997 | |||||||
| chr5:81389163 | C | T | 1 | a0001c0001t0001g0047 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.128-3337G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389163 | |||||||
| chr5:81389280 | G | A | 100 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0170 others(97): Show |
107 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.128-3454C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389280 | |||||||
| chr5:81389665 | T | C | 34 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0021 others(31): Show |
38 | HG00099.hp1 HG01109.hp2 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.128-3839A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389665 | |||||||
| chr5:81389758 | C | G | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.128-3932G>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389758 | |||||||
| chr5:81389770 | GCCTGCCT others(968): Show |
G | 5 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0002c0002t0003g0198 others(2): Show |
6 | HG00323.hp1 HG01243.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+3243_128-3945d others(2): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389770 | |||||||
| chr5:81389792 | A | G | 33 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(30): Show |
35 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.128-3966T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389792 | |||||||
| chr5:81389941 | T | C | 3 | a0001c0001t0003g0232 a0001c0001t0003g0234 a0001c0001t0004g0233 |
3 | HG01891.hp2 HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.127+4047A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389941 | |||||||
| chr5:81389955 | A | AT | 17 | a0001c0001t0001g0098 a0001c0001t0001g0219 a0001c0001t0002g0003 others(14): Show |
17 | HG00423.hp1 HG00438.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.127+4032dupA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389955 | |||||||
| chr5:81389955 | A | T | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+4033T>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389955 | |||||||
| chr5:81389955 | AT | A | 19 | a0001c0001t0001g0132 a0001c0001t0001g0140 a0001c0001t0002g0083 others(16): Show |
20 | HG00558.hp1 HG00609.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.127+4032delA | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81389955 | |||||||
| chr5:81390040 | G | A | 11 | a0001c0001t0003g0014 a0001c0001t0003g0156 a0001c0001t0003g0157 others(8): Show |
12 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.127+3948C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390040 | |||||||
| chr5:81390076 | T | A | 2 | a0001c0001t0003g0232 a0001c0001t0003g0234 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.127+3912A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390076 | |||||||
| chr5:81390172 | G | C | 1 | a0001c0001t0001g0047 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.127+3816C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390172 | |||||||
| chr5:81390199 | C | T | 22 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(19): Show |
24 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.127+3789G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390199 | |||||||
| chr5:81390481 | C | A | 20 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(17): Show |
22 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(19): Show |
intron_variant | MODIFIER | c.127+3507G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390481 | |||||||
| chr5:81390485 | C | T | 1 | a0001c0001t0003g0243 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.127+3503G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390485 | |||||||
| chr5:81390662 | C | A | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0002g0194 |
3 | HG02717.hp2 HG02895.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.127+3326G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390662 | |||||||
| chr5:81390767 | G | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG02015.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.127+3221C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390767 | |||||||
| chr5:81390891 | T | C | 1 | a0001c0001t0003g0189 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.127+3097A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81390891 | |||||||
| chr5:81391121 | A | C | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.127+2867T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391121 | |||||||
| chr5:81391314 | G | A | 1 | a0001c0001t0003g0231 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.127+2674C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391314 | |||||||
| chr5:81391406 | A | C | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+2582T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391406 | |||||||
| chr5:81391426 | G | A | 1 | a0002c0002t0003g0148 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.127+2562C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391426 | |||||||
| chr5:81391438 | G | A | 5 | a0001c0001t0003g0196 a0001c0001t0003g0197 a0002c0002t0003g0198 others(2): Show |
6 | HG00323.hp1 HG01243.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+2550C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391438 | |||||||
| chr5:81391473 | C | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0212 |
4 | HG01258.hp1 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.127+2515G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391473 | |||||||
| chr5:81391576 | G | C | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.127+2412C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391576 | |||||||
| chr5:81391588 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.127+2400C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391588 | |||||||
| chr5:81391685 | C | T | 146 | a0001c0001t0001g0016 a0001c0001t0001g0044 a0001c0001t0001g0170 others(143): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.127+2303G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391685 | |||||||
| chr5:81391754 | G | T | 43 | a0001c0001t0001g0170 a0001c0001t0003g0014 a0001c0001t0003g0149 others(40): Show |
44 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.127+2234C>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391754 | |||||||
| chr5:81391776 | G | A | 1 | a0001c0005t0003g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.127+2212C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391776 | |||||||
| chr5:81391866 | G | C | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+2122C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391866 | |||||||
| chr5:81391870 | A | G | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+2118T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391870 | |||||||
| chr5:81391972 | G | A | 75 | a0001c0001t0001g0170 a0001c0001t0001g0192 a0001c0001t0001g0193 others(72): Show |
80 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.127+2016C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81391972 | |||||||
| chr5:81392030 | T | C | 1 | a0001c0001t0003g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+1958A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392030 | |||||||
| chr5:81392054 | G | A | 1 | a0002c0002t0001g0138 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.127+1934C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392054 | |||||||
| chr5:81392136 | T | G | 1 | a0002c0002t0007g0208 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.127+1852A>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392136 | |||||||
| chr5:81392356 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.127+1632C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392356 | |||||||
| chr5:81392539 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.127+1449C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392539 | |||||||
| chr5:81392750 | TA | T | 68 | a0001c0001t0001g0016 a0001c0001t0001g0041 a0001c0001t0001g0170 others(65): Show |
72 | HG00323.hp1 HG00408.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.127+1237delT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392750 | |||||||
| chr5:81392750 | TAA | T | 28 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(25): Show |
30 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.127+1236_127+1237d others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392750 | |||||||
| chr5:81392902 | A | C | 1 | a0001c0001t0003g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.127+1086T>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392902 | |||||||
| chr5:81392998 | C | T | 1 | a0001c0001t0001g0040 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.127+990G>A | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81392998 | |||||||
| chr5:81393136 | G | C | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.127+852C>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393136 | |||||||
| chr5:81393174 | A | G | 1 | a0001c0001t0005g0141 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.127+814T>C | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393174 | |||||||
| chr5:81393189 | T | A | 145 | a0001c0001t0001g0016 a0001c0001t0001g0170 a0001c0001t0001g0192 others(142): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.127+799A>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393189 | |||||||
| chr5:81393261 | G | A | 1 | a0001c0001t0002g0203 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.127+727C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393261 | |||||||
| chr5:81393279 | T | C | 1 | a0002c0002t0002g0204 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.127+709A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393279 | |||||||
| chr5:81393383 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.127+605A>G | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393383 | |||||||
| chr5:81393623 | G | A | 1 | a0002c0002t0002g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.127+365C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393623 | |||||||
| chr5:81393632 | G | A | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+356C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393632 | |||||||
| chr5:81393653 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.127+335C>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393653 | |||||||
| chr5:81393702 | T | TCAA | 5 | a0001c0001t0001g0016 a0001c0001t0001g0209 a0001c0001t0001g0210 others(2): Show |
6 | HG02258.hp1 NA18957.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.127+283_127+285dup others(3): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393702 | |||||||
| chr5:81393715 | C | CA | 21 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
23 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(20): Show |
intron_variant | MODIFIER | c.127+272dupT | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393715 | |||||||
| chr5:81393715 | C | CAACA | 24 | a0001c0001t0003g0021 a0001c0001t0003g0026 a0001c0001t0003g0028 others(21): Show |
27 | HG00099.hp1 HG01109.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.127+269_127+272dup others(4): Show |
ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393715 | |||||||
| chr5:81393911 | A | AC | 25 | a0001c0001t0003g0018 a0001c0001t0003g0021 a0001c0001t0003g0026 others(22): Show |
28 | HG00099.hp1 HG01109.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.127+76dupG | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393911 | |||||||
| chr5:81393911 | AC | A | 26 | a0001c0001t0003g0004 a0001c0001t0003g0017 a0001c0001t0003g0230 others(23): Show |
29 | HG01106.hp2 HG01123.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.127+76delG | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393911 | |||||||
| chr5:81393917 | C | A | 2 | a0001c0001t0001g0254 a0001c0001t0002g0255 |
2 | HG00140.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.127+71G>T | ACOT12 | ENSG00000172497.9 | transcript | ENST00000307624.8 | protein_coding | 1/14 | chr5 | 81393917 |