Search by Gene
| Item | Value |
|---|---|
| geneid | 80724 |
| ensemblid | ENSG00000111271.15 |
| hgncid | 21597 |
| symbol | ACAD10 |
| name | acyl-CoA dehydrogenase family member 10 |
| refseq_nuc | NM_025247.6 |
| refseq_prot | NP_079523.3 |
| ensembl_nuc | ENST00000313698.9 |
| ensembl_prot | ENSP00000325137.5 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 111686053 |
| end | 111757099 |
| strand | + |
| ver | v1.2 |
| region | chr12:111686053-111757099 |
| region5000 | chr12:111681053-111762099 |
| regionname0 | ACAD10_chr12_111686053_111757099 |
| regionname5000 | ACAD10_chr12_111681053_111762099 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1059 | 311 | 74 | 50 | 150 | 4 | 31 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| a0002 | 0/0 | 1059 | 8 | 7 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| a0003 | 0/0 | 1059 | 6 | 0 | 2 | 0 | 2 | 2 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| a0004 | 0/0 | 1059 | 3 | 0 | 0 | 0 | 0 | 3 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| a0005 | 0/0 | 1005 | 2 | 0 | 1 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1000): Show |
chr12 | 111681053 | 111762099 |
| a0006 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| a0007 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| a0008 | 0/0 | 1059 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| a0009 | 0/0 | 1059 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| a0010 | 0/0 | 1059 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| a0011 | 0/0 | 1059 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | MCVRS others(1054): Show |
chr12 | 111681053 | 111762099 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3177 | 212 | 56 | 38 | 81 | 4 | 31 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0001c0002 | 0/0 | 3177 | 95 | 16 | 11 | 68 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0001c0006 | 0/0 | 3177 | 2 | 2 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0001c0008 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0001c0013 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0002c0003 | 0/0 | 3177 | 8 | 7 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0003c0004 | 0/0 | 3177 | 6 | 0 | 2 | 0 | 2 | 2 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0004c0005 | 0/0 | 3177 | 3 | 0 | 0 | 0 | 0 | 3 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0005c0009 | 0/0 | 3177 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0005c0016 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0006c0015 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0007c0007 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0008c0014 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0009c0012 | 0/0 | 3177 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0010c0011 | 0/0 | 3177 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 | ||
| a0011c0010 | 0/0 | 3177 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ATGTG others(3172): Show |
chr12 | 111681053 | 111762099 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4006 | 210 | 55 | 38 | 81 | 4 | 30 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0001c0001t0004 | 0/0 | 4006 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0001c0001t0005 | 0/0 | 4006 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0001c0002t0002 | 0/0 | 4006 | 95 | 16 | 11 | 68 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0001c0006t0001 | 0/0 | 4006 | 2 | 2 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0001c0008t0001 | 0/0 | 4006 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0001c0013t0001 | 0/0 | 4006 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0002c0003t0003 | 0/0 | 4006 | 8 | 7 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0003c0004t0001 | 0/0 | 4006 | 6 | 0 | 2 | 0 | 2 | 2 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0004c0005t0002 | 0/0 | 4006 | 3 | 0 | 0 | 0 | 0 | 3 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0005c0009t0006 | 0/0 | 4006 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0005c0016t0001 | 0/0 | 4006 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0006c0015t0001 | 0/0 | 4006 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0007c0007t0001 | 0/0 | 4006 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0008c0014t0001 | 0/0 | 4006 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0009c0012t0001 | 0/0 | 4006 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0010c0011t0002 | 0/0 | 4006 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| a0011c0010t0001 | 0/0 | 4006 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | ACTGC others(4001): Show |
chr12 | 111681053 | 111762099 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0262 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0006t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0006t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0008t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0001c0013t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0002c0003t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0002c0003t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0002c0003t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0002c0003t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0002c0003t0003g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0002c0003t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0002c0003t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0002c0003t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0003c0004t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0003c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0003c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0003c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0003c0004t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0003c0004t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0004c0005t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0004c0005t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0004c0005t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0005c0009t0006g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0005c0016t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0006c0015t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0007c0007t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0008c0014t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0009c0012t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0010c0011t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| a0011c0010t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | GBR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0236 | EUR | GBR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00140 | hp1 | a0003 | c0004 | t0001 | g0269 | EUR | GBR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0297 | EUR | GBR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | CHS | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | CHS | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0113 | EAS | CHS | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00738 | hp1 | a0003 | c0004 | t0001 | g0282 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0091 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01106 | hp1 | a0003 | c0004 | t0001 | g0186 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01243 | hp2 | a0005 | c0009 | t0006 | g0198 | AMR | PUR | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0094 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0095 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01884 | hp1 | a0001 | c0002 | t0002 | g0030 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0119 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01943 | hp2 | a0002 | c0003 | t0003 | g0322 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0116 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0118 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0104 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02056 | hp2 | a0001 | c0008 | t0001 | g0065 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02071 | hp1 | a0001 | c0002 | t0002 | g0146 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0114 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0130 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0117 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | CDX | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0017 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02257 | hp2 | a0002 | c0003 | t0003 | g0323 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0123 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02451 | hp1 | a0001 | c0002 | t0002 | g0025 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02630 | hp2 | a0001 | c0006 | t0001 | g0202 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02717 | hp1 | a0002 | c0003 | t0003 | g0320 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0125 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0027 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02809 | hp2 | a0002 | c0003 | t0003 | g0321 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02896 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02897 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02897 | hp2 | a0006 | c0015 | t0001 | g0317 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02965 | hp2 | a0002 | c0003 | t0003 | g0325 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03017 | hp1 | a0004 | c0005 | t0002 | g0109 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03017 | hp2 | a0003 | c0004 | t0001 | g0237 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0016 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03130 | hp2 | a0002 | c0003 | t0003 | g0319 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0201 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03239 | hp2 | a0004 | c0005 | t0002 | g0108 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03540 | hp2 | a0007 | c0007 | t0001 | g0014 | AFR | GWD | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | STU | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | STU | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0310 | SAS | PJL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | BEB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03834 | hp1 | a0008 | c0014 | t0001 | g0226 | SAS | BEB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | STU | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG04204 | hp1 | a0004 | c0005 | t0002 | g0099 | SAS | STU | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | STU | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | STU | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG04228 | hp2 | a0009 | c0012 | t0001 | g0305 | SAS | STU | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | CHB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0101 | EAS | CHB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | YRI | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | YRI | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18946 | hp1 | a0001 | c0002 | t0002 | g0172 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18947 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0181 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18952 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18954 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0096 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18960 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18961 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0183 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18967 | hp1 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18968 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18969 | hp2 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0137 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18978 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18981 | hp2 | a0010 | c0011 | t0002 | g0028 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0158 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18989 | hp1 | a0001 | c0002 | t0002 | g0168 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19009 | hp2 | a0005 | c0016 | t0001 | g0053 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19011 | hp1 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19030 | hp2 | a0002 | c0003 | t0003 | g0318 | AFR | LWK | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19054 | hp1 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19057 | hp2 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0174 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19070 | hp1 | a0001 | c0002 | t0002 | g0160 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19081 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0171 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19088 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0092 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | YRI | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA20129 | hp1 | a0011 | c0010 | t0001 | g0003 | AFR | ASW | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA20129 | hp2 | a0002 | c0003 | t0003 | g0324 | AFR | ASW | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA20752 | hp2 | a0003 | c0004 | t0001 | g0271 | EUR | TSI | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | GIH | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA20905 | hp2 | a0003 | c0004 | t0001 | g0272 | SAS | GIH | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01123 | hp1 | a0001 | c0013 | t0001 | g0258 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0140 | AMR | CLM | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0124 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0115 | AFR | USA | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | LWK | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0252 | REF | REF | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0262 | REF | REF | ACAD10_chr12_111681053_111762099 | ACAD10 | chr12 | 111681053 | 111762099 |
| view | chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111692806 | C | T | 1 | a0005 | 1 | NA19009.hp2 | stop_gained | HIGH | c.97C>T | p.Arg33* | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/21 | 297/4006 | 97/3180 | 33/1059 | chr12 | 111692806 | |||
| chr12:111692854 | A | G | 1 | a0006 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.145A>G | p.Met49Val | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/21 | 345/4006 | 145/3180 | 49/1059 | chr12 | 111692854 | |||
| chr12:111709593 | A | G | 1 | a0002 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.599A>G | p.Gln200Arg | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/21 | 799/4006 | 599/3180 | 200/1059 | chr12 | 111709593 | |||
| chr12:111709640 | A | C | 1 | a0002 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.646A>C | p.Thr216Pro | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/21 | 846/4006 | 646/3180 | 216/1059 | chr12 | 111709640 | |||
| chr12:111712604 | C | T | 1 | a0008 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.797C>T | p.Pro266Leu | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/21 | 997/4006 | 797/3180 | 266/1059 | chr12 | 111712604 | |||
| chr12:111729905 | C | A | 1 | a0004 | 3 | HG03017.hp1 HG03239.hp2 HG04204.hp1 |
missense_variant | MODERATE | c.1343C>A | p.Pro448His | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/21 | 1543/4006 | 1343/3180 | 448/1059 | chr12 | 111729905 | |||
| chr12:111736969 | C | G | 1 | a0002 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.1679C>G | p.Ala560Gly | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/21 | 1879/4006 | 1679/3180 | 560/1059 | chr12 | 111736969 | |||
| chr12:111744850 | A | G | 1 | a0009 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1922A>G | p.Glu641Gly | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/21 | 2122/4006 | 1922/3180 | 641/1059 | chr12 | 111744850 | |||
| chr12:111746229 | A | G | 1 | a0010 | 1 | NA18981.hp2 | missense_variant | MODERATE | c.2201A>G | p.Asn734Ser | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 14/21 | 2401/4006 | 2201/3180 | 734/1059 | chr12 | 111746229 | |||
| chr12:111747061 | T | C | 1 | a0007 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.2269T>C | p.Ser757Pro | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 15/21 | 2469/4006 | 2269/3180 | 757/1059 | chr12 | 111747061 | |||
| chr12:111748470 | C | T | 1 | a0003 | 6 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(3): Show |
missense_variant | MODERATE | c.2639C>T | p.Ala880Val | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 17/21 | 2839/4006 | 2639/3180 | 880/1059 | chr12 | 111748470 | |||
| chr12:111749178 | C | T | 1 | a0011 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.2650C>T | p.His884Tyr | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/21 | 2850/4006 | 2650/3180 | 884/1059 | chr12 | 111749178 | |||
| chr12:111749336 | G | A | 1 | a0007 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.2808G>A | p.Met936Ile | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/21 | 3008/4006 | 2808/3180 | 936/1059 | chr12 | 111749336 | |||
| chr12:111749344 | G | T | 1 | a0002 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.2816G>T | p.Arg939Leu | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/21 | 3016/4006 | 2816/3180 | 939/1059 | chr12 | 111749344 | |||
| chr12:111753865 | C | T | 1 | a0002 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.2911C>T | p.Arg971Trp | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/21 | 3111/4006 | 2911/3180 | 971/1059 | chr12 | 111753865 | |||
| chr12:111755722 | C | T | 1 | a0005 | 1 | HG01243.hp2 | stop_gained | HIGH | c.3016C>T | p.Arg1006* | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 20/21 | 3216/4006 | 3016/3180 | 1006/1059 | chr12 | 111755722 | |||
| chr12:111756433 | G | A | 1 | a0002 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.3140G>A | p.Arg1047Gln | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 21/21 | 3340/4006 | 3140/3180 | 1047/1059 | chr12 | 111756433 |
| view | chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111692760 | A | G | 1 | a0002c0003 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
synonymous_variant | LOW | c.51A>G | p.Arg17Arg | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/21 | 251/4006 | 51/3180 | 17/1059 | chr12 | 111692760 | |||
| chr12:111692862 | A | T | 1 | a0002c0003 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
synonymous_variant | LOW | c.153A>T | p.Gly51Gly | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/21 | 353/4006 | 153/3180 | 51/1059 | chr12 | 111692862 | |||
| chr12:111715957 | G | A | 1 | a0001c0006 | 2 | HG02630.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.987G>A | p.Glu329Glu | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/21 | 1187/4006 | 987/3180 | 329/1059 | chr12 | 111715957 | |||
| chr12:111728052 | A | G | 1 | a0002c0003 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
synonymous_variant | LOW | c.1152A>G | p.Arg384Arg | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/21 | 1352/4006 | 1152/3180 | 384/1059 | chr12 | 111728052 | |||
| chr12:111729901 | C | T | 1 | a0001c0013 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.1339C>T | p.Leu447Leu | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/21 | 1539/4006 | 1339/3180 | 447/1059 | chr12 | 111729901 | |||
| chr12:111736961 | T | A | 1 | a0002c0003 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
synonymous_variant | LOW | c.1671T>A | p.Arg557Arg | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/21 | 1871/4006 | 1671/3180 | 557/1059 | chr12 | 111736961 | |||
| chr12:111753837 | G | A | 3 | a0001c0002a0004c0005a0010c0011 | 99 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(96): Show |
synonymous_variant | LOW | c.2883G>A | p.Ala961Ala | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/21 | 3083/4006 | 2883/3180 | 961/1059 | chr12 | 111753837 | |||
| chr12:111756410 | C | T | 1 | a0001c0008 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.3117C>T | p.Ala1039Ala | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 21/21 | 3317/4006 | 3117/3180 | 1039/1059 | chr12 | 111756410 |
| view | chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111686125 | C | T | 1 | a0005c0009t0006 | 1 | HG01243.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/21 | 6585 | chr12 | 111686125 | ||||||
| chr12:111686141 | C | T | 1 | a0001c0001t0005 | 1 | HG02976.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-112C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/21 | chr12 | 111686141 | |||||||
| chr12:111756554 | G | A | 1 | a0002c0003t0003 | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*81G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 21/21 | 81 | chr12 | 111756554 | ||||||
| chr12:111756617 | T | G | 2 | a0001c0001t0005a0002c0003t0003 | 9 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*144T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 21/21 | 144 | chr12 | 111756617 | ||||||
| chr12:111756832 | A | G | 1 | a0001c0001t0004 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*359A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 21/21 | 359 | chr12 | 111756832 | ||||||
| chr12:111756923 | C | T | 3 | a0001c0002t0002a0004c0005t0002a0010c0011t0002 | 99 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*450C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 21/21 | 450 | chr12 | 111756923 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:111686365 | G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14+126G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111686365 | |||||||
| chr12:111686697 | CAA | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14+459_-14+460del others(2): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111686697 | |||||||
| chr12:111686883 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14+644C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111686883 | |||||||
| chr12:111686986 | G | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0006c0015t0001g0317 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-14+747G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111686986 | |||||||
| chr12:111687418 | C | A | 1 | a0001c0001t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14+1179C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111687418 | |||||||
| chr12:111687433 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-14+1194G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111687433 | |||||||
| chr12:111687512 | CAT | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14+1275_-14+1276d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | 111687512 | ||||||
| chr12:111687562 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-14+1323C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111687562 | |||||||
| chr12:111687620 | C | T | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | NA18959.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-14+1381C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111687620 | |||||||
| chr12:111687671 | T | C | 1 | a0007c0007t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14+1432T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111687671 | |||||||
| chr12:111687829 | T | C | 1 | a0001c0001t0001g0015 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-14+1590T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111687829 | |||||||
| chr12:111687908 | C | T | 1 | a0001c0001t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-14+1669C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111687908 | |||||||
| chr12:111688116 | C | A | 3 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0018 | 3 | HG02257.hp1 HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-14+1877C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688116 | |||||||
| chr12:111688160 | C | T | 1 | a0001c0001t0004g0310 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-14+1921C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688160 | |||||||
| chr12:111688242 | A | G | 1 | a0001c0001t0001g0309 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-14+2003A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688242 | |||||||
| chr12:111688261 | T | C | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(178): Show | 189 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-14+2022T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688261 | |||||||
| chr12:111688467 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14+2228T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688467 | |||||||
| chr12:111688573 | C | T | 1 | a0007c0007t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14+2334C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688573 | |||||||
| chr12:111688655 | A | G | 1 | a0001c0001t0001g0308 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-14+2416A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688655 | |||||||
| chr12:111688750 | C | G | 3 | a0001c0002t0002g0181a0001c0002t0002g0182a0001c0002t0002g0183 | 3 | NA18948.hp1 NA18964.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-14+2511C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688750 | |||||||
| chr12:111688810 | AC | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14+2572delC | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688810 | |||||||
| chr12:111688811 | C | A | 207 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(204): Show | 216 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.-14+2572C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688811 | |||||||
| chr12:111688892 | C | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-14+2653C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111688892 | |||||||
| chr12:111689017 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-14+2778C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689017 | |||||||
| chr12:111689185 | A | G | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-14+2946A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689185 | |||||||
| chr12:111689266 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14+3027A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689266 | |||||||
| chr12:111689287 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-14+3048T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689287 | |||||||
| chr12:111689320 | T | C | 1 | a0007c0007t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-14+3081T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689320 | |||||||
| chr12:111689363 | G | A | 1 | a0003c0004t0001g0186 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-14+3124G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689363 | |||||||
| chr12:111689408 | C | T | 1 | a0009c0012t0001g0305 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-14+3169C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689408 | |||||||
| chr12:111689528 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-3169C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689528 | |||||||
| chr12:111689532 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-3165T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689532 | |||||||
| chr12:111689720 | CTT | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-2965_-13-2964d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | 111689720 | ||||||
| chr12:111689966 | C | T | 4 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 4 | NA18960.hp1 NA18967.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-13-2731C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111689966 | |||||||
| chr12:111690366 | A | G | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0006c0015t0001g0317 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-13-2331A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111690366 | |||||||
| chr12:111690385 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-2312C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111690385 | |||||||
| chr12:111690392 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-13-2305A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111690392 | |||||||
| chr12:111690496 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-13-2201T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111690496 | |||||||
| chr12:111690511 | G | A | 2 | a0001c0002t0002g0020a0001c0002t0002g0021 | 2 | NA18942.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-13-2186G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111690511 | |||||||
| chr12:111690562 | A | C | 1 | a0001c0001t0001g0175 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-13-2135A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111690562 | |||||||
| chr12:111690678 | G | A | 6 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0024others(3): Show | 6 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-2019G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111690678 | |||||||
| chr12:111690740 | G | A | 27 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0187others(24): Show | 28 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.-13-1957G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111690740 | |||||||
| chr12:111690780 | C | CA | 12 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(9): Show | 12 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-13-1898dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | 111690780 | ||||||
| chr12:111690780 | C | CAAAAAAA others(3): Show |
1 | a0002c0003t0003g0325 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-13-1907_-13-1898d others(12): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | 111690780 | ||||||
| chr12:111690780 | C | CAAAAAAA others(4): Show |
6 | a0002c0003t0003g0319a0002c0003t0003g0320a0002c0003t0003g0321others(3): Show | 6 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-13-1908_-13-1898d others(13): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | 111690780 | ||||||
| chr12:111690780 | C | CAAAAAAA others(5): Show |
1 | a0002c0003t0003g0318 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-13-1909_-13-1898d others(14): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | 111690780 | ||||||
| chr12:111690780 | CA | C | 21 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(18): Show | 21 | HG01099.hp2 HG01256.hp1 HG01975.hp2 others(18): Show |
intron_variant | MODIFIER | c.-13-1898delA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | 111690780 | ||||||
| chr12:111691366 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-1331T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111691366 | |||||||
| chr12:111691487 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-1210C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111691487 | |||||||
| chr12:111691520 | G | A | 9 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0024others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-13-1177G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111691520 | |||||||
| chr12:111691541 | G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0006c0015t0001g0317 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-13-1156G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111691541 | |||||||
| chr12:111691594 | A | AT | 43 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(40): Show | 47 | HG00140.hp2 HG00544.hp1 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.-13-1084dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | 111691594 | ||||||
| chr12:111691594 | AT | A | 25 | a0001c0001t0001g0161a0001c0001t0001g0210a0001c0001t0001g0211others(22): Show | 25 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(22): Show |
intron_variant | MODIFIER | c.-13-1084delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr12 | 111691594 | ||||||
| chr12:111691805 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-892A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111691805 | |||||||
| chr12:111691895 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-802C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111691895 | |||||||
| chr12:111691931 | G | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-13-766G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111691931 | |||||||
| chr12:111691969 | T | G | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-13-728T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111691969 | |||||||
| chr12:111692072 | G | A | 20 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(17): Show | 20 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.-13-625G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111692072 | |||||||
| chr12:111692214 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-13-483C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111692214 | |||||||
| chr12:111692247 | A | C | 94 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0016others(91): Show | 99 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.-13-450A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111692247 | |||||||
| chr12:111692395 | G | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(81): Show | 87 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.-13-302G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111692395 | |||||||
| chr12:111692614 | G | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-83G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111692614 | |||||||
| chr12:111692686 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.-13-11T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 1/20 | chr12 | 111692686 | |||||||
| chr12:111692904 | A | G | 94 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0016others(91): Show | 99 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(96): Show |
splice_region_variant&intron_variant | LOW | c.187+8A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111692904 | |||||||
| chr12:111693111 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.187+215G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111693111 | |||||||
| chr12:111693116 | T | C | 6 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(3): Show | 6 | NA18952.hp2 NA18973.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+220T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111693116 | |||||||
| chr12:111693145 | G | A | 1 | a0008c0014t0001g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.187+249G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111693145 | |||||||
| chr12:111693265 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+369A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111693265 | |||||||
| chr12:111693304 | C | T | 1 | a0001c0002t0002g0140 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.187+408C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111693304 | |||||||
| chr12:111693361 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.187+465A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111693361 | |||||||
| chr12:111693894 | G | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(80): Show | 86 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.187+998G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111693894 | |||||||
| chr12:111694017 | A | C | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | NA18984.hp1 NA18986.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.187+1121A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694017 | |||||||
| chr12:111694139 | G | A | 2 | a0001c0002t0002g0004a0001c0002t0002g0091 | 3 | HG01071.hp2 HG01433.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.187+1243G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694139 | |||||||
| chr12:111694271 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.187+1375T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694271 | |||||||
| chr12:111694300 | C | G | 1 | a0001c0001t0001g0291 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.187+1404C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694300 | |||||||
| chr12:111694402 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+1506G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694402 | |||||||
| chr12:111694472 | A | G | 94 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0016others(91): Show | 99 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.187+1576A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694472 | |||||||
| chr12:111694488 | C | CT | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+1598dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111694488 | ||||||
| chr12:111694601 | C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0208a0001c0001t0001g0308 | 3 | HG01884.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.187+1705C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694601 | |||||||
| chr12:111694662 | A | ACT | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+1767_187+1768d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111694662 | ||||||
| chr12:111694666 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.187+1770C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694666 | |||||||
| chr12:111694806 | G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.187+1910G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694806 | |||||||
| chr12:111694828 | C | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(178): Show | 189 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.187+1932C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694828 | |||||||
| chr12:111694837 | C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | NA18971.hp2 NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.187+1941C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694837 | |||||||
| chr12:111694838 | C | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | NA18971.hp2 NA18980.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.187+1942C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111694838 | |||||||
| chr12:111695071 | T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(81): Show | 87 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.187+2175T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111695071 | |||||||
| chr12:111695466 | C | T | 1 | a0001c0002t0002g0140 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.187+2570C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111695466 | |||||||
| chr12:111695581 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.187+2685G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111695581 | |||||||
| chr12:111695589 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+2693A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111695589 | |||||||
| chr12:111695789 | G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.187+2893G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111695789 | |||||||
| chr12:111695979 | G | A | 1 | a0007c0007t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.187+3083G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111695979 | |||||||
| chr12:111695987 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.187+3091T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111695987 | |||||||
| chr12:111696013 | CA | C | 204 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(201): Show | 213 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.187+3130delA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111696013 | ||||||
| chr12:111696026 | A | T | 1 | a0001c0001t0001g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.187+3130A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111696026 | |||||||
| chr12:111696027 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.187+3131G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111696027 | |||||||
| chr12:111696118 | G | A | 2 | a0001c0001t0001g0315a0006c0015t0001g0317 | 2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.187+3222G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111696118 | |||||||
| chr12:111696120 | G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(80): Show | 86 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.187+3224G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111696120 | |||||||
| chr12:111696281 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.187+3385G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111696281 | |||||||
| chr12:111696454 | GAAAATTA others(28): Show |
G | 1 | a0001c0002t0002g0172 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.187+3562_187+3596d others(37): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111696454 | ||||||
| chr12:111696738 | C | G | 1 | a0007c0007t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.187+3842C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111696738 | |||||||
| chr12:111696858 | G | T | 8 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(5): Show | 8 | HG01928.hp1 HG01934.hp2 HG01978.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+3962G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111696858 | |||||||
| chr12:111696864 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+3968G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111696864 | |||||||
| chr12:111696941 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.187+4045C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111696941 | |||||||
| chr12:111697059 | C | T | 2 | a0001c0001t0001g0315a0006c0015t0001g0317 | 2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.187+4163C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697059 | |||||||
| chr12:111697080 | C | CAA | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(173): Show | 184 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(181): Show |
intron_variant | MODIFIER | c.187+4198_187+4199d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111697080 | ||||||
| chr12:111697100 | G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0006c0015t0001g0317 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.187+4204G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697100 | |||||||
| chr12:111697166 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.187+4270G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697166 | |||||||
| chr12:111697167 | G | C | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(80): Show | 86 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.187+4271G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697167 | |||||||
| chr12:111697233 | T | G | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.187+4337T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697233 | |||||||
| chr12:111697235 | C | T | 1 | a0001c0002t0002g0160 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.187+4339C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697235 | |||||||
| chr12:111697255 | A | T | 1 | a0001c0002t0002g0160 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.187+4359A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697255 | |||||||
| chr12:111697362 | CT | C | 10 | a0001c0001t0001g0038a0001c0002t0002g0093a0002c0003t0003g0318others(7): Show | 10 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.187+4482delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111697362 | ||||||
| chr12:111697416 | A | G | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.187+4520A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697416 | |||||||
| chr12:111697471 | G | A | 83 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(80): Show | 86 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.187+4575G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697471 | |||||||
| chr12:111697584 | C | CT | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(180): Show | 191 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.188-4560dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111697584 | ||||||
| chr12:111697584 | C | CTT | 9 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(6): Show | 9 | HG02074.hp2 HG02738.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-4561_188-4560d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111697584 | ||||||
| chr12:111697671 | G | A | 6 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(3): Show | 6 | HG01943.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-4491G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697671 | |||||||
| chr12:111697672 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.188-4490C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111697672 | |||||||
| chr12:111697908 | TCATTTGC others(53): Show |
T | 1 | a0001c0001t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.188-4223_188-4164d others(62): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111697908 | ||||||
| chr12:111697938 | C | CT | 6 | a0001c0001t0001g0054a0001c0001t0001g0295a0001c0001t0001g0298others(3): Show | 6 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-4208dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111697938 | ||||||
| chr12:111697999 | C | CT | 16 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(13): Show | 16 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(13): Show |
intron_variant | MODIFIER | c.188-4150dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111697999 | ||||||
| chr12:111698136 | A | C | 1 | a0001c0002t0002g0158 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.188-4026A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111698136 | |||||||
| chr12:111698297 | C | CT | 13 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0167others(10): Show | 13 | HG01433.hp1 HG02559.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.188-3848dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111698297 | ||||||
| chr12:111698297 | CT | C | 9 | a0001c0001t0001g0090a0002c0003t0003g0318a0002c0003t0003g0319others(6): Show | 9 | HG01175.hp1 HG01943.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-3848delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111698297 | ||||||
| chr12:111698404 | C | CT | 20 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(17): Show | 20 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.188-3743dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111698404 | ||||||
| chr12:111698404 | CT | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 126 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.188-3743delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111698404 | ||||||
| chr12:111698404 | CTT | C | 93 | a0001c0001t0001g0015a0001c0002t0002g0001a0001c0002t0002g0004others(90): Show | 98 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.188-3744_188-3743d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111698404 | ||||||
| chr12:111698477 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.188-3685G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111698477 | |||||||
| chr12:111698612 | G | A | 1 | a0008c0014t0001g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.188-3550G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111698612 | |||||||
| chr12:111698658 | G | C | 1 | a0007c0007t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.188-3504G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111698658 | |||||||
| chr12:111698772 | G | A | 9 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0024others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-3390G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111698772 | |||||||
| chr12:111698779 | C | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.188-3383C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111698779 | |||||||
| chr12:111699319 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-2843A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111699319 | |||||||
| chr12:111699365 | T | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-2797T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111699365 | |||||||
| chr12:111699663 | C | T | 1 | a0001c0001t0001g0234 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.188-2499C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111699663 | |||||||
| chr12:111699796 | T | A | 2 | a0001c0002t0002g0094a0001c0002t0002g0095 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.188-2366T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111699796 | |||||||
| chr12:111699826 | A | T | 1 | a0001c0002t0002g0092 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.188-2336A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111699826 | |||||||
| chr12:111700168 | A | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-1994A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111700168 | |||||||
| chr12:111700649 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.188-1513A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111700649 | |||||||
| chr12:111700723 | T | TTTCCTTC others(17): Show |
7 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(4): Show | 7 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-1418_188-1417i others(26): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111700723 | ||||||
| chr12:111700723 | TTTCC | T | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0006c0015t0001g0317 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.188-1421_188-1418d others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111700723 | ||||||
| chr12:111700741 | T | C | 1 | a0001c0001t0005g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.188-1421T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111700741 | |||||||
| chr12:111700744 | T | TTCCTTCC others(7): Show |
1 | a0002c0003t0003g0324 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.188-1418_188-1417i others(16): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111700744 | |||||||
| chr12:111700748 | C | CT | 21 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076others(18): Show | 21 | HG01361.hp2 HG01952.hp1 HG02027.hp1 others(18): Show |
intron_variant | MODIFIER | c.188-1389dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111700748 | ||||||
| chr12:111700748 | CT | C | 31 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0040others(28): Show | 31 | HG00099.hp1 HG00099.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.188-1389delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111700748 | ||||||
| chr12:111700749 | T | C | 1 | a0002c0003t0003g0324 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.188-1413T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111700749 | |||||||
| chr12:111700883 | C | T | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.188-1279C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111700883 | |||||||
| chr12:111701080 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.188-1082C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111701080 | |||||||
| chr12:111701145 | A | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.188-1017A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111701145 | |||||||
| chr12:111701402 | TCACA | T | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.188-755_188-752del others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111701402 | ||||||
| chr12:111701408 | A | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.188-754A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111701408 | |||||||
| chr12:111701427 | GAGGC | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.188-724_188-721del others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 111701427 | ||||||
| chr12:111701537 | C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0090 | 2 | HG00099.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.188-625C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111701537 | |||||||
| chr12:111701607 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.188-555A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111701607 | |||||||
| chr12:111701616 | G | C | 2 | a0001c0002t0002g0098a0001c0002t0002g0146 | 2 | HG02071.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.188-546G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111701616 | |||||||
| chr12:111701714 | G | A | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0281 | 3 | HG01099.hp1 HG01175.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.188-448G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111701714 | |||||||
| chr12:111701821 | C | T | 2 | a0001c0006t0001g0201a0001c0006t0001g0202 | 2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.188-341C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 2/20 | chr12 | 111701821 | |||||||
| chr12:111702605 | T | C | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(186): Show | 197 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.336+295T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111702605 | |||||||
| chr12:111702755 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.336+445C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111702755 | |||||||
| chr12:111702852 | G | A | 1 | a0001c0002t0002g0091 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.336+542G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111702852 | |||||||
| chr12:111702865 | A | G | 28 | a0001c0002t0002g0001a0001c0002t0002g0029a0001c0002t0002g0033others(25): Show | 32 | HG00544.hp1 HG02071.hp1 HG02129.hp2 others(29): Show |
intron_variant | MODIFIER | c.336+555A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111702865 | |||||||
| chr12:111702881 | C | T | 1 | a0001c0001t0005g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.336+571C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111702881 | |||||||
| chr12:111702930 | C | G | 1 | a0001c0001t0001g0315 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.336+620C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111702930 | |||||||
| chr12:111703008 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.336+698C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703008 | |||||||
| chr12:111703011 | G | A | 79 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0020others(76): Show | 84 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.336+701G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703011 | |||||||
| chr12:111703083 | C | CA | 15 | a0001c0001t0001g0037a0001c0001t0001g0043a0001c0001t0001g0230others(12): Show | 15 | HG01106.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.336+792dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111703083 | ||||||
| chr12:111703083 | C | CAA | 8 | a0001c0001t0001g0042a0002c0003t0003g0318a0002c0003t0003g0319others(5): Show | 8 | HG01943.hp2 HG02717.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.336+791_336+792dup others(2): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111703083 | ||||||
| chr12:111703101 | AATT | A | 76 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0020others(73): Show | 81 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.336+792_336+794del others(3): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703101 | |||||||
| chr12:111703102 | ATT | A | 3 | a0001c0002t0002g0100a0001c0002t0002g0138a0004c0005t0002g0099 | 3 | HG02074.hp2 HG04204.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.336+793_336+794del others(2): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703102 | |||||||
| chr12:111703429 | A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(253): Show | 265 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.336+1119A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703429 | |||||||
| chr12:111703461 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.336+1151T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703461 | |||||||
| chr12:111703766 | G | A | 264 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(261): Show | 273 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.336+1456G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703766 | |||||||
| chr12:111703766 | G | C | 1 | a0001c0001t0001g0185 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.336+1456G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703766 | |||||||
| chr12:111703793 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.336+1483A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703793 | |||||||
| chr12:111703796 | A | T | 1 | a0008c0014t0001g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.336+1486A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703796 | |||||||
| chr12:111703827 | G | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.336+1517G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703827 | |||||||
| chr12:111703870 | A | G | 1 | a0001c0001t0001g0307 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.336+1560A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703870 | |||||||
| chr12:111703905 | T | TTA | 41 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(38): Show | 41 | HG00140.hp1 HG00738.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.336+1614_336+1615d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111703905 | ||||||
| chr12:111703905 | TTA | T | 14 | a0001c0001t0001g0038a0001c0001t0001g0044a0001c0001t0001g0045others(11): Show | 14 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.336+1614_336+1615d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111703905 | ||||||
| chr12:111703943 | G | A | 3 | a0001c0001t0001g0233a0001c0001t0001g0246a0001c0001t0001g0298 | 3 | NA19056.hp2 NA19079.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.336+1633G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111703943 | |||||||
| chr12:111704007 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.336+1697G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111704007 | |||||||
| chr12:111704134 | C | CT | 9 | a0001c0001t0001g0235a0002c0003t0003g0318a0002c0003t0003g0319others(6): Show | 9 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.337-1591dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111704134 | ||||||
| chr12:111704148 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.337-1590A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111704148 | |||||||
| chr12:111704169 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.337-1569T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111704169 | |||||||
| chr12:111704235 | G | A | 1 | a0001c0002t0002g0101 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.337-1503G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111704235 | |||||||
| chr12:111704306 | C | T | 190 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(187): Show | 198 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.337-1432C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111704306 | |||||||
| chr12:111704493 | G | C | 3 | a0001c0001t0001g0194a0001c0001t0001g0208a0001c0001t0001g0308 | 3 | HG01884.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.337-1245G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111704493 | |||||||
| chr12:111704664 | T | TTTTC | 3 | a0001c0001t0001g0013a0001c0001t0001g0242a0001c0006t0001g0202 | 3 | HG02559.hp2 HG02630.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.337-1050_337-1047d others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111704664 | ||||||
| chr12:111704678 | TTCTTTCT others(3): Show |
T | 1 | a0001c0001t0001g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.337-1058_337-1049d others(12): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111704678 | ||||||
| chr12:111704688 | C | CT | 97 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0041others(94): Show | 101 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.337-1033dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111704688 | ||||||
| chr12:111704688 | C | CTT | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(83): Show | 90 | HG00597.hp2 HG00735.hp2 HG01071.hp2 others(87): Show |
intron_variant | MODIFIER | c.337-1034_337-1033d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111704688 | ||||||
| chr12:111704688 | C | CTTT | 9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(6): Show | 9 | HG03688.hp1 HG03927.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.337-1035_337-1033d others(5): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 111704688 | ||||||
| chr12:111704717 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-1021T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111704717 | |||||||
| chr12:111704929 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.337-809T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111704929 | |||||||
| chr12:111705235 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.337-503G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111705235 | |||||||
| chr12:111705404 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.337-334A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111705404 | |||||||
| chr12:111705408 | T | G | 3 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249 | 3 | HG02080.hp2 NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.337-330T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111705408 | |||||||
| chr12:111705718 | G | A | 1 | a0001c0002t0002g0033 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.337-20G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 3/20 | chr12 | 111705718 | |||||||
| chr12:111706140 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.531+208G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706140 | |||||||
| chr12:111706192 | A | G | 1 | a0002c0003t0003g0324 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.531+260A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706192 | |||||||
| chr12:111706404 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.531+472G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706404 | |||||||
| chr12:111706581 | C | T | 20 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(17): Show | 20 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.531+649C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706581 | |||||||
| chr12:111706760 | T | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.531+828T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706760 | |||||||
| chr12:111706762 | T | A | 93 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0016others(90): Show | 98 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.531+830T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706762 | |||||||
| chr12:111706778 | A | AT | 18 | a0001c0001t0001g0015a0001c0001t0001g0037a0001c0001t0001g0039others(15): Show | 18 | HG01167.hp2 HG02273.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.531+847dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111706778 | ||||||
| chr12:111706778 | A | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0311a0007c0007t0001g0014 | 3 | HG00408.hp2 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.531+846A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706778 | |||||||
| chr12:111706780 | A | AT | 124 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0019others(121): Show | 131 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.531+849dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111706780 | ||||||
| chr12:111706780 | A | ATT | 11 | a0001c0001t0001g0068a0001c0001t0001g0080a0001c0002t0002g0094others(8): Show | 11 | HG01256.hp2 HG01258.hp1 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.531+849_531+850ins others(2): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111706780 | ||||||
| chr12:111706780 | A | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0036others(35): Show | 39 | HG00408.hp2 HG01167.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.531+848A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706780 | |||||||
| chr12:111706782 | A | AT | 17 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(14): Show | 17 | HG01884.hp1 HG01934.hp1 HG01934.hp2 others(14): Show |
intron_variant | MODIFIER | c.531+861dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111706782 | ||||||
| chr12:111706782 | A | ATATATTT others(5): Show |
1 | a0002c0003t0003g0325 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.531+851_531+852ins others(12): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111706782 | ||||||
| chr12:111706782 | A | ATATATTT others(6): Show |
3 | a0002c0003t0003g0319a0002c0003t0003g0320a0002c0003t0003g0323 | 3 | HG02257.hp2 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.531+851_531+852ins others(13): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111706782 | ||||||
| chr12:111706782 | A | ATATTTTT others(5): Show |
1 | a0002c0003t0003g0324 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.531+851_531+852ins others(12): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111706782 | ||||||
| chr12:111706782 | A | ATATTTTT others(6): Show |
3 | a0002c0003t0003g0318a0002c0003t0003g0321a0002c0003t0003g0322 | 3 | HG01943.hp2 HG02809.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.531+851_531+852ins others(13): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111706782 | ||||||
| chr12:111706782 | A | ATT | 5 | a0001c0001t0001g0090a0001c0002t0002g0004a0001c0002t0002g0091others(2): Show | 6 | HG00408.hp1 HG01071.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.531+860_531+861dup others(2): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111706782 | ||||||
| chr12:111706782 | A | T | 191 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0012others(188): Show | 199 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(196): Show |
intron_variant | MODIFIER | c.531+850A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706782 | |||||||
| chr12:111706784 | T | A | 3 | a0001c0001t0001g0222a0001c0001t0001g0225a0001c0001t0001g0238 | 3 | HG01175.hp2 HG02451.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.531+852T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706784 | |||||||
| chr12:111706786 | T | A | 1 | a0001c0001t0001g0225 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.531+854T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706786 | |||||||
| chr12:111706842 | C | T | 9 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0024others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.531+910C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706842 | |||||||
| chr12:111706843 | G | A | 2 | a0001c0006t0001g0201a0001c0006t0001g0202 | 2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.531+911G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111706843 | |||||||
| chr12:111707151 | G | A | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.531+1219G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707151 | |||||||
| chr12:111707154 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.531+1222A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707154 | |||||||
| chr12:111707194 | A | G | 1 | a0001c0002t0002g0134 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.531+1262A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707194 | |||||||
| chr12:111707204 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.531+1272C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707204 | |||||||
| chr12:111707296 | C | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(263): Show | 275 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.531+1364C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707296 | |||||||
| chr12:111707412 | A | ATT | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(178): Show | 189 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.531+1480_531+1481i others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707412 | |||||||
| chr12:111707413 | A | T | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(178): Show | 189 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.531+1481A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707413 | |||||||
| chr12:111707417 | G | GT | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.531+1488dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111707417 | ||||||
| chr12:111707657 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.531+1725T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707657 | |||||||
| chr12:111707673 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.531+1741C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707673 | |||||||
| chr12:111707789 | G | A | 1 | a0001c0001t0005g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.532-1737G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111707789 | |||||||
| chr12:111708007 | C | T | 5 | a0001c0001t0001g0052a0001c0001t0001g0177a0001c0001t0001g0178others(2): Show | 5 | NA18960.hp1 NA18967.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-1519C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111708007 | |||||||
| chr12:111708123 | A | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-1403A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111708123 | |||||||
| chr12:111708328 | C | G | 1 | a0001c0001t0001g0042 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.532-1198C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111708328 | |||||||
| chr12:111708401 | G | A | 4 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0224others(1): Show | 4 | HG02135.hp2 NA18954.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.532-1125G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111708401 | |||||||
| chr12:111708470 | A | G | 1 | a0001c0002t0002g0101 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.532-1056A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111708470 | |||||||
| chr12:111708471 | C | CT | 11 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0078others(8): Show | 11 | HG00099.hp1 HG01175.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.532-1044dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111708471 | ||||||
| chr12:111708751 | C | A | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.532-775C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111708751 | |||||||
| chr12:111708904 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.532-622C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111708904 | |||||||
| chr12:111709007 | C | T | 2 | a0001c0002t0002g0114a0001c0002t0002g0120 | 2 | HG02080.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.532-519C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111709007 | |||||||
| chr12:111709045 | C | CA | 13 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 13 | HG01175.hp2 HG02071.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.532-466dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 111709045 | ||||||
| chr12:111709107 | C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(79): Show | 85 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.532-419C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111709107 | |||||||
| chr12:111709160 | C | T | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(252): Show | 264 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.532-366C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 4/20 | chr12 | 111709160 | |||||||
| chr12:111709734 | C | A | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.690+50C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111709734 | |||||||
| chr12:111710172 | C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.690+488C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111710172 | |||||||
| chr12:111710308 | G | A | 9 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0043others(6): Show | 9 | NA18946.hp2 NA18950.hp2 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.690+624G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111710308 | |||||||
| chr12:111710450 | G | A | 3 | a0001c0002t0002g0103a0001c0002t0002g0104a0001c0002t0002g0160 | 3 | HG02040.hp1 NA19070.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.690+766G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111710450 | |||||||
| chr12:111710497 | A | AT | 10 | a0001c0001t0001g0085a0001c0001t0001g0184a0001c0001t0001g0189others(7): Show | 10 | HG02027.hp1 HG02055.hp2 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.690+828dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr12 | 111710497 | ||||||
| chr12:111710639 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.690+955C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111710639 | |||||||
| chr12:111710775 | G | A | 1 | a0001c0002t0002g0105 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.690+1091G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111710775 | |||||||
| chr12:111710862 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.690+1178G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111710862 | |||||||
| chr12:111710917 | G | A | 1 | a0005c0009t0006g0198 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.690+1233G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111710917 | |||||||
| chr12:111710980 | G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.690+1296G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111710980 | |||||||
| chr12:111711294 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.691-1204G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111711294 | |||||||
| chr12:111711447 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.691-1051G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111711447 | |||||||
| chr12:111711522 | A | AT | 15 | a0001c0001t0001g0054a0001c0001t0001g0072a0001c0001t0001g0073others(12): Show | 15 | HG01884.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.691-956dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr12 | 111711522 | ||||||
| chr12:111711522 | AT | A | 20 | a0001c0001t0001g0041a0001c0001t0001g0044a0001c0001t0001g0060others(17): Show | 20 | HG00099.hp1 HG01943.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.691-956delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr12 | 111711522 | ||||||
| chr12:111711586 | C | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-912C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111711586 | |||||||
| chr12:111711804 | G | A | 5 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0190others(2): Show | 5 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.691-694G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111711804 | |||||||
| chr12:111712264 | T | G | 1 | a0001c0001t0001g0274 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.691-234T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111712264 | |||||||
| chr12:111712279 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.691-219G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 5/20 | chr12 | 111712279 | |||||||
| chr12:111712759 | G | A | 1 | a0001c0002t0002g0106 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.850+102G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111712759 | |||||||
| chr12:111712858 | C | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0251 | 2 | NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.850+201C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111712858 | |||||||
| chr12:111713137 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.850+480C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713137 | |||||||
| chr12:111713279 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.850+622C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713279 | |||||||
| chr12:111713316 | GA | G | 10 | a0001c0001t0001g0199a0001c0001t0001g0265a0002c0003t0003g0318others(7): Show | 10 | HG00544.hp2 HG01943.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.850+670delA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 111713316 | ||||||
| chr12:111713448 | A | C | 6 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(3): Show | 6 | NA18952.hp2 NA18973.hp2 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.850+791A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713448 | |||||||
| chr12:111713624 | CA | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0187others(15): Show | 19 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.850+978delA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 111713624 | ||||||
| chr12:111713672 | C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(177): Show | 188 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.850+1015C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713672 | |||||||
| chr12:111713886 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.850+1229A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713886 | |||||||
| chr12:111713933 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.850+1276C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713933 | |||||||
| chr12:111713937 | C | A | 1 | a0005c0009t0006g0198 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.850+1280C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713937 | |||||||
| chr12:111713937 | C | CA | 3 | a0001c0001t0001g0235a0001c0001t0001g0266a0001c0002t0002g0107 | 3 | HG01496.hp2 NA18950.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.850+1280_850+1281i others(3): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713937 | |||||||
| chr12:111713938 | C | A | 297 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(294): Show | 307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.850+1281C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713938 | |||||||
| chr12:111713938 | C | CA | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.850+1291dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 111713938 | ||||||
| chr12:111713950 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.850+1293G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713950 | |||||||
| chr12:111713964 | C | T | 3 | a0001c0001t0001g0194a0001c0001t0001g0208a0001c0001t0001g0308 | 3 | HG01884.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.850+1307C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111713964 | |||||||
| chr12:111714149 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.850+1492A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714149 | |||||||
| chr12:111714229 | A | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.850+1572A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714229 | |||||||
| chr12:111714245 | C | CA | 9 | a0001c0001t0001g0082a0002c0003t0003g0318a0002c0003t0003g0319others(6): Show | 9 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.851-1560dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 111714245 | ||||||
| chr12:111714424 | T | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.851-1397T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714424 | |||||||
| chr12:111714490 | C | A | 1 | a0001c0001t0001g0279 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.851-1331C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714490 | |||||||
| chr12:111714641 | G | A | 7 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG01099.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.851-1180G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714641 | |||||||
| chr12:111714703 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.851-1118T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714703 | |||||||
| chr12:111714722 | T | A | 1 | a0001c0001t0001g0086 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.851-1099T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714722 | |||||||
| chr12:111714798 | C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0077 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.851-1023C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714798 | |||||||
| chr12:111714837 | C | T | 6 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(3): Show | 6 | HG01943.hp2 HG02717.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.851-984C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714837 | |||||||
| chr12:111714962 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.851-859C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714962 | |||||||
| chr12:111714969 | G | A | 1 | a0004c0005t0002g0108 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.851-852G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111714969 | |||||||
| chr12:111715021 | A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0161 | 2 | NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.851-800A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111715021 | |||||||
| chr12:111715058 | C | T | 1 | a0001c0001t0001g0205 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.851-763C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111715058 | |||||||
| chr12:111715262 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.851-559T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111715262 | |||||||
| chr12:111715328 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.851-493A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111715328 | |||||||
| chr12:111715412 | C | T | 2 | a0001c0001t0001g0309a0001c0001t0004g0310 | 2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.851-409C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111715412 | |||||||
| chr12:111715696 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.851-125C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111715696 | |||||||
| chr12:111715739 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.851-82A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 6/20 | chr12 | 111715739 | |||||||
| chr12:111716054 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.992+92T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111716054 | |||||||
| chr12:111716136 | C | G | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.992+174C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111716136 | |||||||
| chr12:111716217 | A | C | 1 | a0001c0001t0001g0297 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.992+255A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111716217 | |||||||
| chr12:111716223 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.992+261A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111716223 | |||||||
| chr12:111716709 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.992+747A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111716709 | |||||||
| chr12:111716797 | A | T | 1 | a0001c0001t0001g0079 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.992+835A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111716797 | |||||||
| chr12:111717151 | G | A | 1 | a0001c0001t0001g0037 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.992+1189G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111717151 | |||||||
| chr12:111717213 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.992+1251C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111717213 | |||||||
| chr12:111717214 | G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0161 | 2 | NA19081.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.992+1252G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111717214 | |||||||
| chr12:111717284 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.992+1322G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111717284 | |||||||
| chr12:111717317 | C | T | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.992+1355C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111717317 | |||||||
| chr12:111717321 | G | A | 2 | a0001c0002t0002g0031a0001c0002t0002g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.992+1359G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111717321 | |||||||
| chr12:111717330 | A | G | 95 | a0001c0001t0001g0042a0001c0002t0002g0001a0001c0002t0002g0004others(92): Show | 100 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.992+1368A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111717330 | |||||||
| chr12:111717346 | C | CA | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(83): Show | 89 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.992+1405dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111717346 | ||||||
| chr12:111717346 | C | CAA | 6 | a0001c0001t0001g0037a0001c0001t0001g0051a0001c0001t0001g0055others(3): Show | 6 | HG01175.hp1 HG03688.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.992+1404_992+1405d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111717346 | ||||||
| chr12:111717346 | CA | C | 14 | a0001c0001t0001g0188a0001c0001t0001g0297a0001c0001t0001g0302others(11): Show | 14 | HG00140.hp2 HG01168.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.992+1405delA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111717346 | ||||||
| chr12:111717570 | A | AT | 15 | a0001c0001t0001g0011a0001c0001t0001g0209a0001c0001t0001g0251others(12): Show | 15 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.992+1624dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111717570 | ||||||
| chr12:111717897 | A | G | 2 | a0001c0001t0001g0034a0001c0001t0001g0078 | 2 | HG01361.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.992+1935A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111717897 | |||||||
| chr12:111718036 | C | CT | 13 | a0001c0001t0001g0013a0001c0001t0001g0209a0001c0001t0001g0228others(10): Show | 13 | HG00741.hp1 HG00741.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.992+2105dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | C | CTTT | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0190others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.992+2103_992+2105d others(5): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | C | CTTTT | 7 | a0001c0001t0001g0005a0001c0001t0001g0189a0001c0001t0001g0191others(4): Show | 8 | HG02886.hp1 HG03098.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.992+2102_992+2105d others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | C | CTTTTTTT others(3): Show |
3 | a0001c0002t0002g0023a0001c0002t0002g0026a0001c0002t0002g0027 | 3 | HG02145.hp2 HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.992+2096_992+2105d others(12): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | C | CTTTTTTT others(26): Show |
1 | a0001c0002t0002g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.992+2105_992+2106i others(35): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | CT | C | 41 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0054others(38): Show | 41 | HG00597.hp2 HG00735.hp2 HG01099.hp2 others(38): Show |
intron_variant | MODIFIER | c.992+2105delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | CTT | C | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(77): Show | 83 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.992+2104_992+2105d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | CTTT | C | 10 | a0001c0001t0001g0015a0001c0001t0001g0038a0001c0001t0001g0161others(7): Show | 10 | HG01099.hp1 HG02109.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.992+2103_992+2105d others(5): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0184a0001c0002t0002g0016a0001c0002t0002g0097others(3): Show | 6 | HG02132.hp2 HG02698.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.992+2098_992+2105d others(10): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | CTTTTTTT others(2): Show |
C | 72 | a0001c0001t0001g0042a0001c0002t0002g0001a0001c0002t0002g0004others(69): Show | 77 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.992+2097_992+2105d others(11): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | CTTTTTTT others(3): Show |
C | 4 | a0001c0002t0002g0105a0001c0002t0002g0106a0001c0002t0002g0156others(1): Show | 4 | NA18982.hp1 NA19062.hp2 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.992+2096_992+2105d others(12): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0294 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.992+2095_992+2105d others(13): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718036 | CTTTTTTT others(9): Show |
C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.992+2090_992+2105d others(18): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111718036 | ||||||
| chr12:111718084 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.992+2122T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718084 | |||||||
| chr12:111718124 | A | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.992+2162A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718124 | |||||||
| chr12:111718148 | C | T | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0281 | 3 | HG01099.hp1 HG01175.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.992+2186C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718148 | |||||||
| chr12:111718613 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.992+2651G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718613 | |||||||
| chr12:111718643 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.992+2681G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718643 | |||||||
| chr12:111718698 | C | T | 3 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0281 | 3 | HG01099.hp1 HG01175.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.992+2736C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718698 | |||||||
| chr12:111718783 | T | C | 80 | a0001c0001t0001g0042a0001c0002t0002g0001a0001c0002t0002g0004others(77): Show | 85 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.992+2821T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718783 | |||||||
| chr12:111718790 | T | C | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.992+2828T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718790 | |||||||
| chr12:111718843 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.993-2828A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718843 | |||||||
| chr12:111718941 | A | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(252): Show | 264 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.993-2730A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718941 | |||||||
| chr12:111718998 | T | A | 40 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(37): Show | 40 | HG00140.hp1 HG00738.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.993-2673T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111718998 | |||||||
| chr12:111719012 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.993-2659G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719012 | |||||||
| chr12:111719120 | CAAAAA | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.993-2545_993-2541d others(7): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111719120 | ||||||
| chr12:111719177 | G | T | 1 | a0008c0014t0001g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.993-2494G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719177 | |||||||
| chr12:111719263 | G | GT | 6 | a0001c0001t0001g0051a0001c0001t0001g0086a0001c0001t0001g0217others(3): Show | 6 | HG02738.hp1 NA18949.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.993-2400dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr12 | 111719263 | ||||||
| chr12:111719311 | T | C | 1 | a0001c0001t0001g0087 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.993-2360T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719311 | |||||||
| chr12:111719458 | C | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 224 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.993-2213C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719458 | |||||||
| chr12:111719693 | A | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.993-1978A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719693 | |||||||
| chr12:111719758 | C | G | 6 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0203others(3): Show | 6 | HG01884.hp2 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.993-1913C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719758 | |||||||
| chr12:111719758 | C | T | 3 | a0001c0001t0001g0040a0001c0001t0001g0043a0001c0001t0001g0076 | 3 | NA18951.hp2 NA18989.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.993-1913C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719758 | |||||||
| chr12:111719790 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.993-1881C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719790 | |||||||
| chr12:111719811 | T | A | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.993-1860T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719811 | |||||||
| chr12:111719813 | C | T | 1 | a0001c0002t0002g0100 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.993-1858C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719813 | |||||||
| chr12:111719973 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.993-1698C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111719973 | |||||||
| chr12:111720060 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.993-1611C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111720060 | |||||||
| chr12:111720110 | C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0207 | 2 | HG02559.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.993-1561C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111720110 | |||||||
| chr12:111720127 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.993-1544A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111720127 | |||||||
| chr12:111720689 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.993-982G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111720689 | |||||||
| chr12:111720792 | A | T | 3 | a0001c0001t0001g0184a0001c0001t0001g0185a0005c0009t0006g0198 | 3 | HG01243.hp2 HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.993-879A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111720792 | |||||||
| chr12:111720831 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.993-840C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111720831 | |||||||
| chr12:111720930 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.993-741C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111720930 | |||||||
| chr12:111720934 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.993-737C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111720934 | |||||||
| chr12:111720990 | G | C | 1 | a0001c0001t0001g0062 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.993-681G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111720990 | |||||||
| chr12:111721138 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.993-533A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111721138 | |||||||
| chr12:111721162 | T | C | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(81): Show | 87 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.993-509T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 7/20 | chr12 | 111721162 | |||||||
| chr12:111722059 | CGGAGTCT others(18): Show |
C | 5 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 5 | HG01099.hp2 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1061+352_1061+376d others(27): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111722059 | ||||||
| chr12:111722060 | G | A | 2 | a0001c0001t0001g0049a0001c0008t0001g0065 | 2 | HG02056.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1061+321G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722060 | |||||||
| chr12:111722162 | A | G | 1 | a0001c0001t0001g0012 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1061+423A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722162 | |||||||
| chr12:111722368 | A | ATTATTTA others(1): Show |
8 | a0001c0001t0001g0005a0001c0001t0001g0187a0001c0001t0001g0188others(5): Show | 9 | HG01168.hp1 HG01169.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1061+629_1061+630i others(10): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722368 | |||||||
| chr12:111722368 | A | ATTATTTA others(5): Show |
5 | a0001c0001t0001g0189a0001c0001t0001g0191a0001c0001t0001g0192others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1061+629_1061+630i others(14): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722368 | |||||||
| chr12:111722369 | C | CTATT | 96 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0042others(93): Show | 101 | HG00408.hp1 HG00544.hp1 HG01071.hp2 others(98): Show |
intron_variant | MODIFIER | c.1061+660_1061+663d others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111722369 | ||||||
| chr12:111722369 | C | CTATTTAT others(1): Show |
4 | a0001c0001t0001g0203a0001c0001t0005g0196a0001c0002t0002g0145others(1): Show | 4 | HG01243.hp2 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1061+656_1061+663d others(10): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111722369 | ||||||
| chr12:111722369 | C | T | 14 | a0001c0001t0001g0005a0001c0001t0001g0187a0001c0001t0001g0188others(11): Show | 15 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.1061+630C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722369 | |||||||
| chr12:111722369 | CTATT | C | 12 | a0001c0001t0001g0315a0001c0001t0001g0316a0001c0002t0002g0025others(9): Show | 12 | HG01943.hp2 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1061+660_1061+663d others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111722369 | ||||||
| chr12:111722403 | T | A | 20 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(17): Show | 20 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.1061+664T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722403 | |||||||
| chr12:111722483 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+744A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722483 | |||||||
| chr12:111722489 | A | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+750A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722489 | |||||||
| chr12:111722516 | A | AG | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+778dupG | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111722516 | ||||||
| chr12:111722538 | C | T | 1 | a0001c0002t0002g0119 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1061+799C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722538 | |||||||
| chr12:111722578 | G | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+839G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722578 | |||||||
| chr12:111722612 | T | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+873T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722612 | |||||||
| chr12:111722696 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1061+957T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722696 | |||||||
| chr12:111722799 | A | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+1060A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722799 | |||||||
| chr12:111722824 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1061+1085T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722824 | |||||||
| chr12:111722914 | C | T | 2 | a0001c0001t0001g0312a0001c0001t0001g0313 | 2 | NA18959.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1061+1175C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722914 | |||||||
| chr12:111722937 | G | C | 2 | a0001c0002t0002g0031a0001c0002t0002g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1061+1198G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111722937 | |||||||
| chr12:111723018 | A | AC | 35 | a0001c0001t0001g0010a0001c0001t0001g0051a0001c0001t0001g0066others(32): Show | 35 | HG00597.hp2 HG01256.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.1061+1288dupC | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111723018 | ||||||
| chr12:111723038 | C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(81): Show | 87 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1061+1299C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723038 | |||||||
| chr12:111723065 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+1326G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723065 | |||||||
| chr12:111723103 | G | GC | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+1368dupC | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111723103 | ||||||
| chr12:111723126 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+1387G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723126 | |||||||
| chr12:111723155 | ACCTCCCT others(42): Show |
A | 1 | a0002c0003t0003g0323 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1061+1447_1061+149 others(53): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111723155 | ||||||
| chr12:111723174 | C | T | 2 | a0001c0001t0001g0218a0001c0001t0001g0223 | 2 | HG03492.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1061+1435C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723174 | |||||||
| chr12:111723218 | C | T | 81 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(78): Show | 84 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1061+1479C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723218 | |||||||
| chr12:111723245 | C | G | 1 | a0001c0001t0001g0306 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1061+1506C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723245 | |||||||
| chr12:111723287 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1061+1548C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723287 | |||||||
| chr12:111723309 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1061+1570C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723309 | |||||||
| chr12:111723310 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1061+1571G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723310 | |||||||
| chr12:111723313 | C | CG | 10 | a0001c0001t0001g0011a0001c0001t0001g0036a0001c0001t0001g0066others(7): Show | 10 | HG00408.hp2 HG00597.hp1 HG00597.hp2 others(7): Show |
intron_variant | MODIFIER | c.1061+1581dupG | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111723313 | ||||||
| chr12:111723313 | C | T | 1 | a0001c0001t0005g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1061+1574C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723313 | |||||||
| chr12:111723314 | GGGGGGGC others(42): Show |
G | 1 | a0001c0001t0001g0191 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1061+1604_1061+165 others(53): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111723314 | ||||||
| chr12:111723392 | G | A | 1 | a0007c0007t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1061+1653G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723392 | |||||||
| chr12:111723427 | C | A | 1 | a0001c0001t0001g0076 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1061+1688C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723427 | |||||||
| chr12:111723429 | C | T | 3 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0027 | 3 | HG02145.hp2 HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1061+1690C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723429 | |||||||
| chr12:111723458 | G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(177): Show | 188 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.1061+1719G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723458 | |||||||
| chr12:111723461 | C | T | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0278 | 3 | HG02572.hp1 HG02630.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1061+1722C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723461 | |||||||
| chr12:111723539 | C | T | 2 | a0001c0001t0001g0315a0006c0015t0001g0317 | 2 | HG02622.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1061+1800C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723539 | |||||||
| chr12:111723588 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+1849T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723588 | |||||||
| chr12:111723621 | G | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(81): Show | 87 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.1061+1882G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723621 | |||||||
| chr12:111723626 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1061+1887G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723626 | |||||||
| chr12:111723651 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1061+1912C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723651 | |||||||
| chr12:111723665 | C | T | 2 | a0001c0002t0002g0031a0001c0002t0002g0032 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1061+1926C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723665 | |||||||
| chr12:111723670 | G | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+1931G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723670 | |||||||
| chr12:111723684 | A | AC | 48 | a0001c0001t0001g0011a0001c0001t0001g0187a0001c0001t0001g0188others(45): Show | 48 | HG00544.hp2 HG00735.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.1061+1956dupC | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111723684 | ||||||
| chr12:111723684 | AC | A | 82 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(79): Show | 85 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1061+1956delC | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111723684 | ||||||
| chr12:111723684 | ACC | A | 89 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0315others(86): Show | 94 | HG00544.hp1 HG01071.hp2 HG01123.hp2 others(91): Show |
intron_variant | MODIFIER | c.1061+1955_1061+195 others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111723684 | ||||||
| chr12:111723693 | C | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG02970.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1061+1954C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723693 | |||||||
| chr12:111723695 | C | CG | 5 | a0002c0003t0003g0320a0002c0003t0003g0321a0002c0003t0003g0322others(2): Show | 5 | HG01943.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1061+1956_1061+195 others(5): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723695 | |||||||
| chr12:111723706 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1061+1967C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723706 | |||||||
| chr12:111723727 | G | C | 3 | a0001c0001t0001g0229a0001c0002t0002g0121a0001c0002t0002g0122 | 3 | HG02683.hp2 NA18943.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1061+1988G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723727 | |||||||
| chr12:111723750 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1061+2011T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723750 | |||||||
| chr12:111723761 | C | T | 2 | a0001c0002t0002g0103a0001c0002t0002g0104 | 2 | HG02040.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1061+2022C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723761 | |||||||
| chr12:111723767 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2028A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723767 | |||||||
| chr12:111723790 | T | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.1061+2051T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723790 | |||||||
| chr12:111723793 | G | C | 1 | a0001c0001t0001g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1061+2054G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723793 | |||||||
| chr12:111723929 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2190C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723929 | |||||||
| chr12:111723930 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1061+2191G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723930 | |||||||
| chr12:111723947 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2208C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723947 | |||||||
| chr12:111723953 | G | A | 1 | a0005c0009t0006g0198 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1061+2214G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723953 | |||||||
| chr12:111723965 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2226G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723965 | |||||||
| chr12:111723973 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2234C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111723973 | |||||||
| chr12:111724005 | CGCTCCTC others(33): Show |
C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2326_1061+236 others(44): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111724005 | ||||||
| chr12:111724113 | T | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2374T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724113 | |||||||
| chr12:111724125 | C | T | 3 | a0001c0002t0002g0093a0001c0002t0002g0134a0001c0002t0002g0169 | 3 | HG02135.hp1 NA18978.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1061+2386C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724125 | |||||||
| chr12:111724280 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1061+2541A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724280 | |||||||
| chr12:111724397 | C | CG | 8 | a0001c0001t0001g0011a0001c0001t0001g0054a0001c0001t0001g0078others(5): Show | 8 | HG00544.hp1 HG01361.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2662dupG | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111724397 | ||||||
| chr12:111724429 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2690A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724429 | |||||||
| chr12:111724453 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1061+2714C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724453 | |||||||
| chr12:111724489 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1061+2750C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724489 | |||||||
| chr12:111724499 | C | G | 12 | a0001c0001t0001g0268a0001c0001t0001g0270a0001c0001t0001g0273others(9): Show | 12 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.1061+2760C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724499 | |||||||
| chr12:111724541 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+2802A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724541 | |||||||
| chr12:111724686 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1061+2947C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724686 | |||||||
| chr12:111724759 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1061+3020G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724759 | |||||||
| chr12:111724796 | GGGGAGAC others(18): Show |
G | 7 | a0001c0001t0001g0013a0001c0001t0001g0206a0001c0001t0001g0207others(4): Show | 7 | HG02559.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1062-3078_1062-305 others(29): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111724796 | ||||||
| chr12:111724796 | GGGGAGAC others(43): Show |
G | 1 | a0001c0001t0001g0059 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1062-3103_1062-305 others(54): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111724796 | ||||||
| chr12:111724820 | GA | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+3082delA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111724820 | |||||||
| chr12:111725337 | A | G | 5 | a0001c0001t0001g0283a0001c0001t0001g0284a0001c0001t0001g0285others(2): Show | 5 | HG01928.hp1 HG01934.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.1062-2625A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111725337 | |||||||
| chr12:111725406 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1062-2556C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111725406 | |||||||
| chr12:111725511 | C | CT | 8 | a0001c0002t0002g0093a0001c0002t0002g0111a0001c0002t0002g0112others(5): Show | 8 | HG00597.hp1 HG02027.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062-2440dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111725511 | ||||||
| chr12:111725596 | G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0006c0015t0001g0317 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1062-2366G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111725596 | |||||||
| chr12:111725781 | C | T | 8 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(5): Show | 8 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.1062-2181C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111725781 | |||||||
| chr12:111725787 | G | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0239 | 3 | HG01978.hp1 HG02683.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1062-2175G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111725787 | |||||||
| chr12:111725842 | T | C | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.1062-2120T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111725842 | |||||||
| chr12:111726067 | A | C | 1 | a0001c0001t0001g0299 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1062-1895A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726067 | |||||||
| chr12:111726069 | C | T | 1 | a0001c0002t0002g0118 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1062-1893C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726069 | |||||||
| chr12:111726101 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062-1861G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726101 | |||||||
| chr12:111726178 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062-1784T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726178 | |||||||
| chr12:111726203 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062-1759A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726203 | |||||||
| chr12:111726208 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062-1754C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726208 | |||||||
| chr12:111726553 | G | A | 1 | a0001c0002t0002g0160 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1062-1409G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726553 | |||||||
| chr12:111726568 | AAAC | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0070a0001c0001t0001g0084 | 3 | HG02723.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1062-1386_1062-138 others(7): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr12 | 111726568 | ||||||
| chr12:111726590 | A | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062-1372A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726590 | |||||||
| chr12:111726745 | C | T | 4 | a0001c0001t0001g0266a0001c0001t0001g0277a0001c0001t0001g0290others(1): Show | 4 | HG01496.hp2 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062-1217C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726745 | |||||||
| chr12:111726816 | G | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(176): Show | 187 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.1062-1146G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726816 | |||||||
| chr12:111726818 | A | G | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 224 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.1062-1144A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726818 | |||||||
| chr12:111726911 | C | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(186): Show | 197 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.1062-1051C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111726911 | |||||||
| chr12:111727057 | C | G | 1 | a0007c0007t0001g0014 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1062-905C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111727057 | |||||||
| chr12:111727182 | C | T | 6 | a0001c0001t0001g0194a0001c0001t0001g0197a0001c0001t0001g0203others(3): Show | 6 | HG01884.hp2 HG02976.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1062-780C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111727182 | |||||||
| chr12:111727262 | C | T | 20 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(17): Show | 20 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.1062-700C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111727262 | |||||||
| chr12:111727375 | T | A | 1 | a0001c0001t0001g0266 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1062-587T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111727375 | |||||||
| chr12:111727384 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1062-578C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111727384 | |||||||
| chr12:111727472 | C | T | 2 | a0001c0001t0001g0250a0001c0001t0001g0296 | 2 | HG01943.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1062-490C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111727472 | |||||||
| chr12:111727608 | C | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062-354C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111727608 | |||||||
| chr12:111727895 | G | C | 1 | a0001c0001t0001g0265 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1062-67G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 8/20 | chr12 | 111727895 | |||||||
| chr12:111728714 | G | A | 1 | a0001c0001t0001g0283 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1243+571G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111728714 | |||||||
| chr12:111728801 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1243+658T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111728801 | |||||||
| chr12:111728892 | A | G | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(186): Show | 197 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.1243+749A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111728892 | |||||||
| chr12:111729123 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244-683A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111729123 | |||||||
| chr12:111729278 | C | T | 1 | a0001c0002t0002g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1244-528C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111729278 | |||||||
| chr12:111729323 | C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(7): Show | 10 | HG01884.hp2 HG02559.hp2 HG02976.hp2 others(7): Show |
intron_variant | MODIFIER | c.1244-483C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111729323 | |||||||
| chr12:111729330 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244-476T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111729330 | |||||||
| chr12:111729480 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1244-326C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111729480 | |||||||
| chr12:111729575 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244-231T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111729575 | |||||||
| chr12:111729649 | A | T | 2 | a0001c0001t0001g0189a0001c0001t0001g0193 | 2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1244-157A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111729649 | |||||||
| chr12:111729738 | G | GT | 6 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0067others(3): Show | 6 | HG01243.hp1 HG01243.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.1244-59dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr12 | 111729738 | ||||||
| chr12:111729795 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244-11A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 9/20 | chr12 | 111729795 | |||||||
| chr12:111729973 | G | A | 6 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0018others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1394+17G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111729973 | |||||||
| chr12:111730205 | G | A | 21 | a0001c0002t0002g0001a0001c0002t0002g0029a0001c0002t0002g0092others(18): Show | 25 | HG00544.hp1 HG02132.hp2 NA18747.hp1 others(22): Show |
intron_variant | MODIFIER | c.1394+249G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111730205 | |||||||
| chr12:111730246 | A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(177): Show | 188 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.1394+290A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111730246 | |||||||
| chr12:111730495 | C | T | 1 | a0001c0002t0002g0182 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1394+539C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111730495 | |||||||
| chr12:111730607 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394+651A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111730607 | |||||||
| chr12:111730754 | C | CTT | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394+813_1394+814d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 111730754 | ||||||
| chr12:111730774 | C | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0251 | 2 | NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1394+818C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111730774 | |||||||
| chr12:111730778 | G | A | 1 | a0001c0002t0002g0102 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1394+822G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111730778 | |||||||
| chr12:111730856 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394+900A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111730856 | |||||||
| chr12:111730931 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1394+975T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111730931 | |||||||
| chr12:111730949 | A | G | 1 | a0001c0006t0001g0202 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1394+993A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111730949 | |||||||
| chr12:111731122 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1394+1166T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111731122 | |||||||
| chr12:111731308 | A | AC | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394+1353dupC | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 111731308 | ||||||
| chr12:111731408 | T | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+1452T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111731408 | |||||||
| chr12:111731811 | G | A | 1 | a0009c0012t0001g0305 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1394+1855G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111731811 | |||||||
| chr12:111731848 | G | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(212): Show | 224 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.1394+1892G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111731848 | |||||||
| chr12:111732085 | A | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0200a0001c0001t0001g0206others(3): Show | 7 | HG02109.hp1 HG02559.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1395-1838A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111732085 | |||||||
| chr12:111732236 | A | G | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1395-1687A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111732236 | |||||||
| chr12:111732338 | G | A | 1 | a0001c0001t0001g0274 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1395-1585G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111732338 | |||||||
| chr12:111732561 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395-1362G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111732561 | |||||||
| chr12:111732711 | G | C | 2 | a0002c0003t0003g0322a0002c0003t0003g0325 | 2 | HG01943.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1395-1212G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111732711 | |||||||
| chr12:111733297 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1395-626T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733297 | |||||||
| chr12:111733628 | G | C | 1 | a0001c0001t0005g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1395-295G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733628 | |||||||
| chr12:111733640 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1395-283C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733640 | |||||||
| chr12:111733641 | G | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395-282G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733641 | |||||||
| chr12:111733791 | G | T | 1 | a0001c0001t0001g0287 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1395-132G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733791 | |||||||
| chr12:111733839 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395-84C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733839 | |||||||
| chr12:111733846 | G | A | 6 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0024others(3): Show | 6 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1395-77G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733846 | |||||||
| chr12:111733859 | C | T | 1 | a0001c0002t0002g0182 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1395-64C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733859 | |||||||
| chr12:111733860 | G | A | 2 | a0001c0001t0001g0214a0001c0001t0001g0301 | 2 | NA18954.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1395-63G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733860 | |||||||
| chr12:111733876 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1395-47C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733876 | |||||||
| chr12:111733877 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1395-46C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 10/20 | chr12 | 111733877 | |||||||
| chr12:111734383 | G | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1540+315G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111734383 | |||||||
| chr12:111734549 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1540+481G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111734549 | |||||||
| chr12:111734646 | A | G | 1 | a0001c0001t0001g0058 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1540+578A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111734646 | |||||||
| chr12:111734711 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1540+643G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111734711 | |||||||
| chr12:111734934 | G | A | 6 | a0001c0001t0001g0006a0001c0001t0001g0233a0001c0001t0001g0246others(3): Show | 7 | NA18942.hp1 NA18948.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.1540+866G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111734934 | |||||||
| chr12:111734945 | C | A | 1 | a0001c0001t0001g0303 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1540+877C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111734945 | |||||||
| chr12:111735038 | A | G | 1 | a0001c0001t0001g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1540+970A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735038 | |||||||
| chr12:111735092 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1540+1024T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735092 | |||||||
| chr12:111735219 | A | G | 1 | a0001c0002t0002g0171 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1540+1151A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735219 | |||||||
| chr12:111735265 | C | T | 94 | a0001c0002t0002g0001a0001c0002t0002g0004a0001c0002t0002g0016others(91): Show | 99 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1540+1197C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735265 | |||||||
| chr12:111735277 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1540+1209T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735277 | |||||||
| chr12:111735459 | A | AT | 6 | a0001c0001t0001g0195a0001c0001t0001g0228a0001c0001t0001g0232others(3): Show | 6 | HG00741.hp2 HG02056.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1541-1358dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 111735459 | ||||||
| chr12:111735459 | ATT | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1541-1359_1541-135 others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 111735459 | ||||||
| chr12:111735519 | G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0064a0001c0001t0001g0071others(1): Show | 4 | NA18979.hp2 NA18985.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1541-1312G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735519 | |||||||
| chr12:111735612 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1541-1219C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735612 | |||||||
| chr12:111735644 | A | G | 181 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(178): Show | 189 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.1541-1187A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735644 | |||||||
| chr12:111735658 | T | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0251 | 2 | NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1541-1173T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735658 | |||||||
| chr12:111735918 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1541-913C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735918 | |||||||
| chr12:111735970 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1541-861C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111735970 | |||||||
| chr12:111736072 | G | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0051 | 2 | NA18945.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1541-759G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111736072 | |||||||
| chr12:111736185 | G | GT | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(94): Show | 101 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.1541-627dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 111736185 | ||||||
| chr12:111736185 | G | GTT | 12 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0062others(9): Show | 12 | HG00597.hp2 HG01934.hp1 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1541-628_1541-627d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 111736185 | ||||||
| chr12:111736185 | GT | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1541-627delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 111736185 | ||||||
| chr12:111736190 | T | G | 2 | a0001c0001t0001g0197a0001c0001t0001g0204 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1541-641T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111736190 | |||||||
| chr12:111736468 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1541-363G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111736468 | |||||||
| chr12:111736608 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1541-223T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111736608 | |||||||
| chr12:111736721 | G | A | 1 | a0001c0001t0001g0292 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1541-110G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 11/20 | chr12 | 111736721 | |||||||
| chr12:111737018 | T | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+14T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111737018 | |||||||
| chr12:111737052 | A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0200 | 3 | HG02109.hp1 HG02886.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1714+48A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111737052 | |||||||
| chr12:111737540 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1714+536T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111737540 | |||||||
| chr12:111737798 | G | A | 1 | a0001c0001t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1714+794G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111737798 | |||||||
| chr12:111737841 | G | GGT | 21 | a0001c0001t0001g0042a0001c0001t0001g0052a0001c0001t0001g0059others(18): Show | 21 | HG01123.hp1 HG01928.hp2 HG01993.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714+864_1714+865d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111737841 | ||||||
| chr12:111737841 | G | GGTGTGTG others(1): Show |
8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+858_1714+865d others(10): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111737841 | ||||||
| chr12:111737841 | GGT | G | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | NA18959.hp1 NA18971.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714+864_1714+865d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111737841 | ||||||
| chr12:111737889 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+885G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111737889 | |||||||
| chr12:111737895 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+891C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111737895 | |||||||
| chr12:111738015 | C | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(252): Show | 264 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.1714+1011C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738015 | |||||||
| chr12:111738109 | G | A | 1 | a0001c0002t0002g0149 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1714+1105G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738109 | |||||||
| chr12:111738155 | C | G | 1 | a0001c0001t0001g0292 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1714+1151C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738155 | |||||||
| chr12:111738302 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1714+1298C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738302 | |||||||
| chr12:111738303 | A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.1714+1299A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738303 | |||||||
| chr12:111738312 | G | T | 1 | a0001c0002t0002g0171 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1714+1308G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738312 | |||||||
| chr12:111738446 | C | CA | 34 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0051others(31): Show | 34 | HG00140.hp1 HG00544.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.1714+1461dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111738446 | ||||||
| chr12:111738506 | A | C | 1 | a0001c0002t0002g0171 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1714+1502A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738506 | |||||||
| chr12:111738520 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1714+1516G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738520 | |||||||
| chr12:111738555 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+1551A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738555 | |||||||
| chr12:111738598 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1714+1594G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738598 | |||||||
| chr12:111738614 | C | T | 1 | a0001c0002t0002g0103 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1714+1610C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738614 | |||||||
| chr12:111738722 | C | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+1718C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738722 | |||||||
| chr12:111738726 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1714+1722G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738726 | |||||||
| chr12:111738998 | T | G | 1 | a0001c0002t0002g0155 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1714+1994T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111738998 | |||||||
| chr12:111738998 | T | TG | 10 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0167others(7): Show | 10 | HG01952.hp2 HG03516.hp2 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.1714+2001dupG | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111738998 | ||||||
| chr12:111739000 | G | C | 1 | a0001c0001t0001g0220 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1714+1996G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111739000 | |||||||
| chr12:111739023 | G | A | 1 | a0008c0014t0001g0226 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1714+2019G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111739023 | |||||||
| chr12:111739211 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+2207G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111739211 | |||||||
| chr12:111739523 | G | A | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01168.hp1 HG01169.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1714+2519G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111739523 | |||||||
| chr12:111739907 | C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0048a0011c0010t0001g0003 | 3 | HG03453.hp1 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1714+2903C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111739907 | |||||||
| chr12:111739971 | T | A | 323 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(320): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.1714+2967T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111739971 | |||||||
| chr12:111739977 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+2973A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111739977 | |||||||
| chr12:111740048 | G | A | 3 | a0001c0002t0002g0096a0001c0002t0002g0097a0001c0002t0002g0168 | 3 | NA18959.hp1 NA18967.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.1714+3044G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740048 | |||||||
| chr12:111740123 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1714+3119C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740123 | |||||||
| chr12:111740176 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1714+3172A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740176 | |||||||
| chr12:111740204 | C | T | 9 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1714+3200C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740204 | |||||||
| chr12:111740254 | G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0200a0001c0006t0001g0201others(1): Show | 5 | HG02109.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1714+3250G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740254 | |||||||
| chr12:111740318 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+3314T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740318 | |||||||
| chr12:111740371 | G | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+3367G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740371 | |||||||
| chr12:111740460 | C | CA | 20 | a0001c0001t0001g0015a0001c0001t0001g0051a0001c0001t0001g0072others(17): Show | 20 | HG01168.hp1 HG01169.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.1714+3473dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111740460 | ||||||
| chr12:111740487 | C | A | 1 | a0001c0001t0001g0221 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1714+3483C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740487 | |||||||
| chr12:111740488 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1714+3484G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740488 | |||||||
| chr12:111740605 | A | C | 1 | a0001c0001t0001g0142 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1714+3601A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740605 | |||||||
| chr12:111740655 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+3651T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740655 | |||||||
| chr12:111740730 | C | G | 1 | a0001c0002t0002g0124 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1714+3726C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740730 | |||||||
| chr12:111740739 | T | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+3735T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740739 | |||||||
| chr12:111740740 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+3736T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740740 | |||||||
| chr12:111740782 | C | CA | 95 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0081others(92): Show | 100 | HG00544.hp1 HG00597.hp1 HG01071.hp2 others(97): Show |
intron_variant | MODIFIER | c.1714+3798dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111740782 | ||||||
| chr12:111740782 | C | CAA | 6 | a0001c0001t0001g0238a0001c0001t0001g0315a0001c0002t0002g0120others(3): Show | 6 | HG01175.hp2 HG02622.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1714+3797_1714+379 others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111740782 | ||||||
| chr12:111740782 | CAA | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714+3797_1714+379 others(6): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111740782 | ||||||
| chr12:111740798 | A | G | 4 | a0001c0001t0001g0189a0001c0001t0001g0193a0001c0001t0001g0227others(1): Show | 4 | HG00738.hp2 HG00741.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1714+3794A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111740798 | |||||||
| chr12:111741103 | A | G | 3 | a0001c0002t0002g0103a0001c0002t0002g0104a0001c0002t0002g0160 | 3 | HG02040.hp1 NA19070.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1715-3540A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111741103 | |||||||
| chr12:111741346 | C | T | 1 | a0002c0003t0003g0324 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1715-3297C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111741346 | |||||||
| chr12:111741352 | G | A | 2 | a0001c0002t0002g0022a0001c0002t0002g0023 | 2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1715-3291G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111741352 | |||||||
| chr12:111741484 | T | C | 2 | a0001c0001t0001g0234a0001c0008t0001g0065 | 2 | HG02056.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1715-3159T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111741484 | |||||||
| chr12:111741667 | T | C | 314 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(311): Show | 324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.1715-2976T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111741667 | |||||||
| chr12:111741668 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1715-2975G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111741668 | |||||||
| chr12:111741808 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1715-2835C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111741808 | |||||||
| chr12:111741860 | T | A | 1 | a0001c0002t0002g0171 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1715-2783T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111741860 | |||||||
| chr12:111741966 | A | C | 1 | a0001c0001t0005g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1715-2677A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111741966 | |||||||
| chr12:111742234 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1715-2409A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111742234 | |||||||
| chr12:111742284 | A | G | 1 | a0001c0001t0001g0203 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1715-2359A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111742284 | |||||||
| chr12:111742337 | G | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1715-2306G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111742337 | |||||||
| chr12:111742373 | A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(185): Show | 196 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.1715-2270A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111742373 | |||||||
| chr12:111742401 | C | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1715-2242C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111742401 | |||||||
| chr12:111742625 | T | G | 20 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(17): Show | 20 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.1715-2018T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111742625 | |||||||
| chr12:111742675 | C | T | 4 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG01167.hp2 HG02723.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1715-1968C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111742675 | |||||||
| chr12:111742731 | C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0070 | 2 | HG02723.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1715-1912C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111742731 | |||||||
| chr12:111742812 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1715-1831C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111742812 | |||||||
| chr12:111743196 | A | T | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1715-1447A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743196 | |||||||
| chr12:111743274 | T | C | 9 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1715-1369T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743274 | |||||||
| chr12:111743368 | T | TG | 5 | a0001c0001t0001g0043a0001c0001t0001g0066a0001c0001t0001g0081others(2): Show | 5 | HG00597.hp2 HG01175.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1715-1274dupG | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111743368 | ||||||
| chr12:111743369 | G | GT | 25 | a0001c0001t0001g0245a0001c0001t0001g0279a0001c0002t0002g0022others(22): Show | 25 | HG01943.hp2 HG02080.hp1 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1715-1257dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111743369 | ||||||
| chr12:111743369 | GT | G | 7 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0214others(4): Show | 7 | HG01167.hp1 HG02896.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.1715-1257delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr12 | 111743369 | ||||||
| chr12:111743370 | T | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(72): Show | 78 | HG00099.hp1 HG00408.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.1715-1273T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743370 | |||||||
| chr12:111743371 | T | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0079 | 2 | NA18985.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1715-1272T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743371 | |||||||
| chr12:111743372 | T | G | 27 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0187others(24): Show | 28 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.1715-1271T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743372 | |||||||
| chr12:111743375 | T | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1715-1268T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743375 | |||||||
| chr12:111743386 | T | A | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG02080.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1715-1257T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743386 | |||||||
| chr12:111743422 | C | T | 86 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(83): Show | 89 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.1715-1221C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743422 | |||||||
| chr12:111743430 | G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(2): Show | 5 | HG02965.hp1 HG02970.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1715-1213G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743430 | |||||||
| chr12:111743722 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1715-921T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743722 | |||||||
| chr12:111743803 | A | G | 1 | a0001c0006t0001g0201 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1715-840A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743803 | |||||||
| chr12:111743840 | A | G | 1 | a0001c0002t0002g0110 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1715-803A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743840 | |||||||
| chr12:111743940 | G | T | 1 | a0001c0001t0001g0311 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1715-703G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111743940 | |||||||
| chr12:111744343 | G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0187a0001c0001t0001g0188others(15): Show | 19 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1715-300G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111744343 | |||||||
| chr12:111744401 | T | G | 1 | a0001c0001t0001g0304 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1715-242T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111744401 | |||||||
| chr12:111744441 | T | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1715-202T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 12/20 | chr12 | 111744441 | |||||||
| chr12:111745093 | T | C | 1 | a0001c0002t0002g0103 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2115+50T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745093 | |||||||
| chr12:111745094 | C | T | 1 | a0001c0002t0002g0103 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2115+51C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745094 | |||||||
| chr12:111745107 | G | A | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0006c0015t0001g0317 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2115+64G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745107 | |||||||
| chr12:111745254 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2115+211C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745254 | |||||||
| chr12:111745433 | A | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0048a0011c0010t0001g0003 | 3 | HG03453.hp1 NA20129.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2115+390A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745433 | |||||||
| chr12:111745600 | C | T | 5 | a0001c0001t0001g0257a0001c0001t0001g0266a0001c0001t0001g0277others(2): Show | 5 | HG01258.hp2 HG01496.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2116-544C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745600 | |||||||
| chr12:111745624 | C | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0077 | 2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2116-520C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745624 | |||||||
| chr12:111745625 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2116-519G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745625 | |||||||
| chr12:111745686 | G | A | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(184): Show | 195 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.2116-458G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745686 | |||||||
| chr12:111745770 | T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(203): Show | 215 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.2116-374T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745770 | |||||||
| chr12:111745835 | C | CT | 27 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0035others(24): Show | 27 | HG00099.hp1 HG01243.hp1 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.2116-285dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr12 | 111745835 | ||||||
| chr12:111745835 | CT | C | 11 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0141others(8): Show | 11 | HG01167.hp1 HG01934.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.2116-285delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr12 | 111745835 | ||||||
| chr12:111745835 | CTT | C | 9 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(6): Show | 9 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.2116-286_2116-285d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr12 | 111745835 | ||||||
| chr12:111745837 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2116-307T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745837 | |||||||
| chr12:111745839 | T | C | 1 | a0002c0003t0003g0324 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2116-305T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745839 | |||||||
| chr12:111745928 | A | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0187a0001c0001t0001g0188others(15): Show | 19 | HG01168.hp1 HG01169.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.2116-216A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111745928 | |||||||
| chr12:111746031 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2116-113G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111746031 | |||||||
| chr12:111746083 | A | G | 95 | a0001c0001t0001g0042a0001c0002t0002g0001a0001c0002t0002g0004others(92): Show | 100 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.2116-61A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 13/20 | chr12 | 111746083 | |||||||
| chr12:111746391 | C | CT | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(172): Show | 183 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.2256+121dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 14/20 | INFO_REALIGN_3_PRIME | chr12 | 111746391 | ||||||
| chr12:111746633 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2256+349C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 14/20 | chr12 | 111746633 | |||||||
| chr12:111746668 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257-381G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 14/20 | chr12 | 111746668 | |||||||
| chr12:111746728 | G | A | 1 | a0001c0002t0002g0104 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2257-321G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 14/20 | chr12 | 111746728 | |||||||
| chr12:111746862 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2257-187A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 14/20 | chr12 | 111746862 | |||||||
| chr12:111746954 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.2257-95C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 14/20 | chr12 | 111746954 | |||||||
| chr12:111747241 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2395-54A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 15/20 | chr12 | 111747241 | |||||||
| chr12:111747249 | C | T | 6 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0024others(3): Show | 6 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2395-46C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 15/20 | chr12 | 111747249 | |||||||
| chr12:111747444 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2485+59C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 16/20 | chr12 | 111747444 | |||||||
| chr12:111747787 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2485+402T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 16/20 | chr12 | 111747787 | |||||||
| chr12:111747993 | T | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2486-324T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 16/20 | chr12 | 111747993 | |||||||
| chr12:111748081 | T | C | 2 | a0002c0003t0003g0322a0002c0003t0003g0325 | 2 | HG01943.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.2486-236T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 16/20 | chr12 | 111748081 | |||||||
| chr12:111748146 | A | G | 3 | a0001c0001t0001g0194a0001c0001t0001g0208a0001c0001t0001g0308 | 3 | HG01884.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2486-171A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 16/20 | chr12 | 111748146 | |||||||
| chr12:111748160 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2486-157C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 16/20 | chr12 | 111748160 | |||||||
| chr12:111748238 | T | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2486-79T>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 16/20 | chr12 | 111748238 | |||||||
| chr12:111748729 | G | A | 4 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0070others(1): Show | 4 | HG01167.hp2 HG02723.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2644+254G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 17/20 | chr12 | 111748729 | |||||||
| chr12:111748824 | C | G | 1 | a0001c0001t0001g0187 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2644+349C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 17/20 | chr12 | 111748824 | |||||||
| chr12:111748825 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2645-348G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 17/20 | chr12 | 111748825 | |||||||
| chr12:111748839 | T | C | 17 | a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0043others(14): Show | 17 | HG02132.hp1 HG02523.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.2645-334T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 17/20 | chr12 | 111748839 | |||||||
| chr12:111749592 | A | AG | 189 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(186): Show | 197 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.2817+249dupG | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111749592 | ||||||
| chr12:111749702 | G | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0233a0001c0001t0001g0246others(3): Show | 7 | NA18942.hp1 NA18948.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.2817+357G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111749702 | |||||||
| chr12:111749763 | C | CA | 7 | a0001c0001t0001g0054a0001c0001t0001g0057a0001c0001t0001g0072others(4): Show | 7 | HG02027.hp1 HG02071.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2817+432dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111749763 | ||||||
| chr12:111749777 | A | AT | 18 | a0001c0001t0001g0051a0001c0001t0001g0076a0001c0001t0001g0086others(15): Show | 18 | HG00140.hp2 HG00741.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.2817+448dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111749777 | ||||||
| chr12:111749778 | T | A | 1 | a0001c0002t0002g0096 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2817+433T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111749778 | |||||||
| chr12:111749997 | T | A | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2817+652T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111749997 | |||||||
| chr12:111749998 | C | T | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2817+653C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111749998 | |||||||
| chr12:111750020 | G | A | 6 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0018others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2817+675G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750020 | |||||||
| chr12:111750033 | A | T | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2817+688A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750033 | |||||||
| chr12:111750036 | A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(87): Show | 93 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.2817+691A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750036 | |||||||
| chr12:111750095 | G | GT | 88 | a0001c0001t0001g0042a0001c0001t0001g0051a0001c0001t0001g0052others(85): Show | 93 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.2817+764dupT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111750095 | ||||||
| chr12:111750095 | G | GTT | 8 | a0001c0002t0002g0100a0001c0002t0002g0113a0001c0002t0002g0124others(5): Show | 8 | HG00597.hp1 HG02074.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2817+763_2817+764d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111750095 | ||||||
| chr12:111750095 | G | T | 2 | a0001c0001t0001g0185a0001c0001t0001g0247 | 2 | HG03654.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.2817+750G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750095 | |||||||
| chr12:111750095 | GT | G | 7 | a0002c0003t0003g0318a0002c0003t0003g0320a0002c0003t0003g0321others(4): Show | 7 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2817+764delT | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111750095 | ||||||
| chr12:111750152 | C | T | 1 | a0001c0002t0002g0025 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2817+807C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750152 | |||||||
| chr12:111750217 | G | A | 2 | a0001c0001t0001g0197a0001c0001t0001g0204 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2817+872G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750217 | |||||||
| chr12:111750341 | C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0204 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2817+996C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750341 | |||||||
| chr12:111750381 | A | G | 1 | a0001c0001t0005g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2817+1036A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750381 | |||||||
| chr12:111750495 | A | T | 1 | a0001c0001t0001g0247 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2817+1150A>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750495 | |||||||
| chr12:111750575 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2817+1230G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111750575 | |||||||
| chr12:111751105 | T | C | 3 | a0001c0001t0001g0315a0001c0001t0001g0316a0006c0015t0001g0317 | 3 | HG02622.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2817+1760T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751105 | |||||||
| chr12:111751197 | G | A | 3 | a0001c0001t0001g0054a0001c0001t0001g0063a0001c0001t0001g0067 | 3 | HG01243.hp1 HG02145.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.2817+1852G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751197 | |||||||
| chr12:111751246 | G | C | 9 | a0001c0002t0002g0022a0001c0002t0002g0023a0001c0002t0002g0024others(6): Show | 9 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2817+1901G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751246 | |||||||
| chr12:111751293 | G | C | 1 | a0001c0001t0001g0264 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2817+1948G>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751293 | |||||||
| chr12:111751560 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2818-2212G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751560 | |||||||
| chr12:111751730 | C | CA | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2818-2031dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111751730 | ||||||
| chr12:111751742 | T | A | 1 | a0001c0002t0002g0101 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2818-2030T>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751742 | |||||||
| chr12:111751773 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2818-1999G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751773 | |||||||
| chr12:111751825 | G | A | 1 | a0001c0002t0002g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2818-1947G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751825 | |||||||
| chr12:111751857 | G | T | 2 | a0001c0002t0002g0103a0001c0002t0002g0104 | 2 | HG02040.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.2818-1915G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751857 | |||||||
| chr12:111751924 | G | A | 4 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(1): Show | 4 | NA18984.hp1 NA18986.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.2818-1848G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751924 | |||||||
| chr12:111751983 | G | A | 6 | a0003c0004t0001g0186a0003c0004t0001g0237a0003c0004t0001g0269others(3): Show | 6 | HG00140.hp1 HG00738.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.2818-1789G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751983 | |||||||
| chr12:111751999 | G | A | 1 | a0001c0001t0005g0196 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2818-1773G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111751999 | |||||||
| chr12:111752058 | C | CA | 76 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(73): Show | 77 | HG00140.hp1 HG00597.hp1 HG00738.hp1 others(74): Show |
intron_variant | MODIFIER | c.2818-1697dupA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111752058 | ||||||
| chr12:111752058 | CA | C | 6 | a0001c0001t0001g0061a0001c0001t0001g0229a0001c0001t0001g0267others(3): Show | 6 | HG01168.hp2 HG02683.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2818-1697delA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111752058 | ||||||
| chr12:111752076 | G | T | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(200): Show | 212 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.2818-1696G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111752076 | |||||||
| chr12:111752096 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2818-1676A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111752096 | |||||||
| chr12:111752278 | TTTG | T | 21 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0001t0001g0212others(18): Show | 21 | HG01993.hp1 HG02074.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.2818-1470_2818-146 others(7): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111752278 | ||||||
| chr12:111752326 | G | A | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2818-1446G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111752326 | |||||||
| chr12:111752608 | T | TCAAA | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2818-1155_2818-115 others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111752608 | ||||||
| chr12:111752629 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2818-1143A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111752629 | |||||||
| chr12:111752634 | C | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(207): Show | 219 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.2818-1138C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111752634 | |||||||
| chr12:111752696 | G | T | 6 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0018others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2818-1076G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111752696 | |||||||
| chr12:111752841 | GA | G | 237 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(234): Show | 246 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.2818-914delA | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111752841 | ||||||
| chr12:111752841 | GAA | G | 10 | a0001c0001t0001g0009a0001c0002t0002g0145a0002c0003t0003g0318others(7): Show | 10 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.2818-915_2818-914d others(4): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 111752841 | ||||||
| chr12:111753166 | A | G | 1 | a0002c0003t0003g0324 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2818-606A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111753166 | |||||||
| chr12:111753208 | AG | A | 3 | a0001c0001t0001g0061a0001c0001t0001g0080a0001c0001t0001g0085 | 3 | HG02027.hp1 NA18949.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2818-563delG | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111753208 | |||||||
| chr12:111753335 | A | G | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(207): Show | 219 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.2818-437A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111753335 | |||||||
| chr12:111753349 | C | T | 2 | a0001c0001t0001g0217a0007c0007t0001g0014 | 2 | HG03540.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.2818-423C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111753349 | |||||||
| chr12:111753376 | C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01175.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.2818-396C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111753376 | |||||||
| chr12:111753400 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2818-372C>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111753400 | |||||||
| chr12:111753613 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2818-159A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 18/20 | chr12 | 111753613 | |||||||
| chr12:111753922 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG02056.hp1 | splice_region_variant&intron_variant | LOW | c.2961+7G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111753922 | |||||||
| chr12:111754289 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2961+374A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111754289 | |||||||
| chr12:111754430 | C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0204 | 2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2961+515C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111754430 | |||||||
| chr12:111754611 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.2961+696C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111754611 | |||||||
| chr12:111754622 | CCATGCT | C | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(179): Show | 190 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(187): Show |
intron_variant | MODIFIER | c.2961+716_2961+721d others(8): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr12 | 111754622 | ||||||
| chr12:111754656 | G | A | 1 | a0001c0002t0002g0030 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2961+741G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111754656 | |||||||
| chr12:111754672 | T | C | 1 | a0005c0016t0001g0053 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2961+757T>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111754672 | |||||||
| chr12:111755185 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2962-483C>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111755185 | |||||||
| chr12:111755196 | G | A | 9 | a0001c0001t0001g0013a0001c0001t0001g0194a0001c0001t0001g0195others(6): Show | 9 | HG01884.hp2 HG02559.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.2962-472G>A | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111755196 | |||||||
| chr12:111755329 | C | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2962-339C>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111755329 | |||||||
| chr12:111755390 | A | C | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2962-278A>C | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111755390 | |||||||
| chr12:111755405 | CTGT | C | 9 | a0001c0002t0002g0093a0001c0002t0002g0106a0001c0002t0002g0111others(6): Show | 9 | HG00597.hp1 HG02027.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.2962-258_2962-256d others(5): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr12 | 111755405 | ||||||
| chr12:111755479 | A | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2962-189A>G | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | chr12 | 111755479 | |||||||
| chr12:111755482 | GC | G | 8 | a0002c0003t0003g0318a0002c0003t0003g0319a0002c0003t0003g0320others(5): Show | 8 | HG01943.hp2 HG02257.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2962-181delC | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr12 | 111755482 | ||||||
| chr12:111755798 | AACTCTCC others(6): Show |
A | 1 | a0001c0001t0001g0307 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3039+54_3039+66del others(13): Show |
ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 20/20 | chr12 | 111755798 | |||||||
| chr12:111756241 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3040-92G>T | ACAD10 | ENSG00000111271.15 | transcript | ENST00000313698.9 | protein_coding | 20/20 | chr12 | 111756241 |