Search by Gene
| Item | Value |
|---|---|
| geneid | 145447 |
| ensemblid | ENSG00000131969.15 |
| hgncid | 19837 |
| symbol | ABHD12B |
| name | abhydrolase domain containing 12B |
| refseq_nuc | NM_001206673.2 |
| refseq_prot | NP_001193602.1 |
| ensembl_nuc | ENST00000337334.7 |
| ensembl_prot | ENSP00000336693.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 50872053 |
| end | 50904970 |
| strand | + |
| ver | v1.2 |
| region | chr14:50872053-50904970 |
| region5000 | chr14:50867053-50909970 |
| regionname0 | ABHD12B_chr14_50872053_50904970 |
| regionname5000 | ABHD12B_chr14_50867053_50909970 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 362 | 187 | 40 | 37 | 77 | 9 | 22 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| a0002 | 0/0 | 362 | 116 | 19 | 14 | 71 | 3 | 9 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| a0003 | 0/0 | 362 | 36 | 10 | 6 | 11 | 0 | 9 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| a0004 | 0/0 | 362 | 18 | 16 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| a0005 | 0/0 | 362 | 13 | 2 | 7 | 4 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| a0006 | 0/0 | 362 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| a0007 | 0/0 | 362 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| a0008 | 0/0 | 362 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| a0009 | 0/0 | 362 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| a0010 | 0/0 | 362 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | MDAQD others(357): Show |
chr14 | 50867053 | 50909970 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1086 | 146 | 26 | 29 | 61 | 9 | 19 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0001c0005 | 0/0 | 1086 | 21 | 3 | 4 | 11 | 0 | 3 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0001c0006 | 0/0 | 1086 | 16 | 9 | 4 | 3 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0001c0011 | 0/0 | 1086 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0001c0013 | 0/0 | 1086 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0002c0002 | 0/0 | 1086 | 89 | 13 | 11 | 53 | 3 | 9 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0002c0004 | 0/0 | 1086 | 27 | 6 | 3 | 18 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0003c0003 | 0/0 | 1086 | 34 | 8 | 6 | 11 | 0 | 9 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0003c0012 | 0/0 | 1086 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0004c0007 | 0/0 | 1086 | 14 | 12 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0004c0009 | 0/0 | 1086 | 4 | 4 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0005c0008 | 0/0 | 1086 | 13 | 2 | 7 | 4 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0006c0010 | 0/0 | 1086 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0007c0015 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0008c0017 | 0/0 | 1086 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0009c0016 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 | ||
| a0010c0014 | 0/0 | 1086 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | ATGGA others(1081): Show |
chr14 | 50867053 | 50909970 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1815 | 134 | 22 | 27 | 58 | 9 | 17 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0001t0003 | 1/0 | 1815 | 9 | 3 | 2 | 1 | 0 | 2 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0001t0004 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0001t0014 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0001t0016 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0005t0004 | 0/0 | 1815 | 17 | 3 | 4 | 9 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0005t0007 | 0/0 | 1815 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0005t0008 | 0/0 | 1815 | 2 | 0 | 0 | 0 | 0 | 2 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0006t0001 | 0/0 | 1815 | 14 | 7 | 4 | 3 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0006t0003 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0006t0013 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0011t0004 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0011t0007 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0001c0013t0003 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0002c0002t0002 | 0/0 | 1815 | 77 | 3 | 10 | 53 | 3 | 8 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0002c0002t0005 | 0/0 | 1815 | 9 | 9 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0002c0002t0006 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0002c0002t0011 | 0/0 | 1815 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0002c0002t0012 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0002c0004t0002 | 0/0 | 1815 | 22 | 1 | 3 | 18 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0002c0004t0005 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0002c0004t0006 | 0/0 | 1815 | 3 | 3 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0002c0004t0010 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0003c0003t0001 | 0/0 | 1815 | 29 | 3 | 6 | 11 | 0 | 9 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0003c0003t0003 | 0/0 | 1815 | 5 | 5 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0003c0012t0001 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0004c0007t0001 | 0/0 | 1815 | 12 | 10 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0004c0007t0003 | 0/0 | 1815 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0004c0009t0001 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0004c0009t0003 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0004c0009t0009 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0004c0009t0015 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0005c0008t0002 | 0/0 | 1815 | 13 | 2 | 7 | 4 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0006c0010t0001 | 0/0 | 1815 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0007c0015t0001 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0008c0017t0006 | 0/0 | 1815 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0009c0016t0002 | 0/0 | 1815 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| a0010c0014t0003 | 0/0 | 1815 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | AGCCT others(1810): Show |
chr14 | 50867053 | 50909970 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0304 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0003g0288 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0014g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0001t0016g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0007g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0008g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0005t0008g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0006t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0011t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0011t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0013t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0001c0013t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0006g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0011g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0002t0012g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0005g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0002c0004t0010g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0003t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0012t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0003c0012t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0007t0003g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0009t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0009t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0009t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0004c0009t0015g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0005c0008t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0006c0010t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0007c0015t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0008c0017t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0009c0016t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| a0010c0014t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0060 | EUR | GBR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | GBR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0306 | EUR | FIN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00280 | hp2 | a0007 | c0015 | t0001 | g0315 | EUR | FIN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00408 | hp1 | a0001 | c0006 | t0001 | g0284 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00408 | hp2 | a0005 | c0008 | t0002 | g0321 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00423 | hp1 | a0001 | c0006 | t0001 | g0268 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00423 | hp2 | a0002 | c0004 | t0002 | g0225 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0117 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0320 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0065 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00597 | hp2 | a0002 | c0004 | t0002 | g0354 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00609 | hp1 | a0002 | c0004 | t0002 | g0269 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00609 | hp2 | a0001 | c0005 | t0004 | g0159 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00621 | hp2 | a0003 | c0003 | t0001 | g0110 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00673 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | CHS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01071 | hp1 | a0001 | c0006 | t0001 | g0219 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0208 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01099 | hp2 | a0002 | c0004 | t0002 | g0090 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0302 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01106 | hp2 | a0004 | c0007 | t0001 | g0124 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01167 | hp1 | a0003 | c0003 | t0001 | g0063 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01167 | hp2 | a0006 | c0010 | t0001 | g0012 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0200 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01169 | hp2 | a0006 | c0010 | t0001 | g0012 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01192 | hp2 | a0001 | c0006 | t0001 | g0218 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0188 | AMR | PUR | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0029 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0121 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01261 | hp2 | a0002 | c0002 | t0011 | g0175 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01346 | hp1 | a0001 | c0006 | t0001 | g0166 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01346 | hp2 | a0005 | c0008 | t0002 | g0149 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01361 | hp1 | a0002 | c0002 | t0002 | g0201 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | IBS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0202 | EUR | IBS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0070 | EUR | IBS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01516 | hp2 | a0002 | c0002 | t0002 | g0096 | EUR | IBS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01884 | hp1 | a0002 | c0002 | t0005 | g0170 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01884 | hp2 | a0001 | c0005 | t0004 | g0125 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01891 | hp1 | a0001 | c0001 | t0004 | g0318 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0105 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01928 | hp2 | a0001 | c0006 | t0001 | g0135 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01934 | hp1 | a0002 | c0004 | t0002 | g0270 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0097 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0334 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01952 | hp1 | a0005 | c0008 | t0002 | g0010 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01952 | hp2 | a0002 | c0004 | t0002 | g0089 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0325 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01975 | hp2 | a0003 | c0003 | t0001 | g0298 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01978 | hp1 | a0005 | c0008 | t0002 | g0150 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0301 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01981 | hp1 | a0001 | c0005 | t0004 | g0017 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01981 | hp2 | a0004 | c0007 | t0001 | g0353 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01993 | hp1 | a0001 | c0005 | t0004 | g0264 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG01993 | hp2 | a0002 | c0002 | t0002 | g0074 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02004 | hp1 | a0001 | c0005 | t0004 | g0137 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02004 | hp2 | a0005 | c0008 | t0002 | g0285 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02055 | hp2 | a0002 | c0002 | t0002 | g0345 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02056 | hp2 | a0001 | c0011 | t0004 | g0087 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02071 | hp1 | a0002 | c0004 | t0002 | g0015 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02071 | hp2 | a0002 | c0004 | t0002 | g0147 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02080 | hp2 | a0003 | c0003 | t0001 | g0061 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0346 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02145 | hp1 | a0002 | c0004 | t0006 | g0228 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0083 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02148 | hp1 | a0005 | c0008 | t0002 | g0152 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0226 | EAS | CDX | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | CDX | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0048 | EAS | CDX | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02258 | hp1 | a0005 | c0008 | t0002 | g0221 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02273 | hp2 | a0005 | c0008 | t0002 | g0151 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02280 | hp1 | a0002 | c0002 | t0005 | g0024 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02280 | hp2 | a0002 | c0002 | t0006 | g0317 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02300 | hp1 | a0005 | c0008 | t0002 | g0010 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02300 | hp2 | a0001 | c0005 | t0004 | g0333 | AMR | PEL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02451 | hp1 | a0004 | c0009 | t0001 | g0289 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02523 | hp2 | a0005 | c0008 | t0002 | g0242 | EAS | KHV | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02572 | hp1 | a0002 | c0004 | t0002 | g0294 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02572 | hp2 | a0003 | c0012 | t0001 | g0130 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0109 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0281 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0142 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02615 | hp2 | a0004 | c0007 | t0003 | g0019 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02622 | hp1 | a0001 | c0006 | t0001 | g0295 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02622 | hp2 | a0002 | c0002 | t0005 | g0022 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02630 | hp1 | a0001 | c0006 | t0013 | g0028 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02630 | hp2 | a0002 | c0002 | t0005 | g0245 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02647 | hp1 | a0003 | c0003 | t0001 | g0290 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02647 | hp2 | a0002 | c0002 | t0005 | g0217 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02717 | hp1 | a0004 | c0009 | t0003 | g0168 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02717 | hp2 | a0002 | c0002 | t0005 | g0153 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0203 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02735 | hp2 | a0001 | c0005 | t0008 | g0212 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0084 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02809 | hp1 | a0001 | c0006 | t0003 | g0198 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02886 | hp1 | a0003 | c0003 | t0003 | g0196 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02886 | hp2 | a0002 | c0004 | t0010 | g0205 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02896 | hp1 | a0004 | c0007 | t0001 | g0293 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02896 | hp2 | a0001 | c0006 | t0001 | g0128 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02922 | hp2 | a0004 | c0007 | t0001 | g0157 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02965 | hp1 | a0004 | c0007 | t0001 | g0243 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02965 | hp2 | a0001 | c0006 | t0001 | g0091 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02970 | hp1 | a0003 | c0003 | t0003 | g0287 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02970 | hp2 | a0002 | c0002 | t0005 | g0244 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02976 | hp1 | a0001 | c0013 | t0003 | g0035 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03041 | hp1 | a0001 | c0006 | t0001 | g0072 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03041 | hp2 | a0001 | c0006 | t0001 | g0176 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03098 | hp1 | a0003 | c0003 | t0003 | g0291 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03098 | hp2 | a0002 | c0004 | t0006 | g0023 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03130 | hp1 | a0003 | c0003 | t0003 | g0075 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03139 | hp1 | a0004 | c0007 | t0001 | g0167 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03195 | hp2 | a0004 | c0007 | t0001 | g0002 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03209 | hp1 | a0004 | c0009 | t0015 | g0177 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03209 | hp2 | a0003 | c0012 | t0001 | g0041 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03225 | hp2 | a0004 | c0007 | t0001 | g0037 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03486 | hp1 | a0002 | c0004 | t0005 | g0071 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03486 | hp2 | a0004 | c0009 | t0009 | g0165 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0140 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03490 | hp2 | a0003 | c0003 | t0001 | g0014 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03492 | hp2 | a0003 | c0003 | t0001 | g0014 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03516 | hp1 | a0002 | c0002 | t0005 | g0179 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03516 | hp2 | a0001 | c0006 | t0001 | g0241 | AFR | ESN | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0227 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03669 | hp2 | a0001 | c0005 | t0008 | g0215 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0276 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0052 | SAS | PJL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0141 | SAS | BEB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0139 | SAS | BEB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03927 | hp2 | a0001 | c0005 | t0004 | g0347 | SAS | BEB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | STU | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG04115 | hp2 | a0002 | c0002 | t0012 | g0214 | SAS | STU | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0092 | SAS | BEB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0077 | SAS | STU | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0267 | SAS | STU | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0232 | SAS | STU | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG04204 | hp2 | a0003 | c0003 | t0001 | g0068 | SAS | STU | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18522 | hp2 | a0002 | c0002 | t0005 | g0171 | AFR | YRI | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | CHB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | CHB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18906 | hp1 | a0004 | c0007 | t0001 | g0116 | AFR | YRI | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18906 | hp2 | a0004 | c0007 | t0003 | g0019 | AFR | YRI | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18942 | hp2 | a0001 | c0005 | t0004 | g0343 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18944 | hp2 | a0001 | c0005 | t0007 | g0005 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18945 | hp1 | a0002 | c0004 | t0002 | g0127 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18946 | hp2 | a0003 | c0003 | t0001 | g0254 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0355 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0033 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18949 | hp1 | a0002 | c0002 | t0002 | g0319 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18949 | hp2 | a0002 | c0004 | t0002 | g0122 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18950 | hp2 | a0002 | c0004 | t0002 | g0279 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0330 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18953 | hp1 | a0002 | c0004 | t0002 | g0204 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0129 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18954 | hp2 | a0002 | c0004 | t0002 | g0008 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18964 | hp2 | a0002 | c0004 | t0002 | g0282 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18966 | hp1 | a0001 | c0006 | t0001 | g0278 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18966 | hp2 | a0002 | c0004 | t0002 | g0088 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0335 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18971 | hp2 | a0001 | c0001 | t0014 | g0349 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18979 | hp1 | a0001 | c0005 | t0004 | g0312 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18979 | hp2 | a0002 | c0004 | t0002 | g0351 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18984 | hp1 | a0002 | c0004 | t0002 | g0008 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18989 | hp1 | a0001 | c0005 | t0004 | g0341 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18990 | hp1 | a0001 | c0005 | t0004 | g0017 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0350 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18994 | hp1 | a0002 | c0004 | t0002 | g0336 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0257 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA18999 | hp2 | a0002 | c0004 | t0002 | g0015 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19004 | hp1 | a0001 | c0001 | t0016 | g0056 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19007 | hp1 | a0001 | c0005 | t0007 | g0005 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0348 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19012 | hp1 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0272 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | LWK | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | LWK | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19043 | hp2 | a0008 | c0017 | t0006 | g0224 | AFR | LWK | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19056 | hp1 | a0003 | c0003 | t0001 | g0100 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19057 | hp2 | a0001 | c0005 | t0004 | g0352 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0102 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19065 | hp2 | a0005 | c0008 | t0002 | g0283 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19074 | hp1 | a0001 | c0011 | t0007 | g0113 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19074 | hp2 | a0001 | c0005 | t0004 | g0328 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19077 | hp1 | a0009 | c0016 | t0002 | g0266 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19077 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19079 | hp1 | a0001 | c0005 | t0004 | g0131 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19081 | hp2 | a0002 | c0004 | t0002 | g0240 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19082 | hp1 | a0005 | c0008 | t0002 | g0178 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19086 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19087 | hp2 | a0001 | c0005 | t0004 | g0261 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19090 | hp1 | a0002 | c0004 | t0002 | g0059 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19091 | hp1 | a0002 | c0002 | t0002 | g0327 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | YRI | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA19240 | hp2 | a0004 | c0007 | t0001 | g0187 | AFR | YRI | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA20129 | hp1 | a0002 | c0004 | t0006 | g0169 | AFR | ASW | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA20129 | hp2 | a0005 | c0008 | t0002 | g0305 | AFR | ASW | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA20805 | hp1 | a0002 | c0002 | t0002 | g0073 | EUR | TSI | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA20805 | hp2 | a0010 | c0014 | t0003 | g0213 | EUR | TSI | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0163 | SAS | GIH | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | GIH | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02109 | hp2 | a0003 | c0003 | t0003 | g0197 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02559 | hp1 | a0004 | c0007 | t0001 | g0002 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | ACB | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03471 | hp1 | a0001 | c0005 | t0004 | g0026 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| HG06807 | hp2 | a0001 | c0006 | t0001 | g0058 | AFR | USA | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA20300 | hp1 | a0004 | c0007 | t0001 | g0115 | AFR | USA | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA20300 | hp2 | a0001 | c0005 | t0004 | g0252 | AFR | USA | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA21309 | hp1 | a0001 | c0013 | t0003 | g0036 | AFR | LWK | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0304 | REF | REF | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0288 | REF | REF | ABHD12B_chr14_50867053_50909970 | ABHD12B | chr14 | 50867053 | 50909970 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50878819 | G | A | 1 | a0010 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.307G>A | p.Val103Ile | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/13 | 429/1815 | 307/1089 | 103/362 | chr14 | 50878819 | |||
| chr14:50885627 | G | A | 3 | a0005a0006a0007 | 16 | HG00280.hp2 HG00408.hp2 HG01167.hp2 others(13): Show |
missense_variant | MODERATE | c.500G>A | p.Gly167Asp | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 6/13 | 622/1815 | 500/1089 | 167/362 | chr14 | 50885627 | |||
| chr14:50885837 | A | G | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.604A>G | p.Thr202Ala | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/13 | 726/1815 | 604/1089 | 202/362 | chr14 | 50885837 | |||
| chr14:50901836 | G | A | 1 | a0009 | 1 | NA19077.hp1 | missense_variant | MODERATE | c.788G>A | p.Arg263Gln | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/13 | 910/1815 | 788/1089 | 263/362 | chr14 | 50901836 | |||
| chr14:50901892 | A | G | 4 | a0002a0005a0008others(1): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
missense_variant | MODERATE | c.844A>G | p.Ile282Val | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/13 | 966/1815 | 844/1089 | 282/362 | chr14 | 50901892 | |||
| chr14:50904131 | T | C | 2 | a0004a0007 | 19 | HG00280.hp2 HG01106.hp2 HG01981.hp2 others(16): Show |
missense_variant | MODERATE | c.1000T>C | p.Phe334Leu | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 12/13 | 1122/1815 | 1000/1089 | 334/362 | chr14 | 50904131 | |||
| chr14:50904134 | C | G | 1 | a0003 | 36 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(33): Show |
missense_variant | MODERATE | c.1003C>G | p.Pro335Ala | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 12/13 | 1125/1815 | 1003/1089 | 335/362 | chr14 | 50904134 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50885848 | A | G | 2 | a0001c0013a0004c0009 | 6 | HG02451.hp1 HG02717.hp1 HG02976.hp1 others(3): Show |
synonymous_variant | LOW | c.615A>G | p.Arg205Arg | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/13 | 737/1815 | 615/1089 | 205/362 | chr14 | 50885848 | |||
| chr14:50885890 | T | C | 5 | a0001c0006a0001c0011a0002c0004others(2): Show | 48 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(45): Show |
synonymous_variant | LOW | c.657T>C | p.Gly219Gly | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/13 | 779/1815 | 657/1089 | 219/362 | chr14 | 50885890 | |||
| chr14:50904363 | A | C | 2 | a0001c0005a0001c0011 | 23 | HG00609.hp2 HG01884.hp2 HG01981.hp1 others(20): Show |
synonymous_variant | LOW | c.1086A>C | p.Ser362Ser | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 1208/1815 | 1086/1089 | 362/362 | chr14 | 50904363 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50872157 | A | C | 26 | a0001c0001t0001a0001c0001t0004a0001c0001t0014others(23): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
5_prime_UTR_variant | MODIFIER | c.-18A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/13 | 18 | chr14 | 50872157 | ||||||
| chr14:50904380 | G | A | 2 | a0001c0005t0007a0001c0011t0007 | 3 | NA18944.hp2 NA19007.hp1 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*14G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 14 | chr14 | 50904380 | ||||||
| chr14:50904403 | C | T | 12 | a0002c0002t0002a0002c0002t0005a0002c0002t0006others(9): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*37C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 37 | chr14 | 50904403 | ||||||
| chr14:50904412 | C | T | 5 | a0002c0002t0002a0002c0002t0012a0002c0004t0002others(2): Show | 114 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*46C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 46 | chr14 | 50904412 | ||||||
| chr14:50904432 | C | T | 12 | a0002c0002t0002a0002c0002t0005a0002c0002t0006others(9): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*66C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 66 | chr14 | 50904432 | ||||||
| chr14:50904582 | T | C | 1 | a0001c0006t0013 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*216T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 216 | chr14 | 50904582 | ||||||
| chr14:50904587 | C | G | 1 | a0001c0001t0016 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*221C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 221 | chr14 | 50904587 | ||||||
| chr14:50904683 | G | T | 7 | a0001c0001t0004a0001c0005t0004a0001c0005t0007others(4): Show | 25 | HG00609.hp2 HG01884.hp2 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*317G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 317 | chr14 | 50904683 | ||||||
| chr14:50904687 | T | C | 4 | a0002c0002t0006a0002c0004t0006a0002c0004t0010others(1): Show | 6 | HG02145.hp1 HG02280.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*321T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 321 | chr14 | 50904687 | ||||||
| chr14:50904692 | C | T | 2 | a0004c0009t0009a0004c0009t0015 | 2 | HG03209.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 326 | chr14 | 50904692 | ||||||
| chr14:50904729 | C | T | 7 | a0002c0002t0005a0002c0002t0006a0002c0002t0011others(4): Show | 17 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*363C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 363 | chr14 | 50904729 | ||||||
| chr14:50904806 | C | T | 5 | a0002c0002t0002a0002c0002t0012a0002c0004t0002others(2): Show | 114 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*440C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 440 | chr14 | 50904806 | ||||||
| chr14:50904820 | C | G | 1 | a0002c0002t0012 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 454 | chr14 | 50904820 | ||||||
| chr14:50904822 | C | T | 1 | a0002c0002t0012 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*456C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 456 | chr14 | 50904822 | ||||||
| chr14:50904823 | T | A | 1 | a0002c0002t0012 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*457T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 457 | chr14 | 50904823 | ||||||
| chr14:50904933 | A | C | 1 | a0001c0001t0014 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*567A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 13/13 | 567 | chr14 | 50904933 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50872346 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.104+68G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50872346 | |||||||
| chr14:50872360 | C | G | 2 | a0002c0002t0002g0355a0002c0004t0002g0354 | 2 | HG00597.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.104+82C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50872360 | |||||||
| chr14:50872379 | G | A | 7 | a0001c0001t0001g0025a0001c0005t0004g0026a0001c0006t0013g0028others(4): Show | 7 | HG02258.hp2 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.104+101G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50872379 | |||||||
| chr14:50872394 | A | G | 1 | a0004c0007t0001g0353 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.104+116A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50872394 | |||||||
| chr14:50872498 | C | G | 1 | a0001c0006t0013g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.104+220C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50872498 | |||||||
| chr14:50872508 | A | G | 36 | a0001c0001t0001g0021a0001c0001t0001g0322a0001c0001t0001g0323others(33): Show | 37 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.104+230A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50872508 | |||||||
| chr14:50872672 | A | AATCTTGG others(11): Show |
1 | a0002c0002t0002g0029 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.104+395_104+412dup others(18): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 50872672 | ||||||
| chr14:50872797 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.104+519T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50872797 | |||||||
| chr14:50872894 | G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.104+616G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50872894 | |||||||
| chr14:50873157 | G | A | 1 | a0002c0002t0002g0033 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.104+879G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873157 | |||||||
| chr14:50873160 | A | G | 2 | a0001c0001t0004g0318a0002c0002t0006g0317 | 2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.104+882A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873160 | |||||||
| chr14:50873197 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.104+919G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873197 | |||||||
| chr14:50873206 | T | C | 2 | a0001c0013t0003g0035a0001c0013t0003g0036 | 2 | HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.104+928T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873206 | |||||||
| chr14:50873222 | C | CTT | 34 | a0001c0001t0001g0021a0001c0001t0001g0316a0001c0001t0001g0322others(31): Show | 35 | HG00597.hp1 HG01943.hp1 HG01975.hp1 others(32): Show |
intron_variant | MODIFIER | c.104+953_104+954dup others(2): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 50873222 | ||||||
| chr14:50873222 | CT | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0005t0004g0026others(6): Show | 9 | HG01169.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.104+954delT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 50873222 | ||||||
| chr14:50873324 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.104+1046T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873324 | |||||||
| chr14:50873370 | T | C | 324 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(321): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.104+1092T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873370 | |||||||
| chr14:50873417 | T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.104+1139T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873417 | |||||||
| chr14:50873476 | T | A | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.104+1198T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873476 | |||||||
| chr14:50873627 | G | A | 32 | a0001c0001t0001g0021a0001c0001t0001g0322a0001c0001t0001g0323others(29): Show | 33 | HG00597.hp1 HG01943.hp1 HG01975.hp1 others(30): Show |
intron_variant | MODIFIER | c.104+1349G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873627 | |||||||
| chr14:50873687 | T | C | 2 | a0001c0001t0001g0039a0004c0007t0001g0002 | 3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.104+1409T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873687 | |||||||
| chr14:50873692 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.104+1414T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873692 | |||||||
| chr14:50873775 | G | A | 6 | a0001c0001t0001g0025a0001c0006t0013g0028a0002c0002t0005g0022others(3): Show | 6 | HG02258.hp2 HG02280.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+1497G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873775 | |||||||
| chr14:50873855 | A | G | 86 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0230others(83): Show | 90 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.104+1577A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873855 | |||||||
| chr14:50873902 | TAGTGAAA others(27): Show |
T | 1 | a0002c0004t0002g0225 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.104+1626_104+1659d others(36): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 50873902 | ||||||
| chr14:50873920 | G | C | 1 | a0002c0002t0002g0136 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.104+1642G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50873920 | |||||||
| chr14:50874055 | C | T | 2 | a0001c0001t0001g0286a0001c0006t0013g0028 | 2 | HG02630.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.104+1777C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874055 | |||||||
| chr14:50874262 | G | A | 1 | a0002c0002t0002g0226 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.104+1984G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874262 | |||||||
| chr14:50874263 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.104+1985G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874263 | |||||||
| chr14:50874368 | A | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0008c0017t0006g0224 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.104+2090A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874368 | |||||||
| chr14:50874372 | G | A | 77 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0230others(74): Show | 81 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.104+2094G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874372 | |||||||
| chr14:50874396 | G | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0008c0017t0006g0224 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.104+2118G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874396 | |||||||
| chr14:50874439 | A | G | 6 | a0001c0001t0001g0220a0001c0001t0001g0222a0001c0001t0001g0223others(3): Show | 6 | HG01071.hp1 HG01175.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.104+2161A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874439 | |||||||
| chr14:50874460 | C | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(96): Show | 107 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.104+2182C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874460 | |||||||
| chr14:50874461 | G | A | 1 | a0003c0003t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.104+2183G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874461 | |||||||
| chr14:50874599 | C | CA | 82 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0039others(79): Show | 87 | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.104+2330dupA | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 50874599 | ||||||
| chr14:50874599 | C | CAA | 7 | a0001c0001t0001g0120a0001c0001t0001g0123a0001c0001t0001g0316others(4): Show | 7 | HG01070.hp1 HG01074.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.104+2329_104+2330d others(4): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 50874599 | ||||||
| chr14:50874609 | T | A | 337 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(334): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.104+2331T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874609 | |||||||
| chr14:50874871 | A | G | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0008c0017t0006g0224 | 3 | HG03225.hp1 HG06807.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.104+2593A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874871 | |||||||
| chr14:50874967 | A | T | 1 | a0002c0002t0002g0350 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.104+2689A>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50874967 | |||||||
| chr14:50875002 | C | T | 7 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0216others(4): Show | 7 | HG02074.hp1 HG02735.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.104+2724C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875002 | |||||||
| chr14:50875113 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.104+2835G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875113 | |||||||
| chr14:50875135 | C | G | 352 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(349): Show | 373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.105-2817C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875135 | |||||||
| chr14:50875155 | T | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0039others(5): Show | 9 | HG01884.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.105-2797T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875155 | |||||||
| chr14:50875164 | G | A | 2 | a0001c0001t0001g0162a0004c0009t0001g0289 | 2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.105-2788G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875164 | |||||||
| chr14:50875169 | T | C | 105 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0045others(102): Show | 109 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.105-2783T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875169 | |||||||
| chr14:50875513 | C | T | 297 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(294): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.105-2439C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875513 | |||||||
| chr14:50875514 | G | A | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0039others(5): Show | 9 | HG01433.hp1 HG02559.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.105-2438G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875514 | |||||||
| chr14:50875579 | C | T | 1 | a0002c0002t0002g0161 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.105-2373C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875579 | |||||||
| chr14:50875602 | C | T | 4 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0277others(1): Show | 4 | HG02135.hp2 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.105-2350C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875602 | |||||||
| chr14:50875758 | T | G | 189 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(186): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.105-2194T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50875758 | |||||||
| chr14:50876293 | C | G | 1 | a0002c0002t0005g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.105-1659C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50876293 | |||||||
| chr14:50876361 | A | G | 1 | a0001c0001t0014g0349 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.105-1591A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50876361 | |||||||
| chr14:50876449 | C | T | 1 | a0002c0002t0002g0043 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.105-1503C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50876449 | |||||||
| chr14:50876492 | G | A | 1 | a0002c0002t0002g0126 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.105-1460G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50876492 | |||||||
| chr14:50876507 | G | C | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.105-1445G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50876507 | |||||||
| chr14:50876672 | G | A | 3 | a0001c0001t0001g0247a0002c0002t0002g0248a0002c0002t0002g0249 | 3 | NA18971.hp1 NA18992.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.105-1280G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50876672 | |||||||
| chr14:50876795 | G | A | 1 | a0003c0003t0001g0027 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.105-1157G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50876795 | |||||||
| chr14:50876881 | A | G | 57 | a0001c0001t0001g0011a0001c0001t0001g0034a0001c0001t0001g0038others(54): Show | 59 | HG00280.hp1 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.105-1071A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50876881 | |||||||
| chr14:50876899 | T | C | 1 | a0002c0002t0002g0250 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.105-1053T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50876899 | |||||||
| chr14:50877047 | G | A | 314 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(311): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.105-905G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50877047 | |||||||
| chr14:50877229 | G | C | 1 | a0002c0002t0002g0335 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.105-723G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50877229 | |||||||
| chr14:50877420 | C | G | 2 | a0001c0001t0001g0025a0002c0002t0005g0024 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.105-532C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50877420 | |||||||
| chr14:50877642 | G | A | 1 | a0003c0003t0001g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.105-310G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50877642 | |||||||
| chr14:50877759 | T | A | 4 | a0001c0006t0001g0295a0002c0002t0006g0317a0002c0004t0006g0169others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.105-193T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | chr14 | 50877759 | |||||||
| chr14:50877866 | C | CAA | 125 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0032others(122): Show | 133 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.105-78_105-77dupAA | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 50877866 | ||||||
| chr14:50877866 | C | CAAA | 217 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(214): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.105-79_105-77dupAA others(1): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr14 | 50877866 | ||||||
| chr14:50878230 | G | T | 5 | a0001c0013t0003g0035a0001c0013t0003g0036a0004c0009t0003g0168others(2): Show | 5 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.232+151G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 2/12 | chr14 | 50878230 | |||||||
| chr14:50878936 | G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0299 | 2 | HG00099.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.335+89G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50878936 | |||||||
| chr14:50878956 | A | G | 4 | a0001c0006t0001g0295a0002c0002t0006g0317a0002c0004t0006g0169others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.335+109A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50878956 | |||||||
| chr14:50879011 | C | G | 36 | a0001c0001t0001g0032a0001c0001t0001g0162a0001c0001t0001g0296others(33): Show | 38 | HG00280.hp2 HG00408.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.335+164C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879011 | |||||||
| chr14:50879056 | G | A | 2 | a0002c0004t0002g0282a0009c0016t0002g0266 | 2 | NA18964.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.335+209G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879056 | |||||||
| chr14:50879100 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.335+253C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879100 | |||||||
| chr14:50879210 | G | A | 1 | a0004c0007t0001g0187 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.335+363G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879210 | |||||||
| chr14:50879368 | A | C | 4 | a0001c0006t0001g0295a0002c0002t0006g0317a0002c0004t0006g0169others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.335+521A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879368 | |||||||
| chr14:50879373 | T | C | 2 | a0001c0005t0004g0347a0002c0002t0002g0267 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.335+526T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879373 | |||||||
| chr14:50879410 | A | G | 1 | a0002c0002t0002g0276 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.335+563A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879410 | |||||||
| chr14:50879603 | G | A | 1 | a0001c0005t0008g0215 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.335+756G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879603 | |||||||
| chr14:50879635 | A | C | 347 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(344): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.335+788A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879635 | |||||||
| chr14:50879659 | T | G | 347 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(344): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.336-793T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879659 | |||||||
| chr14:50879678 | A | G | 1 | a0002c0004t0002g0354 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.336-774A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879678 | |||||||
| chr14:50879692 | T | G | 4 | a0001c0006t0001g0295a0002c0002t0006g0317a0002c0004t0006g0169others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.336-760T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879692 | |||||||
| chr14:50879841 | G | A | 347 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(344): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.336-611G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879841 | |||||||
| chr14:50879876 | C | T | 1 | a0002c0002t0002g0346 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.336-576C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879876 | |||||||
| chr14:50879906 | T | C | 1 | a0008c0017t0006g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.336-546T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879906 | |||||||
| chr14:50879992 | T | A | 347 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(344): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.336-460T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50879992 | |||||||
| chr14:50880083 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.336-369C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50880083 | |||||||
| chr14:50880108 | A | G | 2 | a0001c0001t0001g0025a0002c0002t0005g0024 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.336-344A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50880108 | |||||||
| chr14:50880223 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.336-229G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50880223 | |||||||
| chr14:50880243 | GTC | G | 30 | a0001c0006t0001g0058a0001c0006t0001g0091a0001c0006t0001g0241others(27): Show | 32 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.336-205_336-204del others(2): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr14 | 50880243 | ||||||
| chr14:50880305 | T | C | 273 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(270): Show | 290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.336-147T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50880305 | |||||||
| chr14:50880389 | G | A | 347 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(344): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.336-63G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 3/12 | chr14 | 50880389 | |||||||
| chr14:50880623 | G | A | 1 | a0007c0015t0001g0315 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.455+52G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50880623 | |||||||
| chr14:50880632 | G | A | 2 | a0001c0005t0004g0347a0002c0002t0002g0267 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.455+61G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50880632 | |||||||
| chr14:50880780 | G | T | 1 | a0001c0005t0004g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.455+209G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50880780 | |||||||
| chr14:50880939 | A | C | 1 | a0002c0002t0002g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.455+368A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50880939 | |||||||
| chr14:50880955 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.455+384A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50880955 | |||||||
| chr14:50881017 | A | T | 1 | a0001c0005t0004g0264 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.455+446A>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881017 | |||||||
| chr14:50881027 | C | T | 2 | a0001c0001t0001g0331a0001c0001t0001g0332 | 2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.455+456C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881027 | |||||||
| chr14:50881044 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.455+473G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881044 | |||||||
| chr14:50881154 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.456-442C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881154 | |||||||
| chr14:50881155 | G | A | 2 | a0001c0001t0001g0025a0002c0002t0005g0024 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.456-441G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881155 | |||||||
| chr14:50881168 | A | C | 1 | a0001c0001t0001g0030 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.456-428A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881168 | |||||||
| chr14:50881187 | G | A | 339 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(336): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.456-409G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881187 | |||||||
| chr14:50881209 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.456-387C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881209 | |||||||
| chr14:50881227 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.456-369T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881227 | |||||||
| chr14:50881243 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.456-353G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881243 | |||||||
| chr14:50881282 | G | A | 1 | a0002c0002t0002g0272 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.456-314G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881282 | |||||||
| chr14:50881429 | A | AT | 66 | a0001c0001t0001g0032a0001c0001t0001g0055a0001c0001t0001g0057others(63): Show | 70 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.456-153dupT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 50881429 | ||||||
| chr14:50881458 | C | T | 1 | a0002c0002t0002g0202 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.456-138C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881458 | |||||||
| chr14:50881494 | C | T | 42 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0006t0001g0058others(39): Show | 44 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.456-102C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | chr14 | 50881494 | |||||||
| chr14:50881563 | C | CT | 36 | a0001c0001t0001g0172a0001c0001t0001g0180a0001c0006t0001g0058others(33): Show | 38 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(35): Show |
intron_variant | MODIFIER | c.456-16dupT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 50881563 | ||||||
| chr14:50881563 | C | CTT | 280 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(277): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.456-17_456-16dupTT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 50881563 | ||||||
| chr14:50881563 | C | CTTT | 10 | a0001c0001t0001g0060a0001c0001t0001g0085a0001c0001t0001g0158others(7): Show | 10 | HG00099.hp2 HG00408.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.456-18_456-16dupTT others(1): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 50881563 | ||||||
| chr14:50881563 | CT | C | 15 | a0001c0001t0001g0032a0001c0006t0001g0295a0002c0002t0005g0022others(12): Show | 15 | HG01884.hp1 HG02145.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.456-16delT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr14 | 50881563 | ||||||
| chr14:50881627 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG00140.hp1 | splice_donor_variant&intron_variant | HIGH | c.486+1G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881627 | |||||||
| chr14:50881661 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.486+35T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881661 | |||||||
| chr14:50881696 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.486+70G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881696 | |||||||
| chr14:50881702 | C | A | 1 | a0002c0004t0006g0228 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.486+76C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881702 | |||||||
| chr14:50881703 | G | A | 19 | a0001c0001t0001g0030a0001c0001t0001g0296a0001c0001t0004g0318others(16): Show | 21 | HG00280.hp2 HG00408.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.486+77G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881703 | |||||||
| chr14:50881777 | C | T | 2 | a0002c0004t0002g0127a0002c0004t0002g0147 | 2 | HG02071.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.486+151C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881777 | |||||||
| chr14:50881781 | G | A | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.486+155G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881781 | |||||||
| chr14:50881856 | C | T | 33 | a0001c0006t0001g0058a0001c0006t0001g0091a0001c0006t0001g0128others(30): Show | 35 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.486+230C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881856 | |||||||
| chr14:50881864 | C | A | 1 | a0002c0002t0002g0048 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.486+238C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881864 | |||||||
| chr14:50881926 | GGTT | G | 23 | a0001c0001t0001g0162a0001c0001t0001g0296a0001c0001t0003g0191others(20): Show | 25 | HG00280.hp2 HG00408.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.486+301_486+303del others(3): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50881926 | |||||||
| chr14:50881938 | TGTCGTTG others(5): Show |
T | 23 | a0001c0001t0001g0162a0001c0001t0001g0296a0001c0001t0003g0191others(20): Show | 25 | HG00280.hp2 HG00408.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.486+315_486+326del others(12): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50881938 | ||||||
| chr14:50882054 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.486+428G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882054 | |||||||
| chr14:50882169 | C | G | 5 | a0001c0001t0001g0101a0001c0001t0001g0118a0001c0001t0001g0119others(2): Show | 5 | HG01106.hp2 HG01981.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.486+543C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882169 | |||||||
| chr14:50882189 | G | A | 4 | a0001c0006t0001g0295a0002c0002t0006g0317a0002c0004t0006g0169others(1): Show | 4 | HG02280.hp2 HG02622.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.486+563G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882189 | |||||||
| chr14:50882215 | C | T | 1 | a0002c0002t0002g0330 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.486+589C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882215 | |||||||
| chr14:50882232 | G | A | 1 | a0001c0005t0004g0333 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.486+606G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882232 | |||||||
| chr14:50882281 | G | A | 1 | a0004c0007t0001g0115 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.486+655G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882281 | |||||||
| chr14:50882373 | C | CTT | 68 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0016others(65): Show | 74 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.486+767_486+768dup others(2): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTT | 184 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(181): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.486+766_486+768dup others(3): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTT | 17 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0085others(14): Show | 18 | HG00621.hp1 HG00621.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.486+765_486+768dup others(4): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTTTTT others(5): Show |
17 | a0001c0006t0001g0268a0001c0006t0001g0278a0001c0006t0001g0284others(14): Show | 19 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(16): Show |
intron_variant | MODIFIER | c.486+757_486+768dup others(12): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTTTTT others(6): Show |
9 | a0001c0006t0001g0091a0001c0011t0007g0113a0002c0004t0002g0059others(6): Show | 9 | HG01934.hp1 HG02965.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.486+756_486+768dup others(13): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0004g0318a0003c0003t0001g0027 | 2 | HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.486+755_486+768dup others(14): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTTTTT others(8): Show |
8 | a0001c0001t0001g0296a0001c0006t0001g0058a0001c0006t0001g0128others(5): Show | 8 | HG02056.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+754_486+768dup others(15): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTTTTT others(10): Show |
1 | a0001c0006t0001g0176 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.486+752_486+768dup others(17): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTTTTT others(11): Show |
2 | a0001c0001t0001g0025a0002c0002t0005g0024 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.486+751_486+768dup others(18): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTTTTT others(12): Show |
2 | a0004c0009t0009g0165a0004c0009t0015g0177 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.486+750_486+768dup others(19): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTTTTT others(16): Show |
1 | a0001c0013t0003g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.486+768_486+769ins others(23): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | C | CTTTTTTT others(17): Show |
1 | a0001c0013t0003g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.486+768_486+769ins others(24): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | CT | C | 13 | a0005c0008t0002g0010a0005c0008t0002g0149a0005c0008t0002g0150others(10): Show | 15 | HG00408.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.486+768delT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882373 | CTT | C | 10 | a0002c0002t0005g0022a0002c0002t0005g0153a0002c0002t0005g0170others(7): Show | 10 | HG00280.hp2 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.486+767_486+768del others(2): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882373 | ||||||
| chr14:50882382 | T | TTTTTTTT others(10): Show |
1 | a0001c0001t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.486+768_486+769ins others(17): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882382 | ||||||
| chr14:50882446 | G | A | 316 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.486+820G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882446 | |||||||
| chr14:50882462 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.486+836C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882462 | |||||||
| chr14:50882571 | A | G | 316 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.486+945A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882571 | |||||||
| chr14:50882582 | G | A | 316 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.486+956G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882582 | |||||||
| chr14:50882601 | C | T | 2 | a0001c0001t0001g0025a0002c0002t0005g0024 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.486+975C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882601 | |||||||
| chr14:50882616 | G | A | 316 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.486+990G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882616 | |||||||
| chr14:50882727 | C | T | 2 | a0001c0005t0004g0347a0002c0002t0002g0267 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.486+1101C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882727 | |||||||
| chr14:50882728 | G | A | 316 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.486+1102G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882728 | |||||||
| chr14:50882770 | A | G | 33 | a0001c0006t0001g0058a0001c0006t0001g0091a0001c0006t0001g0128others(30): Show | 35 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.486+1144A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882770 | |||||||
| chr14:50882876 | T | C | 318 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(315): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.486+1250T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50882876 | |||||||
| chr14:50882973 | C | CAAA | 43 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0005t0004g0347others(40): Show | 45 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.486+1361_486+1363d others(5): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882973 | ||||||
| chr14:50882973 | C | CAAAA | 14 | a0001c0001t0001g0042a0001c0001t0001g0120a0001c0001t0001g0180others(11): Show | 14 | HG00099.hp1 HG01074.hp1 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.486+1360_486+1363d others(6): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882973 | ||||||
| chr14:50882973 | C | CAAAAA | 252 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(249): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.486+1359_486+1363d others(7): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882973 | ||||||
| chr14:50882973 | C | CAAAAAA | 7 | a0001c0001t0001g0030a0001c0001t0001g0223a0001c0001t0001g0247others(4): Show | 7 | HG00609.hp2 HG01261.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.486+1358_486+1363d others(8): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882973 | ||||||
| chr14:50882973 | CA | C | 12 | a0001c0001t0001g0162a0001c0001t0003g0191a0001c0001t0003g0192others(9): Show | 12 | HG01884.hp1 HG02559.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.486+1363delA | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50882973 | ||||||
| chr14:50883038 | T | C | 322 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(319): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.486+1412T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50883038 | |||||||
| chr14:50883114 | T | C | 1 | a0003c0003t0001g0068 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.486+1488T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50883114 | |||||||
| chr14:50883306 | T | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0160 | 3 | HG01928.hp1 HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.486+1680T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50883306 | |||||||
| chr14:50883360 | C | G | 5 | a0001c0013t0003g0035a0001c0013t0003g0036a0004c0009t0003g0168others(2): Show | 5 | HG02717.hp1 HG02976.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+1734C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50883360 | |||||||
| chr14:50883364 | T | C | 320 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(317): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.486+1738T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50883364 | |||||||
| chr14:50883617 | C | T | 3 | a0001c0001t0001g0085a0002c0002t0002g0083a0002c0002t0002g0208 | 3 | HG01099.hp1 HG01175.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.486+1991C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50883617 | |||||||
| chr14:50883756 | C | G | 14 | a0005c0008t0002g0010a0005c0008t0002g0149a0005c0008t0002g0150others(11): Show | 16 | HG00280.hp2 HG00408.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.487-1858C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50883756 | |||||||
| chr14:50883849 | C | A | 4 | a0001c0001t0001g0296a0001c0001t0004g0318a0001c0005t0004g0125others(1): Show | 4 | HG01884.hp2 HG01891.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-1765C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50883849 | |||||||
| chr14:50883951 | C | CTA | 336 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(333): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.487-1661_487-1660d others(4): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50883951 | ||||||
| chr14:50883957 | T | C | 351 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(348): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.487-1657T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50883957 | |||||||
| chr14:50884032 | GTCA | G | 301 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(298): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.487-1577_487-1575d others(5): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50884032 | ||||||
| chr14:50884035 | ATC | A | 35 | a0001c0006t0001g0058a0001c0006t0001g0091a0001c0006t0001g0128others(32): Show | 37 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.487-1578_487-1577d others(4): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884035 | |||||||
| chr14:50884038 | A | C | 35 | a0001c0006t0001g0058a0001c0006t0001g0091a0001c0006t0001g0128others(32): Show | 37 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(34): Show |
intron_variant | MODIFIER | c.487-1576A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884038 | |||||||
| chr14:50884228 | A | G | 336 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(333): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.487-1386A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884228 | |||||||
| chr14:50884255 | C | T | 1 | a0001c0005t0004g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.487-1359C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884255 | |||||||
| chr14:50884256 | T | G | 1 | a0001c0005t0004g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.487-1358T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884256 | |||||||
| chr14:50884258 | G | T | 1 | a0001c0005t0004g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.487-1356G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884258 | |||||||
| chr14:50884271 | T | C | 6 | a0001c0013t0003g0035a0001c0013t0003g0036a0004c0009t0001g0289others(3): Show | 6 | HG02451.hp1 HG02717.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-1343T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884271 | |||||||
| chr14:50884303 | T | C | 337 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(334): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.487-1311T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884303 | |||||||
| chr14:50884333 | C | T | 330 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(327): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.487-1281C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884333 | |||||||
| chr14:50884360 | G | A | 6 | a0001c0001t0001g0296a0001c0001t0004g0318a0001c0005t0004g0125others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-1254G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884360 | |||||||
| chr14:50884438 | C | T | 2 | a0001c0005t0004g0347a0002c0002t0002g0267 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.487-1176C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884438 | |||||||
| chr14:50884471 | C | G | 336 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(333): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.487-1143C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884471 | |||||||
| chr14:50884534 | T | A | 6 | a0001c0013t0003g0035a0001c0013t0003g0036a0004c0009t0001g0289others(3): Show | 6 | HG02451.hp1 HG02717.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-1080T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884534 | |||||||
| chr14:50884557 | C | T | 1 | a0003c0003t0001g0188 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.487-1057C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884557 | |||||||
| chr14:50884558 | A | G | 317 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(314): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.487-1056A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884558 | |||||||
| chr14:50884575 | C | T | 336 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(333): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.487-1039C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884575 | |||||||
| chr14:50884630 | T | C | 1 | a0003c0003t0001g0298 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.487-984T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884630 | |||||||
| chr14:50884684 | T | C | 339 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(336): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.487-930T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884684 | |||||||
| chr14:50884702 | CTTTTT | C | 7 | a0002c0002t0005g0022a0002c0002t0005g0153a0002c0002t0005g0170others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.487-884_487-880del others(5): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50884702 | ||||||
| chr14:50884702 | CTTTTTTT | C | 43 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0256others(40): Show | 45 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.487-886_487-880del others(7): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50884702 | ||||||
| chr14:50884702 | CTTTTTTT others(1): Show |
C | 279 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(276): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.487-887_487-880del others(8): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50884702 | ||||||
| chr14:50884702 | CTTTTTTT others(2): Show |
C | 11 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0118others(8): Show | 11 | HG00735.hp1 HG01346.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.487-888_487-880del others(9): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50884702 | ||||||
| chr14:50884702 | CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0001g0030a0001c0001t0001g0296a0001c0001t0004g0318others(2): Show | 5 | HG01891.hp1 HG02965.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.487-890_487-880del others(11): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50884702 | ||||||
| chr14:50884702 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0046 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.487-893_487-880del others(14): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50884702 | ||||||
| chr14:50884702 | CTTTTTTT others(12): Show |
C | 3 | a0001c0001t0003g0191a0001c0001t0003g0192a0008c0017t0006g0224 | 3 | HG02559.hp2 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.487-898_487-880del others(19): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr14 | 50884702 | ||||||
| chr14:50884711 | T | C | 1 | a0009c0016t0002g0266 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.487-903T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884711 | |||||||
| chr14:50884712 | T | C | 43 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0256others(40): Show | 45 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.487-902T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884712 | |||||||
| chr14:50884713 | T | C | 279 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(276): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.487-901T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884713 | |||||||
| chr14:50884714 | T | C | 12 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0118others(9): Show | 12 | HG00735.hp1 HG01346.hp2 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.487-900T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884714 | |||||||
| chr14:50884715 | T | C | 43 | a0001c0001t0001g0181a0001c0001t0001g0189a0001c0001t0001g0256others(40): Show | 45 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.487-899T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884715 | |||||||
| chr14:50884716 | T | C | 284 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(281): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.487-898T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884716 | |||||||
| chr14:50884717 | T | C | 11 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0118others(8): Show | 11 | HG00735.hp1 HG01346.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.487-897T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884717 | |||||||
| chr14:50884740 | A | G | 339 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(336): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.487-874A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884740 | |||||||
| chr14:50884818 | C | A | 1 | a0001c0001t0001g0050 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.487-796C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884818 | |||||||
| chr14:50884939 | G | A | 9 | a0002c0002t0005g0022a0002c0002t0005g0153a0002c0002t0005g0170others(6): Show | 9 | HG01884.hp1 HG02280.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.487-675G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884939 | |||||||
| chr14:50884944 | C | T | 6 | a0001c0001t0001g0296a0001c0001t0004g0318a0001c0005t0004g0125others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-670C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884944 | |||||||
| chr14:50884959 | T | C | 6 | a0001c0001t0001g0296a0001c0001t0004g0318a0001c0005t0004g0125others(3): Show | 6 | HG01884.hp2 HG01891.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-655T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884959 | |||||||
| chr14:50884962 | A | G | 33 | a0001c0006t0001g0058a0001c0006t0001g0091a0001c0006t0001g0128others(30): Show | 35 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.487-652A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884962 | |||||||
| chr14:50884989 | C | T | 2 | a0001c0005t0004g0347a0002c0002t0002g0267 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.487-625C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50884989 | |||||||
| chr14:50885010 | G | A | 337 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(334): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.487-604G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885010 | |||||||
| chr14:50885094 | C | T | 3 | a0001c0001t0001g0296a0001c0001t0004g0318a0003c0003t0001g0027 | 3 | HG01891.hp1 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.487-520C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885094 | |||||||
| chr14:50885114 | G | A | 1 | a0001c0001t0001g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.487-500G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885114 | |||||||
| chr14:50885138 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.487-476G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885138 | |||||||
| chr14:50885171 | C | T | 6 | a0001c0013t0003g0035a0001c0013t0003g0036a0004c0009t0001g0289others(3): Show | 6 | HG02451.hp1 HG02717.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-443C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885171 | |||||||
| chr14:50885172 | G | A | 1 | a0002c0002t0002g0051 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.487-442G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885172 | |||||||
| chr14:50885233 | A | G | 338 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(335): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.487-381A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885233 | |||||||
| chr14:50885256 | G | A | 338 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(335): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.487-358G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885256 | |||||||
| chr14:50885341 | G | A | 1 | a0008c0017t0006g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.487-273G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885341 | |||||||
| chr14:50885441 | C | T | 338 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(335): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.487-173C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885441 | |||||||
| chr14:50885474 | T | C | 4 | a0001c0006t0001g0072a0001c0006t0003g0198a0002c0004t0005g0071others(1): Show | 4 | HG02809.hp1 HG03041.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-140T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 5/12 | chr14 | 50885474 | |||||||
| chr14:50886096 | A | G | 1 | a0002c0002t0002g0053 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.662+201A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/12 | chr14 | 50886096 | |||||||
| chr14:50886164 | G | T | 1 | a0002c0002t0006g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.662+269G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/12 | chr14 | 50886164 | |||||||
| chr14:50886171 | C | G | 1 | a0002c0002t0002g0044 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.662+276C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/12 | chr14 | 50886171 | |||||||
| chr14:50886236 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.662+341G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/12 | chr14 | 50886236 | |||||||
| chr14:50886409 | C | CAGCCTGG others(1): Show |
6 | a0001c0013t0003g0035a0001c0013t0003g0036a0004c0009t0001g0289others(3): Show | 6 | HG02451.hp1 HG02717.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.663-237_663-230dup others(8): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr14 | 50886409 | ||||||
| chr14:50886440 | C | CA | 8 | a0001c0001t0001g0013a0001c0001t0001g0039a0001c0001t0001g0104others(5): Show | 9 | HG01261.hp2 HG02071.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.663-189dupA | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr14 | 50886440 | ||||||
| chr14:50886440 | CA | C | 14 | a0001c0001t0001g0162a0005c0008t0002g0010a0005c0008t0002g0149others(11): Show | 16 | HG00280.hp2 HG00408.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.663-189delA | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr14 | 50886440 | ||||||
| chr14:50886518 | G | A | 17 | a0001c0001t0001g0032a0001c0001t0001g0162a0005c0008t0002g0010others(14): Show | 19 | HG00280.hp2 HG00408.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.663-129G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 7/12 | chr14 | 50886518 | |||||||
| chr14:50886775 | T | C | 339 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(336): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.700+91T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50886775 | |||||||
| chr14:50886906 | G | C | 2 | a0001c0005t0004g0347a0002c0002t0002g0267 | 2 | HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.700+222G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50886906 | |||||||
| chr14:50886938 | C | T | 339 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(336): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.700+254C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50886938 | |||||||
| chr14:50886981 | T | C | 339 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(336): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.700+297T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50886981 | |||||||
| chr14:50886986 | T | C | 339 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(336): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.700+302T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50886986 | |||||||
| chr14:50886987 | G | A | 4 | a0001c0001t0001g0324a0002c0002t0002g0020a0002c0002t0002g0346others(1): Show | 5 | HG02135.hp1 NA18990.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.700+303G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50886987 | |||||||
| chr14:50887011 | C | T | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.700+327C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887011 | |||||||
| chr14:50887111 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.700+427G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887111 | |||||||
| chr14:50887191 | G | A | 1 | a0002c0002t0002g0134 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.700+507G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887191 | |||||||
| chr14:50887211 | C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0174a0001c0001t0001g0206a0001c0005t0004g0261others(11): Show | 14 | HG01256.hp1 HG01257.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.700+538_700+545dup others(8): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 50887211 | ||||||
| chr14:50887211 | C | CAAAAAAA others(2): Show |
204 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(201): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.700+537_700+545dup others(9): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 50887211 | ||||||
| chr14:50887211 | C | CAAAAAAA others(3): Show |
46 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0030others(43): Show | 47 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.700+536_700+545dup others(10): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 50887211 | ||||||
| chr14:50887211 | C | CAAAAAAA others(4): Show |
10 | a0001c0001t0001g0162a0001c0001t0001g0182a0001c0001t0003g0191others(7): Show | 11 | HG01167.hp2 HG01169.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.700+535_700+545dup others(11): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 50887211 | ||||||
| chr14:50887211 | C | CAAAAAAA others(5): Show |
17 | a0001c0001t0001g0032a0001c0001t0004g0318a0001c0006t0001g0295others(14): Show | 17 | HG00280.hp2 HG00408.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.700+534_700+545dup others(12): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 50887211 | ||||||
| chr14:50887211 | C | CAAAAAAA others(6): Show |
36 | a0001c0005t0004g0125a0001c0006t0001g0058a0001c0006t0001g0072others(33): Show | 38 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.700+533_700+545dup others(13): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 50887211 | ||||||
| chr14:50887211 | C | CAAAAAAA others(7): Show |
14 | a0001c0005t0004g0347a0001c0006t0001g0241a0001c0006t0001g0268others(11): Show | 15 | HG00423.hp1 HG00423.hp2 HG01952.hp2 others(12): Show |
intron_variant | MODIFIER | c.700+532_700+545dup others(14): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 50887211 | ||||||
| chr14:50887211 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0296a0003c0003t0001g0027 | 2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.700+531_700+545dup others(15): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 50887211 | ||||||
| chr14:50887277 | A | T | 2 | a0001c0001t0001g0025a0002c0002t0005g0024 | 2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.700+593A>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887277 | |||||||
| chr14:50887599 | A | G | 339 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(336): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.700+915A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887599 | |||||||
| chr14:50887603 | C | T | 351 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(348): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.700+919C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887603 | |||||||
| chr14:50887732 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.700+1048G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887732 | |||||||
| chr14:50887787 | A | C | 7 | a0001c0001t0001g0032a0001c0013t0003g0035a0001c0013t0003g0036others(4): Show | 7 | HG02451.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.701-1037A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887787 | |||||||
| chr14:50887798 | G | A | 333 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(330): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.701-1026G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887798 | |||||||
| chr14:50887801 | G | A | 4 | a0001c0001t0001g0296a0001c0001t0004g0318a0001c0005t0004g0125others(1): Show | 4 | HG01884.hp2 HG01891.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.701-1023G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50887801 | |||||||
| chr14:50888208 | C | CT | 270 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(267): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.701-602dupT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr14 | 50888208 | ||||||
| chr14:50888313 | T | C | 334 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.701-511T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888313 | |||||||
| chr14:50888328 | C | T | 334 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.701-496C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888328 | |||||||
| chr14:50888444 | C | T | 264 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(261): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.701-380C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888444 | |||||||
| chr14:50888452 | G | T | 351 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(348): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.701-372G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888452 | |||||||
| chr14:50888468 | C | A | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.701-356C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888468 | |||||||
| chr14:50888615 | G | A | 1 | a0002c0004t0002g0354 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.701-209G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888615 | |||||||
| chr14:50888726 | G | A | 2 | a0001c0001t0001g0337a0001c0001t0001g0338 | 2 | NA19054.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.701-98G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888726 | |||||||
| chr14:50888786 | G | T | 2 | a0001c0001t0001g0040a0001c0001t0001g0231 | 2 | HG02109.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.701-38G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888786 | |||||||
| chr14:50888799 | C | A | 196 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(193): Show | 208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.701-25C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888799 | |||||||
| chr14:50888803 | C | A | 1 | a0001c0005t0004g0131 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.701-21C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 8/12 | chr14 | 50888803 | |||||||
| chr14:50888941 | G | C | 1 | a0002c0002t0002g0313 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.780+38G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50888941 | |||||||
| chr14:50889096 | T | C | 1 | a0002c0002t0002g0280 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.780+193T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889096 | |||||||
| chr14:50889205 | G | A | 15 | a0001c0001t0001g0296a0005c0008t0002g0010a0005c0008t0002g0149others(12): Show | 17 | HG00280.hp2 HG00408.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.780+302G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889205 | |||||||
| chr14:50889405 | T | C | 334 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.780+502T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889405 | |||||||
| chr14:50889425 | G | T | 3 | a0001c0001t0004g0318a0001c0005t0004g0125a0003c0003t0001g0027 | 3 | HG01884.hp2 HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.780+522G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889425 | |||||||
| chr14:50889463 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.780+560C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889463 | |||||||
| chr14:50889466 | C | T | 18 | a0001c0001t0001g0007a0001c0001t0001g0070a0001c0001t0001g0145others(15): Show | 20 | HG01074.hp2 HG01168.hp2 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.780+563C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889466 | |||||||
| chr14:50889503 | C | T | 351 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(348): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.780+600C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889503 | |||||||
| chr14:50889516 | T | C | 334 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.780+613T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889516 | |||||||
| chr14:50889586 | T | C | 351 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(348): Show | 372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.780+683T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889586 | |||||||
| chr14:50889615 | C | T | 7 | a0001c0001t0001g0032a0001c0013t0003g0035a0001c0013t0003g0036others(4): Show | 7 | HG02451.hp1 HG02717.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.780+712C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889615 | |||||||
| chr14:50889632 | G | A | 8 | a0002c0002t0005g0022a0002c0002t0005g0153a0002c0002t0005g0170others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+729G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889632 | |||||||
| chr14:50889669 | A | T | 5 | a0001c0001t0003g0216a0002c0002t0002g0077a0002c0002t0002g0203others(2): Show | 5 | HG02735.hp1 HG03490.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+766A>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889669 | |||||||
| chr14:50889727 | C | T | 5 | a0001c0001t0004g0318a0001c0005t0004g0125a0001c0005t0004g0347others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+824C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889727 | |||||||
| chr14:50889914 | A | G | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02559.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.780+1011A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50889914 | |||||||
| chr14:50890025 | A | T | 1 | a0002c0004t0006g0023 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.780+1122A>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890025 | |||||||
| chr14:50890027 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.780+1124T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890027 | |||||||
| chr14:50890281 | G | A | 7 | a0002c0002t0005g0022a0002c0002t0005g0153a0002c0002t0005g0170others(4): Show | 7 | HG01884.hp1 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.780+1378G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890281 | |||||||
| chr14:50890439 | T | C | 8 | a0002c0002t0005g0022a0002c0002t0005g0153a0002c0002t0005g0170others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+1536T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890439 | |||||||
| chr14:50890632 | T | G | 8 | a0002c0002t0005g0022a0002c0002t0005g0153a0002c0002t0005g0170others(5): Show | 8 | HG01884.hp1 HG02280.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+1729T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890632 | |||||||
| chr14:50890668 | T | G | 334 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.780+1765T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890668 | |||||||
| chr14:50890683 | A | G | 334 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.780+1780A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890683 | |||||||
| chr14:50890802 | C | A | 1 | a0005c0008t0002g0305 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.780+1899C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890802 | |||||||
| chr14:50890814 | C | T | 1 | a0001c0005t0008g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.780+1911C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890814 | |||||||
| chr14:50890850 | A | C | 1 | a0001c0001t0001g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.780+1947A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890850 | |||||||
| chr14:50890875 | C | A | 335 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(332): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.780+1972C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890875 | |||||||
| chr14:50890977 | A | G | 335 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(332): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.780+2074A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890977 | |||||||
| chr14:50890992 | A | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0160 | 3 | HG01928.hp1 HG02148.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.780+2089A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50890992 | |||||||
| chr14:50891111 | T | C | 5 | a0001c0001t0004g0318a0001c0005t0004g0125a0001c0005t0004g0347others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+2208T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891111 | |||||||
| chr14:50891161 | T | G | 1 | a0001c0001t0001g0021 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.780+2258T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891161 | |||||||
| chr14:50891237 | T | C | 334 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(331): Show | 355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.780+2334T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891237 | |||||||
| chr14:50891250 | CT | C | 348 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(345): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.780+2357delT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50891250 | ||||||
| chr14:50891331 | T | C | 1 | a0002c0002t0002g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.780+2428T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891331 | |||||||
| chr14:50891335 | C | T | 1 | a0002c0002t0002g0129 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.780+2432C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891335 | |||||||
| chr14:50891336 | G | A | 348 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(345): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.780+2433G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891336 | |||||||
| chr14:50891338 | G | A | 1 | a0008c0017t0006g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.780+2435G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891338 | |||||||
| chr14:50891399 | T | C | 2 | a0002c0002t0002g0029a0002c0002t0002g0121 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.780+2496T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891399 | |||||||
| chr14:50891469 | T | A | 84 | a0001c0001t0001g0025a0001c0001t0001g0101a0001c0001t0001g0118others(81): Show | 90 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.780+2566T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891469 | |||||||
| chr14:50891485 | C | T | 1 | a0001c0006t0001g0091 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.780+2582C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891485 | |||||||
| chr14:50891490 | A | G | 4 | a0002c0002t0002g0001a0002c0002t0002g0199a0002c0004t0002g0282others(1): Show | 6 | HG03098.hp2 NA18964.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+2587A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891490 | |||||||
| chr14:50891532 | C | A | 8 | a0001c0001t0001g0078a0001c0001t0001g0311a0001c0001t0003g0216others(5): Show | 8 | HG02735.hp1 HG03831.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.780+2629C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891532 | |||||||
| chr14:50891532 | C | G | 1 | a0003c0003t0003g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.780+2629C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891532 | |||||||
| chr14:50891653 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.780+2750T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891653 | |||||||
| chr14:50891658 | T | G | 1 | a0003c0003t0003g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.780+2755T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891658 | |||||||
| chr14:50891725 | T | G | 1 | a0002c0002t0005g0244 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.780+2822T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891725 | |||||||
| chr14:50891752 | G | A | 1 | a0005c0008t0002g0242 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.780+2849G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891752 | |||||||
| chr14:50891843 | T | C | 4 | a0002c0002t0002g0083a0002c0002t0002g0096a0002c0002t0002g0276others(1): Show | 4 | HG01516.hp2 HG02145.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+2940T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50891843 | |||||||
| chr14:50892076 | C | T | 198 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(195): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.780+3173C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892076 | |||||||
| chr14:50892113 | A | C | 344 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(341): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.780+3210A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892113 | |||||||
| chr14:50892276 | G | C | 32 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0038others(29): Show | 33 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.780+3373G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892276 | |||||||
| chr14:50892382 | C | G | 87 | a0001c0001t0001g0104a0001c0005t0004g0159a0001c0005t0004g0328others(84): Show | 94 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.780+3479C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892382 | |||||||
| chr14:50892382 | C | T | 2 | a0004c0009t0009g0165a0004c0009t0015g0177 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.780+3479C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892382 | |||||||
| chr14:50892389 | A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0076a0001c0001t0001g0235others(1): Show | 5 | HG02622.hp1 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+3486A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892389 | |||||||
| chr14:50892461 | G | A | 1 | a0001c0005t0004g0343 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.780+3558G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892461 | |||||||
| chr14:50892487 | G | A | 1 | a0001c0001t0001g0326 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.780+3584G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892487 | |||||||
| chr14:50892497 | C | T | 8 | a0001c0001t0001g0040a0001c0001t0001g0101a0001c0001t0001g0185others(5): Show | 8 | HG00140.hp1 HG02109.hp1 HG03834.hp2 others(5): Show |
intron_variant | MODIFIER | c.780+3594C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892497 | |||||||
| chr14:50892498 | G | A | 1 | a0003c0003t0003g0196 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.780+3595G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892498 | |||||||
| chr14:50892505 | C | T | 112 | a0001c0001t0001g0031a0001c0001t0001g0104a0001c0001t0001g0207others(109): Show | 119 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.780+3602C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892505 | |||||||
| chr14:50892582 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.780+3679C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892582 | |||||||
| chr14:50892625 | T | C | 84 | a0001c0001t0001g0104a0001c0005t0004g0159a0001c0005t0004g0328others(81): Show | 91 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.780+3722T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892625 | |||||||
| chr14:50892777 | T | A | 2 | a0001c0013t0003g0035a0001c0013t0003g0036 | 2 | HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.780+3874T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892777 | |||||||
| chr14:50892879 | C | T | 13 | a0001c0001t0001g0182a0001c0001t0004g0318a0002c0002t0005g0022others(10): Show | 13 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.780+3976C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892879 | |||||||
| chr14:50892940 | T | G | 98 | a0001c0001t0001g0104a0001c0005t0004g0343a0002c0002t0002g0001others(95): Show | 106 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.780+4037T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50892940 | |||||||
| chr14:50893009 | G | A | 1 | a0008c0017t0006g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.780+4106G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893009 | |||||||
| chr14:50893021 | T | C | 1 | a0002c0002t0012g0214 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.780+4118T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893021 | |||||||
| chr14:50893044 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+4141C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893044 | |||||||
| chr14:50893075 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.780+4172T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893075 | |||||||
| chr14:50893128 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+4225C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893128 | |||||||
| chr14:50893133 | G | A | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+4230G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893133 | |||||||
| chr14:50893192 | C | A | 1 | a0001c0001t0003g0211 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.780+4289C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893192 | |||||||
| chr14:50893194 | C | T | 30 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0038others(27): Show | 31 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.780+4291C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893194 | |||||||
| chr14:50893217 | C | A | 194 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(191): Show | 207 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(204): Show |
intron_variant | MODIFIER | c.780+4314C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893217 | |||||||
| chr14:50893335 | T | A | 15 | a0004c0007t0001g0002a0004c0007t0001g0037a0004c0007t0001g0115others(12): Show | 17 | HG00280.hp2 HG01106.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.780+4432T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893335 | |||||||
| chr14:50893369 | C | A | 1 | a0002c0002t0002g0301 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.780+4466C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893369 | |||||||
| chr14:50893477 | A | G | 1 | a0002c0004t0010g0205 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.780+4574A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893477 | |||||||
| chr14:50893520 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+4617C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893520 | |||||||
| chr14:50893532 | A | G | 126 | a0001c0001t0001g0104a0001c0005t0004g0343a0002c0002t0002g0001others(123): Show | 134 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.780+4629A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893532 | |||||||
| chr14:50893603 | G | A | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+4700G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893603 | |||||||
| chr14:50893604 | C | T | 3 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02055.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.780+4701C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893604 | |||||||
| chr14:50893638 | G | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+4735G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893638 | |||||||
| chr14:50893640 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+4737C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893640 | |||||||
| chr14:50893641 | C | T | 1 | a0001c0005t0004g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.780+4738C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893641 | |||||||
| chr14:50893679 | G | C | 2 | a0001c0005t0004g0026a0001c0011t0004g0087 | 2 | HG02056.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.780+4776G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893679 | |||||||
| chr14:50893724 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.780+4821C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893724 | |||||||
| chr14:50893826 | A | G | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+4923A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893826 | |||||||
| chr14:50893850 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.780+4947T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893850 | |||||||
| chr14:50893912 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.780+5009C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893912 | |||||||
| chr14:50893973 | A | G | 1 | a0001c0001t0004g0318 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.780+5070A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893973 | |||||||
| chr14:50893985 | A | G | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5082A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50893985 | |||||||
| chr14:50894048 | GTCCTTCA others(182): Show |
G | 2 | a0002c0002t0005g0153a0002c0002t0005g0245 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.780+5176_780+5364d others(2): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50894048 | ||||||
| chr14:50894147 | GAGGGGCA others(57): Show |
G | 27 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(24): Show | 27 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.780+5278_780+5341d others(66): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50894147 | ||||||
| chr14:50894162 | C | T | 1 | a0001c0005t0008g0215 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.780+5259C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894162 | |||||||
| chr14:50894284 | C | T | 2 | a0001c0013t0003g0035a0001c0013t0003g0036 | 2 | HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.780+5381C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894284 | |||||||
| chr14:50894293 | G | A | 2 | a0001c0001t0001g0331a0001c0001t0001g0332 | 2 | NA18942.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.780+5390G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894293 | |||||||
| chr14:50894302 | T | C | 23 | a0001c0001t0001g0182a0001c0001t0004g0318a0001c0006t0013g0028others(20): Show | 23 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.780+5399T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894302 | |||||||
| chr14:50894348 | C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0277 | 2 | HG01192.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.780+5445C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894348 | |||||||
| chr14:50894394 | C | G | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5491C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894394 | |||||||
| chr14:50894533 | T | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5630T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894533 | |||||||
| chr14:50894558 | A | G | 1 | a0001c0011t0004g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.780+5655A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894558 | |||||||
| chr14:50894562 | C | T | 1 | a0001c0011t0004g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.780+5659C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894562 | |||||||
| chr14:50894582 | C | T | 1 | a0002c0002t0006g0317 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.780+5679C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894582 | |||||||
| chr14:50894655 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.780+5752T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894655 | |||||||
| chr14:50894732 | C | A | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5829C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894732 | |||||||
| chr14:50894772 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.780+5869G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894772 | |||||||
| chr14:50894782 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5879C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894782 | |||||||
| chr14:50894800 | G | A | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5897G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894800 | |||||||
| chr14:50894802 | C | T | 1 | a0002c0002t0002g0301 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.780+5899C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894802 | |||||||
| chr14:50894838 | G | A | 197 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(194): Show | 210 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.780+5935G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894838 | |||||||
| chr14:50894851 | C | CTTCCTCC others(8): Show |
29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5948_780+5949i others(17): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894851 | |||||||
| chr14:50894852 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5949C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894852 | |||||||
| chr14:50894871 | A | G | 1 | a0002c0002t0002g0195 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.780+5968A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894871 | |||||||
| chr14:50894874 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5971C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894874 | |||||||
| chr14:50894876 | T | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5973T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894876 | |||||||
| chr14:50894894 | C | G | 1 | a0005c0008t0002g0242 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.780+5991C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894894 | |||||||
| chr14:50894895 | T | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+5992T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894895 | |||||||
| chr14:50894895 | T | G | 1 | a0005c0008t0002g0242 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.780+5992T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894895 | |||||||
| chr14:50894911 | A | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0340a0005c0008t0002g0242 | 3 | HG02523.hp2 NA18961.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.780+6008A>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894911 | |||||||
| chr14:50894923 | G | A | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6020G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894923 | |||||||
| chr14:50894947 | T | C | 28 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(25): Show | 28 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.780+6044T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894947 | |||||||
| chr14:50894964 | C | G | 23 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(20): Show | 23 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.780+6061C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894964 | |||||||
| chr14:50894964 | C | T | 4 | a0004c0007t0001g0002a0004c0007t0001g0115a0004c0007t0001g0116others(1): Show | 5 | HG02559.hp1 HG02922.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+6061C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50894964 | |||||||
| chr14:50895000 | T | C | 99 | a0001c0001t0001g0104a0001c0005t0004g0343a0002c0002t0002g0001others(96): Show | 107 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.780+6097T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895000 | |||||||
| chr14:50895021 | T | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6118T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895021 | |||||||
| chr14:50895029 | T | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6126T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895029 | |||||||
| chr14:50895058 | T | C | 99 | a0001c0001t0001g0104a0001c0005t0004g0343a0002c0002t0002g0001others(96): Show | 107 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.780+6155T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895058 | |||||||
| chr14:50895067 | A | G | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6164A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895067 | |||||||
| chr14:50895074 | A | G | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6171A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895074 | |||||||
| chr14:50895090 | A | G | 31 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0038others(28): Show | 32 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.780+6187A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895090 | |||||||
| chr14:50895132 | G | A | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6229G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895132 | |||||||
| chr14:50895179 | C | T | 2 | a0001c0005t0004g0026a0001c0011t0004g0087 | 2 | HG02056.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.780+6276C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895179 | |||||||
| chr14:50895180 | C | T | 28 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(25): Show | 28 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.780+6277C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895180 | |||||||
| chr14:50895181 | A | G | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6278A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895181 | |||||||
| chr14:50895208 | G | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6305G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895208 | |||||||
| chr14:50895219 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6316C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895219 | |||||||
| chr14:50895248 | G | A | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6345G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895248 | |||||||
| chr14:50895252 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6349C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895252 | |||||||
| chr14:50895258 | C | T | 1 | a0002c0002t0002g0302 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.780+6355C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895258 | |||||||
| chr14:50895291 | C | T | 2 | a0001c0001t0001g0220a0001c0001t0001g0234 | 2 | HG01175.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.780+6388C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895291 | |||||||
| chr14:50895305 | A | C | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.780+6402A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895305 | |||||||
| chr14:50895325 | A | G | 1 | a0001c0001t0003g0164 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.780+6422A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895325 | |||||||
| chr14:50895397 | G | A | 2 | a0003c0003t0001g0027a0003c0003t0003g0075 | 2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.781-6432G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895397 | |||||||
| chr14:50895453 | G | A | 1 | a0001c0001t0003g0211 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.781-6376G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895453 | |||||||
| chr14:50895483 | C | T | 3 | a0001c0001t0001g0162a0001c0013t0003g0035a0001c0013t0003g0036 | 3 | HG02818.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.781-6346C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895483 | |||||||
| chr14:50895490 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.781-6339C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895490 | |||||||
| chr14:50895507 | C | T | 64 | a0001c0001t0001g0104a0001c0005t0004g0343a0002c0002t0002g0003others(61): Show | 67 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.781-6322C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895507 | |||||||
| chr14:50895553 | T | A | 15 | a0004c0007t0001g0002a0004c0007t0001g0037a0004c0007t0001g0115others(12): Show | 17 | HG00280.hp2 HG01106.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.781-6276T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895553 | |||||||
| chr14:50895592 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.781-6237C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895592 | |||||||
| chr14:50895618 | C | G | 15 | a0004c0007t0001g0002a0004c0007t0001g0037a0004c0007t0001g0115others(12): Show | 17 | HG00280.hp2 HG01106.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.781-6211C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895618 | |||||||
| chr14:50895628 | C | T | 3 | a0001c0001t0001g0237a0001c0001t0001g0340a0002c0002t0005g0179 | 3 | HG03516.hp1 NA18961.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.781-6201C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895628 | |||||||
| chr14:50895636 | C | T | 29 | a0001c0001t0001g0031a0001c0001t0001g0182a0001c0001t0001g0207others(26): Show | 29 | HG01261.hp2 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.781-6193C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895636 | |||||||
| chr14:50895657 | C | G | 5 | a0002c0004t0002g0008a0002c0004t0002g0059a0002c0004t0002g0088others(2): Show | 6 | HG00597.hp2 NA18954.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-6172C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895657 | |||||||
| chr14:50895662 | G | A | 136 | a0001c0001t0001g0104a0001c0001t0001g0162a0001c0005t0004g0017others(133): Show | 148 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.781-6167G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895662 | |||||||
| chr14:50895692 | G | T | 98 | a0001c0001t0001g0104a0001c0005t0004g0343a0002c0002t0002g0001others(95): Show | 106 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.781-6137G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895692 | |||||||
| chr14:50895726 | G | A | 2 | a0002c0002t0002g0102a0002c0002t0002g0280 | 2 | NA18945.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.781-6103G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895726 | |||||||
| chr14:50895731 | G | A | 9 | a0002c0002t0005g0022a0002c0002t0005g0170a0002c0002t0005g0171others(6): Show | 9 | HG01261.hp2 HG01884.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.781-6098G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895731 | |||||||
| chr14:50895751 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.781-6078G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895751 | |||||||
| chr14:50895767 | C | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0303 | 2 | HG01074.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.781-6062C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895767 | |||||||
| chr14:50895775 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.781-6054T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895775 | |||||||
| chr14:50895790 | T | C | 1 | a0001c0001t0014g0349 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.781-6039T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895790 | |||||||
| chr14:50895829 | T | C | 2 | a0001c0001t0001g0231a0002c0002t0002g0048 | 2 | HG02165.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.781-6000T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895829 | |||||||
| chr14:50895880 | A | G | 11 | a0001c0001t0004g0318a0002c0002t0005g0022a0002c0002t0005g0024others(8): Show | 11 | HG01261.hp2 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.781-5949A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895880 | |||||||
| chr14:50895929 | G | T | 1 | a0001c0006t0013g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.781-5900G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895929 | |||||||
| chr14:50895973 | T | C | 3 | a0001c0001t0001g0162a0001c0013t0003g0035a0001c0013t0003g0036 | 3 | HG02818.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.781-5856T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50895973 | |||||||
| chr14:50896098 | T | C | 1 | a0002c0004t0002g0225 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.781-5731T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896098 | |||||||
| chr14:50896102 | C | G | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.781-5727C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896102 | |||||||
| chr14:50896157 | C | G | 1 | a0001c0001t0001g0340 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.781-5672C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896157 | |||||||
| chr14:50896169 | G | A | 1 | a0001c0001t0001g0340 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.781-5660G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896169 | |||||||
| chr14:50896173 | T | C | 1 | a0001c0001t0001g0340 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.781-5656T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896173 | |||||||
| chr14:50896180 | T | C | 36 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0038others(33): Show | 37 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.781-5649T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896180 | |||||||
| chr14:50896181 | G | A | 33 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0079others(30): Show | 34 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.781-5648G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896181 | |||||||
| chr14:50896252 | T | C | 101 | a0001c0001t0001g0104a0002c0002t0002g0001a0002c0002t0002g0003others(98): Show | 109 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.781-5577T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896252 | |||||||
| chr14:50896314 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.781-5515C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896314 | |||||||
| chr14:50896395 | C | T | 1 | a0001c0006t0013g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.781-5434C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896395 | |||||||
| chr14:50896503 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.781-5326C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896503 | |||||||
| chr14:50896542 | C | CCTGCCCC others(50): Show |
1 | a0001c0006t0013g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.781-5256_781-5255i others(59): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50896542 | ||||||
| chr14:50896542 | CCTGCCCC others(50): Show |
C | 1 | a0001c0011t0004g0087 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.781-5255_781-5199d others(59): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50896542 | ||||||
| chr14:50896574 | T | C | 1 | a0001c0006t0013g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.781-5255T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896574 | |||||||
| chr14:50896574 | TGAATTTC others(50): Show |
T | 101 | a0001c0001t0001g0104a0002c0002t0002g0001a0002c0002t0002g0003others(98): Show | 109 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.781-5227_781-5171d others(59): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50896574 | ||||||
| chr14:50896663 | C | G | 2 | a0003c0003t0001g0290a0003c0003t0003g0291 | 2 | HG02647.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.781-5166C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896663 | |||||||
| chr14:50896711 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.781-5118C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896711 | |||||||
| chr14:50896782 | T | A | 98 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(95): Show | 103 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.781-5047T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896782 | |||||||
| chr14:50896789 | G | T | 199 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(196): Show | 212 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.781-5040G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896789 | |||||||
| chr14:50896864 | C | A | 20 | a0002c0002t0005g0022a0002c0002t0005g0024a0002c0002t0005g0153others(17): Show | 20 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.781-4965C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896864 | |||||||
| chr14:50896938 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.781-4891A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50896938 | |||||||
| chr14:50897051 | T | A | 5 | a0002c0002t0002g0054a0002c0002t0002g0111a0002c0002t0002g0112others(2): Show | 5 | NA18946.hp1 NA18948.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.781-4778T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897051 | |||||||
| chr14:50897071 | G | GT | 6 | a0001c0001t0001g0049a0001c0001t0001g0194a0001c0001t0001g0332others(3): Show | 6 | HG03710.hp2 NA18989.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.781-4740dupT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50897071 | ||||||
| chr14:50897071 | GT | G | 7 | a0001c0001t0001g0133a0001c0001t0001g0260a0001c0001t0001g0309others(4): Show | 7 | HG01943.hp1 HG02155.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.781-4740delT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50897071 | ||||||
| chr14:50897071 | GTT | G | 200 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(197): Show | 213 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.781-4741_781-4740d others(4): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50897071 | ||||||
| chr14:50897112 | A | G | 103 | a0001c0001t0001g0018a0001c0001t0001g0025a0001c0001t0001g0031others(100): Show | 108 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.781-4717A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897112 | |||||||
| chr14:50897134 | G | A | 1 | a0002c0002t0002g0232 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.781-4695G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897134 | |||||||
| chr14:50897554 | TAAATAGG | T | 3 | a0002c0002t0006g0317a0002c0004t0006g0023a0002c0004t0006g0228 | 3 | HG02145.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.781-4273_781-4267d others(9): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50897554 | ||||||
| chr14:50897640 | T | C | 19 | a0002c0002t0005g0022a0002c0002t0005g0024a0002c0002t0005g0153others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.781-4189T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897640 | |||||||
| chr14:50897653 | T | C | 101 | a0001c0001t0001g0104a0002c0002t0002g0001a0002c0002t0002g0003others(98): Show | 109 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.781-4176T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897653 | |||||||
| chr14:50897728 | G | C | 1 | a0002c0002t0002g0229 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.781-4101G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897728 | |||||||
| chr14:50897764 | G | A | 19 | a0002c0002t0005g0022a0002c0002t0005g0024a0002c0002t0005g0153others(16): Show | 19 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.781-4065G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897764 | |||||||
| chr14:50897773 | G | C | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.781-4056G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897773 | |||||||
| chr14:50897782 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.781-4047A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897782 | |||||||
| chr14:50897801 | T | A | 4 | a0002c0004t0006g0169a0002c0004t0010g0205a0004c0007t0001g0167others(1): Show | 4 | HG02886.hp2 HG03139.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-4028T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897801 | |||||||
| chr14:50897860 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.781-3969C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50897860 | |||||||
| chr14:50898244 | C | A | 3 | a0001c0001t0001g0162a0001c0013t0003g0035a0001c0013t0003g0036 | 3 | HG02818.hp1 HG02976.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.781-3585C>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50898244 | |||||||
| chr14:50898630 | C | T | 120 | a0001c0001t0001g0104a0002c0002t0002g0001a0002c0002t0002g0003others(117): Show | 128 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.781-3199C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50898630 | |||||||
| chr14:50898751 | A | T | 1 | a0003c0003t0001g0067 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.781-3078A>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50898751 | |||||||
| chr14:50898775 | A | G | 1 | a0002c0002t0002g0163 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.781-3054A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50898775 | |||||||
| chr14:50898921 | G | A | 24 | a0001c0001t0004g0318a0001c0005t0004g0017a0001c0005t0004g0026others(21): Show | 26 | HG00609.hp2 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.781-2908G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50898921 | |||||||
| chr14:50899013 | C | T | 120 | a0001c0001t0001g0104a0002c0002t0002g0001a0002c0002t0002g0003others(117): Show | 128 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.781-2816C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50899013 | |||||||
| chr14:50899031 | A | G | 120 | a0001c0001t0001g0104a0002c0002t0002g0001a0002c0002t0002g0003others(117): Show | 128 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.781-2798A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50899031 | |||||||
| chr14:50899118 | G | A | 101 | a0001c0001t0001g0104a0002c0002t0002g0001a0002c0002t0002g0003others(98): Show | 109 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.781-2711G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50899118 | |||||||
| chr14:50899140 | C | T | 120 | a0001c0001t0001g0104a0002c0002t0002g0001a0002c0002t0002g0003others(117): Show | 128 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.781-2689C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50899140 | |||||||
| chr14:50899242 | A | C | 4 | a0002c0004t0006g0169a0002c0004t0010g0205a0004c0007t0001g0167others(1): Show | 4 | HG02886.hp2 HG03139.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.781-2587A>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50899242 | |||||||
| chr14:50899329 | T | C | 6 | a0001c0001t0001g0031a0001c0001t0001g0207a0001c0001t0003g0191others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-2500T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50899329 | |||||||
| chr14:50899857 | C | T | 119 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(116): Show | 127 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(124): Show |
intron_variant | MODIFIER | c.781-1972C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50899857 | |||||||
| chr14:50899901 | A | G | 125 | a0001c0001t0001g0025a0001c0001t0001g0182a0002c0002t0002g0001others(122): Show | 133 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.781-1928A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50899901 | |||||||
| chr14:50900025 | G | T | 105 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(102): Show | 113 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.781-1804G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900025 | |||||||
| chr14:50900082 | A | G | 1 | a0001c0001t0004g0318 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.781-1747A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900082 | |||||||
| chr14:50900145 | C | T | 121 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(118): Show | 129 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.781-1684C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900145 | |||||||
| chr14:50900237 | C | G | 1 | a0001c0001t0001g0322 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.781-1592C>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900237 | |||||||
| chr14:50900279 | T | C | 2 | a0004c0009t0009g0165a0004c0009t0015g0177 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.781-1550T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900279 | |||||||
| chr14:50900330 | A | G | 1 | a0001c0006t0001g0135 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.781-1499A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900330 | |||||||
| chr14:50900604 | C | T | 2 | a0002c0002t0005g0153a0002c0002t0005g0245 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.781-1225C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900604 | |||||||
| chr14:50900610 | C | T | 64 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(61): Show | 67 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.781-1219C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900610 | |||||||
| chr14:50900891 | T | C | 3 | a0002c0002t0002g0161a0002c0002t0002g0248a0002c0002t0002g0249 | 3 | NA18971.hp1 NA18992.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.781-938T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900891 | |||||||
| chr14:50900942 | G | C | 6 | a0001c0001t0001g0031a0001c0001t0001g0207a0001c0001t0003g0191others(3): Show | 6 | HG02559.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-887G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50900942 | |||||||
| chr14:50901147 | C | T | 1 | a0002c0002t0002g0081 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.781-682C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50901147 | |||||||
| chr14:50901415 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.781-414A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50901415 | |||||||
| chr14:50901511 | A | AT | 123 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(120): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.781-314dupT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50901511 | ||||||
| chr14:50901684 | T | C | 12 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0118others(9): Show | 12 | HG00280.hp1 HG00642.hp2 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.781-145T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50901684 | |||||||
| chr14:50901763 | AAGACTAT others(5): Show |
A | 2 | a0001c0001t0001g0138a0001c0001t0001g0145 | 2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.781-62_781-51delCT others(10): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr14 | 50901763 | ||||||
| chr14:50901777 | G | A | 123 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(120): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.781-52G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 9/12 | chr14 | 50901777 | |||||||
| chr14:50901967 | CA | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0047 | 3 | HG02055.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.863+58delA | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr14 | 50901967 | ||||||
| chr14:50901974 | C | T | 1 | a0002c0002t0002g0053 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.863+63C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50901974 | |||||||
| chr14:50901998 | T | A | 1 | a0001c0006t0013g0028 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.863+87T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50901998 | |||||||
| chr14:50902015 | C | T | 10 | a0003c0003t0001g0061a0003c0003t0001g0065a0003c0003t0001g0066others(7): Show | 10 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.863+104C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902015 | |||||||
| chr14:50902038 | T | A | 123 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(120): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.863+127T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902038 | |||||||
| chr14:50902202 | CT | C | 205 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(202): Show | 218 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.863+293delT | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr14 | 50902202 | ||||||
| chr14:50902205 | G | C | 2 | a0003c0003t0001g0052a0003c0003t0001g0092 | 2 | HG03710.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.863+294G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902205 | |||||||
| chr14:50902212 | T | A | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.863+301T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902212 | |||||||
| chr14:50902267 | G | A | 11 | a0002c0002t0005g0022a0002c0002t0005g0024a0002c0002t0005g0153others(8): Show | 11 | HG01261.hp2 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.863+356G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902267 | |||||||
| chr14:50902292 | G | A | 82 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(79): Show | 87 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.863+381G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902292 | |||||||
| chr14:50902294 | G | A | 17 | a0002c0002t0005g0022a0002c0002t0005g0024a0002c0002t0005g0153others(14): Show | 17 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.863+383G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902294 | |||||||
| chr14:50902322 | A | T | 17 | a0002c0002t0005g0022a0002c0002t0005g0024a0002c0002t0005g0153others(14): Show | 17 | HG01261.hp2 HG01884.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.863+411A>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902322 | |||||||
| chr14:50902363 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.863+452C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902363 | |||||||
| chr14:50902433 | G | A | 123 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(120): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.863+522G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902433 | |||||||
| chr14:50902463 | G | T | 42 | a0001c0001t0001g0018a0001c0001t0001g0031a0001c0001t0001g0034others(39): Show | 43 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.863+552G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902463 | |||||||
| chr14:50902606 | T | C | 17 | a0004c0007t0001g0002a0004c0007t0001g0037a0004c0007t0001g0115others(14): Show | 19 | HG00280.hp2 HG01106.hp2 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.863+695T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902606 | |||||||
| chr14:50902660 | C | T | 23 | a0001c0001t0004g0318a0001c0005t0004g0017a0001c0005t0004g0026others(20): Show | 25 | HG00609.hp2 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.864-729C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902660 | |||||||
| chr14:50902859 | T | G | 1 | a0008c0017t0006g0224 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.864-530T>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902859 | |||||||
| chr14:50902908 | C | T | 2 | a0002c0004t0006g0169a0002c0004t0010g0205 | 2 | HG02886.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.864-481C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50902908 | |||||||
| chr14:50903052 | T | A | 31 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0038others(28): Show | 32 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.864-337T>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50903052 | |||||||
| chr14:50903110 | G | T | 1 | a0001c0001t0001g0260 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.864-279G>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50903110 | |||||||
| chr14:50903110 | GTTTTTT | G | 123 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(120): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.864-272_864-267del others(6): Show |
ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr14 | 50903110 | ||||||
| chr14:50903162 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.864-227A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50903162 | |||||||
| chr14:50903229 | G | A | 31 | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0038others(28): Show | 32 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.864-160G>A | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 10/12 | chr14 | 50903229 | |||||||
| chr14:50903774 | C | T | 2 | a0002c0002t0002g0009a0002c0002t0012g0214 | 3 | HG00642.hp1 HG01243.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.943-300C>T | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 11/12 | chr14 | 50903774 | |||||||
| chr14:50903789 | T | C | 1 | a0001c0001t0001g0006 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.943-285T>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 11/12 | chr14 | 50903789 | |||||||
| chr14:50903804 | A | G | 1 | a0001c0001t0001g0339 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.943-270A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 11/12 | chr14 | 50903804 | |||||||
| chr14:50903821 | A | G | 123 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(120): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.943-253A>G | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 11/12 | chr14 | 50903821 | |||||||
| chr14:50904066 | G | C | 123 | a0002c0002t0002g0001a0002c0002t0002g0003a0002c0002t0002g0009others(120): Show | 131 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(128): Show |
splice_region_variant&intron_variant | LOW | c.943-8G>C | ABHD12B | ENSG00000131969.15 | transcript | ENST00000337334.7 | protein_coding | 11/12 | chr14 | 50904066 |