Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 201562 |
| ensemblid | ENSG00000206527.10 |
| hgncid | 9640 |
| symbol | HACD2 |
| name | 3-hydroxyacyl-CoA dehydratase 2 |
| refseq_nuc | NM_198402.5 |
| refseq_prot | NP_940684.1 |
| ensembl_nuc | ENST00000383657.10 |
| ensembl_prot | ENSP00000373153.5 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 123491554 |
| end | 123585053 |
| strand | - |
| ver | v1.2 |
| region | chr3:123491554-123585053 |
| region5000 | chr3:123486554-123590053 |
| regionname0 | HACD2_chr3_123491554_123585053 |
| regionname5000 | HACD2_chr3_123486554_123590053 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 254 | 349 | 88 | 60 | 151 | 12 | 36 | 119 | HACD2_chr3_123486554_123590053 | HACD2 | MAAVA others(249): Show |
chr3 | 123486554 | 123590053 |
| a0002 | 0/0 | 254 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | MAAVA others(249): Show |
chr3 | 123486554 | 123590053 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 762 | 152 | 43 | 32 | 47 | 7 | 21 | HACD2_chr3_123486554_123590053 | HACD2 | ATGGC others(757): Show |
chr3 | 123486554 | 123590053 | ||
| a0001c0002 | 0/0 | 762 | 102 | 17 | 14 | 65 | 1 | 5 | HACD2_chr3_123486554_123590053 | HACD2 | ATGGC others(757): Show |
chr3 | 123486554 | 123590053 | ||
| a0001c0003 | 0/0 | 762 | 94 | 27 | 14 | 39 | 4 | 10 | HACD2_chr3_123486554_123590053 | HACD2 | ATGGC others(757): Show |
chr3 | 123486554 | 123590053 | ||
| a0001c0004 | 0/0 | 762 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | ATGGC others(757): Show |
chr3 | 123486554 | 123590053 | ||
| a0002c0005 | 0/0 | 762 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | ATGGC others(757): Show |
chr3 | 123486554 | 123590053 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4125 | 11 | 5 | 5 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0002 | 0/0 | 4125 | 64 | 9 | 9 | 37 | 2 | 7 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0003 | 0/0 | 4125 | 2 | 0 | 0 | 1 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0004 | 0/0 | 4125 | 32 | 0 | 12 | 5 | 3 | 12 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0005 | 0/0 | 4125 | 6 | 2 | 3 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0006 | 1/0 | 4125 | 24 | 20 | 3 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0009 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0013 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0015 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0018 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0019 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0026 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0027 | 0/0 | 4071 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4066): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0028 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0029 | 0/1 | 4125 | 1 | 0 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0030 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0001t0031 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0001 | 0/0 | 4125 | 65 | 0 | 7 | 53 | 1 | 4 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0002 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0003 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0004 | 0/0 | 4125 | 6 | 0 | 1 | 5 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0005 | 0/0 | 4125 | 17 | 10 | 3 | 4 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0008 | 0/0 | 4125 | 7 | 6 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0009 | 0/0 | 4125 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0020 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0022 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0002t0023 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0001 | 0/0 | 4125 | 10 | 0 | 3 | 0 | 3 | 4 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0003 | 0/0 | 4125 | 58 | 13 | 5 | 37 | 0 | 3 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0005 | 0/0 | 4125 | 3 | 3 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0007 | 0/0 | 4125 | 8 | 0 | 5 | 1 | 1 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0009 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0010 | 0/0 | 4125 | 4 | 4 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0011 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0012 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0014 | 0/0 | 4125 | 2 | 2 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0016 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0021 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0024 | 0/0 | 4125 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0003t0025 | 0/0 | 4125 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0001c0004t0017 | 0/0 | 4125 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| a0002c0005t0001 | 0/0 | 4125 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | AGGAG others(4120): Show |
chr3 | 123486554 | 123590053 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0160 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0009g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0013g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0013g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0015g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0015g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0018g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0019g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0026g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0027g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0028g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0029g0189 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0030g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0001t0031g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0005g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0009g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0009g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0020g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0022g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0002t0023g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0005g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0007g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0009g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0010g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0010g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0010g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0010g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0011g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0011g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0012g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0012g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0014g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0014g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0016g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0021g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0024g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0003t0025g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0001c0004t0017g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| a0002c0005t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0007 | g0307 | EUR | GBR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0203 | EUR | GBR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0319 | EUR | GBR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00140 | hp2 | a0001 | c0001 | t0004 | g0181 | EUR | GBR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0118 | EUR | FIN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00323 | hp2 | a0001 | c0003 | t0001 | g0328 | EUR | FIN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0039 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00544 | hp2 | a0001 | c0003 | t0003 | g0266 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0062 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0064 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0180 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00642 | hp2 | a0001 | c0003 | t0007 | g0312 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00673 | hp2 | a0001 | c0002 | t0005 | g0067 | EAS | CHS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00735 | hp1 | a0001 | c0003 | t0007 | g0305 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00735 | hp2 | a0001 | c0002 | t0008 | g0013 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0199 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0258 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0098 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01167 | hp1 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01168 | hp1 | a0001 | c0001 | t0004 | g0109 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01169 | hp1 | a0001 | c0001 | t0006 | g0228 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01169 | hp2 | a0001 | c0001 | t0004 | g0110 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0219 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01243 | hp2 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01255 | hp2 | a0001 | c0003 | t0007 | g0309 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01256 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0008 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0182 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01261 | hp2 | a0001 | c0003 | t0007 | g0308 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01346 | hp1 | a0001 | c0003 | t0007 | g0311 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01358 | hp1 | a0001 | c0001 | t0005 | g0113 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0185 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0114 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01433 | hp2 | a0001 | c0002 | t0005 | g0094 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0205 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01515 | hp1 | a0001 | c0001 | t0031 | g0342 | EUR | IBS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | IBS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01516 | hp1 | a0001 | c0001 | t0004 | g0178 | EUR | IBS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0314 | EUR | IBS | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01884 | hp1 | a0001 | c0003 | t0012 | g0303 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01928 | hp2 | a0001 | c0003 | t0025 | g0261 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01943 | hp1 | a0001 | c0003 | t0003 | g0279 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01943 | hp2 | a0001 | c0003 | t0001 | g0318 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0212 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01993 | hp1 | a0001 | c0003 | t0003 | g0265 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01993 | hp2 | a0001 | c0002 | t0020 | g0056 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02004 | hp1 | a0001 | c0003 | t0003 | g0264 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02004 | hp2 | a0001 | c0002 | t0023 | g0058 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02055 | hp1 | a0001 | c0003 | t0014 | g0299 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0289 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02080 | hp2 | a0001 | c0003 | t0003 | g0274 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0043 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02083 | hp2 | a0001 | c0003 | t0003 | g0263 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02129 | hp1 | a0001 | c0003 | t0007 | g0306 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02129 | hp2 | a0001 | c0003 | t0003 | g0270 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02132 | hp2 | a0001 | c0003 | t0003 | g0294 | EAS | KHV | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02145 | hp2 | a0001 | c0003 | t0003 | g0313 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | CDX | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0037 | EAS | CDX | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0218 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0244 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02258 | hp1 | a0001 | c0003 | t0005 | g0302 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02258 | hp2 | a0001 | c0004 | t0017 | g0107 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0332 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02293 | hp1 | a0001 | c0003 | t0003 | g0268 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | PEL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02451 | hp1 | a0001 | c0003 | t0010 | g0340 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02572 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0147 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0173 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0229 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02622 | hp1 | a0001 | c0002 | t0008 | g0077 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02622 | hp2 | a0001 | c0003 | t0016 | g0321 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0231 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02647 | hp1 | a0001 | c0003 | t0012 | g0304 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02647 | hp2 | a0001 | c0001 | t0015 | g0224 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0204 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02683 | hp2 | a0001 | c0003 | t0021 | g0316 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0155 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02698 | hp2 | a0001 | c0003 | t0001 | g0317 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02723 | hp1 | a0001 | c0002 | t0005 | g0074 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02809 | hp1 | a0001 | c0003 | t0003 | g0329 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0079 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02818 | hp1 | a0001 | c0002 | t0005 | g0076 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0238 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0327 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02896 | hp2 | a0001 | c0003 | t0003 | g0335 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0334 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02897 | hp2 | a0001 | c0001 | t0006 | g0237 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02922 | hp1 | a0001 | c0001 | t0019 | g0217 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02922 | hp2 | a0001 | c0002 | t0008 | g0065 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0115 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02965 | hp2 | a0001 | c0003 | t0010 | g0338 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02970 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02970 | hp2 | a0001 | c0001 | t0006 | g0233 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02976 | hp1 | a0001 | c0002 | t0008 | g0071 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0235 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0325 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0108 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0097 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03098 | hp1 | a0001 | c0002 | t0005 | g0066 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03098 | hp2 | a0001 | c0003 | t0005 | g0301 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03139 | hp1 | a0001 | c0003 | t0010 | g0339 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0226 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03209 | hp1 | a0001 | c0002 | t0005 | g0096 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0242 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03225 | hp2 | a0001 | c0003 | t0014 | g0298 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03239 | hp1 | a0001 | c0003 | t0007 | g0310 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0209 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03453 | hp1 | a0001 | c0003 | t0003 | g0336 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03486 | hp1 | a0001 | c0002 | t0008 | g0070 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03486 | hp2 | a0001 | c0003 | t0003 | g0256 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0206 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0044 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0202 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0175 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03516 | hp1 | a0001 | c0003 | t0011 | g0323 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0073 | AFR | ESN | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03540 | hp2 | a0001 | c0001 | t0015 | g0223 | AFR | GWD | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03579 | hp2 | a0001 | c0003 | t0003 | g0330 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0315 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0208 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0176 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | PJL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03831 | hp1 | a0001 | c0003 | t0003 | g0260 | SAS | BEB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0041 | SAS | BEB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03942 | hp1 | a0001 | c0003 | t0001 | g0324 | SAS | BEB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04115 | hp1 | a0001 | c0001 | t0028 | g0163 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0045 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04199 | hp2 | a0001 | c0003 | t0024 | g0326 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0187 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04204 | hp2 | a0001 | c0003 | t0003 | g0259 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0188 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG04228 | hp2 | a0001 | c0003 | t0003 | g0276 | SAS | STU | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0116 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | CHB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | CHB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18747 | hp2 | a0001 | c0003 | t0009 | g0267 | EAS | CHB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18906 | hp1 | a0001 | c0003 | t0005 | g0300 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0240 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18939 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18939 | hp2 | a0001 | c0001 | t0009 | g0138 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18942 | hp1 | a0002 | c0005 | t0001 | g0341 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18945 | hp1 | a0001 | c0003 | t0003 | g0295 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18946 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18948 | hp1 | a0001 | c0003 | t0003 | g0006 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18957 | hp2 | a0001 | c0003 | t0003 | g0281 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18959 | hp2 | a0001 | c0003 | t0003 | g0273 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18960 | hp1 | a0001 | c0003 | t0003 | g0293 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18961 | hp2 | a0001 | c0003 | t0003 | g0290 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18962 | hp2 | a0001 | c0003 | t0003 | g0269 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18964 | hp1 | a0001 | c0002 | t0009 | g0086 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18968 | hp1 | a0001 | c0001 | t0027 | g0119 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18968 | hp2 | a0001 | c0003 | t0003 | g0254 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18970 | hp1 | a0001 | c0002 | t0004 | g0099 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18971 | hp2 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18973 | hp1 | a0001 | c0003 | t0003 | g0007 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18978 | hp2 | a0001 | c0003 | t0003 | g0285 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18979 | hp1 | a0001 | c0002 | t0004 | g0103 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18979 | hp2 | a0001 | c0003 | t0003 | g0287 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18981 | hp2 | a0001 | c0003 | t0003 | g0271 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18985 | hp1 | a0001 | c0003 | t0003 | g0262 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0184 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18992 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18994 | hp2 | a0001 | c0002 | t0005 | g0020 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18998 | hp1 | a0001 | c0003 | t0003 | g0282 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18999 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA18999 | hp2 | a0001 | c0003 | t0003 | g0288 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19000 | hp2 | a0001 | c0003 | t0003 | g0253 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19002 | hp1 | a0001 | c0003 | t0003 | g0283 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19003 | hp1 | a0001 | c0002 | t0009 | g0100 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19012 | hp1 | a0001 | c0003 | t0003 | g0296 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19030 | hp1 | a0001 | c0003 | t0011 | g0322 | AFR | LWK | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0197 | AFR | LWK | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0331 | AFR | LWK | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19043 | hp2 | a0001 | c0002 | t0008 | g0078 | AFR | LWK | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19054 | hp1 | a0001 | c0003 | t0003 | g0275 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19057 | hp1 | a0001 | c0002 | t0005 | g0091 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19058 | hp1 | a0001 | c0003 | t0003 | g0255 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19058 | hp2 | a0001 | c0002 | t0022 | g0019 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19062 | hp1 | a0001 | c0002 | t0004 | g0102 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19062 | hp2 | a0001 | c0003 | t0003 | g0286 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19066 | hp2 | a0001 | c0003 | t0003 | g0284 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19070 | hp1 | a0001 | c0003 | t0003 | g0272 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19074 | hp1 | a0001 | c0003 | t0003 | g0280 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19080 | hp2 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19081 | hp2 | a0001 | c0001 | t0026 | g0121 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19082 | hp1 | a0001 | c0003 | t0003 | g0297 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19085 | hp1 | a0001 | c0002 | t0005 | g0021 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19085 | hp2 | a0001 | c0003 | t0003 | g0277 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19086 | hp2 | a0001 | c0003 | t0003 | g0292 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19090 | hp1 | a0001 | c0003 | t0003 | g0278 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19091 | hp1 | a0001 | c0003 | t0003 | g0291 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0245 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA19240 | hp2 | a0001 | c0001 | t0018 | g0230 | AFR | YRI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20129 | hp1 | a0001 | c0003 | t0003 | g0257 | AFR | ASW | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20129 | hp2 | a0001 | c0001 | t0006 | g0232 | AFR | ASW | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0030 | EUR | TSI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | TSI | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0207 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02109 | hp1 | a0001 | c0002 | t0003 | g0075 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0241 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02486 | hp1 | a0001 | c0003 | t0003 | g0320 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0333 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02559 | hp1 | a0001 | c0002 | t0008 | g0072 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG02559 | hp2 | a0001 | c0001 | t0030 | g0252 | AFR | ACB | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03471 | hp1 | a0001 | c0002 | t0005 | g0069 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG03471 | hp2 | a0001 | c0003 | t0010 | g0337 | AFR | MSL | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0200 | AFR | USA | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | USA | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0095 | AFR | USA | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| NA20300 | hp2 | a0001 | c0001 | t0006 | g0236 | AFR | USA | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0029 | g0189 | REF | REF | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0160 | REF | REF | HACD2_chr3_123486554_123590053 | HACD2 | chr3 | 123486554 | 123590053 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123585009 | T | A | 1 | a0002 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.19A>T | p.Thr7Ser | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 45/4125 | 19/765 | 7/254 | chr3 | 123585009 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123584965 | C | T | 1 | a0001c0004 | 1 | HG02258.hp2 | synonymous_variant | LOW | c.63G>A | p.Gly21Gly | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 89/4125 | 63/765 | 21/254 | chr3 | 123584965 | |||
| chr3:123584974 | G | C | 3 | a0001c0002 a0001c0003 a0002c0005 |
197 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(194): Show |
synonymous_variant | LOW | c.54C>G | p.Gly18Gly | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 80/4125 | 54/765 | 18/254 | chr3 | 123584974 | |||
| chr3:123584977 | A | G | 2 | a0001c0002 a0002c0005 |
103 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(100): Show |
synonymous_variant | LOW | c.51T>C | p.Gly17Gly | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 77/4125 | 51/765 | 17/254 | chr3 | 123584977 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123491817 | C | T | 3 | a0001c0001t0013 a0001c0003t0007 a0001c0003t0014 |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3071G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 3071 | chr3 | 123491817 | ||||||
| chr3:123491852 | C | A | 1 | a0001c0003t0025 | 1 | HG01928.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3036G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 3036 | chr3 | 123491852 | ||||||
| chr3:123491968 | A | T | 4 | a0001c0001t0009 a0001c0002t0009 a0001c0002t0022 others(1): Show |
5 | NA18747.hp2 NA18939.hp2 NA18964.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2920T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2920 | chr3 | 123491968 | ||||||
| chr3:123492030 | C | G | 1 | a0001c0002t0023 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2858G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2858 | chr3 | 123492030 | ||||||
| chr3:123492046 | C | G | 1 | a0001c0001t0030 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2842G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2842 | chr3 | 123492046 | ||||||
| chr3:123492111 | C | T | 1 | a0001c0002t0020 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2777G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2777 | chr3 | 123492111 | ||||||
| chr3:123492131 | T | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*2757A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2757 | chr3 | 123492131 | ||||||
| chr3:123492168 | C | G | 3 | a0001c0001t0013 a0001c0003t0007 a0001c0003t0014 |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2720G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2720 | chr3 | 123492168 | ||||||
| chr3:123492168 | C | T | 1 | a0001c0001t0028 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2720G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2720 | chr3 | 123492168 | ||||||
| chr3:123492178 | T | C | 1 | a0001c0003t0024 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2710A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2710 | chr3 | 123492178 | ||||||
| chr3:123492217 | G | T | 3 | a0001c0001t0004 a0001c0001t0031 a0001c0002t0004 |
39 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*2671C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2671 | chr3 | 123492217 | ||||||
| chr3:123492301 | CCTTTGAC others(47): Show |
C | 1 | a0001c0001t0027 | 1 | NA18968.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2533_*2586delTTTT others(50): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2533 | chr3 | 123492301 | ||||||
| chr3:123492448 | G | A | 3 | a0001c0001t0005 a0001c0002t0005 a0001c0003t0005 |
26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2440C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2440 | chr3 | 123492448 | ||||||
| chr3:123492568 | C | T | 1 | a0001c0003t0007 | 8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2320G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 2320 | chr3 | 123492568 | ||||||
| chr3:123493006 | C | T | 1 | a0001c0002t0022 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1882G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1882 | chr3 | 123493006 | ||||||
| chr3:123493022 | A | G | 1 | a0001c0001t0026 | 1 | NA19081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1866T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1866 | chr3 | 123493022 | ||||||
| chr3:123493032 | A | G | 1 | a0001c0001t0030 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1856T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1856 | chr3 | 123493032 | ||||||
| chr3:123493120 | T | C | 3 | a0001c0001t0013 a0001c0003t0007 a0001c0003t0014 |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1768A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1768 | chr3 | 123493120 | ||||||
| chr3:123493190 | T | C | 3 | a0001c0001t0013 a0001c0003t0007 a0001c0003t0014 |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1698A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1698 | chr3 | 123493190 | ||||||
| chr3:123493196 | T | C | 12 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0026 others(9): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*1692A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1692 | chr3 | 123493196 | ||||||
| chr3:123493205 | A | C | 1 | a0001c0001t0018 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1683T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1683 | chr3 | 123493205 | ||||||
| chr3:123493225 | A | G | 1 | a0001c0003t0021 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1663T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1663 | chr3 | 123493225 | ||||||
| chr3:123493229 | A | G | 1 | a0001c0003t0021 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1659T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1659 | chr3 | 123493229 | ||||||
| chr3:123493304 | T | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*1584A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1584 | chr3 | 123493304 | ||||||
| chr3:123493335 | A | G | 1 | a0001c0002t0020 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1553T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1553 | chr3 | 123493335 | ||||||
| chr3:123493342 | C | T | 1 | a0001c0002t0008 | 7 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1546G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1546 | chr3 | 123493342 | ||||||
| chr3:123493351 | G | A | 1 | a0001c0001t0019 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1537C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1537 | chr3 | 123493351 | ||||||
| chr3:123493423 | A | T | 1 | a0001c0003t0010 | 4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1465T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1465 | chr3 | 123493423 | ||||||
| chr3:123493716 | A | G | 12 | a0001c0001t0001 a0001c0001t0009 a0001c0002t0001 others(9): Show |
96 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*1172T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1172 | chr3 | 123493716 | ||||||
| chr3:123493847 | A | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*1041T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1041 | chr3 | 123493847 | ||||||
| chr3:123493848 | G | A | 1 | a0001c0001t0030 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1040C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 1040 | chr3 | 123493848 | ||||||
| chr3:123493985 | C | T | 3 | a0001c0001t0013 a0001c0003t0007 a0001c0003t0014 |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*903G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 903 | chr3 | 123493985 | ||||||
| chr3:123494025 | C | T | 1 | a0001c0004t0017 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*863G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 863 | chr3 | 123494025 | ||||||
| chr3:123494079 | C | T | 1 | a0001c0003t0012 | 2 | HG01884.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*809G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 809 | chr3 | 123494079 | ||||||
| chr3:123494086 | T | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
3_prime_UTR_variant | MODIFIER | c.*802A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 802 | chr3 | 123494086 | ||||||
| chr3:123494172 | T | C | 1 | a0001c0003t0014 | 2 | HG02055.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*716A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 716 | chr3 | 123494172 | ||||||
| chr3:123494456 | C | G | 1 | a0001c0004t0017 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 432 | chr3 | 123494456 | ||||||
| chr3:123494478 | C | T | 2 | a0001c0003t0011 a0001c0003t0016 |
3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 410 | chr3 | 123494478 | ||||||
| chr3:123494589 | A | G | 1 | a0001c0003t0016 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*299T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 299 | chr3 | 123494589 | ||||||
| chr3:123494702 | T | C | 1 | a0001c0001t0015 | 2 | HG02647.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*186A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 7/7 | 186 | chr3 | 123494702 | ||||||
| chr3:123585028 | G | A | 1 | a0001c0001t0031 | 1 | HG01515.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/7 | 1 | chr3 | 123585028 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:123495048 | T | C | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.683-78A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495048 | |||||||
| chr3:123495122 | A | G | 1 | a0001c0002t0001g0048 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.683-152T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495122 | |||||||
| chr3:123495181 | T | C | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.683-211A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495181 | |||||||
| chr3:123495243 | C | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-273G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495243 | |||||||
| chr3:123495260 | C | T | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.683-290G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495260 | |||||||
| chr3:123495523 | C | T | 3 | a0001c0003t0011g0322 a0001c0003t0011g0323 a0001c0003t0016g0321 |
3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.683-553G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495523 | |||||||
| chr3:123495596 | TA | T | 81 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(78): Show |
83 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.683-627delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495596 | |||||||
| chr3:123495596 | TAAAA | T | 220 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(217): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.683-630_683-627del others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495596 | |||||||
| chr3:123495740 | T | C | 1 | a0001c0001t0004g0208 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.683-770A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495740 | |||||||
| chr3:123495785 | G | A | 1 | a0001c0003t0003g0296 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.683-815C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495785 | |||||||
| chr3:123495903 | G | T | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.683-933C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495903 | |||||||
| chr3:123495943 | G | GTTT | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.683-974_683-973ins others(3): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123495943 | |||||||
| chr3:123496105 | T | C | 313 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.683-1135A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496105 | |||||||
| chr3:123496113 | T | G | 1 | a0001c0001t0004g0204 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.683-1143A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496113 | |||||||
| chr3:123496175 | C | T | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-1205G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496175 | |||||||
| chr3:123496270 | G | A | 110 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(107): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.683-1300C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496270 | |||||||
| chr3:123496434 | A | T | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.683-1464T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496434 | |||||||
| chr3:123496458 | C | T | 1 | a0001c0002t0005g0067 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.683-1488G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496458 | |||||||
| chr3:123496462 | G | A | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-1492C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496462 | |||||||
| chr3:123496600 | G | A | 107 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(104): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.683-1630C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496600 | |||||||
| chr3:123496656 | C | G | 4 | a0001c0001t0006g0238 a0001c0001t0006g0241 a0001c0001t0006g0245 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-1686G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496656 | |||||||
| chr3:123496685 | A | G | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.683-1715T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496685 | |||||||
| chr3:123496764 | T | A | 313 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.683-1794A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496764 | |||||||
| chr3:123496901 | C | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-1931G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123496901 | |||||||
| chr3:123497179 | C | A | 1 | a0001c0003t0003g0256 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.683-2209G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497179 | |||||||
| chr3:123497261 | C | T | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-2291G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497261 | |||||||
| chr3:123497346 | A | T | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.683-2376T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497346 | |||||||
| chr3:123497367 | C | T | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-2397G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497367 | |||||||
| chr3:123497375 | G | A | 1 | a0001c0001t0006g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.683-2405C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497375 | |||||||
| chr3:123497952 | G | A | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.682+2563C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123497952 | |||||||
| chr3:123498242 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.682+2273G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498242 | |||||||
| chr3:123498248 | T | C | 1 | a0001c0003t0021g0316 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.682+2267A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498248 | |||||||
| chr3:123498358 | A | T | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.682+2157T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498358 | |||||||
| chr3:123498402 | A | G | 222 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(219): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.682+2113T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498402 | |||||||
| chr3:123498461 | G | A | 7 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 others(4): Show |
7 | HG02258.hp2 HG02451.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+2054C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498461 | |||||||
| chr3:123498495 | C | A | 108 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(105): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.682+2020G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498495 | |||||||
| chr3:123498505 | T | G | 108 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(105): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.682+2010A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498505 | |||||||
| chr3:123498625 | G | A | 1 | a0001c0002t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.682+1890C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498625 | |||||||
| chr3:123498657 | C | T | 1 | a0001c0002t0001g0022 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.682+1858G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498657 | |||||||
| chr3:123498839 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.682+1676G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498839 | |||||||
| chr3:123498860 | T | C | 1 | a0001c0003t0001g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.682+1655A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498860 | |||||||
| chr3:123498885 | G | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+1630C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498885 | |||||||
| chr3:123498897 | C | G | 1 | a0001c0001t0002g0005 | 2 | HG01070.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.682+1618G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498897 | |||||||
| chr3:123498922 | A | G | 26 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(23): Show |
26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+1593T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123498922 | |||||||
| chr3:123499001 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.682+1514A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499001 | |||||||
| chr3:123499201 | T | G | 3 | a0001c0001t0002g0220 a0001c0001t0013g0115 a0001c0001t0013g0116 |
3 | HG02630.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.682+1314A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499201 | |||||||
| chr3:123499261 | T | TA | 46 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(43): Show |
48 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(45): Show |
intron_variant | MODIFIER | c.682+1253dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499261 | |||||||
| chr3:123499298 | C | T | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+1217G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499298 | |||||||
| chr3:123499366 | T | C | 1 | a0001c0001t0002g0140 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.682+1149A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499366 | |||||||
| chr3:123499382 | G | C | 26 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(23): Show |
26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+1133C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499382 | |||||||
| chr3:123499484 | C | A | 1 | a0001c0002t0005g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.682+1031G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499484 | |||||||
| chr3:123499578 | T | C | 1 | a0001c0001t0004g0190 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.682+937A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499578 | |||||||
| chr3:123499607 | C | G | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+908G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499607 | |||||||
| chr3:123499629 | G | C | 1 | a0001c0001t0002g0142 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.682+886C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499629 | |||||||
| chr3:123499677 | TTAAAA | T | 26 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(23): Show |
26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.682+833_682+837del others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499677 | |||||||
| chr3:123499704 | T | G | 3 | a0001c0003t0003g0253 a0001c0003t0003g0283 a0001c0003t0003g0284 |
3 | NA19000.hp2 NA19002.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.682+811A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499704 | |||||||
| chr3:123499801 | T | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+714A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123499801 | |||||||
| chr3:123500131 | T | A | 1 | a0001c0002t0004g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.682+384A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123500131 | |||||||
| chr3:123500132 | C | T | 1 | a0001c0002t0004g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.682+383G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123500132 | |||||||
| chr3:123500133 | T | C | 1 | a0001c0002t0004g0102 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.682+382A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123500133 | |||||||
| chr3:123500290 | G | A | 222 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(219): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.682+225C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 6/6 | chr3 | 123500290 | |||||||
| chr3:123500910 | C | T | 1 | a0001c0002t0003g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.504-217G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123500910 | |||||||
| chr3:123501172 | T | A | 26 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(23): Show |
26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.504-479A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501172 | |||||||
| chr3:123501178 | TC | T | 26 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(23): Show |
26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.504-486delG | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501178 | |||||||
| chr3:123501218 | A | G | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.504-525T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501218 | |||||||
| chr3:123501391 | C | T | 1 | a0001c0003t0003g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.504-698G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501391 | |||||||
| chr3:123501417 | T | C | 107 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(104): Show |
109 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.504-724A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501417 | |||||||
| chr3:123501443 | T | G | 1 | a0001c0001t0002g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.504-750A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501443 | |||||||
| chr3:123501587 | GA | G | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.504-895delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501587 | |||||||
| chr3:123501589 | A | G | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.504-896T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501589 | |||||||
| chr3:123501714 | G | A | 78 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(75): Show |
80 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.503+846C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501714 | |||||||
| chr3:123501741 | T | C | 1 | a0001c0001t0005g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.503+819A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123501741 | |||||||
| chr3:123502229 | T | C | 107 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(104): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.503+331A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123502229 | |||||||
| chr3:123502289 | A | ATTTTTT | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.503+265_503+270dup others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123502289 | |||||||
| chr3:123502342 | T | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.503+218A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 5/6 | chr3 | 123502342 | |||||||
| chr3:123502781 | G | A | 2 | a0001c0001t0015g0223 a0001c0001t0015g0224 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.382-100C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123502781 | |||||||
| chr3:123502936 | C | T | 3 | a0001c0003t0005g0300 a0001c0003t0005g0301 a0001c0003t0005g0302 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382-255G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123502936 | |||||||
| chr3:123502955 | G | A | 1 | a0001c0002t0001g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.382-274C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123502955 | |||||||
| chr3:123503188 | C | T | 17 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(14): Show |
18 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.382-507G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503188 | |||||||
| chr3:123503250 | G | A | 1 | a0001c0003t0001g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.382-569C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503250 | |||||||
| chr3:123503262 | C | CA | 45 | a0001c0001t0002g0132 a0001c0001t0002g0137 a0001c0001t0002g0213 others(42): Show |
45 | HG00099.hp1 HG00597.hp2 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.382-582dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503262 | |||||||
| chr3:123503292 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.382-611A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503292 | |||||||
| chr3:123503447 | C | G | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-766G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503447 | |||||||
| chr3:123503458 | T | C | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-777A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503458 | |||||||
| chr3:123503521 | A | G | 15 | a0001c0001t0004g0175 a0001c0001t0004g0180 a0001c0001t0004g0182 others(12): Show |
15 | HG00099.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.382-840T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503521 | |||||||
| chr3:123503708 | C | CA | 18 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0002g0133 others(15): Show |
18 | HG00597.hp1 HG01884.hp2 HG02155.hp1 others(15): Show |
intron_variant | MODIFIER | c.382-1028dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | |||||||
| chr3:123503708 | C | CAA | 16 | a0001c0001t0002g0221 a0001c0001t0002g0251 a0001c0002t0001g0026 others(13): Show |
16 | HG02145.hp2 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.382-1029_382-1028d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | |||||||
| chr3:123503708 | C | CAAA | 94 | a0001c0001t0002g0220 a0001c0001t0005g0113 a0001c0001t0005g0114 others(91): Show |
95 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-1030_382-1028d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | |||||||
| chr3:123503708 | C | CAAAA | 14 | a0001c0002t0001g0015 a0001c0002t0001g0082 a0001c0002t0020g0056 others(11): Show |
14 | HG01993.hp2 HG02080.hp2 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.382-1031_382-1028d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | |||||||
| chr3:123503708 | C | CAAAAA | 40 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(37): Show |
42 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(39): Show |
intron_variant | MODIFIER | c.382-1032_382-1028d others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | |||||||
| chr3:123503708 | CA | C | 10 | a0001c0001t0001g0152 a0001c0001t0002g0126 a0001c0001t0002g0141 others(7): Show |
10 | HG00558.hp1 HG01884.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-1028delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503708 | |||||||
| chr3:123503716 | A | C | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-1035T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503716 | |||||||
| chr3:123503761 | C | T | 1 | a0001c0002t0005g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.382-1080G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503761 | |||||||
| chr3:123503765 | C | T | 1 | a0001c0003t0003g0290 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.382-1084G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503765 | |||||||
| chr3:123503773 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.382-1092G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123503773 | |||||||
| chr3:123504192 | A | G | 3 | a0001c0003t0011g0322 a0001c0003t0011g0323 a0001c0003t0016g0321 |
3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.382-1511T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504192 | |||||||
| chr3:123504293 | G | A | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-1612C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504293 | |||||||
| chr3:123504322 | A | T | 3 | a0001c0003t0011g0322 a0001c0003t0011g0323 a0001c0003t0016g0321 |
3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.382-1641T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504322 | |||||||
| chr3:123504453 | T | G | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-1772A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504453 | |||||||
| chr3:123504503 | G | A | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.382-1822C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504503 | |||||||
| chr3:123504530 | T | TA | 14 | a0001c0001t0002g0128 a0001c0001t0006g0239 a0001c0003t0003g0256 others(11): Show |
14 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.382-1850dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504530 | |||||||
| chr3:123504560 | C | T | 1 | a0001c0003t0003g0275 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.382-1879G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504560 | |||||||
| chr3:123504774 | C | G | 315 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(312): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.382-2093G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504774 | |||||||
| chr3:123504832 | A | G | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.382-2151T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504832 | |||||||
| chr3:123504887 | A | AAATGT | 339 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(336): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.382-2207_382-2206i others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123504887 | |||||||
| chr3:123505041 | G | A | 18 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(15): Show |
18 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.382-2360C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505041 | |||||||
| chr3:123505223 | G | A | 5 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-2542C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505223 | |||||||
| chr3:123505315 | A | G | 1 | a0001c0002t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.382-2634T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505315 | |||||||
| chr3:123505516 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.382-2835C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505516 | |||||||
| chr3:123505601 | A | G | 1 | a0001c0001t0004g0203 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.382-2920T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505601 | |||||||
| chr3:123505700 | T | C | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-3019A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505700 | |||||||
| chr3:123505904 | T | C | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.382-3223A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123505904 | |||||||
| chr3:123506007 | C | T | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.382-3326G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506007 | |||||||
| chr3:123506041 | G | A | 26 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(23): Show |
26 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.382-3360C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506041 | |||||||
| chr3:123506058 | A | G | 114 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(111): Show |
118 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.382-3377T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506058 | |||||||
| chr3:123506377 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-3696G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506377 | |||||||
| chr3:123506447 | C | G | 27 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.382-3766G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506447 | |||||||
| chr3:123506617 | T | C | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-3936A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506617 | |||||||
| chr3:123506776 | GT | G | 3 | a0001c0003t0003g0256 a0001c0003t0003g0257 a0001c0003t0003g0258 |
3 | HG01109.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.382-4096delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506776 | |||||||
| chr3:123506924 | A | G | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(3): Show |
6 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.382-4243T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506924 | |||||||
| chr3:123506965 | A | G | 1 | a0001c0002t0020g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.382-4284T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123506965 | |||||||
| chr3:123507006 | C | T | 107 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(104): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.382-4325G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507006 | |||||||
| chr3:123507069 | C | A | 1 | a0001c0002t0001g0050 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.382-4388G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507069 | |||||||
| chr3:123507085 | C | T | 1 | a0001c0001t0009g0138 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.382-4404G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507085 | |||||||
| chr3:123507169 | T | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-4488A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507169 | |||||||
| chr3:123507388 | G | GAT | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-4709_382-4708d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507388 | |||||||
| chr3:123507507 | A | T | 1 | a0001c0001t0002g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.382-4826T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507507 | |||||||
| chr3:123507509 | C | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-4828G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507509 | |||||||
| chr3:123507533 | C | T | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-4852G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507533 | |||||||
| chr3:123507705 | A | G | 1 | a0001c0001t0031g0342 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.382-5024T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507705 | |||||||
| chr3:123507730 | T | A | 2 | a0001c0003t0003g0329 a0001c0003t0003g0336 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.382-5049A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507730 | |||||||
| chr3:123507746 | A | T | 312 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(309): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.382-5065T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507746 | |||||||
| chr3:123507892 | G | A | 36 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(33): Show |
36 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.382-5211C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507892 | |||||||
| chr3:123507993 | T | C | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.382-5312A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123507993 | |||||||
| chr3:123508006 | G | GA | 5 | a0001c0002t0001g0050 a0001c0003t0010g0337 a0001c0003t0010g0338 others(2): Show |
5 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5326dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508006 | |||||||
| chr3:123508006 | GA | G | 20 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(17): Show |
21 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.382-5326delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508006 | |||||||
| chr3:123508149 | T | C | 1 | a0001c0001t0013g0116 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.382-5468A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508149 | |||||||
| chr3:123508198 | T | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-5517A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508198 | |||||||
| chr3:123508221 | G | C | 2 | a0001c0001t0015g0223 a0001c0001t0015g0224 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.382-5540C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508221 | |||||||
| chr3:123508357 | G | A | 1 | a0001c0003t0021g0316 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.382-5676C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508357 | |||||||
| chr3:123508641 | A | C | 5 | a0001c0001t0005g0139 a0001c0002t0005g0020 a0001c0002t0005g0021 others(2): Show |
5 | HG00673.hp2 NA18994.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-5960T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508641 | |||||||
| chr3:123508827 | T | G | 1 | a0001c0001t0004g0004 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.382-6146A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508827 | |||||||
| chr3:123508848 | C | A | 1 | a0001c0003t0005g0302 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.382-6167G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508848 | |||||||
| chr3:123508862 | G | A | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-6181C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508862 | |||||||
| chr3:123508867 | G | T | 1 | a0001c0002t0005g0095 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382-6186C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508867 | |||||||
| chr3:123508997 | A | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-6316T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123508997 | |||||||
| chr3:123509020 | T | C | 1 | a0001c0001t0002g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.382-6339A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509020 | |||||||
| chr3:123509034 | C | T | 3 | a0001c0001t0006g0233 a0001c0001t0006g0237 a0001c0001t0006g0242 |
3 | HG02897.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.382-6353G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509034 | |||||||
| chr3:123509094 | C | T | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.382-6413G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509094 | |||||||
| chr3:123509284 | C | T | 3 | a0001c0001t0004g0180 a0001c0001t0004g0182 a0001c0001t0004g0185 |
3 | HG00642.hp1 HG01261.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.382-6603G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509284 | |||||||
| chr3:123509288 | A | G | 25 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.382-6607T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509288 | |||||||
| chr3:123509428 | G | A | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-6747C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509428 | |||||||
| chr3:123509500 | TTC | T | 107 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(104): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.382-6821_382-6820d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509500 | |||||||
| chr3:123509502 | CT | C | 208 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(205): Show |
212 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(209): Show |
intron_variant | MODIFIER | c.382-6822delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509502 | |||||||
| chr3:123509502 | CTT | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-6823_382-6822d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509502 | |||||||
| chr3:123509532 | T | C | 8 | a0001c0002t0001g0015 a0001c0002t0001g0081 a0001c0002t0001g0082 others(5): Show |
8 | NA18962.hp1 NA18972.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-6851A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509532 | |||||||
| chr3:123509599 | C | T | 268 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(265): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.382-6918G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509599 | |||||||
| chr3:123509623 | T | C | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-6942A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509623 | |||||||
| chr3:123509641 | G | A | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-6960C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509641 | |||||||
| chr3:123509652 | C | A | 8 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0330 others(5): Show |
8 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.382-6971G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509652 | |||||||
| chr3:123509662 | C | A | 1 | a0001c0001t0006g0231 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.382-6981G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509662 | |||||||
| chr3:123509701 | G | A | 1 | a0001c0003t0005g0302 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.382-7020C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509701 | |||||||
| chr3:123509706 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.382-7025T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509706 | |||||||
| chr3:123509745 | C | T | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-7064G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509745 | |||||||
| chr3:123509787 | G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-7106C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509787 | |||||||
| chr3:123509863 | G | A | 3 | a0001c0003t0005g0300 a0001c0003t0005g0301 a0001c0003t0005g0302 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.382-7182C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509863 | |||||||
| chr3:123509864 | G | GGGAGAAG others(9): Show |
2 | a0001c0003t0003g0329 a0001c0003t0003g0336 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.382-7199_382-7184d others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509864 | |||||||
| chr3:123509940 | G | C | 2 | a0001c0001t0004g0109 a0001c0001t0004g0110 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.382-7259C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123509940 | |||||||
| chr3:123510333 | C | T | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-7652G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510333 | |||||||
| chr3:123510340 | C | T | 2 | a0001c0003t0003g0334 a0001c0003t0003g0335 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.382-7659G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510340 | |||||||
| chr3:123510341 | G | T | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-7660C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510341 | |||||||
| chr3:123510395 | C | G | 3 | a0001c0003t0003g0269 a0001c0003t0003g0270 a0001c0003t0003g0272 |
3 | HG02129.hp2 NA18962.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.382-7714G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510395 | |||||||
| chr3:123510456 | C | T | 6 | a0001c0002t0001g0014 a0001c0002t0001g0080 a0001c0002t0001g0085 others(3): Show |
6 | NA18959.hp1 NA18964.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.382-7775G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510456 | |||||||
| chr3:123510465 | C | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-7784G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510465 | |||||||
| chr3:123510473 | C | G | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-7792G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510473 | |||||||
| chr3:123510535 | A | C | 1 | a0001c0001t0002g0155 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.382-7854T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510535 | |||||||
| chr3:123510541 | G | A | 1 | a0001c0002t0020g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.382-7860C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510541 | |||||||
| chr3:123510631 | T | C | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-7950A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510631 | |||||||
| chr3:123510716 | G | T | 97 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(94): Show |
99 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.382-8035C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510716 | |||||||
| chr3:123510818 | T | A | 1 | a0001c0002t0001g0027 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.382-8137A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510818 | |||||||
| chr3:123510932 | GT | G | 257 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(254): Show |
263 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.382-8252delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510932 | |||||||
| chr3:123510932 | GTT | G | 58 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 others(55): Show |
60 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(57): Show |
intron_variant | MODIFIER | c.382-8253_382-8252d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510932 | |||||||
| chr3:123510932 | GTTT | G | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-8254_382-8252d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510932 | |||||||
| chr3:123510933 | T | G | 3 | a0001c0002t0001g0044 a0001c0002t0001g0089 a0001c0002t0001g0090 |
3 | HG03490.hp2 NA18972.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.382-8252A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510933 | |||||||
| chr3:123510934 | T | G | 109 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(106): Show |
111 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.382-8253A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510934 | |||||||
| chr3:123510935 | T | G | 1 | a0001c0003t0003g0331 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.382-8254A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510935 | |||||||
| chr3:123510944 | T | G | 5 | a0001c0001t0002g0129 a0001c0001t0006g0218 a0001c0001t0006g0244 others(2): Show |
5 | HG01358.hp2 HG02257.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-8263A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510944 | |||||||
| chr3:123510945 | G | T | 5 | a0001c0001t0002g0129 a0001c0001t0006g0218 a0001c0001t0006g0244 others(2): Show |
5 | HG01358.hp2 HG02257.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.382-8264C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510945 | |||||||
| chr3:123510955 | G | T | 1 | a0001c0001t0005g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.382-8274C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510955 | |||||||
| chr3:123510955 | GT | G | 81 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(78): Show |
83 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.382-8275delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510955 | |||||||
| chr3:123510955 | GTT | G | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-8276_382-8275d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510955 | |||||||
| chr3:123510956 | T | G | 1 | a0001c0001t0005g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.382-8275A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510956 | |||||||
| chr3:123510963 | T | G | 7 | a0001c0002t0008g0013 a0001c0002t0008g0065 a0001c0002t0008g0070 others(4): Show |
7 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-8282A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123510963 | |||||||
| chr3:123511007 | A | G | 93 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(90): Show |
95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-8326T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511007 | |||||||
| chr3:123511047 | G | C | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-8366C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511047 | |||||||
| chr3:123511159 | C | T | 4 | a0001c0001t0005g0139 a0001c0002t0005g0020 a0001c0002t0005g0021 others(1): Show |
4 | NA18994.hp2 NA19057.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-8478G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511159 | |||||||
| chr3:123511278 | T | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-8597A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511278 | |||||||
| chr3:123511496 | T | C | 7 | a0001c0002t0008g0013 a0001c0002t0008g0065 a0001c0002t0008g0070 others(4): Show |
7 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.382-8815A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511496 | |||||||
| chr3:123511618 | G | A | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-8937C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511618 | |||||||
| chr3:123511726 | G | A | 1 | a0001c0002t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.382-9045C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511726 | |||||||
| chr3:123511808 | C | G | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-9127G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511808 | |||||||
| chr3:123511930 | C | T | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.382-9249G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511930 | |||||||
| chr3:123511954 | C | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-9273G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123511954 | |||||||
| chr3:123512221 | C | T | 5 | a0001c0002t0005g0094 a0001c0002t0005g0095 a0001c0002t0005g0096 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.382-9540G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512221 | |||||||
| chr3:123512288 | G | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.382-9607C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512288 | |||||||
| chr3:123512305 | A | C | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-9624T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512305 | |||||||
| chr3:123512413 | C | T | 1 | a0001c0001t0004g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.382-9732G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512413 | |||||||
| chr3:123512487 | A | T | 97 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(94): Show |
99 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.382-9806T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512487 | |||||||
| chr3:123512883 | G | T | 4 | a0001c0001t0005g0139 a0001c0002t0005g0020 a0001c0002t0005g0021 others(1): Show |
4 | NA18994.hp2 NA19057.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.382-10202C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123512883 | |||||||
| chr3:123513058 | A | G | 107 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(104): Show |
111 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.382-10377T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513058 | |||||||
| chr3:123513287 | T | C | 93 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(90): Show |
95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-10606A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513287 | |||||||
| chr3:123513354 | C | G | 1 | a0001c0001t0006g0245 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.382-10673G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513354 | |||||||
| chr3:123513404 | T | C | 93 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(90): Show |
95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-10723A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513404 | |||||||
| chr3:123513470 | C | T | 1 | a0001c0003t0003g0294 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.382-10789G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513470 | |||||||
| chr3:123513789 | C | T | 1 | a0001c0001t0004g0188 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.382-11108G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513789 | |||||||
| chr3:123513846 | T | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.382-11165A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513846 | |||||||
| chr3:123513860 | G | C | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.382-11179C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123513860 | |||||||
| chr3:123514052 | A | T | 52 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(49): Show |
54 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(51): Show |
intron_variant | MODIFIER | c.382-11371T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514052 | |||||||
| chr3:123514100 | C | T | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-11419G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514100 | |||||||
| chr3:123514189 | C | T | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-11508G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514189 | |||||||
| chr3:123514350 | G | A | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.382-11669C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514350 | |||||||
| chr3:123514360 | T | C | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.382-11679A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514360 | |||||||
| chr3:123514361 | G | A | 1 | a0001c0001t0006g0238 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.382-11680C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514361 | |||||||
| chr3:123514419 | AATTGTTT others(3): Show |
A | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-11748_382-1173 others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514419 | |||||||
| chr3:123514429 | T | TA | 220 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(217): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.382-11749dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514429 | |||||||
| chr3:123514430 | A | C | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.382-11749T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514430 | |||||||
| chr3:123514480 | A | C | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.382-11799T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514480 | |||||||
| chr3:123514608 | T | C | 93 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(90): Show |
95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.382-11927A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514608 | |||||||
| chr3:123514926 | G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.382-12245C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123514926 | |||||||
| chr3:123515101 | T | C | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.382-12420A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515101 | |||||||
| chr3:123515113 | C | T | 1 | a0001c0002t0001g0054 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.382-12432G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515113 | |||||||
| chr3:123515138 | G | A | 46 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0118 others(43): Show |
47 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.382-12457C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515138 | |||||||
| chr3:123515202 | A | C | 2 | a0001c0003t0010g0338 a0001c0003t0010g0339 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.382-12521T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515202 | |||||||
| chr3:123515267 | T | C | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.382-12586A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515267 | |||||||
| chr3:123515274 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.382-12593A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515274 | |||||||
| chr3:123515290 | C | G | 2 | a0001c0002t0001g0014 a0001c0002t0001g0080 |
2 | NA18959.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.382-12609G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515290 | |||||||
| chr3:123515623 | C | A | 1 | a0001c0002t0001g0052 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.381+12763G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515623 | |||||||
| chr3:123515625 | T | G | 2 | a0001c0001t0006g0226 a0001c0001t0006g0232 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.381+12761A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515625 | |||||||
| chr3:123515715 | T | C | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.381+12671A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515715 | |||||||
| chr3:123515724 | A | T | 1 | a0001c0003t0003g0264 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.381+12662T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515724 | |||||||
| chr3:123515744 | T | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381+12642A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515744 | |||||||
| chr3:123515757 | G | T | 111 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(108): Show |
113 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.381+12629C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515757 | |||||||
| chr3:123515900 | G | A | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+12486C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515900 | |||||||
| chr3:123515917 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.381+12469G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515917 | |||||||
| chr3:123515947 | A | G | 1 | a0001c0002t0005g0097 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.381+12439T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515947 | |||||||
| chr3:123515949 | G | A | 1 | a0001c0001t0002g0124 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.381+12437C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515949 | |||||||
| chr3:123515989 | A | G | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+12397T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123515989 | |||||||
| chr3:123516135 | G | C | 1 | a0001c0003t0003g0295 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.381+12251C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516135 | |||||||
| chr3:123516164 | T | C | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+12222A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516164 | |||||||
| chr3:123516213 | G | C | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+12173C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516213 | |||||||
| chr3:123516233 | A | AT | 13 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0225 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+12152dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516233 | |||||||
| chr3:123516233 | A | ATTT | 8 | a0001c0001t0013g0116 a0001c0003t0007g0305 a0001c0003t0007g0306 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+12150_381+1215 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516233 | |||||||
| chr3:123516233 | AT | A | 57 | a0001c0001t0002g0143 a0001c0001t0002g0170 a0001c0001t0003g0112 others(54): Show |
59 | HG00544.hp2 HG00642.hp1 HG01109.hp1 others(56): Show |
intron_variant | MODIFIER | c.381+12152delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516233 | |||||||
| chr3:123516233 | ATT | A | 212 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(209): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.381+12151_381+1215 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516233 | |||||||
| chr3:123516380 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.381+12006C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516380 | |||||||
| chr3:123516383 | C | T | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+12003G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516383 | |||||||
| chr3:123516542 | A | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+11844T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516542 | |||||||
| chr3:123516555 | A | C | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+11831T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516555 | |||||||
| chr3:123516625 | G | A | 1 | a0001c0001t0002g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.381+11761C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516625 | |||||||
| chr3:123516782 | C | G | 1 | a0001c0002t0001g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.381+11604G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516782 | |||||||
| chr3:123516858 | T | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+11528A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516858 | |||||||
| chr3:123516863 | G | A | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+11523C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123516863 | |||||||
| chr3:123517053 | T | C | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+11333A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517053 | |||||||
| chr3:123517276 | T | C | 1 | a0001c0001t0019g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.381+11110A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517276 | |||||||
| chr3:123517359 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+11027G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517359 | |||||||
| chr3:123517371 | G | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+11015C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517371 | |||||||
| chr3:123517498 | T | C | 1 | a0001c0003t0024g0326 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.381+10888A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517498 | |||||||
| chr3:123517546 | A | T | 1 | a0001c0001t0004g0205 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.381+10840T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517546 | |||||||
| chr3:123517899 | TAAAAATA others(308): Show |
T | 313 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.381+10172_381+1048 others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123517899 | |||||||
| chr3:123518191 | C | CAA | 9 | a0001c0001t0006g0219 a0001c0001t0006g0225 a0001c0001t0006g0226 others(6): Show |
9 | HG01167.hp1 HG01243.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.381+10193_381+1019 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518191 | |||||||
| chr3:123518338 | C | G | 42 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(39): Show |
42 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.381+10048G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518338 | |||||||
| chr3:123518368 | T | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+10018A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518368 | |||||||
| chr3:123518433 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+9953G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518433 | |||||||
| chr3:123518521 | AGTTATTT others(6): Show |
A | 4 | a0001c0003t0003g0260 a0001c0003t0003g0263 a0001c0003t0003g0271 others(1): Show |
4 | HG02080.hp2 HG02083.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+9852_381+9864d others(15): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518521 | |||||||
| chr3:123518551 | A | T | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+9835T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518551 | |||||||
| chr3:123518654 | A | T | 1 | a0001c0002t0005g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.381+9732T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518654 | |||||||
| chr3:123518670 | A | G | 110 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(107): Show |
114 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.381+9716T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518670 | |||||||
| chr3:123518905 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.381+9481C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518905 | |||||||
| chr3:123518945 | C | T | 1 | a0001c0003t0003g0294 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.381+9441G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518945 | |||||||
| chr3:123518952 | G | A | 1 | a0001c0002t0002g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.381+9434C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518952 | |||||||
| chr3:123518993 | A | G | 1 | a0001c0002t0003g0075 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.381+9393T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518993 | |||||||
| chr3:123518995 | T | TA | 18 | a0001c0001t0002g0145 a0001c0001t0002g0155 a0001c0001t0002g0161 others(15): Show |
18 | HG00140.hp1 HG00735.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.381+9390dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518995 | |||||||
| chr3:123518995 | TA | T | 145 | a0001c0001t0002g0133 a0001c0001t0002g0144 a0001c0001t0002g0221 others(142): Show |
148 | HG00423.hp2 HG00544.hp2 HG00558.hp2 others(145): Show |
intron_variant | MODIFIER | c.381+9390delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123518995 | |||||||
| chr3:123519086 | T | C | 2 | a0001c0001t0005g0113 a0001c0001t0005g0114 |
2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.381+9300A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519086 | |||||||
| chr3:123519209 | T | C | 1 | a0001c0003t0001g0318 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.381+9177A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519209 | |||||||
| chr3:123519267 | C | T | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.381+9119G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519267 | |||||||
| chr3:123519664 | G | A | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+8722C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519664 | |||||||
| chr3:123519805 | G | A | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+8581C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519805 | |||||||
| chr3:123519890 | T | C | 1 | a0001c0001t0004g0206 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.381+8496A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519890 | |||||||
| chr3:123519902 | A | G | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.381+8484T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519902 | |||||||
| chr3:123519935 | A | T | 2 | a0001c0003t0003g0256 a0001c0003t0003g0258 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.381+8451T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123519935 | |||||||
| chr3:123520012 | G | T | 1 | a0001c0003t0009g0267 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.381+8374C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520012 | |||||||
| chr3:123520096 | C | T | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+8290G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520096 | |||||||
| chr3:123520099 | G | A | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.381+8287C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520099 | |||||||
| chr3:123520343 | C | T | 1 | a0001c0002t0001g0010 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.381+8043G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520343 | |||||||
| chr3:123520403 | T | G | 1 | a0001c0001t0002g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.381+7983A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520403 | |||||||
| chr3:123520518 | C | A | 1 | a0001c0002t0001g0035 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.381+7868G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520518 | |||||||
| chr3:123520571 | A | G | 3 | a0001c0002t0008g0072 a0001c0002t0008g0077 a0001c0002t0008g0078 |
3 | HG02559.hp1 HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.381+7815T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123520571 | |||||||
| chr3:123521106 | T | C | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.381+7280A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521106 | |||||||
| chr3:123521152 | A | C | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+7234T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521152 | |||||||
| chr3:123521256 | C | T | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+7130G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521256 | |||||||
| chr3:123521283 | T | C | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.381+7103A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521283 | |||||||
| chr3:123521416 | C | G | 27 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+6970G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521416 | |||||||
| chr3:123521449 | C | T | 1 | a0001c0002t0020g0056 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.381+6937G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521449 | |||||||
| chr3:123521568 | A | G | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 |
3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.381+6818T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521568 | |||||||
| chr3:123521600 | C | CA | 13 | a0001c0001t0004g0110 a0001c0001t0013g0115 a0001c0001t0013g0116 others(10): Show |
13 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.381+6785dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521600 | |||||||
| chr3:123521600 | CA | C | 34 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(31): Show |
34 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.381+6785delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521600 | |||||||
| chr3:123521634 | T | G | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+6752A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521634 | |||||||
| chr3:123521698 | G | C | 1 | a0001c0003t0003g0258 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.381+6688C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521698 | |||||||
| chr3:123521749 | A | G | 4 | a0001c0002t0004g0002 a0001c0002t0004g0099 a0001c0002t0004g0102 others(1): Show |
5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+6637T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521749 | |||||||
| chr3:123521874 | T | C | 1 | a0001c0003t0003g0255 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.381+6512A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521874 | |||||||
| chr3:123521906 | CA | C | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+6479delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123521906 | |||||||
| chr3:123522332 | C | CA | 131 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(128): Show |
135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.381+6053dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522332 | |||||||
| chr3:123522332 | C | CAA | 52 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(49): Show |
54 | HG00544.hp2 HG00738.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.381+6052_381+6053d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522332 | |||||||
| chr3:123522337 | A | AG | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.381+6048_381+6049i others(3): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522337 | |||||||
| chr3:123522348 | A | G | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+6038T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522348 | |||||||
| chr3:123522349 | AG | A | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+6036delC | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522349 | |||||||
| chr3:123522433 | A | T | 111 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(108): Show |
115 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.381+5953T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522433 | |||||||
| chr3:123522455 | G | C | 2 | a0001c0003t0005g0301 a0001c0003t0005g0302 |
2 | HG02258.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.381+5931C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522455 | |||||||
| chr3:123522581 | A | G | 327 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(324): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.381+5805T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522581 | |||||||
| chr3:123522657 | G | A | 1 | a0001c0001t0006g0244 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.381+5729C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522657 | |||||||
| chr3:123522662 | C | CT | 147 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0248 others(144): Show |
151 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.381+5723dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522662 | |||||||
| chr3:123522662 | C | CTT | 94 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(91): Show |
96 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.381+5722_381+5723d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522662 | |||||||
| chr3:123522741 | A | T | 3 | a0001c0003t0003g0256 a0001c0003t0003g0257 a0001c0003t0003g0258 |
3 | HG01109.hp1 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.381+5645T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522741 | |||||||
| chr3:123522875 | T | C | 27 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+5511A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123522875 | |||||||
| chr3:123523161 | A | G | 25 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.381+5225T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523161 | |||||||
| chr3:123523243 | A | C | 5 | a0001c0002t0005g0094 a0001c0002t0005g0095 a0001c0002t0005g0096 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+5143T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523243 | |||||||
| chr3:123523253 | C | T | 3 | a0001c0001t0001g0150 a0001c0002t0001g0038 a0001c0002t0001g0039 |
3 | HG00423.hp2 HG00738.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.381+5133G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523253 | |||||||
| chr3:123523254 | G | A | 5 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.381+5132C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523254 | |||||||
| chr3:123523262 | G | C | 6 | a0001c0002t0001g0014 a0001c0002t0001g0080 a0001c0002t0001g0085 others(3): Show |
6 | NA18959.hp1 NA18964.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.381+5124C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523262 | |||||||
| chr3:123523373 | G | A | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+5013C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523373 | |||||||
| chr3:123523427 | T | C | 10 | a0001c0001t0006g0219 a0001c0001t0006g0225 a0001c0001t0006g0226 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.381+4959A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523427 | |||||||
| chr3:123523698 | G | A | 2 | a0001c0003t0003g0332 a0001c0003t0003g0333 |
2 | HG02280.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.381+4688C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523698 | |||||||
| chr3:123523777 | C | T | 1 | a0001c0003t0003g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.381+4609G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123523777 | |||||||
| chr3:123524052 | A | C | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.381+4334T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524052 | |||||||
| chr3:123524312 | G | A | 1 | a0001c0001t0006g0250 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.381+4074C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524312 | |||||||
| chr3:123524376 | G | C | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.381+4010C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524376 | |||||||
| chr3:123524535 | C | T | 1 | a0001c0001t0018g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.381+3851G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524535 | |||||||
| chr3:123524579 | C | T | 108 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(105): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.381+3807G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524579 | |||||||
| chr3:123524606 | C | T | 1 | a0001c0003t0005g0302 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.381+3780G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524606 | |||||||
| chr3:123524797 | T | C | 2 | a0001c0002t0005g0074 a0001c0002t0005g0076 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.381+3589A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524797 | |||||||
| chr3:123524827 | T | C | 4 | a0001c0002t0004g0002 a0001c0002t0004g0099 a0001c0002t0004g0102 others(1): Show |
5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.381+3559A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524827 | |||||||
| chr3:123524968 | G | A | 33 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(30): Show |
33 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.381+3418C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524968 | |||||||
| chr3:123524980 | C | T | 220 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(217): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.381+3406G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123524980 | |||||||
| chr3:123525190 | A | G | 1 | a0001c0001t0002g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.381+3196T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525190 | |||||||
| chr3:123525269 | A | T | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.381+3117T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525269 | |||||||
| chr3:123525404 | C | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.381+2982G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525404 | |||||||
| chr3:123525481 | A | C | 1 | a0001c0002t0005g0066 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.381+2905T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525481 | |||||||
| chr3:123525644 | A | G | 1 | a0001c0001t0004g0187 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.381+2742T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525644 | |||||||
| chr3:123525722 | A | G | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381+2664T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525722 | |||||||
| chr3:123525749 | T | C | 1 | a0001c0003t0010g0337 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.381+2637A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123525749 | |||||||
| chr3:123526022 | C | T | 25 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.381+2364G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526022 | |||||||
| chr3:123526041 | GAGCAAGC others(47): Show |
G | 3 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0001g0325 |
3 | HG02965.hp1 HG03017.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+2291_381+2344d others(56): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526041 | |||||||
| chr3:123526262 | A | G | 27 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.381+2124T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526262 | |||||||
| chr3:123526264 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0151 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.381+2122C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526264 | |||||||
| chr3:123526305 | G | A | 112 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(109): Show |
116 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.381+2081C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526305 | |||||||
| chr3:123526527 | CTTTTCCT others(10): Show |
C | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.381+1842_381+1858d others(19): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526527 | |||||||
| chr3:123526533 | CTT | C | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.381+1851_381+1852d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526533 | |||||||
| chr3:123526627 | G | T | 219 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.381+1759C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526627 | |||||||
| chr3:123526628 | T | G | 219 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(216): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.381+1758A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123526628 | |||||||
| chr3:123527155 | C | T | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.381+1231G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527155 | |||||||
| chr3:123527230 | T | C | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.381+1156A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527230 | |||||||
| chr3:123527250 | G | A | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+1136C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527250 | |||||||
| chr3:123527278 | C | T | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+1108G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527278 | |||||||
| chr3:123527592 | G | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.381+794C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527592 | |||||||
| chr3:123527639 | G | C | 1 | a0001c0003t0003g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.381+747C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527639 | |||||||
| chr3:123527663 | T | C | 1 | a0001c0001t0019g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.381+723A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527663 | |||||||
| chr3:123527731 | G | T | 71 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(68): Show |
72 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.381+655C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527731 | |||||||
| chr3:123527790 | T | C | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.381+596A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527790 | |||||||
| chr3:123527831 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.381+555C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527831 | |||||||
| chr3:123527874 | C | T | 73 | a0001c0001t0009g0138 a0001c0001t0013g0115 a0001c0001t0013g0116 others(70): Show |
74 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.381+512G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527874 | |||||||
| chr3:123527931 | C | T | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.381+455G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123527931 | |||||||
| chr3:123528304 | T | C | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.381+82A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123528304 | |||||||
| chr3:123528367 | G | A | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.381+19C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123528367 | |||||||
| chr3:123528374 | A | G | 2 | a0001c0001t0002g0003 a0001c0001t0002g0145 |
3 | NA18994.hp1 NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.381+12T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 4/6 | chr3 | 123528374 | |||||||
| chr3:123528522 | C | T | 6 | a0001c0002t0001g0014 a0001c0002t0001g0080 a0001c0002t0001g0085 others(3): Show |
6 | NA18959.hp1 NA18964.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-48G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123528522 | |||||||
| chr3:123528607 | T | C | 93 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(90): Show |
95 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(92): Show |
intron_variant | MODIFIER | c.293-133A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123528607 | |||||||
| chr3:123528630 | T | C | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-156A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123528630 | |||||||
| chr3:123528767 | T | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-293A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123528767 | |||||||
| chr3:123529006 | CT | C | 274 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(271): Show |
282 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.293-533delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529006 | |||||||
| chr3:123529006 | CTT | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-534_293-533del others(2): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529006 | |||||||
| chr3:123529008 | T | C | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-534A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529008 | |||||||
| chr3:123529241 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-767G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529241 | |||||||
| chr3:123529329 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.293-855A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529329 | |||||||
| chr3:123529596 | C | T | 71 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(68): Show |
72 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.293-1122G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529596 | |||||||
| chr3:123529800 | G | A | 2 | a0001c0001t0009g0138 a0001c0002t0009g0100 |
2 | NA18939.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.293-1326C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529800 | |||||||
| chr3:123529817 | G | A | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-1343C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529817 | |||||||
| chr3:123529893 | GA | G | 5 | a0001c0002t0005g0094 a0001c0002t0005g0095 a0001c0002t0005g0096 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-1420delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529893 | |||||||
| chr3:123529924 | A | T | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-1450T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123529924 | |||||||
| chr3:123530046 | T | G | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1572A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530046 | |||||||
| chr3:123530054 | C | A | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1580G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530054 | |||||||
| chr3:123530056 | A | C | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1582T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530056 | |||||||
| chr3:123530058 | T | C | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1584A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530058 | |||||||
| chr3:123530061 | G | A | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1587C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530061 | |||||||
| chr3:123530064 | A | T | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1590T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530064 | |||||||
| chr3:123530081 | T | A | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1607A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530081 | |||||||
| chr3:123530082 | A | G | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1608T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530082 | |||||||
| chr3:123530083 | A | ACATTAGT others(30): Show |
1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1610_293-1609i others(39): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530083 | |||||||
| chr3:123530100 | T | C | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1626A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530100 | |||||||
| chr3:123530111 | G | A | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1637C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530111 | |||||||
| chr3:123530115 | GATTAATG others(38): Show |
G | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1686_293-1642d others(47): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530115 | |||||||
| chr3:123530125 | G | A | 1 | a0001c0003t0003g0260 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.293-1651C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530125 | |||||||
| chr3:123530141 | C | T | 1 | a0001c0001t0004g0181 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.293-1667G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530141 | |||||||
| chr3:123530167 | A | T | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1693T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530167 | |||||||
| chr3:123530177 | A | G | 1 | a0001c0002t0009g0086 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.293-1703T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530177 | |||||||
| chr3:123530261 | A | T | 5 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-1787T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530261 | |||||||
| chr3:123530394 | C | T | 1 | a0001c0003t0003g0295 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.293-1920G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530394 | |||||||
| chr3:123530408 | A | AT | 101 | a0001c0001t0002g0132 a0001c0001t0003g0112 a0001c0001t0003g0154 others(98): Show |
103 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.293-1935dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530408 | |||||||
| chr3:123530408 | A | T | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.293-1934T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530408 | |||||||
| chr3:123530433 | G | A | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293-1959C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530433 | |||||||
| chr3:123530554 | A | G | 1 | a0001c0002t0001g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.293-2080T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530554 | |||||||
| chr3:123530615 | G | A | 1 | a0001c0002t0001g0082 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.293-2141C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530615 | |||||||
| chr3:123530663 | T | G | 1 | a0001c0002t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.293-2189A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530663 | |||||||
| chr3:123530696 | T | A | 107 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(104): Show |
109 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.293-2222A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530696 | |||||||
| chr3:123530702 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-2228G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530702 | |||||||
| chr3:123530781 | A | G | 92 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(89): Show |
94 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.293-2307T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530781 | |||||||
| chr3:123530862 | TTTG | T | 3 | a0001c0001t0004g0164 a0001c0001t0004g0183 a0001c0001t0004g0184 |
3 | NA18949.hp2 NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.293-2391_293-2389d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530862 | |||||||
| chr3:123530895 | T | G | 1 | a0001c0002t0005g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.293-2421A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530895 | |||||||
| chr3:123530907 | G | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.293-2433C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123530907 | |||||||
| chr3:123531317 | TTTTTC | T | 108 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(105): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.293-2848_293-2844d others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123531317 | |||||||
| chr3:123531406 | G | A | 1 | a0001c0003t0005g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.293-2932C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123531406 | |||||||
| chr3:123531468 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-2994G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123531468 | |||||||
| chr3:123532075 | C | G | 14 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0080 others(11): Show |
14 | NA18959.hp1 NA18962.hp1 NA18964.hp2 others(11): Show |
intron_variant | MODIFIER | c.293-3601G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532075 | |||||||
| chr3:123532137 | A | G | 2 | a0001c0001t0002g0193 a0001c0003t0003g0006 |
3 | HG01256.hp1 NA18939.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.293-3663T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532137 | |||||||
| chr3:123532150 | A | G | 2 | a0001c0003t0003g0256 a0001c0003t0003g0258 |
2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-3676T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532150 | |||||||
| chr3:123532275 | C | T | 2 | a0001c0002t0005g0074 a0001c0002t0005g0076 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.293-3801G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532275 | |||||||
| chr3:123532391 | T | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-3917A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532391 | |||||||
| chr3:123532407 | T | C | 1 | a0001c0002t0001g0024 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.293-3933A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532407 | |||||||
| chr3:123532432 | G | C | 1 | a0001c0003t0003g0292 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.293-3958C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532432 | |||||||
| chr3:123532435 | T | G | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.293-3961A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532435 | |||||||
| chr3:123532445 | A | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293-3971T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532445 | |||||||
| chr3:123532552 | C | T | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.293-4078G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532552 | |||||||
| chr3:123532566 | T | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-4092A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532566 | |||||||
| chr3:123532569 | G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-4095C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532569 | |||||||
| chr3:123532670 | T | A | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.293-4196A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532670 | |||||||
| chr3:123532705 | A | G | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-4231T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532705 | |||||||
| chr3:123532783 | G | A | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-4309C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532783 | |||||||
| chr3:123532784 | A | C | 1 | a0001c0003t0003g0262 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.293-4310T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532784 | |||||||
| chr3:123532826 | T | C | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-4352A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532826 | |||||||
| chr3:123532833 | C | CA | 15 | a0001c0001t0002g0167 a0001c0001t0006g0233 a0001c0001t0006g0236 others(12): Show |
15 | HG01109.hp2 HG02080.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.293-4360dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532833 | |||||||
| chr3:123532833 | CA | C | 194 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(191): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.293-4360delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532833 | |||||||
| chr3:123532833 | CAA | C | 10 | a0001c0001t0002g0171 a0001c0001t0004g0109 a0001c0001t0013g0115 others(7): Show |
10 | HG01168.hp1 HG01168.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-4361_293-4360d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532833 | |||||||
| chr3:123532833 | CAAA | C | 13 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(10): Show |
13 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.293-4362_293-4360d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532833 | |||||||
| chr3:123532917 | T | C | 1 | a0001c0002t0005g0067 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.293-4443A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532917 | |||||||
| chr3:123532946 | A | G | 25 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.293-4472T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123532946 | |||||||
| chr3:123533059 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.293-4585C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533059 | |||||||
| chr3:123533114 | G | C | 265 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(262): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.293-4640C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533114 | |||||||
| chr3:123533118 | T | A | 1 | a0001c0002t0001g0029 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.293-4644A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533118 | |||||||
| chr3:123533213 | ATCATGGC others(11): Show |
A | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-4757_293-4740d others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533213 | |||||||
| chr3:123533321 | G | A | 1 | a0001c0001t0015g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.293-4847C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533321 | |||||||
| chr3:123533349 | A | G | 1 | a0001c0003t0005g0301 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.293-4875T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533349 | |||||||
| chr3:123533377 | A | G | 1 | a0001c0001t0002g0157 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.293-4903T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533377 | |||||||
| chr3:123533395 | C | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-4921G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533395 | |||||||
| chr3:123533428 | C | T | 33 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(30): Show |
33 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.293-4954G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533428 | |||||||
| chr3:123533443 | T | G | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293-4969A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533443 | |||||||
| chr3:123533800 | C | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-5326G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123533800 | |||||||
| chr3:123534029 | A | AGT | 224 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(221): Show |
231 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.293-5557_293-5556d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | |||||||
| chr3:123534029 | A | AGTGT | 36 | a0001c0001t0002g0124 a0001c0001t0002g0130 a0001c0001t0002g0136 others(33): Show |
36 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.293-5559_293-5556d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | |||||||
| chr3:123534029 | A | AGTGTGT | 31 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(28): Show |
32 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.293-5561_293-5556d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | |||||||
| chr3:123534029 | A | AGTGTGTG others(1): Show |
5 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-5563_293-5556d others(10): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | |||||||
| chr3:123534029 | A | AGTGTGTG others(3): Show |
3 | a0001c0003t0005g0300 a0001c0003t0005g0301 a0001c0003t0005g0302 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.293-5565_293-5556d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534029 | |||||||
| chr3:123534153 | A | G | 45 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(42): Show |
45 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.293-5679T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534153 | |||||||
| chr3:123534366 | C | T | 27 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-5892G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534366 | |||||||
| chr3:123534721 | G | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.293-6247C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534721 | |||||||
| chr3:123534793 | T | C | 3 | a0001c0003t0005g0300 a0001c0003t0005g0301 a0001c0003t0005g0302 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.293-6319A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534793 | |||||||
| chr3:123534798 | T | TTGTGTGT others(7): Show |
49 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0002t0003g0075 others(46): Show |
51 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(48): Show |
intron_variant | MODIFIER | c.293-6338_293-6325d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | |||||||
| chr3:123534798 | T | TTGTGTGT others(9): Show |
236 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(233): Show |
242 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.293-6325_293-6324i others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | |||||||
| chr3:123534798 | T | TTGTGTGT others(11): Show |
11 | a0001c0001t0002g0201 a0001c0001t0002g0213 a0001c0001t0002g0220 others(8): Show |
11 | HG01516.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.293-6325_293-6324i others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | |||||||
| chr3:123534798 | T | TTGTGTGT others(13): Show |
3 | a0001c0001t0013g0115 a0001c0003t0014g0298 a0001c0003t0014g0299 |
3 | HG02055.hp1 HG02965.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-6325_293-6324i others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | |||||||
| chr3:123534798 | T | TTGTGTGT others(15): Show |
8 | a0001c0001t0013g0116 a0001c0003t0007g0305 a0001c0003t0007g0306 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-6325_293-6324i others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | |||||||
| chr3:123534798 | T | TTGTGTGT others(17): Show |
1 | a0001c0003t0007g0310 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.293-6325_293-6324i others(26): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | |||||||
| chr3:123534798 | T | TTGTGTGT others(19): Show |
2 | a0001c0003t0010g0338 a0001c0003t0010g0339 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.293-6325_293-6324i others(28): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | |||||||
| chr3:123534798 | T | TTGTGTGT others(23): Show |
2 | a0001c0003t0010g0337 a0001c0003t0010g0340 |
2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.293-6325_293-6324i others(32): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534798 | |||||||
| chr3:123534877 | T | C | 20 | a0001c0001t0002g0117 a0001c0001t0002g0122 a0001c0001t0002g0123 others(17): Show |
20 | HG00423.hp1 HG00558.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.293-6403A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123534877 | |||||||
| chr3:123535068 | G | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.293-6594C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535068 | |||||||
| chr3:123535219 | G | A | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-6745C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535219 | |||||||
| chr3:123535264 | G | A | 1 | a0001c0003t0009g0267 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.293-6790C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535264 | |||||||
| chr3:123535351 | A | G | 27 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-6877T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535351 | |||||||
| chr3:123535352 | T | C | 1 | a0001c0002t0001g0080 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.293-6878A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535352 | |||||||
| chr3:123535670 | G | T | 3 | a0001c0003t0005g0300 a0001c0003t0005g0301 a0001c0003t0005g0302 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.293-7196C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535670 | |||||||
| chr3:123535752 | T | C | 327 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(324): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.293-7278A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535752 | |||||||
| chr3:123535763 | A | G | 1 | a0001c0002t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.293-7289T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535763 | |||||||
| chr3:123535907 | G | T | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-7433C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535907 | |||||||
| chr3:123535985 | T | C | 1 | a0001c0001t0002g0161 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.293-7511A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123535985 | |||||||
| chr3:123536186 | C | T | 2 | a0001c0001t0004g0180 a0001c0001t0004g0182 |
2 | HG00642.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.293-7712G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536186 | |||||||
| chr3:123536281 | G | A | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-7807C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536281 | |||||||
| chr3:123536326 | G | A | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-7852C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536326 | |||||||
| chr3:123536515 | C | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-8041G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536515 | |||||||
| chr3:123536640 | A | G | 1 | a0001c0003t0024g0326 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.293-8166T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536640 | |||||||
| chr3:123536649 | G | T | 1 | a0001c0003t0001g0328 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.293-8175C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536649 | |||||||
| chr3:123536651 | C | T | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-8177G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536651 | |||||||
| chr3:123536756 | A | G | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-8282T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536756 | |||||||
| chr3:123536896 | G | A | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-8422C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536896 | |||||||
| chr3:123536908 | C | T | 4 | a0001c0002t0004g0002 a0001c0002t0004g0099 a0001c0002t0004g0102 others(1): Show |
5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-8434G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536908 | |||||||
| chr3:123536930 | G | A | 35 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.293-8456C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536930 | |||||||
| chr3:123536996 | G | A | 4 | a0001c0003t0003g0260 a0001c0003t0003g0263 a0001c0003t0003g0271 others(1): Show |
4 | HG02080.hp2 HG02083.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-8522C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123536996 | |||||||
| chr3:123537042 | T | C | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | NA18966.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.293-8568A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537042 | |||||||
| chr3:123537074 | A | G | 8 | a0001c0002t0001g0015 a0001c0002t0001g0081 a0001c0002t0001g0082 others(5): Show |
8 | NA18962.hp1 NA18972.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-8600T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537074 | |||||||
| chr3:123537108 | A | G | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-8634T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537108 | |||||||
| chr3:123537110 | A | G | 3 | a0001c0003t0005g0300 a0001c0003t0005g0301 a0001c0003t0005g0302 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.293-8636T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537110 | |||||||
| chr3:123537279 | A | C | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.293-8805T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537279 | |||||||
| chr3:123537329 | A | G | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-8855T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537329 | |||||||
| chr3:123537331 | C | T | 1 | a0001c0001t0002g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.293-8857G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537331 | |||||||
| chr3:123537418 | A | T | 4 | a0001c0001t0006g0238 a0001c0001t0006g0241 a0001c0001t0006g0245 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-8944T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537418 | |||||||
| chr3:123537556 | C | T | 220 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(217): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.293-9082G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537556 | |||||||
| chr3:123537576 | AATACAC | A | 11 | a0001c0001t0005g0139 a0001c0001t0005g0173 a0001c0002t0005g0020 others(8): Show |
11 | HG00673.hp2 HG01109.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.293-9108_293-9103d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537576 | |||||||
| chr3:123537578 | T | TAC | 73 | a0001c0001t0001g0248 a0001c0001t0001g0249 a0001c0001t0002g0162 others(70): Show |
76 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.293-9106_293-9105d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | |||||||
| chr3:123537578 | T | TACAC | 16 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0222 others(13): Show |
16 | HG01884.hp2 HG01928.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-9108_293-9105d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | |||||||
| chr3:123537578 | T | TACACACA others(3): Show |
1 | a0001c0003t0014g0299 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.293-9105_293-9104i others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | |||||||
| chr3:123537578 | T | TACACACA others(7): Show |
1 | a0001c0003t0007g0305 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.293-9105_293-9104i others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | |||||||
| chr3:123537578 | T | TACACACA others(9): Show |
7 | a0001c0003t0007g0306 a0001c0003t0007g0307 a0001c0003t0007g0308 others(4): Show |
7 | HG00099.hp1 HG00642.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-9105_293-9104i others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | |||||||
| chr3:123537578 | TACACATA others(3): Show |
T | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-9114_293-9105d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537578 | |||||||
| chr3:123537580 | CACAT | C | 16 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0199 others(13): Show |
16 | HG00639.hp2 HG00738.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.293-9110_293-9107d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537580 | |||||||
| chr3:123537582 | CAT | C | 20 | a0001c0001t0006g0219 a0001c0001t0006g0225 a0001c0001t0006g0226 others(17): Show |
20 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.293-9110_293-9109d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537582 | |||||||
| chr3:123537584 | T | C | 232 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(229): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.293-9110A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537584 | |||||||
| chr3:123537627 | A | T | 1 | a0001c0003t0003g0285 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.293-9153T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537627 | |||||||
| chr3:123537630 | AT | A | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-9157delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537630 | |||||||
| chr3:123537884 | AATC | A | 27 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-9413_293-9411d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537884 | |||||||
| chr3:123537921 | T | C | 2 | a0001c0003t0007g0308 a0001c0003t0007g0309 |
2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.293-9447A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537921 | |||||||
| chr3:123537963 | A | C | 2 | a0001c0003t0007g0308 a0001c0003t0007g0309 |
2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.293-9489T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123537963 | |||||||
| chr3:123538053 | A | G | 1 | a0001c0001t0006g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.293-9579T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538053 | |||||||
| chr3:123538218 | T | C | 4 | a0001c0002t0004g0002 a0001c0002t0004g0099 a0001c0002t0004g0102 others(1): Show |
5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-9744A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538218 | |||||||
| chr3:123538258 | T | C | 108 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(105): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.293-9784A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538258 | |||||||
| chr3:123538623 | A | G | 1 | a0001c0001t0006g0250 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.293-10149T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538623 | |||||||
| chr3:123538635 | C | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02071.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.293-10161G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538635 | |||||||
| chr3:123538666 | T | C | 108 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0108 others(105): Show |
112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.293-10192A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538666 | |||||||
| chr3:123538747 | C | T | 1 | a0001c0002t0001g0045 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.293-10273G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538747 | |||||||
| chr3:123538862 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0129 a0001c0001t0002g0135 |
3 | HG01346.hp2 HG01358.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.293-10388C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123538862 | |||||||
| chr3:123539154 | T | C | 220 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(217): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.293-10680A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539154 | |||||||
| chr3:123539364 | G | A | 71 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(68): Show |
72 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.293-10890C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539364 | |||||||
| chr3:123539493 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.293-11019G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539493 | |||||||
| chr3:123539513 | T | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0145 |
3 | NA18994.hp1 NA18995.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.293-11039A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539513 | |||||||
| chr3:123539564 | G | T | 1 | a0001c0002t0001g0022 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.293-11090C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539564 | |||||||
| chr3:123539613 | C | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.293-11139G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539613 | |||||||
| chr3:123539911 | T | TA | 32 | a0001c0001t0002g0251 a0001c0001t0006g0218 a0001c0001t0006g0219 others(29): Show |
32 | HG00099.hp1 HG00642.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.293-11438dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123539911 | T | TAA | 57 | a0001c0001t0004g0205 a0001c0001t0006g0226 a0001c0001t0009g0138 others(54): Show |
58 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.293-11439_293-1143 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123539911 | T | TAAA | 67 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(64): Show |
68 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.293-11440_293-1143 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123539911 | T | TAAAA | 55 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(52): Show |
58 | HG00140.hp2 HG00323.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.293-11441_293-1143 others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123539911 | T | TAAAAA | 18 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0127 others(15): Show |
18 | HG00423.hp1 HG00544.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.293-11442_293-1143 others(9): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123539911 | T | TAAAAAA | 9 | a0001c0001t0002g0172 a0001c0001t0002g0174 a0001c0001t0002g0191 others(6): Show |
9 | HG00140.hp1 HG01071.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.293-11443_293-1143 others(10): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123539911 | T | TAAAAAAA others(1): Show |
8 | a0001c0001t0002g0005 a0001c0003t0003g0327 a0001c0003t0003g0329 others(5): Show |
9 | HG01070.hp2 HG01081.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-11445_293-1143 others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123539911 | T | TAAAAAAA others(3): Show |
1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.293-11447_293-1143 others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123539911 | TA | T | 25 | a0001c0001t0003g0154 a0001c0001t0015g0223 a0001c0001t0015g0224 others(22): Show |
27 | HG00639.hp2 HG01109.hp1 HG02080.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-11438delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123539911 | TAAAAAAA others(3): Show |
T | 4 | a0001c0002t0001g0081 a0001c0002t0001g0082 a0001c0002t0001g0084 others(1): Show |
4 | NA18982.hp2 NA19002.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-11447_293-1143 others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123539911 | |||||||
| chr3:123540007 | G | A | 1 | a0001c0001t0002g0144 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.293-11533C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540007 | |||||||
| chr3:123540235 | C | T | 45 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(42): Show |
45 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.293-11761G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540235 | |||||||
| chr3:123540423 | T | C | 1 | a0001c0001t0006g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.293-11949A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540423 | |||||||
| chr3:123540490 | A | G | 1 | a0001c0001t0005g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.293-12016T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540490 | |||||||
| chr3:123540492 | G | C | 4 | a0001c0002t0001g0016 a0001c0002t0001g0024 a0001c0002t0001g0048 others(1): Show |
4 | NA18973.hp2 NA18983.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-12018C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540492 | |||||||
| chr3:123540512 | C | T | 5 | a0001c0002t0001g0010 a0001c0002t0001g0059 a0001c0002t0001g0060 others(2): Show |
5 | HG01123.hp2 HG01255.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-12038G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540512 | |||||||
| chr3:123540513 | G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-12039C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540513 | |||||||
| chr3:123540569 | G | A | 3 | a0001c0003t0010g0338 a0001c0003t0010g0339 a0001c0003t0010g0340 |
3 | HG02451.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.293-12095C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540569 | |||||||
| chr3:123540578 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.293-12104A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540578 | |||||||
| chr3:123540591 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.293-12117T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540591 | |||||||
| chr3:123540633 | G | T | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-12159C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540633 | |||||||
| chr3:123540677 | T | C | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-12203A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540677 | |||||||
| chr3:123540855 | A | G | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-12381T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123540855 | |||||||
| chr3:123541055 | G | A | 2 | a0001c0001t0006g0233 a0001c0001t0006g0242 |
2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.293-12581C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541055 | |||||||
| chr3:123541145 | C | T | 1 | a0001c0002t0022g0019 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.293-12671G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541145 | |||||||
| chr3:123541243 | A | C | 338 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(335): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.293-12769T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541243 | |||||||
| chr3:123541292 | T | C | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.293-12818A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541292 | |||||||
| chr3:123541697 | T | G | 1 | a0001c0001t0004g0211 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.293-13223A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541697 | |||||||
| chr3:123541837 | A | G | 1 | a0001c0001t0006g0225 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.293-13363T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541837 | |||||||
| chr3:123541918 | C | T | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-13444G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541918 | |||||||
| chr3:123541953 | C | T | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-13479G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123541953 | |||||||
| chr3:123542019 | C | T | 1 | a0001c0003t0001g0324 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.293-13545G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542019 | |||||||
| chr3:123542126 | G | A | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 |
3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-13652C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542126 | |||||||
| chr3:123542142 | G | A | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-13668C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542142 | |||||||
| chr3:123542146 | C | CA | 187 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(184): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.293-13673dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAA | 18 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0248 others(15): Show |
18 | HG01884.hp2 HG02258.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.293-13674_293-1367 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAA | 47 | a0001c0001t0001g0222 a0001c0001t0003g0112 a0001c0001t0003g0154 others(44): Show |
49 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(46): Show |
intron_variant | MODIFIER | c.293-13675_293-1367 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(4): Show |
1 | a0001c0002t0005g0020 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.293-13683_293-1367 others(15): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(6): Show |
1 | a0001c0002t0005g0021 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.293-13685_293-1367 others(17): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(7): Show |
2 | a0001c0002t0005g0096 a0001c0002t0005g0097 |
2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.293-13686_293-1367 others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(8): Show |
2 | a0001c0002t0005g0094 a0001c0002t0005g0095 |
2 | HG01433.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.293-13687_293-1367 others(19): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0005g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.293-13688_293-1367 others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(10): Show |
1 | a0001c0002t0005g0098 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.293-13689_293-1367 others(21): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(11): Show |
1 | a0001c0002t0005g0064 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.293-13690_293-1367 others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0005g0113 a0001c0001t0005g0173 |
2 | HG01358.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.293-13691_293-1367 others(23): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(13): Show |
3 | a0001c0001t0005g0114 a0001c0002t0005g0066 a0001c0002t0005g0079 |
3 | HG01361.hp2 HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.293-13692_293-1367 others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(14): Show |
2 | a0001c0002t0005g0068 a0001c0002t0005g0069 |
2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.293-13693_293-1367 others(25): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(16): Show |
1 | a0001c0002t0005g0073 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293-13695_293-1367 others(27): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(18): Show |
4 | a0001c0001t0005g0139 a0001c0001t0005g0200 a0001c0002t0005g0067 others(1): Show |
4 | HG00673.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-13697_293-1367 others(29): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | C | CAAAAAAA others(20): Show |
1 | a0001c0002t0005g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.293-13673_293-1367 others(31): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542146 | CAAA | C | 10 | a0001c0001t0013g0115 a0001c0003t0007g0305 a0001c0003t0007g0306 others(7): Show |
10 | HG00642.hp2 HG00735.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-13675_293-1367 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542146 | |||||||
| chr3:123542165 | A | AG | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 |
3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-13692_293-1369 others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542165 | |||||||
| chr3:123542194 | T | A | 313 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(310): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.293-13720A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542194 | |||||||
| chr3:123542223 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.293-13749C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542223 | |||||||
| chr3:123542435 | A | G | 317 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(314): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.293-13961T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542435 | |||||||
| chr3:123542543 | C | T | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.293-14069G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542543 | |||||||
| chr3:123542666 | A | T | 5 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-14192T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542666 | |||||||
| chr3:123542778 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-14304G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542778 | |||||||
| chr3:123542959 | T | C | 1 | a0001c0003t0005g0302 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.293-14485A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123542959 | |||||||
| chr3:123543121 | C | T | 117 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(114): Show |
118 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.293-14647G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543121 | |||||||
| chr3:123543189 | T | C | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.293-14715A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543189 | |||||||
| chr3:123543349 | A | G | 1 | a0001c0001t0002g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.293-14875T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543349 | |||||||
| chr3:123543420 | CA | C | 27 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(24): Show |
27 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.293-14947delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543420 | |||||||
| chr3:123543509 | C | A | 2 | a0001c0002t0005g0074 a0001c0002t0005g0076 |
2 | HG02723.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.293-15035G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543509 | |||||||
| chr3:123543513 | G | A | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-15039C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543513 | |||||||
| chr3:123543807 | C | CT | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 |
3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-15334dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123543807 | |||||||
| chr3:123544018 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.293-15544T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544018 | |||||||
| chr3:123544100 | C | T | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-15626G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544100 | |||||||
| chr3:123544112 | G | A | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-15638C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544112 | |||||||
| chr3:123544272 | A | G | 13 | a0001c0001t0006g0233 a0001c0001t0006g0234 a0001c0001t0006g0235 others(10): Show |
13 | HG02109.hp2 HG02572.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-15798T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544272 | |||||||
| chr3:123544394 | C | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG00738.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.293-15920G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544394 | |||||||
| chr3:123544394 | C | T | 37 | a0001c0001t0002g0179 a0001c0001t0004g0004 a0001c0001t0004g0109 others(34): Show |
39 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.293-15920G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544394 | |||||||
| chr3:123544408 | G | T | 35 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.293-15934C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544408 | |||||||
| chr3:123544435 | T | A | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.293-15961A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544435 | |||||||
| chr3:123544559 | A | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-16085T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544559 | |||||||
| chr3:123544617 | T | C | 4 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-16143A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544617 | |||||||
| chr3:123544742 | T | C | 75 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0006g0218 others(72): Show |
77 | HG00544.hp2 HG01109.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.293-16268A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544742 | |||||||
| chr3:123544766 | TA | T | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-16293delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544766 | |||||||
| chr3:123544986 | A | G | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.293-16512T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123544986 | |||||||
| chr3:123545007 | G | A | 1 | a0001c0002t0005g0073 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293-16533C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545007 | |||||||
| chr3:123545034 | C | CA | 139 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(136): Show |
142 | HG00140.hp1 HG00558.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.293-16561dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545034 | |||||||
| chr3:123545034 | C | CAA | 25 | a0001c0001t0003g0112 a0001c0002t0001g0017 a0001c0002t0001g0039 others(22): Show |
26 | HG00423.hp2 HG00544.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.293-16562_293-1656 others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545034 | |||||||
| chr3:123545034 | CA | C | 16 | a0001c0001t0002g0120 a0001c0001t0004g0175 a0001c0001t0004g0206 others(13): Show |
16 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.293-16561delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545034 | |||||||
| chr3:123545099 | G | T | 2 | a0001c0001t0005g0113 a0001c0001t0005g0114 |
2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.293-16625C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545099 | |||||||
| chr3:123545139 | G | GT | 42 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(39): Show |
42 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.293-16666dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545139 | |||||||
| chr3:123545139 | GT | G | 10 | a0001c0001t0002g0220 a0001c0001t0015g0223 a0001c0001t0015g0224 others(7): Show |
10 | HG00597.hp2 HG02630.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.293-16666delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545139 | |||||||
| chr3:123545170 | T | C | 80 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(77): Show |
81 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.293-16696A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545170 | |||||||
| chr3:123545286 | C | G | 45 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(42): Show |
45 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.293-16812G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545286 | |||||||
| chr3:123545363 | T | C | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0006g0236 |
3 | HG02976.hp2 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.293-16889A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545363 | |||||||
| chr3:123545376 | G | A | 3 | a0001c0003t0003g0253 a0001c0003t0003g0283 a0001c0003t0003g0284 |
3 | NA19000.hp2 NA19002.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.293-16902C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545376 | |||||||
| chr3:123545460 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.293-16986G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545460 | |||||||
| chr3:123545486 | A | AAAAT | 10 | a0001c0001t0002g0159 a0001c0001t0002g0251 a0001c0001t0006g0233 others(7): Show |
10 | HG00642.hp2 HG02109.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.293-17016_293-1701 others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | |||||||
| chr3:123545486 | A | AAAATAAA others(1): Show |
75 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0006g0218 others(72): Show |
77 | HG00544.hp2 HG00639.hp2 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.293-17020_293-1701 others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | |||||||
| chr3:123545486 | A | AAAATAAA others(5): Show |
23 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(20): Show |
23 | HG00099.hp1 HG00673.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-17024_293-1701 others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | |||||||
| chr3:123545486 | A | AAAATAAA others(9): Show |
7 | a0001c0001t0005g0173 a0001c0001t0005g0199 a0001c0001t0005g0200 others(4): Show |
7 | HG00738.hp2 HG01167.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-17028_293-1701 others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | |||||||
| chr3:123545486 | A | AAAATAAA others(13): Show |
2 | a0001c0002t0005g0094 a0001c0002t0005g0096 |
2 | HG01433.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.293-17032_293-1701 others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | |||||||
| chr3:123545486 | AAAAT | A | 209 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(206): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.293-17016_293-1701 others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | |||||||
| chr3:123545486 | AAAATAAA others(5): Show |
A | 1 | a0001c0002t0001g0083 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.293-17024_293-1701 others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545486 | |||||||
| chr3:123545490 | T | TAAATAAA others(10910): Show |
1 | a0001c0002t0008g0070 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.293-17017_293-1701 others(10921): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545490 | |||||||
| chr3:123545548 | T | TA | 9 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0001g0325 others(6): Show |
9 | HG00544.hp2 HG02965.hp1 HG03017.hp1 others(6): Show |
intron_variant | MODIFIER | c.293-17075dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545548 | |||||||
| chr3:123545548 | TA | T | 51 | a0001c0001t0002g0118 a0001c0001t0002g0193 a0001c0001t0002g0198 others(48): Show |
52 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.293-17075delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545548 | |||||||
| chr3:123545647 | A | G | 1 | a0001c0002t0005g0067 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.293-17173T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545647 | |||||||
| chr3:123545690 | C | A | 33 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(30): Show |
33 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.293-17216G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545690 | |||||||
| chr3:123545713 | A | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-17239T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545713 | |||||||
| chr3:123545715 | A | AT | 7 | a0001c0001t0002g0155 a0001c0001t0002g0179 a0001c0001t0002g0215 others(4): Show |
7 | HG01515.hp2 HG02155.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-17242dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123545715 | |||||||
| chr3:123546251 | T | C | 1 | a0001c0001t0002g0165 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.293-17777A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546251 | |||||||
| chr3:123546267 | G | A | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-17793C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546267 | |||||||
| chr3:123546308 | G | A | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 |
3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-17834C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546308 | |||||||
| chr3:123546484 | C | G | 15 | a0001c0002t0001g0001 a0001c0002t0001g0010 a0001c0002t0001g0040 others(12): Show |
16 | HG00558.hp2 HG00673.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.293-18010G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546484 | |||||||
| chr3:123546569 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.293-18095C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546569 | |||||||
| chr3:123546775 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-18301G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546775 | |||||||
| chr3:123546928 | A | G | 4 | a0001c0002t0004g0002 a0001c0002t0004g0099 a0001c0002t0004g0102 others(1): Show |
5 | NA18946.hp2 NA18970.hp1 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-18454T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546928 | |||||||
| chr3:123546977 | T | C | 162 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(159): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.293-18503A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123546977 | |||||||
| chr3:123547023 | C | G | 3 | a0001c0001t0004g0147 a0001c0001t0004g0175 a0001c0001t0004g0190 |
3 | HG01257.hp2 HG02602.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.293-18549G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547023 | |||||||
| chr3:123547063 | AT | A | 3 | a0001c0002t0005g0068 a0001c0002t0005g0069 a0001c0002t0005g0073 |
3 | HG02970.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.293-18590delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547063 | |||||||
| chr3:123547233 | T | C | 116 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(113): Show |
119 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.293-18759A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547233 | |||||||
| chr3:123547510 | G | A | 24 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(21): Show |
24 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.293-19036C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547510 | |||||||
| chr3:123547803 | C | T | 228 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(225): Show |
232 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.293-19329G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547803 | |||||||
| chr3:123547904 | C | T | 1 | a0001c0003t0001g0314 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.293-19430G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547904 | |||||||
| chr3:123547986 | C | G | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.293-19512G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123547986 | |||||||
| chr3:123548092 | G | A | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-19618C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548092 | |||||||
| chr3:123548211 | A | G | 1 | a0001c0002t0001g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.292+19551T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548211 | |||||||
| chr3:123548250 | T | C | 80 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(77): Show |
81 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.292+19512A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548250 | |||||||
| chr3:123548338 | C | T | 71 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(68): Show |
72 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.292+19424G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548338 | |||||||
| chr3:123548417 | A | G | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+19345T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548417 | |||||||
| chr3:123548428 | C | T | 2 | a0001c0003t0001g0008 a0001c0003t0001g0319 |
3 | HG00140.hp1 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.292+19334G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548428 | |||||||
| chr3:123548556 | T | C | 75 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0006g0218 others(72): Show |
77 | HG00544.hp2 HG01109.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.292+19206A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548556 | |||||||
| chr3:123548644 | A | G | 1 | a0001c0002t0005g0079 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.292+19118T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548644 | |||||||
| chr3:123548740 | G | T | 1 | a0001c0003t0003g0270 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.292+19022C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548740 | |||||||
| chr3:123548821 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.292+18941G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548821 | |||||||
| chr3:123548826 | T | C | 4 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0027 others(1): Show |
4 | HG00597.hp2 NA18946.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+18936A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548826 | |||||||
| chr3:123548833 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+18929G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548833 | |||||||
| chr3:123548892 | T | A | 1 | a0001c0001t0002g0132 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.292+18870A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123548892 | |||||||
| chr3:123549009 | A | G | 229 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(226): Show |
233 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.292+18753T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549009 | |||||||
| chr3:123549181 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.292+18581G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549181 | |||||||
| chr3:123549184 | T | C | 1 | a0001c0001t0026g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.292+18578A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549184 | |||||||
| chr3:123549295 | A | C | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+18467T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549295 | |||||||
| chr3:123549391 | G | A | 170 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(167): Show |
172 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.292+18371C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549391 | |||||||
| chr3:123549426 | G | A | 23 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(20): Show |
23 | HG00639.hp2 HG00673.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.292+18336C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549426 | |||||||
| chr3:123549500 | C | A | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.292+18262G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549500 | |||||||
| chr3:123549542 | G | A | 1 | a0001c0001t0002g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.292+18220C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549542 | |||||||
| chr3:123549653 | T | C | 1 | a0001c0003t0003g0291 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.292+18109A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549653 | |||||||
| chr3:123549661 | T | C | 5 | a0001c0002t0005g0094 a0001c0002t0005g0095 a0001c0002t0005g0096 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+18101A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549661 | |||||||
| chr3:123549663 | G | T | 27 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0225 others(24): Show |
27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+18099C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549663 | |||||||
| chr3:123549672 | T | C | 2 | a0001c0003t0003g0320 a0001c0003t0005g0301 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.292+18090A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549672 | |||||||
| chr3:123549686 | T | A | 1 | a0001c0002t0001g0052 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.292+18076A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549686 | |||||||
| chr3:123549751 | AAAC | A | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 |
3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.292+18008_292+1801 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549751 | |||||||
| chr3:123549866 | TGGGG | T | 4 | a0001c0001t0004g0204 a0001c0001t0004g0210 a0001c0001t0004g0212 others(1): Show |
4 | HG00639.hp1 HG01978.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+17892_292+1789 others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549866 | |||||||
| chr3:123549885 | A | C | 5 | a0001c0003t0003g0264 a0001c0003t0003g0265 a0001c0003t0003g0268 others(2): Show |
5 | HG01928.hp2 HG01943.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+17877T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123549885 | |||||||
| chr3:123550086 | A | C | 27 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0225 others(24): Show |
27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+17676T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550086 | |||||||
| chr3:123550120 | G | A | 27 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0225 others(24): Show |
27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+17642C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550120 | |||||||
| chr3:123550149 | A | C | 2 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
2 | HG00099.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.292+17613T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550149 | |||||||
| chr3:123550154 | C | A | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+17608G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550154 | |||||||
| chr3:123550236 | C | G | 75 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0006g0218 others(72): Show |
77 | HG00544.hp2 HG01109.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.292+17526G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550236 | |||||||
| chr3:123550289 | T | C | 2 | a0001c0002t0001g0017 a0001c0002t0001g0057 |
2 | NA18944.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.292+17473A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550289 | |||||||
| chr3:123550293 | C | T | 9 | a0001c0001t0015g0224 a0001c0003t0007g0305 a0001c0003t0007g0306 others(6): Show |
9 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+17469G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550293 | |||||||
| chr3:123550315 | G | A | 1 | a0001c0001t0006g0250 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.292+17447C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550315 | |||||||
| chr3:123550667 | C | A | 1 | a0001c0003t0012g0303 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+17095G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550667 | |||||||
| chr3:123550686 | G | A | 1 | a0001c0002t0001g0084 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.292+17076C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550686 | |||||||
| chr3:123550836 | T | C | 4 | a0001c0002t0001g0029 a0001c0002t0001g0037 a0001c0002t0001g0038 others(1): Show |
4 | HG00423.hp2 HG02027.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+16926A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550836 | |||||||
| chr3:123550866 | G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292+16896C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550866 | |||||||
| chr3:123550925 | T | C | 1 | a0001c0001t0002g0133 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.292+16837A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550925 | |||||||
| chr3:123550977 | G | A | 1 | a0001c0002t0001g0034 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.292+16785C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123550977 | |||||||
| chr3:123551127 | G | A | 4 | a0001c0002t0001g0011 a0001c0002t0001g0026 a0001c0002t0001g0027 others(1): Show |
4 | HG00597.hp2 NA18946.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+16635C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551127 | |||||||
| chr3:123551265 | A | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+16497T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551265 | |||||||
| chr3:123551311 | T | C | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+16451A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551311 | |||||||
| chr3:123551346 | C | T | 2 | a0001c0002t0001g0030 a0001c0002t0001g0045 |
2 | HG04115.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.292+16416G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551346 | |||||||
| chr3:123551424 | G | A | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.292+16338C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551424 | |||||||
| chr3:123551456 | T | TA | 5 | a0001c0001t0005g0139 a0001c0002t0005g0020 a0001c0002t0005g0021 others(2): Show |
5 | HG00673.hp2 NA18994.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+16305dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551456 | |||||||
| chr3:123551464 | A | T | 85 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(82): Show |
88 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.292+16298T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551464 | |||||||
| chr3:123551494 | G | A | 3 | a0001c0003t0003g0289 a0001c0003t0003g0334 a0001c0003t0003g0335 |
3 | HG02071.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.292+16268C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551494 | |||||||
| chr3:123551599 | G | A | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | NA18966.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.292+16163C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551599 | |||||||
| chr3:123551917 | A | C | 1 | a0001c0001t0002g0129 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.292+15845T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123551917 | |||||||
| chr3:123552085 | T | C | 1 | a0001c0001t0006g0244 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.292+15677A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552085 | |||||||
| chr3:123552238 | C | T | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+15524G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552238 | |||||||
| chr3:123552245 | C | A | 87 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.292+15517G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552245 | |||||||
| chr3:123552837 | A | G | 131 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(128): Show |
134 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.292+14925T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552837 | |||||||
| chr3:123552960 | G | A | 1 | a0001c0002t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.292+14802C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123552960 | |||||||
| chr3:123553114 | T | C | 1 | a0001c0003t0003g0260 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.292+14648A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553114 | |||||||
| chr3:123553244 | G | C | 1 | a0001c0001t0002g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.292+14518C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553244 | |||||||
| chr3:123553449 | A | G | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+14313T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553449 | |||||||
| chr3:123553517 | T | C | 2 | a0001c0001t0002g0128 a0001c0001t0002g0134 |
2 | HG02071.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.292+14245A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553517 | |||||||
| chr3:123553571 | G | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.292+14191C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553571 | |||||||
| chr3:123553952 | T | A | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+13810A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553952 | |||||||
| chr3:123553960 | A | T | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+13802T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123553960 | |||||||
| chr3:123554076 | C | T | 17 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(14): Show |
18 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.292+13686G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554076 | |||||||
| chr3:123554134 | A | AAAGAATA others(135): Show |
1 | a0001c0003t0003g0295 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.292+13627_292+1362 others(146): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554134 | |||||||
| chr3:123554335 | G | T | 34 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(31): Show |
34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+13427C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554335 | |||||||
| chr3:123554490 | C | T | 2 | a0001c0002t0001g0012 a0001c0002t0001g0044 |
2 | HG02738.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.292+13272G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554490 | |||||||
| chr3:123554687 | C | T | 1 | a0001c0003t0001g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.292+13075G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554687 | |||||||
| chr3:123554798 | G | A | 1 | a0001c0001t0006g0231 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.292+12964C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554798 | |||||||
| chr3:123554828 | AT | A | 27 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0225 others(24): Show |
27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+12933delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554828 | |||||||
| chr3:123554987 | C | T | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+12775G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123554987 | |||||||
| chr3:123555087 | T | C | 34 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(31): Show |
34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+12675A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555087 | |||||||
| chr3:123555139 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.292+12623C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555139 | |||||||
| chr3:123555167 | G | A | 1 | a0001c0002t0001g0105 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.292+12595C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555167 | |||||||
| chr3:123555377 | C | T | 1 | a0001c0002t0001g0043 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.292+12385G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555377 | |||||||
| chr3:123555431 | A | G | 34 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(31): Show |
34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+12331T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555431 | |||||||
| chr3:123555476 | T | TA | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+12285dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555476 | |||||||
| chr3:123555611 | T | A | 2 | a0001c0003t0003g0329 a0001c0003t0003g0336 |
2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.292+12151A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123555611 | |||||||
| chr3:123556006 | A | C | 7 | a0001c0002t0001g0015 a0001c0002t0001g0081 a0001c0002t0001g0082 others(4): Show |
7 | NA18962.hp1 NA18972.hp1 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.292+11756T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556006 | |||||||
| chr3:123556232 | T | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+11530A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556232 | |||||||
| chr3:123556320 | C | G | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.292+11442G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556320 | |||||||
| chr3:123556332 | G | T | 75 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(72): Show |
76 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.292+11430C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556332 | |||||||
| chr3:123556363 | G | T | 1 | a0001c0002t0004g0062 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.292+11399C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556363 | |||||||
| chr3:123556381 | G | A | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.292+11381C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556381 | |||||||
| chr3:123556425 | A | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+11337T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556425 | |||||||
| chr3:123556436 | C | CA | 7 | a0001c0001t0004g0164 a0001c0001t0004g0183 a0001c0001t0004g0184 others(4): Show |
7 | HG01884.hp1 HG02647.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+11325dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556436 | |||||||
| chr3:123556436 | CA | C | 203 | a0001c0001t0001g0248 a0001c0001t0002g0117 a0001c0001t0002g0124 others(200): Show |
206 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.292+11325delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556436 | |||||||
| chr3:123556453 | T | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+11309A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556453 | |||||||
| chr3:123556539 | C | A | 5 | a0001c0002t0005g0094 a0001c0002t0005g0095 a0001c0002t0005g0096 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+11223G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556539 | |||||||
| chr3:123556551 | A | G | 73 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(70): Show |
74 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.292+11211T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556551 | |||||||
| chr3:123556875 | T | C | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.292+10887A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556875 | |||||||
| chr3:123556938 | C | T | 2 | a0001c0001t0005g0113 a0001c0001t0005g0114 |
2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.292+10824G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123556938 | |||||||
| chr3:123557011 | T | A | 3 | a0001c0003t0011g0322 a0001c0003t0011g0323 a0001c0003t0016g0321 |
3 | HG02622.hp2 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.292+10751A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557011 | |||||||
| chr3:123557112 | CGCA | C | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+10647_292+1064 others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557112 | |||||||
| chr3:123557310 | C | T | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.292+10452G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557310 | |||||||
| chr3:123557388 | C | T | 12 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0003t0007g0305 others(9): Show |
12 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+10374G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557388 | |||||||
| chr3:123557667 | A | G | 1 | a0001c0003t0011g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292+10095T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557667 | |||||||
| chr3:123557713 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.292+10049C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557713 | |||||||
| chr3:123557756 | C | G | 1 | a0001c0002t0005g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.292+10006G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557756 | |||||||
| chr3:123557869 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.292+9893G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123557869 | |||||||
| chr3:123558166 | G | A | 5 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG01884.hp2 HG02055.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+9596C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558166 | |||||||
| chr3:123558169 | G | A | 1 | a0001c0001t0005g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.292+9593C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558169 | |||||||
| chr3:123558233 | G | A | 1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+9529C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558233 | |||||||
| chr3:123558508 | G | A | 37 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(34): Show |
38 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.292+9254C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558508 | |||||||
| chr3:123558702 | T | C | 9 | a0001c0001t0002g0005 a0001c0001t0002g0171 a0001c0001t0002g0172 others(6): Show |
10 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+9060A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558702 | |||||||
| chr3:123558849 | C | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.292+8913G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558849 | |||||||
| chr3:123558972 | G | C | 240 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(237): Show |
244 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.292+8790C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123558972 | |||||||
| chr3:123559073 | C | T | 1 | a0001c0002t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.292+8689G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559073 | |||||||
| chr3:123559094 | C | G | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 |
3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.292+8668G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559094 | |||||||
| chr3:123559183 | T | G | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+8579A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559183 | |||||||
| chr3:123559253 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.292+8509C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559253 | |||||||
| chr3:123559285 | GTGT | G | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+8474_292+8476d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559285 | |||||||
| chr3:123559540 | G | A | 1 | a0001c0003t0012g0303 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+8222C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559540 | |||||||
| chr3:123559552 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.292+8210T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559552 | |||||||
| chr3:123559750 | C | T | 10 | a0001c0001t0006g0219 a0001c0001t0006g0225 a0001c0001t0006g0226 others(7): Show |
10 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+8012G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559750 | |||||||
| chr3:123559845 | G | A | 34 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(31): Show |
34 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.292+7917C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123559845 | |||||||
| chr3:123560143 | G | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+7619C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560143 | |||||||
| chr3:123560180 | G | A | 35 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+7582C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560180 | |||||||
| chr3:123560234 | G | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+7528C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560234 | |||||||
| chr3:123560255 | G | T | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.292+7507C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560255 | |||||||
| chr3:123560377 | G | A | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+7385C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560377 | |||||||
| chr3:123560417 | A | G | 1 | a0001c0002t0001g0035 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.292+7345T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560417 | |||||||
| chr3:123560679 | C | G | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+7083G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560679 | |||||||
| chr3:123560786 | CT | C | 72 | a0001c0001t0009g0138 a0001c0002t0001g0001 a0001c0002t0001g0009 others(69): Show |
73 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.292+6975delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560786 | |||||||
| chr3:123560873 | G | A | 35 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+6889C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560873 | |||||||
| chr3:123560876 | G | A | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+6886C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123560876 | |||||||
| chr3:123561040 | A | G | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+6722T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561040 | |||||||
| chr3:123561079 | G | T | 1 | a0001c0001t0002g0159 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.292+6683C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561079 | |||||||
| chr3:123561081 | G | C | 1 | a0001c0001t0006g0243 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292+6681C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561081 | |||||||
| chr3:123561129 | C | G | 27 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0225 others(24): Show |
27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+6633G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561129 | |||||||
| chr3:123561167 | G | A | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG01168.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.292+6595C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561167 | |||||||
| chr3:123561226 | T | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+6536A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561226 | |||||||
| chr3:123561254 | G | A | 162 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(159): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.292+6508C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561254 | |||||||
| chr3:123561315 | C | T | 1 | a0001c0001t0002g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.292+6447G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561315 | |||||||
| chr3:123561316 | T | C | 1 | a0001c0001t0002g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.292+6446A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561316 | |||||||
| chr3:123561412 | G | A | 1 | a0001c0003t0003g0297 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.292+6350C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561412 | |||||||
| chr3:123561488 | A | G | 1 | a0001c0002t0005g0074 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.292+6274T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561488 | |||||||
| chr3:123561551 | T | TCACATCT others(21): Show |
2 | a0001c0002t0001g0023 a0001c0002t0001g0042 |
2 | HG01081.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.292+6183_292+6210d others(30): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561551 | |||||||
| chr3:123561602 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+6160G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561602 | |||||||
| chr3:123561613 | A | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+6149T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561613 | |||||||
| chr3:123561614 | G | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+6148C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561614 | |||||||
| chr3:123561689 | C | G | 1 | a0001c0002t0001g0030 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.292+6073G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561689 | |||||||
| chr3:123561776 | C | T | 2 | a0001c0001t0015g0223 a0001c0001t0015g0224 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.292+5986G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561776 | |||||||
| chr3:123561777 | G | A | 9 | a0001c0003t0003g0327 a0001c0003t0003g0329 a0001c0003t0003g0330 others(6): Show |
9 | HG02280.hp1 HG02486.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+5985C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561777 | |||||||
| chr3:123561778 | G | A | 1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.292+5984C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561778 | |||||||
| chr3:123561778 | G | GA | 19 | a0001c0001t0002g0134 a0001c0001t0002g0145 a0001c0001t0002g0157 others(16): Show |
19 | HG00099.hp1 HG00323.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.292+5983dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561778 | |||||||
| chr3:123561779 | A | G | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+5983T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561779 | |||||||
| chr3:123561791 | A | C | 36 | a0001c0001t0002g0179 a0001c0001t0004g0004 a0001c0001t0004g0109 others(33): Show |
38 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.292+5971T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561791 | |||||||
| chr3:123561864 | T | C | 1 | a0001c0001t0004g0178 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.292+5898A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561864 | |||||||
| chr3:123561881 | G | A | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.292+5881C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561881 | |||||||
| chr3:123561905 | G | A | 27 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0225 others(24): Show |
27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+5857C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561905 | |||||||
| chr3:123561959 | C | G | 1 | a0001c0001t0002g0214 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.292+5803G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561959 | |||||||
| chr3:123561984 | G | A | 1 | a0001c0001t0028g0163 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.292+5778C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123561984 | |||||||
| chr3:123562091 | T | A | 1 | a0001c0001t0002g0146 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.292+5671A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562091 | |||||||
| chr3:123562104 | G | A | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.292+5658C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562104 | |||||||
| chr3:123562161 | A | C | 35 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+5601T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562161 | |||||||
| chr3:123562252 | T | C | 1 | a0002c0005t0001g0341 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.292+5510A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562252 | |||||||
| chr3:123562297 | G | T | 2 | a0001c0003t0003g0290 a0001c0003t0003g0291 |
2 | NA18961.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.292+5465C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562297 | |||||||
| chr3:123562315 | T | G | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 |
3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.292+5447A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562315 | |||||||
| chr3:123562376 | G | A | 2 | a0001c0002t0001g0053 a0001c0002t0001g0054 |
2 | HG02074.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.292+5386C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562376 | |||||||
| chr3:123562406 | C | G | 1 | a0001c0002t0001g0034 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.292+5356G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562406 | |||||||
| chr3:123562415 | G | C | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.292+5347C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562415 | |||||||
| chr3:123562517 | ATAT | A | 135 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+5242_292+5244d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562517 | |||||||
| chr3:123562556 | G | C | 135 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+5206C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562556 | |||||||
| chr3:123562623 | T | G | 6 | a0001c0001t0004g0147 a0001c0001t0004g0175 a0001c0001t0004g0176 others(3): Show |
6 | HG01257.hp2 HG01516.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+5139A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562623 | |||||||
| chr3:123562652 | T | C | 135 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+5110A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562652 | |||||||
| chr3:123562908 | C | A | 1 | a0001c0003t0011g0323 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.292+4854G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562908 | |||||||
| chr3:123562957 | C | T | 25 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.292+4805G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123562957 | |||||||
| chr3:123563053 | T | C | 1 | a0001c0001t0004g0182 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.292+4709A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563053 | |||||||
| chr3:123563145 | A | C | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.292+4617T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563145 | |||||||
| chr3:123563210 | T | A | 1 | a0001c0001t0004g0190 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.292+4552A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563210 | |||||||
| chr3:123563250 | A | G | 135 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+4512T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563250 | |||||||
| chr3:123563292 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.292+4470C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563292 | |||||||
| chr3:123563455 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.292+4307G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563455 | |||||||
| chr3:123563533 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.292+4229G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563533 | |||||||
| chr3:123563581 | C | G | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | HG01168.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.292+4181G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563581 | |||||||
| chr3:123563638 | TATATATA others(3): Show |
T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+4114_292+4123d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563638 | |||||||
| chr3:123563640 | TATATACA others(3): Show |
T | 1 | a0001c0003t0012g0304 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.292+4112_292+4121d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563640 | |||||||
| chr3:123563640 | TATATACA others(5): Show |
T | 79 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0005g0113 others(76): Show |
81 | HG00544.hp2 HG00639.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.292+4110_292+4121d others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563640 | |||||||
| chr3:123563640 | TATATACA others(7): Show |
T | 3 | a0001c0003t0005g0300 a0001c0003t0005g0301 a0001c0003t0005g0302 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.292+4108_292+4121d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563640 | |||||||
| chr3:123563640 | TATATACA others(13): Show |
T | 1 | a0001c0001t0005g0199 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.292+4102_292+4121d others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563640 | |||||||
| chr3:123563642 | T | TAC | 5 | a0001c0001t0002g0179 a0001c0001t0004g0004 a0001c0001t0004g0109 others(2): Show |
6 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+4119_292+4120i others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | |||||||
| chr3:123563642 | TATAC | T | 6 | a0001c0001t0004g0187 a0001c0002t0001g0018 a0001c0002t0001g0031 others(3): Show |
6 | HG03669.hp1 HG04204.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.292+4116_292+4119d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | |||||||
| chr3:123563642 | TATACACA others(3): Show |
T | 5 | a0001c0003t0003g0329 a0001c0003t0010g0337 a0001c0003t0010g0340 others(2): Show |
5 | HG02451.hp1 HG02683.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+4110_292+4119d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | |||||||
| chr3:123563642 | TATACACA others(5): Show |
T | 31 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0151 others(28): Show |
32 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.292+4108_292+4119d others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | |||||||
| chr3:123563642 | TATACACA others(7): Show |
T | 6 | a0001c0001t0001g0149 a0001c0003t0007g0306 a0001c0003t0010g0338 others(3): Show |
6 | HG02055.hp1 HG02129.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+4106_292+4119d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | |||||||
| chr3:123563642 | TATACACA others(9): Show |
T | 7 | a0001c0003t0007g0305 a0001c0003t0007g0307 a0001c0003t0007g0308 others(4): Show |
7 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.292+4104_292+4119d others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563642 | |||||||
| chr3:123563644 | T | C | 8 | a0001c0001t0002g0130 a0001c0001t0002g0170 a0001c0001t0002g0179 others(5): Show |
9 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.292+4118A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | |||||||
| chr3:123563644 | T | TAC | 20 | a0001c0001t0002g0108 a0001c0001t0002g0133 a0001c0001t0002g0143 others(17): Show |
21 | HG00140.hp2 HG00544.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.292+4116_292+4117d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | |||||||
| chr3:123563644 | T | TACAC | 7 | a0001c0001t0002g0005 a0001c0001t0004g0183 a0001c0001t0004g0190 others(4): Show |
8 | HG00099.hp2 HG01070.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+4114_292+4117d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | |||||||
| chr3:123563644 | T | TACACAC | 8 | a0001c0001t0004g0185 a0001c0001t0004g0204 a0001c0001t0004g0207 others(5): Show |
8 | HG00639.hp1 HG01123.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+4112_292+4117d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | |||||||
| chr3:123563644 | TAC | T | 29 | a0001c0001t0002g0146 a0001c0001t0006g0219 a0001c0001t0006g0225 others(26): Show |
29 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.292+4116_292+4117d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | |||||||
| chr3:123563644 | TACAC | T | 39 | a0001c0001t0009g0138 a0001c0002t0001g0012 a0001c0002t0001g0014 others(36): Show |
39 | HG00423.hp2 HG01081.hp1 HG01978.hp2 others(36): Show |
intron_variant | MODIFIER | c.292+4114_292+4117d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | |||||||
| chr3:123563644 | TACACAC | T | 5 | a0001c0001t0002g0125 a0001c0001t0004g0182 a0001c0002t0001g0034 others(2): Show |
5 | HG01261.hp1 HG02015.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+4112_292+4117d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | |||||||
| chr3:123563644 | TACACACA others(3): Show |
T | 15 | a0001c0002t0001g0001 a0001c0002t0001g0010 a0001c0002t0001g0040 others(12): Show |
16 | HG00558.hp2 HG00673.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.292+4108_292+4117d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563644 | |||||||
| chr3:123563695 | G | A | 3 | a0001c0001t0004g0211 a0001c0001t0013g0115 a0001c0001t0013g0116 |
3 | HG02738.hp1 HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+4067C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563695 | |||||||
| chr3:123563814 | C | A | 1 | a0001c0003t0001g0328 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.292+3948G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563814 | |||||||
| chr3:123563834 | C | T | 135 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+3928G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563834 | |||||||
| chr3:123563876 | T | TTTAAGAA others(17): Show |
1 | a0001c0001t0002g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.292+3862_292+3885d others(26): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563876 | |||||||
| chr3:123563937 | C | T | 135 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+3825G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563937 | |||||||
| chr3:123563951 | T | C | 1 | a0001c0001t0005g0200 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.292+3811A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563951 | |||||||
| chr3:123563957 | G | A | 162 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(159): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.292+3805C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563957 | |||||||
| chr3:123563996 | C | T | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+3766G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123563996 | |||||||
| chr3:123564067 | G | A | 1 | a0001c0001t0015g0224 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.292+3695C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564067 | |||||||
| chr3:123564071 | C | G | 135 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+3691G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564071 | |||||||
| chr3:123564073 | T | G | 135 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.292+3689A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564073 | |||||||
| chr3:123564183 | G | A | 3 | a0001c0003t0005g0300 a0001c0003t0005g0301 a0001c0003t0005g0302 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.292+3579C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564183 | |||||||
| chr3:123564217 | C | T | 27 | a0001c0001t0006g0218 a0001c0001t0006g0219 a0001c0001t0006g0225 others(24): Show |
27 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.292+3545G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564217 | |||||||
| chr3:123564462 | G | A | 75 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(72): Show |
76 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.292+3300C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564462 | |||||||
| chr3:123564499 | C | G | 35 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+3263G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564499 | |||||||
| chr3:123564503 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.292+3259C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564503 | |||||||
| chr3:123564647 | A | C | 1 | a0001c0002t0001g0042 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.292+3115T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123564647 | |||||||
| chr3:123565089 | C | T | 1 | a0001c0002t0001g0081 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.292+2673G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565089 | |||||||
| chr3:123565431 | CT | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+2330delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565431 | |||||||
| chr3:123565572 | A | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+2190T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565572 | |||||||
| chr3:123565593 | G | T | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+2169C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565593 | |||||||
| chr3:123565751 | T | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.292+2011A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565751 | |||||||
| chr3:123565883 | G | A | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.292+1879C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123565883 | |||||||
| chr3:123566039 | T | G | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+1723A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566039 | |||||||
| chr3:123566051 | C | T | 87 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.292+1711G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566051 | |||||||
| chr3:123566132 | T | C | 1 | a0001c0003t0012g0303 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.292+1630A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566132 | |||||||
| chr3:123566159 | G | A | 31 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0139 others(28): Show |
31 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.292+1603C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566159 | |||||||
| chr3:123566272 | C | T | 1 | a0001c0003t0003g0297 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.292+1490G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566272 | |||||||
| chr3:123566450 | C | T | 1 | a0001c0002t0001g0029 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.292+1312G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566450 | |||||||
| chr3:123566503 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.292+1259G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566503 | |||||||
| chr3:123566727 | T | C | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+1035A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566727 | |||||||
| chr3:123566853 | A | G | 3 | a0001c0001t0004g0164 a0001c0001t0004g0183 a0001c0001t0004g0184 |
3 | NA18949.hp2 NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.292+909T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566853 | |||||||
| chr3:123566895 | A | G | 1 | a0001c0001t0002g0123 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.292+867T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123566895 | |||||||
| chr3:123567009 | C | T | 35 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.292+753G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567009 | |||||||
| chr3:123567254 | T | G | 162 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(159): Show |
165 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.292+508A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567254 | |||||||
| chr3:123567312 | C | T | 1 | a0001c0001t0006g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.292+450G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567312 | |||||||
| chr3:123567346 | A | G | 1 | a0001c0001t0004g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.292+416T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567346 | |||||||
| chr3:123567369 | A | G | 75 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0001t0006g0218 others(72): Show |
77 | HG00544.hp2 HG01109.hp1 HG01167.hp1 others(74): Show |
intron_variant | MODIFIER | c.292+393T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 3/6 | chr3 | 123567369 | |||||||
| chr3:123567946 | C | A | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.274-166G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123567946 | |||||||
| chr3:123567951 | T | C | 1 | a0001c0003t0001g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.274-171A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123567951 | |||||||
| chr3:123567966 | A | G | 7 | a0001c0002t0008g0013 a0001c0002t0008g0065 a0001c0002t0008g0070 others(4): Show |
7 | HG00735.hp2 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-186T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123567966 | |||||||
| chr3:123568105 | A | G | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-325T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568105 | |||||||
| chr3:123568128 | A | G | 1 | a0001c0001t0002g0191 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.274-348T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568128 | |||||||
| chr3:123568152 | C | T | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-372G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568152 | |||||||
| chr3:123568194 | T | C | 1 | a0001c0003t0003g0289 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.274-414A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568194 | |||||||
| chr3:123568197 | C | A | 1 | a0001c0001t0002g0135 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.274-417G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568197 | |||||||
| chr3:123568372 | C | T | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.274-592G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568372 | |||||||
| chr3:123568424 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.274-644C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568424 | |||||||
| chr3:123568519 | C | T | 135 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(132): Show |
138 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.274-739G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568519 | |||||||
| chr3:123568618 | C | G | 2 | a0001c0001t0002g0201 a0001c0001t0002g0213 |
2 | HG02145.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.274-838G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568618 | |||||||
| chr3:123568618 | C | T | 1 | a0001c0002t0002g0041 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.274-838G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568618 | |||||||
| chr3:123568713 | T | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.274-933A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568713 | |||||||
| chr3:123568865 | C | G | 1 | a0001c0003t0001g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.274-1085G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568865 | |||||||
| chr3:123568959 | T | C | 37 | a0001c0001t0002g0179 a0001c0001t0004g0004 a0001c0001t0004g0109 others(34): Show |
39 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.274-1179A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568959 | |||||||
| chr3:123568970 | T | G | 4 | a0001c0001t0002g0197 a0001c0003t0005g0300 a0001c0003t0005g0301 others(1): Show |
4 | HG02258.hp1 HG03098.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-1190A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123568970 | |||||||
| chr3:123569046 | A | G | 48 | a0001c0001t0003g0112 a0001c0001t0003g0154 a0001c0003t0003g0006 others(45): Show |
50 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(47): Show |
intron_variant | MODIFIER | c.274-1266T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569046 | |||||||
| chr3:123569103 | G | A | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-1323C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569103 | |||||||
| chr3:123569165 | C | G | 2 | a0001c0001t0006g0226 a0001c0001t0006g0232 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.274-1385G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569165 | |||||||
| chr3:123569305 | G | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.274-1525C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569305 | |||||||
| chr3:123569491 | A | AGCTGGGA others(15): Show |
1 | a0001c0001t0006g0218 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.274-1733_274-1712d others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569491 | |||||||
| chr3:123569512 | C | T | 1 | a0001c0003t0001g0325 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.274-1732G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569512 | |||||||
| chr3:123569605 | G | A | 1 | a0001c0002t0001g0088 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.274-1825C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569605 | |||||||
| chr3:123569699 | C | A | 106 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 others(103): Show |
107 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.274-1919G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569699 | |||||||
| chr3:123569725 | C | T | 2 | a0001c0001t0004g0109 a0001c0001t0004g0110 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.274-1945G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569725 | |||||||
| chr3:123569748 | G | A | 35 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(32): Show |
36 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.274-1968C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569748 | |||||||
| chr3:123569813 | C | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.274-2033G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569813 | |||||||
| chr3:123569850 | A | G | 3 | a0001c0002t0005g0068 a0001c0002t0005g0069 a0001c0002t0005g0073 |
3 | HG02970.hp1 HG03471.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.274-2070T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569850 | |||||||
| chr3:123569888 | C | T | 6 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 others(3): Show |
6 | HG02258.hp2 HG02451.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-2108G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569888 | |||||||
| chr3:123569942 | T | C | 1 | a0001c0003t0003g0276 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.274-2162A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569942 | |||||||
| chr3:123569988 | C | CA | 6 | a0001c0001t0002g0165 a0001c0001t0002g0197 a0001c0001t0004g0187 others(3): Show |
6 | HG02080.hp1 HG03239.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-2209dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CA | C | 17 | a0001c0001t0002g0156 a0001c0001t0002g0157 a0001c0001t0002g0167 others(14): Show |
17 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.274-2209delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAA | C | 9 | a0001c0001t0002g0005 a0001c0001t0002g0108 a0001c0001t0002g0166 others(6): Show |
11 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-2210_274-2209d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAA | C | 6 | a0001c0001t0002g0155 a0001c0001t0002g0196 a0001c0002t0005g0097 others(3): Show |
6 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-2211_274-2209d others(5): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAA | C | 9 | a0001c0001t0002g0169 a0001c0001t0005g0113 a0001c0001t0005g0114 others(6): Show |
9 | HG00544.hp1 HG01358.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-2212_274-2209d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAA | C | 13 | a0001c0001t0002g0120 a0001c0001t0002g0168 a0001c0001t0005g0199 others(10): Show |
13 | HG00735.hp2 HG00738.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.274-2213_274-2209d others(7): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAA | C | 7 | a0001c0001t0005g0173 a0001c0002t0005g0064 a0001c0002t0005g0066 others(4): Show |
7 | HG00639.hp2 HG00673.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-2214_274-2209d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(2): Show |
C | 14 | a0001c0001t0003g0154 a0001c0001t0013g0115 a0001c0001t0013g0116 others(11): Show |
14 | HG00673.hp1 HG02083.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.274-2217_274-2209d others(11): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(3): Show |
C | 44 | a0001c0001t0003g0112 a0001c0001t0015g0223 a0001c0002t0001g0034 others(41): Show |
46 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.274-2218_274-2209d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(4): Show |
C | 5 | a0001c0003t0001g0008 a0001c0003t0003g0269 a0001c0003t0003g0293 others(2): Show |
6 | HG01257.hp1 HG01258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-2219_274-2209d others(13): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(5): Show |
C | 20 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(17): Show |
20 | HG00738.hp1 HG01071.hp2 HG01516.hp2 others(17): Show |
intron_variant | MODIFIER | c.274-2220_274-2209d others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(6): Show |
C | 27 | a0001c0001t0001g0148 a0001c0001t0002g0220 a0001c0001t0002g0251 others(24): Show |
27 | HG00323.hp2 HG00735.hp1 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.274-2221_274-2209d others(15): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(7): Show |
C | 86 | a0001c0001t0006g0219 a0001c0001t0006g0225 a0001c0001t0006g0228 others(83): Show |
87 | HG00099.hp1 HG00558.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.274-2222_274-2209d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(8): Show |
C | 5 | a0001c0001t0006g0226 a0001c0001t0006g0227 a0001c0001t0006g0237 others(2): Show |
5 | HG01167.hp1 HG02897.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-2223_274-2209d others(17): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0002g0191 a0001c0002t0004g0099 |
2 | HG01433.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.274-2224_274-2209d others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(10): Show |
C | 2 | a0001c0001t0002g0198 a0001c0002t0005g0020 |
2 | HG02280.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.274-2225_274-2209d others(19): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(11): Show |
C | 6 | a0001c0001t0004g0147 a0001c0001t0004g0175 a0001c0001t0004g0176 others(3): Show |
6 | HG01516.hp1 HG02602.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-2226_274-2209d others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(12): Show |
C | 3 | a0001c0001t0002g0137 a0001c0001t0004g0190 a0001c0002t0001g0029 |
3 | HG01257.hp2 HG02027.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.274-2227_274-2209d others(21): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123569988 | CAAAAAAA others(13): Show |
C | 35 | a0001c0001t0002g0003 a0001c0001t0002g0117 a0001c0001t0002g0118 others(32): Show |
36 | HG00323.hp1 HG00423.hp1 HG00558.hp1 others(33): Show |
intron_variant | MODIFIER | c.274-2228_274-2209d others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123569988 | |||||||
| chr3:123570079 | A | G | 5 | a0001c0002t0005g0094 a0001c0003t0010g0337 a0001c0003t0010g0338 others(2): Show |
5 | HG01433.hp2 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-2299T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570079 | |||||||
| chr3:123570264 | T | C | 9 | a0001c0001t0031g0342 a0001c0003t0007g0305 a0001c0003t0007g0306 others(6): Show |
9 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-2484A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570264 | |||||||
| chr3:123570504 | A | C | 23 | a0001c0001t0003g0112 a0001c0003t0003g0253 a0001c0003t0003g0254 others(20): Show |
23 | HG00544.hp2 HG01928.hp2 HG01943.hp1 others(20): Show |
intron_variant | MODIFIER | c.274-2724T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570504 | |||||||
| chr3:123570656 | C | T | 1 | a0001c0003t0003g0330 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.274-2876G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570656 | |||||||
| chr3:123570724 | C | T | 1 | a0001c0001t0019g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.274-2944G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570724 | |||||||
| chr3:123570748 | C | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.274-2968G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570748 | |||||||
| chr3:123570832 | T | G | 226 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(223): Show |
230 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.274-3052A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570832 | |||||||
| chr3:123570867 | G | A | 5 | a0001c0003t0003g0286 a0001c0003t0003g0287 a0001c0003t0003g0288 others(2): Show |
5 | HG02071.hp1 NA18945.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3087C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570867 | |||||||
| chr3:123570917 | T | TAC | 44 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(41): Show |
45 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.274-3139_274-3138d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACAC | 6 | a0001c0001t0002g0195 a0001c0001t0006g0250 a0001c0001t0015g0223 others(3): Show |
6 | HG00639.hp2 HG01167.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-3141_274-3138d others(6): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(1): Show |
30 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0199 others(27): Show |
31 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.274-3145_274-3138d others(10): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(3): Show |
15 | a0001c0001t0005g0173 a0001c0002t0001g0011 a0001c0002t0001g0024 others(12): Show |
15 | HG00597.hp2 HG02132.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.274-3147_274-3138d others(12): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(5): Show |
24 | a0001c0002t0001g0028 a0001c0002t0001g0029 a0001c0002t0001g0030 others(21): Show |
24 | HG00423.hp2 HG01884.hp1 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.274-3149_274-3138d others(14): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(7): Show |
35 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0012 others(32): Show |
36 | HG00558.hp2 HG00673.hp1 HG01978.hp2 others(33): Show |
intron_variant | MODIFIER | c.274-3151_274-3138d others(16): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(9): Show |
22 | a0001c0001t0013g0115 a0001c0001t0013g0116 a0001c0002t0001g0010 others(19): Show |
23 | HG00140.hp1 HG00323.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.274-3153_274-3138d others(18): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(11): Show |
12 | a0001c0001t0003g0112 a0001c0002t0001g0059 a0001c0002t0001g0060 others(9): Show |
12 | HG00639.hp1 HG01255.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.274-3155_274-3138d others(20): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(13): Show |
21 | a0001c0002t0001g0090 a0001c0003t0003g0254 a0001c0003t0003g0255 others(18): Show |
21 | HG00544.hp2 HG01109.hp1 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.274-3157_274-3138d others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(15): Show |
15 | a0001c0001t0030g0252 a0001c0003t0003g0007 a0001c0003t0003g0253 others(12): Show |
16 | HG01943.hp1 HG02071.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.274-3159_274-3138d others(24): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(17): Show |
2 | a0001c0003t0003g0290 a0001c0003t0003g0291 |
2 | NA18961.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.274-3161_274-3138d others(26): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(19): Show |
1 | a0001c0003t0003g0292 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.274-3163_274-3138d others(28): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570917 | T | TACACACA others(21): Show |
1 | a0001c0001t0002g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.274-3138_274-3137i others(30): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570917 | |||||||
| chr3:123570943 | C | CACACACA others(17): Show |
1 | a0001c0001t0002g0221 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.274-3164_274-3163i others(26): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570943 | |||||||
| chr3:123570943 | C | CACACACA others(13): Show |
1 | a0001c0001t0002g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.274-3164_274-3163i others(22): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570943 | |||||||
| chr3:123570945 | T | C | 2 | a0001c0001t0002g0221 a0001c0001t0002g0251 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.274-3165A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123570945 | |||||||
| chr3:123571054 | G | A | 3 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 |
3 | HG02451.hp2 HG02630.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.274-3274C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571054 | |||||||
| chr3:123571124 | T | C | 6 | a0001c0002t0001g0101 a0001c0002t0004g0002 a0001c0002t0004g0099 others(3): Show |
7 | NA18946.hp2 NA18964.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-3344A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571124 | |||||||
| chr3:123571259 | G | A | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-3479C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571259 | |||||||
| chr3:123571376 | A | G | 72 | a0001c0001t0003g0112 a0001c0003t0001g0008 a0001c0003t0001g0314 others(69): Show |
75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.274-3596T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571376 | |||||||
| chr3:123571420 | C | A | 2 | a0001c0001t0015g0223 a0001c0001t0015g0224 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.274-3640G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571420 | |||||||
| chr3:123571470 | C | G | 4 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-3690G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571470 | |||||||
| chr3:123571526 | G | A | 108 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(105): Show |
109 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.274-3746C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571526 | |||||||
| chr3:123571568 | C | T | 32 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(29): Show |
32 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.274-3788G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571568 | |||||||
| chr3:123571609 | G | A | 1 | a0001c0003t0003g0293 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.274-3829C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571609 | |||||||
| chr3:123571774 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.274-3994C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571774 | |||||||
| chr3:123571821 | A | G | 33 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(30): Show |
33 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.274-4041T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123571821 | |||||||
| chr3:123572244 | A | G | 231 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(228): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.274-4464T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572244 | |||||||
| chr3:123572260 | C | T | 103 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(100): Show |
104 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.274-4480G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572260 | |||||||
| chr3:123572316 | C | T | 108 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(105): Show |
109 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.274-4536G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572316 | |||||||
| chr3:123572511 | G | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-4731C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572511 | |||||||
| chr3:123572619 | T | A | 231 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(228): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.274-4839A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572619 | |||||||
| chr3:123572649 | C | T | 18 | a0001c0001t0002g0117 a0001c0001t0002g0123 a0001c0001t0002g0124 others(15): Show |
18 | HG00423.hp1 HG00558.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.274-4869G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572649 | |||||||
| chr3:123572662 | T | C | 1 | a0001c0001t0002g0170 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.274-4882A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572662 | |||||||
| chr3:123572713 | GTTCAAT | G | 45 | a0001c0001t0003g0112 a0001c0003t0003g0006 a0001c0003t0003g0007 others(42): Show |
47 | HG00544.hp2 HG01928.hp2 HG01943.hp1 others(44): Show |
intron_variant | MODIFIER | c.274-4939_274-4934d others(8): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572713 | |||||||
| chr3:123572772 | G | C | 192 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(189): Show |
196 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.274-4992C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572772 | |||||||
| chr3:123572861 | C | T | 3 | a0001c0001t0006g0234 a0001c0001t0006g0235 a0001c0001t0006g0236 |
3 | HG02976.hp2 NA18522.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.274-5081G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572861 | |||||||
| chr3:123572940 | G | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.274-5160C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123572940 | |||||||
| chr3:123573081 | A | C | 1 | a0001c0001t0006g0233 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.274-5301T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573081 | |||||||
| chr3:123573184 | T | G | 25 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0173 others(22): Show |
25 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.274-5404A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573184 | |||||||
| chr3:123573212 | T | C | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-5432A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573212 | |||||||
| chr3:123573222 | G | A | 33 | a0001c0001t0005g0113 a0001c0001t0005g0114 a0001c0001t0005g0173 others(30): Show |
33 | HG00639.hp2 HG00673.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-5442C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573222 | |||||||
| chr3:123573337 | C | T | 1 | a0001c0001t0006g0225 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.274-5557G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573337 | |||||||
| chr3:123573439 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.274-5659C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573439 | |||||||
| chr3:123573636 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.274-5856A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573636 | |||||||
| chr3:123573737 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-5957C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573737 | |||||||
| chr3:123573737 | G | C | 1 | a0001c0003t0003g0294 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.274-5957C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573737 | |||||||
| chr3:123573920 | G | C | 5 | a0001c0002t0005g0094 a0001c0002t0005g0095 a0001c0002t0005g0096 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-6140C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573920 | |||||||
| chr3:123573941 | G | A | 10 | a0001c0003t0003g0313 a0001c0003t0003g0327 a0001c0003t0003g0329 others(7): Show |
10 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-6161C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123573941 | |||||||
| chr3:123574036 | A | G | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-6256T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574036 | |||||||
| chr3:123574160 | A | C | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.274-6380T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574160 | |||||||
| chr3:123574257 | G | A | 103 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(100): Show |
104 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.274-6477C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574257 | |||||||
| chr3:123574444 | T | C | 231 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(228): Show |
235 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.274-6664A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574444 | |||||||
| chr3:123574459 | T | C | 3 | a0001c0001t0002g0120 a0001c0001t0002g0168 a0001c0001t0002g0169 |
3 | HG00544.hp1 NA18942.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.274-6679A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574459 | |||||||
| chr3:123574637 | G | A | 1 | a0001c0003t0003g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.274-6857C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574637 | |||||||
| chr3:123574680 | CAT | C | 11 | a0001c0003t0001g0008 a0001c0003t0001g0314 a0001c0003t0001g0315 others(8): Show |
12 | HG00140.hp1 HG00323.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.274-6902_274-6901d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574680 | |||||||
| chr3:123574742 | C | T | 109 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(106): Show |
110 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.274-6962G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574742 | |||||||
| chr3:123574754 | A | T | 1 | a0001c0003t0001g0315 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.274-6974T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123574754 | |||||||
| chr3:123575011 | T | C | 1 | a0001c0001t0004g0111 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.273+7201A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575011 | |||||||
| chr3:123575068 | A | G | 1 | a0001c0002t0001g0022 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.273+7144T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575068 | |||||||
| chr3:123575110 | AT | A | 125 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(122): Show |
128 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.273+7101delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575110 | |||||||
| chr3:123575384 | T | C | 1 | a0001c0001t0026g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.273+6828A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575384 | |||||||
| chr3:123575506 | C | G | 5 | a0001c0002t0005g0094 a0001c0002t0005g0095 a0001c0002t0005g0096 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+6706G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575506 | |||||||
| chr3:123575622 | T | C | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+6590A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575622 | |||||||
| chr3:123575689 | T | G | 186 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(183): Show |
190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+6523A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575689 | |||||||
| chr3:123575739 | C | T | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+6473G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575739 | |||||||
| chr3:123575917 | G | A | 14 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0080 others(11): Show |
14 | NA18959.hp1 NA18962.hp1 NA18964.hp1 others(11): Show |
intron_variant | MODIFIER | c.273+6295C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575917 | |||||||
| chr3:123575938 | T | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+6274A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123575938 | |||||||
| chr3:123576059 | T | C | 1 | a0001c0003t0003g0336 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.273+6153A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576059 | |||||||
| chr3:123576186 | T | A | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+6026A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576186 | |||||||
| chr3:123576249 | CT | C | 225 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(222): Show |
229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+5962delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576249 | |||||||
| chr3:123576266 | T | C | 1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.273+5946A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576266 | |||||||
| chr3:123576726 | C | T | 1 | a0001c0002t0001g0016 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.273+5486G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576726 | |||||||
| chr3:123576849 | A | C | 2 | a0001c0001t0015g0223 a0001c0001t0015g0224 |
2 | HG02647.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.273+5363T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576849 | |||||||
| chr3:123576970 | A | C | 1 | a0001c0001t0026g0121 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.273+5242T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576970 | |||||||
| chr3:123576974 | C | G | 225 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(222): Show |
229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+5238G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123576974 | |||||||
| chr3:123577040 | T | TCAATTCC others(19): Show |
1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+5146_273+5171d others(28): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577040 | |||||||
| chr3:123577094 | A | G | 72 | a0001c0003t0001g0008 a0001c0003t0001g0314 a0001c0003t0001g0315 others(69): Show |
75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.273+5118T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577094 | |||||||
| chr3:123577105 | C | T | 186 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(183): Show |
190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+5107G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577105 | |||||||
| chr3:123577211 | T | C | 1 | a0001c0001t0004g0190 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.273+5001A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577211 | |||||||
| chr3:123577326 | T | C | 176 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(173): Show |
180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.273+4886A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577326 | |||||||
| chr3:123577396 | C | T | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+4816G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577396 | |||||||
| chr3:123577424 | A | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.273+4788T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577424 | |||||||
| chr3:123577437 | T | C | 225 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(222): Show |
229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+4775A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577437 | |||||||
| chr3:123577471 | A | G | 1 | a0001c0004t0017g0107 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.273+4741T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577471 | |||||||
| chr3:123577481 | T | C | 225 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(222): Show |
229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+4731A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577481 | |||||||
| chr3:123577620 | C | CA | 35 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(32): Show |
35 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.273+4591dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577620 | |||||||
| chr3:123577620 | CA | C | 172 | a0001c0001t0002g0120 a0001c0001t0013g0115 a0001c0001t0013g0116 others(169): Show |
176 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.273+4591delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577620 | |||||||
| chr3:123577620 | CAA | C | 7 | a0001c0002t0001g0018 a0001c0002t0005g0020 a0001c0002t0005g0021 others(4): Show |
7 | HG01516.hp2 NA18957.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+4590_273+4591d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577620 | |||||||
| chr3:123577629 | A | C | 8 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(5): Show |
8 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.273+4583T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577629 | |||||||
| chr3:123577846 | A | G | 225 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(222): Show |
229 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.273+4366T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577846 | |||||||
| chr3:123577896 | C | T | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.273+4316G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577896 | |||||||
| chr3:123577927 | C | G | 1 | a0001c0001t0001g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.273+4285G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577927 | |||||||
| chr3:123577930 | G | C | 176 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(173): Show |
180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.273+4282C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123577930 | |||||||
| chr3:123578028 | ACCCCACT others(4): Show |
A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4173_273+4183d others(13): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578028 | |||||||
| chr3:123578038 | C | G | 3 | a0001c0003t0005g0300 a0001c0003t0005g0301 a0001c0003t0005g0302 |
3 | HG02258.hp1 HG03098.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.273+4174G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578038 | |||||||
| chr3:123578052 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4160G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578052 | |||||||
| chr3:123578059 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4153T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578059 | |||||||
| chr3:123578060 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4152A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578060 | |||||||
| chr3:123578061 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4151A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578061 | |||||||
| chr3:123578063 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4149G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578063 | |||||||
| chr3:123578064 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4148A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578064 | |||||||
| chr3:123578066 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4146A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578066 | |||||||
| chr3:123578067 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4145T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578067 | |||||||
| chr3:123578076 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4136G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578076 | |||||||
| chr3:123578106 | TTATAAAT others(4): Show |
T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4095_273+4105d others(13): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578106 | |||||||
| chr3:123578118 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4094A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578118 | |||||||
| chr3:123578120 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4092T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578120 | |||||||
| chr3:123578121 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4091A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578121 | |||||||
| chr3:123578143 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4069G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578143 | |||||||
| chr3:123578147 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4065G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578147 | |||||||
| chr3:123578148 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4064A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578148 | |||||||
| chr3:123578150 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4062G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578150 | |||||||
| chr3:123578151 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4061A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578151 | |||||||
| chr3:123578152 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4060A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578152 | |||||||
| chr3:123578156 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4056G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578156 | |||||||
| chr3:123578170 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4042T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578170 | |||||||
| chr3:123578171 | G | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4041C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578171 | |||||||
| chr3:123578175 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4037A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578175 | |||||||
| chr3:123578176 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4036T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578176 | |||||||
| chr3:123578196 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4016A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578196 | |||||||
| chr3:123578209 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+4003T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578209 | |||||||
| chr3:123578214 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3998A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578214 | |||||||
| chr3:123578221 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3991T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578221 | |||||||
| chr3:123578232 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3980G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578232 | |||||||
| chr3:123578233 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3979G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578233 | |||||||
| chr3:123578234 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3978T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578234 | |||||||
| chr3:123578235 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3977A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578235 | |||||||
| chr3:123578239 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3973G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578239 | |||||||
| chr3:123578257 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3955A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578257 | |||||||
| chr3:123578262 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3950A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578262 | |||||||
| chr3:123578271 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3941A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578271 | |||||||
| chr3:123578273 | G | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3939C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578273 | |||||||
| chr3:123578275 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3937A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578275 | |||||||
| chr3:123578277 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3935G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578277 | |||||||
| chr3:123578279 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3933A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578279 | |||||||
| chr3:123578280 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3932A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578280 | |||||||
| chr3:123578281 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3931A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578281 | |||||||
| chr3:123578290 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3922T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578290 | |||||||
| chr3:123578299 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3913G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578299 | |||||||
| chr3:123578302 | G | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3910C>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578302 | |||||||
| chr3:123578303 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3909G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578303 | |||||||
| chr3:123578305 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3907G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578305 | |||||||
| chr3:123578306 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3906A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578306 | |||||||
| chr3:123578312 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3900G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578312 | |||||||
| chr3:123578321 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3891T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578321 | |||||||
| chr3:123578323 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3889A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578323 | |||||||
| chr3:123578324 | G | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3888C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578324 | |||||||
| chr3:123578326 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3886T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578326 | |||||||
| chr3:123578332 | A | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3880T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578332 | |||||||
| chr3:123578339 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3873A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578339 | |||||||
| chr3:123578342 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3870G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578342 | |||||||
| chr3:123578343 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3869A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578343 | |||||||
| chr3:123578344 | C | T | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3868G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578344 | |||||||
| chr3:123578345 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3867T>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578345 | |||||||
| chr3:123578353 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3859G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578353 | |||||||
| chr3:123578354 | T | C | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3858A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578354 | |||||||
| chr3:123578361 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3851G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578361 | |||||||
| chr3:123578376 | T | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3836A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578376 | |||||||
| chr3:123578377 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3835G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578377 | |||||||
| chr3:123578378 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3834G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578378 | |||||||
| chr3:123578379 | T | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3833A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578379 | |||||||
| chr3:123578384 | C | A | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3828G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578384 | |||||||
| chr3:123578387 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3825G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578387 | |||||||
| chr3:123578394 | C | G | 1 | a0001c0001t0002g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+3818G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578394 | |||||||
| chr3:123578415 | C | T | 4 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0002g0251 others(1): Show |
4 | HG02258.hp2 HG02451.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+3797G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578415 | |||||||
| chr3:123578559 | T | C | 100 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(97): Show |
101 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.273+3653A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578559 | |||||||
| chr3:123578589 | T | C | 223 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(220): Show |
227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.273+3623A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578589 | |||||||
| chr3:123578664 | T | C | 186 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(183): Show |
190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+3548A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578664 | |||||||
| chr3:123578893 | G | C | 176 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(173): Show |
180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.273+3319C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123578893 | |||||||
| chr3:123579093 | T | C | 2 | a0001c0003t0012g0303 a0001c0003t0012g0304 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.273+3119A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579093 | |||||||
| chr3:123579211 | G | A | 1 | a0001c0001t0004g0212 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.273+3001C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579211 | |||||||
| chr3:123579299 | G | GT | 13 | a0001c0001t0002g0005 a0001c0001t0002g0171 a0001c0001t0002g0172 others(10): Show |
14 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.273+2912dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579299 | |||||||
| chr3:123579369 | G | A | 95 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(92): Show |
96 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.273+2843C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579369 | |||||||
| chr3:123579450 | C | T | 1 | a0001c0003t0003g0254 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.273+2762G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579450 | |||||||
| chr3:123579474 | A | T | 1 | a0001c0002t0001g0016 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.273+2738T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579474 | |||||||
| chr3:123579523 | C | T | 37 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(34): Show |
37 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.273+2689G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579523 | |||||||
| chr3:123579586 | T | C | 1 | a0001c0002t0005g0091 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.273+2626A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579586 | |||||||
| chr3:123579768 | T | C | 186 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(183): Show |
190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+2444A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579768 | |||||||
| chr3:123579772 | G | A | 1 | a0001c0003t0001g0328 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.273+2440C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579772 | |||||||
| chr3:123579824 | G | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+2388C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579824 | |||||||
| chr3:123579887 | G | A | 1 | a0001c0003t0003g0327 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.273+2325C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579887 | |||||||
| chr3:123579999 | T | C | 11 | a0001c0001t0002g0005 a0001c0001t0002g0171 a0001c0001t0002g0172 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+2213A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123579999 | |||||||
| chr3:123580166 | C | CA | 48 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(45): Show |
49 | HG00140.hp1 HG01167.hp1 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.273+2045dupT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580166 | |||||||
| chr3:123580174 | A | G | 98 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(95): Show |
99 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.273+2038T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580174 | |||||||
| chr3:123580275 | A | G | 186 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(183): Show |
190 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.273+1937T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580275 | |||||||
| chr3:123580358 | C | T | 1 | a0001c0003t0005g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.273+1854G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580358 | |||||||
| chr3:123580389 | T | C | 32 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(29): Show |
32 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.273+1823A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580389 | |||||||
| chr3:123580620 | T | C | 1 | a0001c0001t0005g0173 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.273+1592A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580620 | |||||||
| chr3:123580733 | C | T | 176 | a0001c0002t0001g0001 a0001c0002t0001g0009 a0001c0002t0001g0010 others(173): Show |
180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.273+1479G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580733 | |||||||
| chr3:123580791 | GA | G | 98 | a0001c0001t0002g0117 a0001c0002t0001g0001 a0001c0002t0001g0009 others(95): Show |
99 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.273+1420delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580791 | |||||||
| chr3:123580853 | AT | A | 243 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(240): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.273+1358delA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580853 | |||||||
| chr3:123580853 | ATT | A | 15 | a0001c0001t0002g0251 a0001c0002t0001g0093 a0001c0003t0007g0306 others(12): Show |
15 | HG00099.hp1 HG00642.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.273+1357_273+1358d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580853 | |||||||
| chr3:123580878 | CAG | C | 5 | a0001c0002t0005g0094 a0001c0002t0005g0095 a0001c0002t0005g0096 others(2): Show |
5 | HG01109.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+1332_273+1333d others(4): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580878 | |||||||
| chr3:123580916 | C | T | 2 | a0001c0001t0013g0115 a0001c0001t0013g0116 |
2 | HG02965.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.273+1296G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123580916 | |||||||
| chr3:123581010 | C | T | 2 | a0001c0001t0005g0113 a0001c0001t0005g0114 |
2 | HG01358.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.273+1202G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581010 | |||||||
| chr3:123581035 | C | T | 2 | a0001c0001t0006g0218 a0001c0001t0019g0217 |
2 | HG02257.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.273+1177G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581035 | |||||||
| chr3:123581118 | C | T | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+1094G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581118 | |||||||
| chr3:123581119 | G | A | 2 | a0001c0001t0005g0199 a0001c0001t0005g0200 |
2 | HG00738.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.273+1093C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581119 | |||||||
| chr3:123581363 | A | G | 1 | a0001c0001t0003g0112 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.273+849T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581363 | |||||||
| chr3:123581451 | T | C | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+761A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581451 | |||||||
| chr3:123581501 | T | C | 1 | a0001c0001t0030g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.273+711A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581501 | |||||||
| chr3:123581657 | T | C | 1 | a0001c0003t0001g0328 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.273+555A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581657 | |||||||
| chr3:123581839 | C | G | 7 | a0001c0003t0001g0008 a0001c0003t0001g0314 a0001c0003t0001g0315 others(4): Show |
8 | HG00140.hp1 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.273+373G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581839 | |||||||
| chr3:123581878 | C | A | 9 | a0001c0003t0003g0313 a0001c0003t0003g0329 a0001c0003t0003g0330 others(6): Show |
9 | HG02145.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+334G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581878 | |||||||
| chr3:123581940 | T | C | 37 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(34): Show |
37 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.273+272A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123581940 | |||||||
| chr3:123582009 | A | G | 1 | a0001c0002t0001g0010 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.273+203T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123582009 | |||||||
| chr3:123582159 | G | C | 1 | a0001c0003t0003g0295 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.273+53C>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123582159 | |||||||
| chr3:123582177 | G | A | 10 | a0001c0003t0007g0305 a0001c0003t0007g0306 a0001c0003t0007g0307 others(7): Show |
10 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+35C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 2/6 | chr3 | 123582177 | |||||||
| chr3:123582395 | C | G | 223 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(220): Show |
227 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.156-66G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582395 | |||||||
| chr3:123582537 | G | A | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.156-208C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582537 | |||||||
| chr3:123582589 | C | G | 3 | a0001c0001t0004g0109 a0001c0001t0004g0110 a0001c0001t0004g0111 |
3 | HG01168.hp1 HG01169.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.156-260G>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582589 | |||||||
| chr3:123582654 | G | A | 1 | a0001c0003t0003g0296 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.156-325C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582654 | |||||||
| chr3:123582671 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.156-342G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582671 | |||||||
| chr3:123582692 | A | G | 1 | a0001c0002t0001g0009 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.156-363T>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582692 | |||||||
| chr3:123582791 | T | C | 25 | a0001c0003t0001g0008 a0001c0003t0001g0314 a0001c0003t0001g0315 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.156-462A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582791 | |||||||
| chr3:123582839 | T | C | 1 | a0001c0001t0002g0201 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.156-510A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123582839 | |||||||
| chr3:123583083 | G | A | 11 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0204 others(8): Show |
11 | HG00099.hp2 HG01123.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.156-754C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583083 | |||||||
| chr3:123583109 | T | C | 1 | a0001c0002t0001g0104 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.156-780A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583109 | |||||||
| chr3:123583202 | TA | T | 72 | a0001c0003t0001g0008 a0001c0003t0001g0314 a0001c0003t0001g0315 others(69): Show |
75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.156-874delT | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583202 | |||||||
| chr3:123583430 | G | GT | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-1102dupA | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583430 | |||||||
| chr3:123583437 | T | A | 2 | a0001c0001t0031g0342 a0001c0002t0001g0105 |
2 | HG01515.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.156-1108A>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583437 | |||||||
| chr3:123583688 | T | C | 37 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(34): Show |
37 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.155+1185A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583688 | |||||||
| chr3:123583847 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.155+1026C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123583847 | |||||||
| chr3:123584146 | T | C | 1 | a0001c0003t0003g0297 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.155+727A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584146 | |||||||
| chr3:123584245 | A | T | 1 | a0001c0003t0003g0313 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.155+628T>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584245 | |||||||
| chr3:123584440 | C | T | 2 | a0001c0003t0014g0298 a0001c0003t0014g0299 |
2 | HG02055.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.155+433G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584440 | |||||||
| chr3:123584457 | ACT | A | 3 | a0001c0001t0002g0214 a0001c0001t0002g0215 a0001c0001t0002g0216 |
3 | HG00597.hp1 HG02155.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.155+414_155+415del others(2): Show |
HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584457 | |||||||
| chr3:123584476 | T | C | 25 | a0001c0003t0001g0008 a0001c0003t0001g0314 a0001c0003t0001g0315 others(22): Show |
26 | HG00140.hp1 HG00323.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.155+397A>G | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584476 | |||||||
| chr3:123584508 | G | A | 1 | a0001c0002t0001g0106 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.155+365C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584508 | |||||||
| chr3:123584639 | C | A | 37 | a0001c0001t0001g0222 a0001c0001t0001g0246 a0001c0001t0001g0247 others(34): Show |
37 | HG01167.hp1 HG01169.hp1 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.155+234G>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584639 | |||||||
| chr3:123584650 | G | A | 47 | a0001c0003t0003g0006 a0001c0003t0003g0007 a0001c0003t0003g0253 others(44): Show |
49 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(46): Show |
intron_variant | MODIFIER | c.155+223C>T | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584650 | |||||||
| chr3:123584744 | T | G | 4 | a0001c0003t0010g0337 a0001c0003t0010g0338 a0001c0003t0010g0339 others(1): Show |
4 | HG02451.hp1 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.155+129A>C | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584744 | |||||||
| chr3:123584806 | C | T | 47 | a0001c0003t0003g0006 a0001c0003t0003g0007 a0001c0003t0003g0253 others(44): Show |
49 | HG00544.hp2 HG01109.hp1 HG01928.hp2 others(46): Show |
intron_variant | MODIFIER | c.155+67G>A | HACD2 | ENSG00000206527.10 | transcript | ENST00000383657.10 | protein_coding | 1/6 | chr3 | 123584806 |