Search by Gene
| Item | Value |
|---|---|
| geneid | 28976 |
| ensemblid | ENSG00000177646.20 |
| hgncid | 21497 |
| symbol | ACAD9 |
| name | acyl-CoA dehydrogenase family member 9 |
| refseq_nuc | NM_014049.5 |
| refseq_prot | NP_054768.2 |
| ensembl_nuc | ENST00000308982.12 |
| ensembl_prot | ENSP00000312618.7 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 128879620 |
| end | 128913114 |
| strand | + |
| ver | v1.2 |
| region | chr3:128879620-128913114 |
| region5000 | chr3:128874620-128918114 |
| regionname0 | ACAD9_chr3_128879620_128913114 |
| regionname5000 | ACAD9_chr3_128874620_128918114 |
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 | 1/0 | 621 | 362 | 89 | 71 | 143 | 18 | 40 | ACAD9_chr3_128874620_128918114 | ACAD9 | MSGCG others(616): Show |
chr3 | 128874620 | 128918114 |
| a0002 | 0/0 | 621 | 3 | 0 | 0 | 3 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | MSGCG others(616): Show |
chr3 | 128874620 | 128918114 |
| a0003 | 0/0 | 621 | 2 | 0 | 1 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | MSGCG others(616): Show |
chr3 | 128874620 | 128918114 |
| a0004 | 0/0 | 621 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | MSGCG others(616): Show |
chr3 | 128874620 | 128918114 |
| a0005 | 0/0 | 621 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | MSGCG others(616): Show |
chr3 | 128874620 | 128918114 |
| a0006 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | MSGCG others(616): Show |
chr3 | 128874620 | 128918114 |
| a0007 | 0/0 | 621 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | MSGCG others(616): Show |
chr3 | 128874620 | 128918114 |
| a0008 | 0/1 | 621 | 1 | 0 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | MSGCG others(616): Show |
chr3 | 128874620 | 128918114 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1863 | 136 | 15 | 31 | 57 | 10 | 22 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0001c0002 | 0/0 | 1863 | 134 | 16 | 27 | 74 | 6 | 11 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0001c0003 | 0/0 | 1863 | 68 | 46 | 13 | 3 | 2 | 4 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0001c0004 | 0/0 | 1863 | 19 | 8 | 0 | 8 | 0 | 3 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0001c0007 | 0/0 | 1863 | 2 | 2 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0001c0012 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0001c0014 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0001c0015 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0002c0005 | 0/0 | 1863 | 3 | 0 | 0 | 3 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0003c0006 | 0/0 | 1863 | 2 | 0 | 1 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0004c0013 | 0/0 | 1863 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0005c0011 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0006c0009 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0007c0010 | 0/0 | 1863 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 | ||
| a0008c0008 | 0/1 | 1863 | 1 | 0 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATGAG others(1858): Show |
chr3 | 128874620 | 128918114 |
| acthapid | grch38/chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2445 | 136 | 15 | 31 | 57 | 10 | 22 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2440): Show |
chr3 | 128874620 | 128918114 |
| a0001c0002t0002 | 0/0 | 2443 | 129 | 14 | 26 | 74 | 6 | 9 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2438): Show |
chr3 | 128874620 | 128918114 |
| a0001c0002t0007 | 0/0 | 2443 | 3 | 2 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2438): Show |
chr3 | 128874620 | 128918114 |
| a0001c0002t0008 | 0/0 | 2443 | 2 | 0 | 0 | 0 | 0 | 2 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2438): Show |
chr3 | 128874620 | 128918114 |
| a0001c0003t0001 | 0/0 | 2445 | 5 | 0 | 2 | 3 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2440): Show |
chr3 | 128874620 | 128918114 |
| a0001c0003t0002 | 0/0 | 2443 | 13 | 11 | 2 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2438): Show |
chr3 | 128874620 | 128918114 |
| a0001c0003t0003 | 0/0 | 2443 | 35 | 29 | 5 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2438): Show |
chr3 | 128874620 | 128918114 |
| a0001c0003t0004 | 0/0 | 2449 | 3 | 0 | 0 | 0 | 0 | 3 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2444): Show |
chr3 | 128874620 | 128918114 |
| a0001c0003t0005 | 0/0 | 2449 | 6 | 6 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2444): Show |
chr3 | 128874620 | 128918114 |
| a0001c0003t0006 | 0/0 | 2441 | 6 | 0 | 4 | 0 | 2 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2436): Show |
chr3 | 128874620 | 128918114 |
| a0001c0004t0004 | 0/0 | 2449 | 19 | 8 | 0 | 8 | 0 | 3 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2444): Show |
chr3 | 128874620 | 128918114 |
| a0001c0007t0001 | 0/0 | 2445 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2440): Show |
chr3 | 128874620 | 128918114 |
| a0001c0007t0002 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2438): Show |
chr3 | 128874620 | 128918114 |
| a0001c0012t0004 | 0/0 | 2449 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2444): Show |
chr3 | 128874620 | 128918114 |
| a0001c0014t0005 | 0/0 | 2449 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2444): Show |
chr3 | 128874620 | 128918114 |
| a0001c0015t0002 | 0/0 | 2443 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2438): Show |
chr3 | 128874620 | 128918114 |
| a0002c0005t0001 | 0/0 | 2445 | 3 | 0 | 0 | 3 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2440): Show |
chr3 | 128874620 | 128918114 |
| a0003c0006t0001 | 0/0 | 2445 | 2 | 0 | 1 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2440): Show |
chr3 | 128874620 | 128918114 |
| a0004c0013t0004 | 0/0 | 2449 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2444): Show |
chr3 | 128874620 | 128918114 |
| a0005c0011t0004 | 0/0 | 2449 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2444): Show |
chr3 | 128874620 | 128918114 |
| a0006c0009t0001 | 0/0 | 2445 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2440): Show |
chr3 | 128874620 | 128918114 |
| a0007c0010t0001 | 0/0 | 2445 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2440): Show |
chr3 | 128874620 | 128918114 |
| a0008c0008t0001 | 0/1 | 2445 | 1 | 0 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | ATCAG others(2440): Show |
chr3 | 128874620 | 128918114 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 0 | 0 | 14 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0008 | 0/0 | 4 | 1 | 0 | 1 | 1 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0009 | 1/0 | 5 | 0 | 3 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0011 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0020 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0003 | 0/0 | 9 | 0 | 2 | 7 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0005 | 0/0 | 7 | 2 | 1 | 0 | 0 | 4 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0014 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0015 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0007g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0008g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0002t0008g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0002g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0044 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0005g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0005g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0005g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0006g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0006g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0003t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0004t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0007t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0007t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0012t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0014t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0001c0015t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0002c0005t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0002c0005t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0002c0005t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0003c0006t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0003c0006t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0004c0013t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0005c0011t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0006c0009t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0007c0010t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| a0008c0008t0001g0018 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0160 | EUR | GBR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00140 | hp1 | a0001 | c0002 | t0002 | g0161 | EUR | GBR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0039 | EUR | FIN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | FIN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00423 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0094 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00639 | hp1 | a0001 | c0003 | t0006 | g0255 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00639 | hp2 | a0001 | c0003 | t0003 | g0069 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0088 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0120 | EAS | CHS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0142 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0104 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01069 | hp2 | a0001 | c0003 | t0003 | g0253 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0150 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0149 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01109 | hp1 | a0001 | c0003 | t0003 | g0044 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0026 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0114 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01243 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | PUR | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01255 | hp1 | a0001 | c0002 | t0007 | g0159 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0123 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01256 | hp2 | a0001 | c0003 | t0006 | g0046 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01258 | hp1 | a0001 | c0003 | t0006 | g0046 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0100 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01261 | hp1 | a0001 | c0003 | t0003 | g0251 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0031 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01433 | hp1 | a0003 | c0006 | t0001 | g0234 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0131 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0015 | EUR | IBS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01516 | hp1 | a0001 | c0003 | t0006 | g0045 | EUR | IBS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0102 | EUR | IBS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01517 | hp1 | a0001 | c0003 | t0006 | g0045 | EUR | IBS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0015 | EUR | IBS | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01884 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0005 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01891 | hp2 | a0001 | c0003 | t0002 | g0089 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01934 | hp1 | a0001 | c0003 | t0001 | g0212 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0140 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0116 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01975 | hp2 | a0001 | c0002 | t0002 | g0144 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01981 | hp1 | a0001 | c0003 | t0006 | g0254 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0143 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02015 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02015 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02040 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02040 | hp2 | a0001 | c0004 | t0004 | g0052 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02055 | hp1 | a0001 | c0003 | t0003 | g0081 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02055 | hp2 | a0001 | c0004 | t0004 | g0060 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0125 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02056 | hp2 | a0001 | c0004 | t0004 | g0057 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0117 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02080 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02083 | hp2 | a0001 | c0003 | t0001 | g0017 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02129 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0128 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0139 | EAS | CDX | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0079 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02257 | hp2 | a0001 | c0003 | t0002 | g0004 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02258 | hp1 | a0001 | c0004 | t0004 | g0048 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02258 | hp2 | a0001 | c0003 | t0005 | g0037 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02273 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0085 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02280 | hp2 | a0001 | c0007 | t0001 | g0256 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02293 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02451 | hp1 | a0001 | c0004 | t0004 | g0063 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02451 | hp2 | a0001 | c0015 | t0002 | g0087 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02572 | hp1 | a0001 | c0003 | t0003 | g0078 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02572 | hp2 | a0001 | c0014 | t0005 | g0190 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02615 | hp2 | a0001 | c0003 | t0003 | g0077 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0066 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02622 | hp2 | a0001 | c0003 | t0005 | g0188 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02630 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02630 | hp2 | a0001 | c0007 | t0002 | g0187 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02647 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0092 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02683 | hp1 | a0004 | c0013 | t0004 | g0259 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02698 | hp2 | a0001 | c0003 | t0003 | g0252 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02717 | hp2 | a0001 | c0002 | t0002 | g0118 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02735 | hp1 | a0001 | c0002 | t0002 | g0126 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0156 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02809 | hp2 | a0001 | c0003 | t0002 | g0004 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02818 | hp1 | a0001 | c0003 | t0003 | g0067 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02886 | hp2 | a0001 | c0003 | t0003 | g0027 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0097 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02895 | hp2 | a0001 | c0003 | t0002 | g0004 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0082 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02896 | hp2 | a0001 | c0003 | t0003 | g0007 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0065 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0098 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02922 | hp1 | a0001 | c0003 | t0003 | g0027 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02922 | hp2 | a0005 | c0011 | t0004 | g0024 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02965 | hp2 | a0001 | c0003 | t0002 | g0186 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02970 | hp1 | a0001 | c0004 | t0004 | g0024 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02970 | hp2 | a0001 | c0003 | t0005 | g0191 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02976 | hp1 | a0001 | c0003 | t0003 | g0070 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03017 | hp1 | a0001 | c0002 | t0008 | g0103 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03017 | hp2 | a0003 | c0006 | t0001 | g0229 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03041 | hp1 | a0001 | c0003 | t0003 | g0072 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03098 | hp1 | a0001 | c0003 | t0003 | g0073 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0113 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03139 | hp1 | a0001 | c0003 | t0003 | g0075 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03139 | hp2 | a0001 | c0002 | t0002 | g0086 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03209 | hp1 | a0001 | c0003 | t0003 | g0068 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03209 | hp2 | a0001 | c0004 | t0004 | g0062 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0044 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03225 | hp2 | a0001 | c0002 | t0007 | g0157 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03453 | hp2 | a0001 | c0003 | t0003 | g0074 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03486 | hp1 | a0001 | c0003 | t0003 | g0083 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0112 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03491 | hp2 | a0001 | c0003 | t0004 | g0061 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0093 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03516 | hp2 | a0001 | c0003 | t0005 | g0037 | AFR | ESN | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03579 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03669 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03704 | hp1 | a0001 | c0003 | t0004 | g0050 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03710 | hp2 | a0001 | c0002 | t0002 | g0141 | SAS | PJL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03927 | hp1 | a0001 | c0004 | t0004 | g0055 | SAS | BEB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03942 | hp2 | a0001 | c0003 | t0004 | g0054 | SAS | BEB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04115 | hp1 | a0001 | c0002 | t0002 | g0137 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04184 | hp2 | a0001 | c0002 | t0002 | g0005 | SAS | BEB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0005 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04199 | hp2 | a0001 | c0002 | t0008 | g0110 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04204 | hp2 | a0001 | c0004 | t0004 | g0022 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04228 | hp1 | a0001 | c0004 | t0004 | g0022 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18522 | hp1 | a0001 | c0003 | t0003 | g0028 | AFR | YRI | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0130 | AFR | YRI | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18612 | hp1 | a0001 | c0003 | t0001 | g0017 | EAS | CHB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | CHB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18747 | hp1 | a0001 | c0002 | t0002 | g0108 | EAS | CHB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18906 | hp1 | a0001 | c0003 | t0005 | g0189 | AFR | YRI | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18906 | hp2 | a0001 | c0003 | t0003 | g0076 | AFR | YRI | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18939 | hp2 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18941 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18943 | hp1 | a0002 | c0005 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18943 | hp2 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18950 | hp1 | a0001 | c0004 | t0004 | g0051 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18950 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18951 | hp1 | a0001 | c0003 | t0001 | g0237 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18951 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0151 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18959 | hp2 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18962 | hp1 | a0001 | c0004 | t0004 | g0021 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0164 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18963 | hp2 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18964 | hp1 | a0001 | c0002 | t0002 | g0127 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18965 | hp1 | a0001 | c0002 | t0002 | g0135 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0138 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18973 | hp1 | a0006 | c0009 | t0001 | g0008 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0152 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18974 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0136 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18978 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18988 | hp1 | a0001 | c0004 | t0004 | g0021 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18988 | hp2 | a0001 | c0002 | t0002 | g0147 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18992 | hp2 | a0001 | c0002 | t0002 | g0032 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0148 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18995 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18995 | hp2 | a0001 | c0002 | t0002 | g0146 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18999 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19002 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19003 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19010 | hp1 | a0007 | c0010 | t0001 | g0203 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19010 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19030 | hp1 | a0001 | c0004 | t0004 | g0049 | AFR | LWK | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19030 | hp2 | a0001 | c0003 | t0003 | g0007 | AFR | LWK | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19043 | hp1 | a0001 | c0003 | t0003 | g0007 | AFR | LWK | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19043 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | LWK | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19057 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19057 | hp2 | a0002 | c0005 | t0001 | g0220 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19058 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0132 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19063 | hp2 | a0001 | c0004 | t0004 | g0056 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19065 | hp2 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19066 | hp1 | a0001 | c0004 | t0004 | g0053 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19072 | hp1 | a0001 | c0004 | t0004 | g0023 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19076 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19083 | hp1 | a0001 | c0002 | t0002 | g0145 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0033 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19085 | hp1 | a0001 | c0002 | t0002 | g0029 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19091 | hp1 | a0001 | c0012 | t0004 | g0023 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20129 | hp1 | a0001 | c0003 | t0005 | g0192 | AFR | ASW | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20129 | hp2 | a0001 | c0004 | t0004 | g0058 | AFR | ASW | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | TSI | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0031 | EUR | TSI | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | GIH | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | GIH | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG01123 | hp2 | a0001 | c0003 | t0003 | g0084 | AMR | CLM | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02109 | hp1 | a0001 | c0003 | t0003 | g0080 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02486 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02486 | hp2 | a0001 | c0003 | t0003 | g0028 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02559 | hp1 | a0001 | c0002 | t0007 | g0158 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG02559 | hp2 | a0001 | c0003 | t0003 | g0071 | AFR | ACB | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03471 | hp1 | a0001 | c0003 | t0002 | g0004 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0193 | AFR | MSL | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | USA | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| HG06807 | hp2 | a0001 | c0004 | t0004 | g0059 | AFR | USA | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18955 | hp1 | a0002 | c0005 | t0001 | g0232 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA18955 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0030 | AFR | USA | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| homoSapiens | chm13v2 | a0008 | c0008 | t0001 | g0018 | REF | REF | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0009 | REF | REF | ACAD9_chr3_128874620_128918114 | ACAD9 | chr3 | 128874620 | 128918114 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:128897655 | G | A | 1 | a0005 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.578G>A | p.Arg193Gln | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/18 | 650/2445 | 578/1866 | 193/621 | chr3 | 128897655 | |||
| chr3:128904079 | G | A | 1 | a0003 | 2 | HG01433.hp1 HG03017.hp2 |
missense_variant | MODERATE | c.976G>A | p.Ala326Thr | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 10/18 | 1048/2445 | 976/1866 | 326/621 | chr3 | 128904079 | |||
| chr3:128904091 | A | C | 1 | a0002 | 3 | NA18943.hp1 NA18955.hp1 NA19057.hp2 |
missense_variant | MODERATE | c.988A>C | p.Lys330Gln | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 10/18 | 1060/2445 | 988/1866 | 330/621 | chr3 | 128904091 | |||
| chr3:128906146 | A | T | 1 | a0007 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.1175A>T | p.Gln392Leu | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/18 | 1247/2445 | 1175/1866 | 392/621 | chr3 | 128906146 | |||
| chr3:128908237 | C | T | 1 | a0004 | 1 | HG02683.hp1 | missense_variant | MODERATE | c.1331C>T | p.Ala444Val | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/18 | 1403/2445 | 1331/1866 | 444/621 | chr3 | 128908237 | |||
| chr3:128910132 | C | A | 1 | a0006 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.1675C>A | p.Arg559Ser | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/18 | 1747/2445 | 1675/1866 | 559/621 | chr3 | 128910132 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:128895342 | A | C | 9 | a0001c0002a0001c0003a0001c0004others(6): Show | 228 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(225): Show |
synonymous_variant | LOW | c.379A>C | p.Arg127Arg | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/18 | 451/2445 | 379/1866 | 127/621 | chr3 | 128895342 | |||
| chr3:128896495 | C | T | 1 | a0001c0015 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.513C>T | p.Ser171Ser | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/18 | 585/2445 | 513/1866 | 171/621 | chr3 | 128896495 | |||
| chr3:128899440 | T | C | 4 | a0001c0004a0001c0012a0004c0013others(1): Show | 22 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(19): Show |
synonymous_variant | LOW | c.787T>C | p.Leu263Leu | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/18 | 859/2445 | 787/1866 | 263/621 | chr3 | 128899440 | |||
| chr3:128904123 | A | G | 1 | a0001c0014 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1020A>G | p.Gly340Gly | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 10/18 | 1092/2445 | 1020/1866 | 340/621 | chr3 | 128904123 | |||
| chr3:128909090 | C | T | 1 | a0001c0002 | 134 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(131): Show |
synonymous_variant | LOW | c.1476C>T | p.Pro492Pro | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 14/18 | 1548/2445 | 1476/1866 | 492/621 | chr3 | 128909090 | |||
| chr3:128910140 | C | T | 1 | a0001c0007 | 2 | HG02280.hp2 HG02630.hp2 |
synonymous_variant | LOW | c.1683C>T | p.His561His | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/18 | 1755/2445 | 1683/1866 | 561/621 | chr3 | 128910140 | |||
| chr3:128912598 | G | A | 1 | a0001c0012 | 1 | NA19091.hp1 | synonymous_variant | LOW | c.1857G>A | p.Arg619Arg | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 18/18 | 1929/2445 | 1857/1866 | 619/621 | chr3 | 128912598 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:128879626 | CGT | C | 8 | a0001c0002t0002a0001c0002t0007a0001c0002t0008others(5): Show | 190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
5_prime_UTR_variant | MODIFIER | c.-57_-56delGT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/18 | 56 | INFO_REALIGN_3_PRIME | chr3 | 128879626 | |||||
| chr3:128879647 | C | CTAAG | 7 | a0001c0003t0004a0001c0003t0005a0001c0004t0004others(4): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
5_prime_UTR_variant | MODIFIER | c.-44_-41dupTAAG | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/18 | 40 | INFO_REALIGN_3_PRIME | chr3 | 128879647 | |||||
| chr3:128912633 | C | T | 1 | a0001c0002t0008 | 2 | HG03017.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*26C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 18/18 | 26 | chr3 | 128912633 | ||||||
| chr3:128912638 | G | A | 1 | a0001c0003t0003 | 35 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*31G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 18/18 | 31 | chr3 | 128912638 | ||||||
| chr3:128912675 | C | T | 2 | a0001c0003t0005a0001c0014t0005 | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*68C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 18/18 | 68 | chr3 | 128912675 | ||||||
| chr3:128912829 | GGA | G | 1 | a0001c0003t0006 | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*231_*232delGA | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 18/18 | 231 | INFO_REALIGN_3_PRIME | chr3 | 128912829 | |||||
| chr3:128912938 | T | G | 1 | a0001c0002t0007 | 3 | HG01255.hp1 HG02559.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*331T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 18/18 | 331 | chr3 | 128912938 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:128879928 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.150+87C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128879928 | |||||||
| chr3:128880000 | A | T | 1 | a0004c0013t0004g0259 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.150+159A>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128880000 | |||||||
| chr3:128880063 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.150+222C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128880063 | |||||||
| chr3:128880121 | A | G | 2 | a0001c0002t0002g0047a0001c0002t0002g0257 | 3 | NA18963.hp2 NA19066.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.150+280A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128880121 | |||||||
| chr3:128880202 | C | T | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150+361C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128880202 | |||||||
| chr3:128880267 | C | G | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+426C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128880267 | |||||||
| chr3:128880300 | T | C | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.150+459T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128880300 | |||||||
| chr3:128880342 | G | C | 1 | a0001c0001t0001g0025 | 2 | NA18942.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.150+501G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128880342 | |||||||
| chr3:128880433 | CAG | C | 4 | a0001c0003t0003g0044a0001c0003t0003g0251a0001c0003t0003g0252others(1): Show | 5 | HG01069.hp2 HG01109.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+595_150+596del others(2): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 128880433 | ||||||
| chr3:128880548 | CT | C | 174 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(171): Show | 243 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.150+720delT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 128880548 | ||||||
| chr3:128880593 | T | C | 1 | a0001c0002t0002g0064 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.150+752T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128880593 | |||||||
| chr3:128881011 | A | G | 1 | a0001c0003t0004g0061 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.150+1170A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881011 | |||||||
| chr3:128881123 | T | C | 1 | a0001c0002t0002g0026 | 2 | HG00642.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.150+1282T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881123 | |||||||
| chr3:128881136 | A | G | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.150+1295A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881136 | |||||||
| chr3:128881183 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.150+1342A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881183 | |||||||
| chr3:128881324 | C | G | 1 | a0001c0001t0001g0250 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.150+1483C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881324 | |||||||
| chr3:128881330 | C | T | 1 | a0001c0003t0002g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.150+1489C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881330 | |||||||
| chr3:128881386 | G | A | 162 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(159): Show | 223 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.150+1545G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881386 | |||||||
| chr3:128881395 | G | C | 190 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(187): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.150+1554G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881395 | |||||||
| chr3:128881521 | A | G | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150+1680A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881521 | |||||||
| chr3:128881533 | T | C | 28 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0028others(25): Show | 35 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.150+1692T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881533 | |||||||
| chr3:128881617 | T | G | 1 | a0001c0007t0002g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.150+1776T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881617 | |||||||
| chr3:128881620 | G | C | 1 | a0001c0002t0002g0086 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.150+1779G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881620 | |||||||
| chr3:128881677 | A | G | 1 | a0001c0002t0002g0164 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.150+1836A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881677 | |||||||
| chr3:128881730 | C | T | 6 | a0001c0003t0003g0028a0001c0003t0003g0081a0001c0003t0003g0082others(3): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+1889C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881730 | |||||||
| chr3:128881742 | C | G | 94 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(91): Show | 143 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.150+1901C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881742 | |||||||
| chr3:128881762 | T | C | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+1921T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881762 | |||||||
| chr3:128881828 | G | A | 1 | a0001c0002t0002g0090 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.150+1987G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881828 | |||||||
| chr3:128881863 | A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0185 | 2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.150+2022A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881863 | |||||||
| chr3:128881984 | C | G | 1 | a0001c0002t0002g0163 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.150+2143C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128881984 | |||||||
| chr3:128882003 | C | G | 1 | a0001c0001t0001g0249 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.150+2162C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128882003 | |||||||
| chr3:128882042 | C | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(25): Show | 39 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.150+2201C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128882042 | |||||||
| chr3:128882053 | A | G | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150+2212A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128882053 | |||||||
| chr3:128882106 | TA | T | 162 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(159): Show | 223 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.150+2267delA | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 128882106 | ||||||
| chr3:128882163 | C | A | 1 | a0001c0002t0002g0091 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.150+2322C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128882163 | |||||||
| chr3:128882207 | A | G | 132 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(129): Show | 190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.150+2366A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128882207 | |||||||
| chr3:128882369 | C | T | 1 | a0001c0003t0003g0044 | 2 | HG01109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.151-2284C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128882369 | |||||||
| chr3:128882619 | G | C | 1 | a0001c0001t0001g0250 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.151-2034G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128882619 | |||||||
| chr3:128882792 | T | C | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.151-1861T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128882792 | |||||||
| chr3:128882812 | C | G | 3 | a0001c0002t0002g0160a0001c0002t0002g0161a0001c0002t0002g0162 | 3 | HG00099.hp2 HG00140.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.151-1841C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128882812 | |||||||
| chr3:128883073 | GT | G | 160 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(157): Show | 221 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(218): Show |
intron_variant | MODIFIER | c.151-1565delT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 128883073 | ||||||
| chr3:128883092 | G | GT | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.151-1551dupT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 128883092 | ||||||
| chr3:128883102 | T | C | 6 | a0001c0003t0003g0007a0001c0003t0003g0065a0001c0003t0003g0066others(3): Show | 10 | HG00639.hp2 HG01884.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.151-1551T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883102 | |||||||
| chr3:128883246 | C | T | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.151-1407C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883246 | |||||||
| chr3:128883292 | G | T | 35 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186others(32): Show | 44 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.151-1361G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883292 | |||||||
| chr3:128883424 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.151-1229C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883424 | |||||||
| chr3:128883481 | C | T | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.151-1172C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883481 | |||||||
| chr3:128883489 | C | G | 22 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0044others(19): Show | 28 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-1164C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883489 | |||||||
| chr3:128883504 | C | T | 6 | a0001c0003t0003g0007a0001c0003t0003g0065a0001c0003t0003g0066others(3): Show | 10 | HG00639.hp2 HG01884.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.151-1149C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883504 | |||||||
| chr3:128883591 | C | T | 7 | a0001c0004t0004g0024a0001c0004t0004g0058a0001c0004t0004g0059others(4): Show | 7 | HG02055.hp2 HG02451.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.151-1062C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883591 | |||||||
| chr3:128883603 | G | A | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.151-1050G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883603 | |||||||
| chr3:128883683 | C | T | 132 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(129): Show | 190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.151-970C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883683 | |||||||
| chr3:128883715 | G | A | 132 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(129): Show | 190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.151-938G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883715 | |||||||
| chr3:128883885 | C | T | 1 | a0001c0003t0002g0156 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.151-768C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883885 | |||||||
| chr3:128883905 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.151-748C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128883905 | |||||||
| chr3:128884004 | A | G | 132 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(129): Show | 190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.151-649A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128884004 | |||||||
| chr3:128884021 | G | A | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-632G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128884021 | |||||||
| chr3:128884114 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.151-539A>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128884114 | |||||||
| chr3:128884237 | T | G | 95 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(92): Show | 144 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.151-416T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128884237 | |||||||
| chr3:128884307 | G | T | 162 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(159): Show | 223 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(220): Show |
intron_variant | MODIFIER | c.151-346G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128884307 | |||||||
| chr3:128884403 | A | C | 4 | a0001c0004t0004g0023a0001c0004t0004g0056a0001c0004t0004g0057others(1): Show | 4 | HG02056.hp2 NA19063.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-250A>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128884403 | |||||||
| chr3:128884440 | C | T | 1 | a0001c0003t0006g0046 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.151-213C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128884440 | |||||||
| chr3:128884453 | T | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.151-200T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 1/17 | chr3 | 128884453 | |||||||
| chr3:128884773 | C | T | 1 | a0001c0003t0003g0080 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.244+27C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128884773 | |||||||
| chr3:128884798 | G | A | 2 | a0001c0003t0002g0193a0001c0007t0002g0187 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.244+52G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128884798 | |||||||
| chr3:128885002 | A | G | 1 | a0001c0002t0002g0155 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.244+256A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128885002 | |||||||
| chr3:128885042 | G | A | 2 | a0001c0003t0003g0028a0001c0003t0003g0081 | 3 | HG02055.hp1 HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.244+296G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128885042 | |||||||
| chr3:128885170 | T | A | 1 | a0001c0002t0002g0029 | 2 | NA18943.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.244+424T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128885170 | |||||||
| chr3:128885217 | G | C | 1 | a0001c0003t0002g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.244+471G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128885217 | |||||||
| chr3:128885356 | A | T | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244+610A>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128885356 | |||||||
| chr3:128885455 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.244+709C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128885455 | |||||||
| chr3:128885483 | T | C | 257 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0010others(254): Show | 358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.244+737T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128885483 | |||||||
| chr3:128885940 | C | T | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+1194C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128885940 | |||||||
| chr3:128886032 | A | T | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+1286A>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886032 | |||||||
| chr3:128886167 | A | G | 1 | a0001c0003t0003g0253 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.244+1421A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886167 | |||||||
| chr3:128886303 | A | G | 2 | a0001c0001t0001g0240a0001c0001t0001g0241 | 2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.244+1557A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886303 | |||||||
| chr3:128886364 | G | A | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.244+1618G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886364 | |||||||
| chr3:128886480 | G | T | 28 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0028others(25): Show | 35 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.244+1734G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886480 | |||||||
| chr3:128886563 | C | T | 1 | a0001c0002t0002g0154 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.244+1817C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886563 | |||||||
| chr3:128886575 | G | T | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+1829G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886575 | |||||||
| chr3:128886577 | A | G | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+1831A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886577 | |||||||
| chr3:128886647 | G | A | 2 | a0001c0003t0002g0193a0001c0007t0002g0187 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.244+1901G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886647 | |||||||
| chr3:128886668 | AC | A | 132 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(129): Show | 190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.244+1923delC | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886668 | |||||||
| chr3:128886733 | A | G | 1 | a0001c0002t0002g0153 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.244+1987A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886733 | |||||||
| chr3:128886736 | T | TA | 18 | a0001c0001t0001g0165a0001c0003t0004g0050a0001c0003t0004g0054others(15): Show | 20 | HG02040.hp2 HG02056.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.244+2003dupA | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128886736 | ||||||
| chr3:128886736 | T | TAA | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.244+2002_244+2003d others(4): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128886736 | ||||||
| chr3:128886920 | G | C | 190 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(187): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.244+2174G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128886920 | |||||||
| chr3:128887067 | A | AG | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+2322dupG | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887067 | ||||||
| chr3:128887168 | G | T | 1 | a0001c0001t0001g0239 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.244+2422G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887168 | |||||||
| chr3:128887224 | C | T | 28 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0028others(25): Show | 35 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.244+2478C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887224 | |||||||
| chr3:128887225 | G | A | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.244+2479G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887225 | |||||||
| chr3:128887334 | G | A | 3 | a0001c0002t0002g0030a0001c0002t0002g0092a0001c0002t0002g0093 | 4 | HG02647.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+2588G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887334 | |||||||
| chr3:128887450 | T | G | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+2704T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887450 | |||||||
| chr3:128887451 | T | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+2705T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887451 | |||||||
| chr3:128887463 | C | A | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244+2717C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887463 | |||||||
| chr3:128887479 | C | T | 132 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(129): Show | 190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.244+2733C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887479 | |||||||
| chr3:128887618 | T | A | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+2872T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887618 | |||||||
| chr3:128887619 | A | T | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+2873A>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887619 | |||||||
| chr3:128887630 | T | A | 1 | a0001c0002t0002g0094 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.244+2884T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887630 | |||||||
| chr3:128887630 | TAAAA | T | 6 | a0001c0003t0002g0193a0001c0003t0006g0045a0001c0003t0006g0046others(3): Show | 8 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.244+2888_244+2891d others(6): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887630 | ||||||
| chr3:128887634 | A | T | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+2888A>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887634 | |||||||
| chr3:128887638 | T | A | 6 | a0001c0002t0002g0095a0001c0002t0007g0157a0001c0002t0007g0158others(3): Show | 6 | HG01255.hp1 HG02559.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.244+2892T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887638 | |||||||
| chr3:128887644 | A | AAT | 9 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(6): Show | 9 | HG00673.hp1 HG00741.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.244+2921_244+2922d others(4): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | A | AATAAATA others(7): Show |
1 | a0001c0014t0005g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.244+2901_244+2902i others(16): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | A | AATAAATA others(13): Show |
2 | a0001c0003t0005g0188a0001c0003t0005g0189 | 2 | HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.244+2901_244+2902i others(22): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | A | AATAT | 8 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0178others(5): Show | 14 | HG00735.hp2 HG00738.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.244+2919_244+2922d others(6): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | A | AATATAT | 12 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0035others(9): Show | 17 | HG00423.hp1 HG01346.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.244+2917_244+2922d others(8): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | A | AATATATA others(1): Show |
5 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0169others(2): Show | 5 | HG00323.hp2 HG01515.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.244+2915_244+2922d others(10): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | A | AATATATA others(3): Show |
1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244+2913_244+2922d others(12): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0166 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.244+2909_244+2922d others(16): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | A | AATATATA others(17): Show |
2 | a0001c0003t0005g0037a0001c0003t0005g0192 | 3 | HG02258.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.244+2899_244+2922d others(26): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | AAT | A | 28 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0028others(25): Show | 35 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.244+2921_244+2922d others(4): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | AATAT | A | 98 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(95): Show | 147 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.244+2919_244+2922d others(6): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887644 | AATATATA others(1): Show |
A | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+2915_244+2922d others(10): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887644 | ||||||
| chr3:128887648 | T | A | 7 | a0001c0001t0001g0008a0001c0003t0002g0193a0001c0003t0006g0045others(4): Show | 9 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.244+2902T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887648 | |||||||
| chr3:128887650 | T | A | 28 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0028others(25): Show | 35 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.244+2904T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887650 | |||||||
| chr3:128887652 | T | A | 104 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(101): Show | 155 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.244+2906T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887652 | |||||||
| chr3:128887656 | T | A | 29 | a0001c0002t0002g0090a0001c0002t0002g0096a0001c0002t0002g0097others(26): Show | 38 | HG01243.hp2 HG02040.hp2 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.244+2910T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887656 | |||||||
| chr3:128887660 | T | A | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+2914T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887660 | |||||||
| chr3:128887667 | A | ATATATAT others(23): Show |
1 | a0001c0003t0005g0191 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.244+2922_244+2923i others(32): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128887667 | ||||||
| chr3:128887687 | C | T | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.244+2941C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887687 | |||||||
| chr3:128887872 | C | T | 1 | a0001c0002t0002g0047 | 2 | NA19066.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.244+3126C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887872 | |||||||
| chr3:128887920 | G | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+3174G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128887920 | |||||||
| chr3:128888106 | ACCTAAGA others(13): Show |
A | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.244+3364_244+3383d others(22): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128888106 | ||||||
| chr3:128888309 | T | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.244+3563T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128888309 | |||||||
| chr3:128888391 | C | T | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+3645C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128888391 | |||||||
| chr3:128888451 | C | T | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.244+3705C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128888451 | |||||||
| chr3:128888536 | G | A | 5 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(2): Show | 7 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.244+3790G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128888536 | |||||||
| chr3:128888541 | T | G | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0205 | 5 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.244+3795T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128888541 | |||||||
| chr3:128888625 | C | A | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.244+3879C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128888625 | |||||||
| chr3:128888678 | T | TA | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.244+3933dupA | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128888678 | ||||||
| chr3:128888717 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.244+3971G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128888717 | |||||||
| chr3:128888803 | CT | C | 4 | a0001c0002t0002g0099a0001c0002t0002g0100a0001c0002t0002g0101others(1): Show | 4 | HG01167.hp1 HG01175.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.244+4064delT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128888803 | ||||||
| chr3:128888899 | GT | G | 190 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(187): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.244+4166delT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128888899 | ||||||
| chr3:128888970 | C | T | 1 | a0001c0002t0002g0151 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.244+4224C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128888970 | |||||||
| chr3:128889143 | TTTTTG | T | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.245-4397_245-4393d others(7): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128889143 | ||||||
| chr3:128889166 | T | TA | 27 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0002t0002g0104others(24): Show | 29 | HG01069.hp1 HG02040.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.245-4376dupA | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128889166 | ||||||
| chr3:128889166 | TA | T | 6 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0002t0002g0148others(3): Show | 6 | HG01074.hp1 HG01106.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.245-4376delA | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128889166 | ||||||
| chr3:128889178 | A | C | 2 | a0001c0002t0002g0015a0001c0002t0002g0150 | 4 | HG01070.hp2 HG01175.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-4377A>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889178 | |||||||
| chr3:128889179 | AC | A | 2 | a0001c0003t0005g0037a0001c0003t0005g0191 | 3 | HG02258.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.245-4375delC | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889179 | |||||||
| chr3:128889180 | C | A | 3 | a0001c0003t0005g0188a0001c0003t0005g0189a0001c0014t0005g0190 | 3 | HG02572.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.245-4375C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889180 | |||||||
| chr3:128889227 | T | C | 2 | a0001c0004t0004g0048a0001c0004t0004g0049 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.245-4328T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889227 | |||||||
| chr3:128889305 | C | T | 1 | a0001c0003t0003g0079 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.245-4250C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889305 | |||||||
| chr3:128889310 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.245-4245G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889310 | |||||||
| chr3:128889353 | C | T | 22 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0044others(19): Show | 28 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.245-4202C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889353 | |||||||
| chr3:128889457 | G | A | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.245-4098G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889457 | |||||||
| chr3:128889496 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.245-4059C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889496 | |||||||
| chr3:128889498 | T | G | 95 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(92): Show | 144 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.245-4057T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889498 | |||||||
| chr3:128889514 | A | G | 1 | a0001c0003t0003g0085 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.245-4041A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889514 | |||||||
| chr3:128889736 | T | G | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(25): Show | 39 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.245-3819T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889736 | |||||||
| chr3:128889908 | G | C | 132 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(129): Show | 190 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(187): Show |
intron_variant | MODIFIER | c.245-3647G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128889908 | |||||||
| chr3:128890173 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.245-3382C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890173 | |||||||
| chr3:128890183 | G | A | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-3372G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890183 | |||||||
| chr3:128890258 | G | A | 1 | a0001c0003t0003g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.245-3297G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890258 | |||||||
| chr3:128890306 | G | A | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.245-3249G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890306 | |||||||
| chr3:128890332 | C | T | 5 | a0001c0002t0002g0143a0001c0002t0002g0144a0001c0002t0002g0145others(2): Show | 5 | HG01975.hp2 HG01993.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.245-3223C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890332 | |||||||
| chr3:128890355 | G | A | 28 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0028others(25): Show | 35 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.245-3200G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890355 | |||||||
| chr3:128890357 | A | G | 1 | a0001c0002t0002g0164 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.245-3198A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890357 | |||||||
| chr3:128890377 | C | T | 1 | a0001c0015t0002g0087 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.245-3178C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890377 | |||||||
| chr3:128890412 | T | A | 35 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186others(32): Show | 44 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.245-3143T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890412 | |||||||
| chr3:128890441 | G | A | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-3114G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890441 | |||||||
| chr3:128890468 | C | T | 130 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(127): Show | 188 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(185): Show |
intron_variant | MODIFIER | c.245-3087C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890468 | |||||||
| chr3:128890477 | C | T | 1 | a0001c0001t0001g0043 | 2 | HG00558.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.245-3078C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890477 | |||||||
| chr3:128890484 | T | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.245-3071T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890484 | |||||||
| chr3:128890660 | C | T | 1 | a0001c0002t0002g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.245-2895C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890660 | |||||||
| chr3:128890680 | C | T | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.245-2875C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890680 | |||||||
| chr3:128890681 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.245-2874G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890681 | |||||||
| chr3:128890712 | G | T | 3 | a0001c0003t0003g0077a0001c0003t0003g0078a0001c0003t0003g0080 | 3 | HG02109.hp1 HG02572.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.245-2843G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890712 | |||||||
| chr3:128890728 | G | T | 1 | a0001c0002t0002g0141 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.245-2827G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890728 | |||||||
| chr3:128890836 | T | C | 6 | a0001c0003t0003g0028a0001c0003t0003g0081a0001c0003t0003g0082others(3): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-2719T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890836 | |||||||
| chr3:128890843 | A | AT | 58 | a0001c0001t0001g0183a0001c0001t0001g0235a0001c0002t0002g0140others(55): Show | 69 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.245-2696dupT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128890843 | ||||||
| chr3:128890843 | A | ATT | 8 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(5): Show | 9 | HG02055.hp2 HG02258.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.245-2697_245-2696d others(4): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128890843 | ||||||
| chr3:128890859 | T | G | 1 | a0001c0001t0001g0211 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.245-2696T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890859 | |||||||
| chr3:128890890 | G | A | 1 | a0001c0003t0003g0251 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.245-2665G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890890 | |||||||
| chr3:128890903 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.245-2652G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890903 | |||||||
| chr3:128890930 | C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0176a0001c0001t0001g0182 | 4 | HG00423.hp1 NA18960.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.245-2625C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128890930 | |||||||
| chr3:128891134 | C | T | 6 | a0001c0003t0003g0028a0001c0003t0003g0081a0001c0003t0003g0082others(3): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.245-2421C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891134 | |||||||
| chr3:128891172 | A | G | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.245-2383A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891172 | |||||||
| chr3:128891332 | A | G | 1 | a0001c0003t0002g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.245-2223A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891332 | |||||||
| chr3:128891362 | C | T | 1 | a0001c0002t0002g0090 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.245-2193C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891362 | |||||||
| chr3:128891418 | C | T | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.245-2137C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891418 | |||||||
| chr3:128891450 | G | A | 1 | a0001c0003t0001g0212 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.245-2105G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891450 | |||||||
| chr3:128891540 | G | A | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.245-2015G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891540 | |||||||
| chr3:128891600 | G | C | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.245-1955G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891600 | |||||||
| chr3:128891668 | G | A | 2 | a0001c0002t0002g0012a0001c0002t0002g0105 | 4 | NA18951.hp2 NA18961.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-1887G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891668 | |||||||
| chr3:128891721 | C | G | 1 | a0001c0015t0002g0087 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.245-1834C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891721 | |||||||
| chr3:128891751 | T | C | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.245-1804T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891751 | |||||||
| chr3:128891786 | T | C | 193 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(190): Show | 267 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.245-1769T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891786 | |||||||
| chr3:128891965 | A | C | 2 | a0001c0003t0002g0193a0001c0007t0002g0187 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.245-1590A>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128891965 | |||||||
| chr3:128892384 | G | A | 1 | a0001c0004t0004g0051 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.245-1171G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128892384 | |||||||
| chr3:128893101 | T | A | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.245-454T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128893101 | |||||||
| chr3:128893184 | G | GA | 8 | a0001c0001t0001g0213a0001c0002t0002g0106a0001c0002t0002g0107others(5): Show | 8 | HG00423.hp2 HG00558.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.245-355dupA | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128893184 | ||||||
| chr3:128893242 | CATG | C | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.245-311_245-309del others(3): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 128893242 | ||||||
| chr3:128893270 | A | C | 95 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(92): Show | 144 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.245-285A>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128893270 | |||||||
| chr3:128893291 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.245-264G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128893291 | |||||||
| chr3:128893386 | A | T | 28 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0028others(25): Show | 35 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.245-169A>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 2/17 | chr3 | 128893386 | |||||||
| chr3:128893719 | A | G | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.346+63A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128893719 | |||||||
| chr3:128893756 | G | A | 1 | a0001c0015t0002g0087 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.346+100G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128893756 | |||||||
| chr3:128893816 | G | C | 135 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(132): Show | 195 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.346+160G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128893816 | |||||||
| chr3:128893987 | C | A | 135 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(132): Show | 195 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(192): Show |
intron_variant | MODIFIER | c.346+331C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128893987 | |||||||
| chr3:128894157 | T | C | 6 | a0001c0003t0001g0017a0001c0003t0001g0212a0001c0003t0001g0237others(3): Show | 8 | HG01069.hp2 HG01261.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.346+501T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894157 | |||||||
| chr3:128894221 | C | T | 2 | a0001c0002t0002g0097a0001c0002t0002g0098 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.346+565C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894221 | |||||||
| chr3:128894227 | A | G | 2 | a0001c0002t0002g0139a0001c0002t0002g0141 | 2 | HG02165.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.346+571A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894227 | |||||||
| chr3:128894269 | C | G | 2 | a0001c0003t0002g0193a0001c0007t0002g0187 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.346+613C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894269 | |||||||
| chr3:128894287 | G | T | 2 | a0001c0003t0002g0193a0001c0007t0002g0187 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.346+631G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894287 | |||||||
| chr3:128894300 | A | G | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.346+644A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894300 | |||||||
| chr3:128894433 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.346+777C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894433 | |||||||
| chr3:128894533 | C | CT | 10 | a0001c0001t0001g0019a0001c0001t0001g0205a0001c0001t0001g0208others(7): Show | 12 | HG00735.hp1 HG01433.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.347-758dupT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 128894533 | ||||||
| chr3:128894533 | CT | C | 8 | a0001c0001t0001g0178a0001c0001t0001g0214a0001c0001t0001g0215others(5): Show | 10 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.347-758delT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 128894533 | ||||||
| chr3:128894548 | T | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(25): Show | 39 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.347-762T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894548 | |||||||
| chr3:128894569 | C | T | 1 | a0001c0002t0002g0137 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.347-741C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894569 | |||||||
| chr3:128894681 | G | A | 19 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0199others(16): Show | 34 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.347-629G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894681 | |||||||
| chr3:128894684 | C | T | 3 | a0001c0002t0007g0157a0001c0002t0007g0158a0001c0002t0007g0159 | 3 | HG01255.hp1 HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.347-626C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894684 | |||||||
| chr3:128894685 | G | A | 2 | a0001c0002t0008g0103a0001c0002t0008g0110 | 2 | HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.347-625G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894685 | |||||||
| chr3:128894702 | A | G | 3 | a0001c0002t0002g0134a0001c0002t0002g0135a0001c0002t0002g0136 | 3 | NA18965.hp1 NA18975.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.347-608A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894702 | |||||||
| chr3:128894716 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.347-594G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894716 | |||||||
| chr3:128894872 | A | AT | 21 | a0001c0001t0001g0042a0001c0001t0001g0176a0001c0001t0001g0204others(18): Show | 25 | HG00639.hp1 HG00673.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.347-416dupT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 128894872 | ||||||
| chr3:128894872 | A | ATT | 23 | a0001c0003t0001g0017a0001c0003t0001g0212a0001c0003t0001g0237others(20): Show | 31 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.347-417_347-416dup others(2): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 128894872 | ||||||
| chr3:128894872 | AT | A | 88 | a0001c0001t0001g0222a0001c0001t0001g0223a0001c0001t0001g0242others(85): Show | 135 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.347-416delT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 128894872 | ||||||
| chr3:128894872 | ATT | A | 8 | a0001c0002t0002g0026a0001c0002t0002g0031a0001c0002t0002g0097others(5): Show | 10 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.347-417_347-416del others(2): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 128894872 | ||||||
| chr3:128894872 | ATTT | A | 28 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(25): Show | 31 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.347-418_347-416del others(3): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 128894872 | ||||||
| chr3:128894894 | T | G | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.347-416T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894894 | |||||||
| chr3:128894923 | C | G | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.347-387C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894923 | |||||||
| chr3:128894981 | A | T | 2 | a0001c0004t0004g0048a0001c0004t0004g0049 | 2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.347-329A>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128894981 | |||||||
| chr3:128895001 | T | C | 30 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(27): Show | 33 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(30): Show |
intron_variant | MODIFIER | c.347-309T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128895001 | |||||||
| chr3:128895066 | G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0213a0001c0001t0001g0222 | 5 | NA18747.hp2 NA18941.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.347-244G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128895066 | |||||||
| chr3:128895161 | G | A | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.347-149G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128895161 | |||||||
| chr3:128895172 | C | T | 1 | a0003c0006t0001g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.347-138C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128895172 | |||||||
| chr3:128895232 | G | GA | 165 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(162): Show | 228 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.347-68dupA | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 128895232 | ||||||
| chr3:128895290 | C | T | 193 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(190): Show | 267 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.347-20C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 3/17 | chr3 | 128895290 | |||||||
| chr3:128895575 | C | T | 1 | a0001c0003t0004g0054 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.453+159C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | chr3 | 128895575 | |||||||
| chr3:128895697 | C | T | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.453+281C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | chr3 | 128895697 | |||||||
| chr3:128895720 | T | TCTC | 193 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(190): Show | 267 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.453+305_453+307dup others(3): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 128895720 | ||||||
| chr3:128895767 | A | C | 1 | a0001c0002t0002g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.453+351A>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | chr3 | 128895767 | |||||||
| chr3:128895797 | G | T | 1 | a0001c0002t0002g0140 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.453+381G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | chr3 | 128895797 | |||||||
| chr3:128895927 | G | A | 166 | a0001c0001t0001g0038a0001c0002t0002g0002a0001c0002t0002g0003others(163): Show | 230 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(227): Show |
intron_variant | MODIFIER | c.454-509G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | chr3 | 128895927 | |||||||
| chr3:128896035 | G | A | 1 | a0001c0003t0002g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.454-401G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | chr3 | 128896035 | |||||||
| chr3:128896175 | A | G | 1 | a0001c0003t0003g0044 | 2 | HG01109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.454-261A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | chr3 | 128896175 | |||||||
| chr3:128896244 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.454-192C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | chr3 | 128896244 | |||||||
| chr3:128896417 | C | A | 2 | a0001c0003t0002g0193a0001c0007t0002g0187 | 2 | HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.454-19C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 4/17 | chr3 | 128896417 | |||||||
| chr3:128896556 | G | A | 1 | a0001c0007t0001g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.554+20G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128896556 | |||||||
| chr3:128896807 | A | T | 1 | a0001c0001t0001g0245 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.554+271A>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128896807 | |||||||
| chr3:128896987 | A | G | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.554+451A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128896987 | |||||||
| chr3:128897054 | C | A | 1 | a0001c0002t0002g0106 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.554+518C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897054 | |||||||
| chr3:128897055 | A | C | 2 | a0001c0004t0004g0060a0001c0004t0004g0063 | 2 | HG02055.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.554+519A>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897055 | |||||||
| chr3:128897161 | A | G | 1 | a0001c0003t0003g0069 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.555-471A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897161 | |||||||
| chr3:128897193 | G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0217a0001c0001t0001g0258 | 4 | HG00558.hp2 HG02135.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.555-439G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897193 | |||||||
| chr3:128897270 | C | T | 3 | a0001c0002t0002g0006a0001c0002t0002g0112a0001c0002t0002g0129 | 8 | HG02080.hp2 HG03490.hp1 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.555-362C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897270 | |||||||
| chr3:128897295 | C | T | 1 | a0001c0015t0002g0087 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.555-337C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897295 | |||||||
| chr3:128897458 | TGAG | T | 3 | a0001c0002t0002g0128a0001c0002t0002g0160a0001c0002t0002g0161 | 3 | HG00099.hp2 HG00140.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.555-169_555-167del others(3): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 128897458 | ||||||
| chr3:128897482 | C | T | 190 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(187): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.555-150C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897482 | |||||||
| chr3:128897516 | C | G | 94 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(91): Show | 143 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.555-116C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897516 | |||||||
| chr3:128897554 | C | T | 2 | a0001c0003t0006g0045a0001c0003t0006g0255 | 3 | HG00639.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.555-78C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897554 | |||||||
| chr3:128897619 | T | C | 1 | a0001c0002t0007g0157 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.555-13T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 5/17 | chr3 | 128897619 | |||||||
| chr3:128897873 | T | A | 1 | a0001c0001t0001g0020 | 3 | HG02735.hp2 HG04204.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.633+163T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128897873 | |||||||
| chr3:128897909 | G | A | 28 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(25): Show | 39 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.633+199G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128897909 | |||||||
| chr3:128897986 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.633+276A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128897986 | |||||||
| chr3:128898316 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.633+606G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128898316 | |||||||
| chr3:128898406 | T | G | 14 | a0001c0001t0001g0010a0001c0001t0001g0165a0001c0001t0001g0178others(11): Show | 21 | HG00639.hp2 HG01255.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.633+696T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128898406 | |||||||
| chr3:128898459 | G | GCAGTGGC others(21): Show |
23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.633+751_633+778dup others(28): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 128898459 | ||||||
| chr3:128898468 | C | CGATCTTG others(21): Show |
7 | a0001c0002t0002g0113a0001c0003t0005g0037a0001c0003t0005g0188others(4): Show | 8 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.633+778_633+779ins others(28): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 128898468 | ||||||
| chr3:128898515 | C | G | 1 | a0001c0002t0002g0127 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.634-772C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128898515 | |||||||
| chr3:128898569 | A | AT | 10 | a0001c0001t0001g0010a0001c0001t0001g0165a0001c0001t0001g0178others(7): Show | 17 | HG00639.hp2 HG01346.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.634-708dupT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr3 | 128898569 | ||||||
| chr3:128898583 | A | G | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.634-704A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128898583 | |||||||
| chr3:128898651 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.634-636C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128898651 | |||||||
| chr3:128898677 | G | C | 1 | a0001c0003t0003g0044 | 2 | HG01109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.634-610G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128898677 | |||||||
| chr3:128898947 | T | G | 29 | a0001c0001t0001g0224a0001c0001t0001g0246a0001c0002t0002g0086others(26): Show | 31 | HG01243.hp1 HG02040.hp2 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.634-340T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128898947 | |||||||
| chr3:128899047 | T | C | 1 | a0001c0007t0002g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.634-240T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128899047 | |||||||
| chr3:128899127 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.634-160T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 6/17 | chr3 | 128899127 | |||||||
| chr3:128899478 | C | T | 1 | a0001c0003t0002g0156 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.808+17C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128899478 | |||||||
| chr3:128899483 | G | A | 2 | a0001c0002t0002g0116a0001c0002t0002g0140 | 2 | HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.808+22G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128899483 | |||||||
| chr3:128899522 | C | CCGTG | 3 | a0001c0003t0005g0037a0001c0003t0005g0191a0001c0003t0005g0192 | 4 | HG02258.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.808+61_808+62insCG others(2): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128899522 | |||||||
| chr3:128899522 | C | CCGTGTGT others(3): Show |
1 | a0001c0003t0005g0188 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.808+61_808+62insCG others(8): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128899522 | |||||||
| chr3:128899522 | C | CTG | 4 | a0001c0004t0004g0048a0001c0004t0004g0049a0001c0004t0004g0052others(1): Show | 4 | HG02040.hp2 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.808+61_808+62insTG | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128899522 | |||||||
| chr3:128899522 | CGGTG | C | 3 | a0001c0004t0004g0051a0001c0004t0004g0053a0001c0004t0004g0062 | 3 | HG03209.hp2 NA18950.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.808+62_808+65delGG others(2): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128899522 | |||||||
| chr3:128899523 | G | GGT | 44 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0038others(41): Show | 57 | HG00140.hp2 HG00280.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.808+101_808+102dup others(2): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899523 | G | GGTGT | 33 | a0001c0001t0001g0215a0001c0001t0001g0241a0001c0002t0002g0005others(30): Show | 45 | HG00099.hp2 HG00140.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.808+99_808+102dupG others(3): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899523 | G | GGTGTGT | 37 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0029others(34): Show | 57 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.808+97_808+102dupG others(5): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899523 | G | GGTGTGTG others(1): Show |
9 | a0001c0002t0002g0033a0001c0002t0002g0064a0001c0002t0002g0109others(6): Show | 10 | HG00558.hp1 HG01123.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.808+95_808+102dupG others(7): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899523 | G | GGTGTGTG others(3): Show |
4 | a0001c0002t0002g0124a0001c0002t0002g0136a0001c0003t0003g0028others(1): Show | 5 | HG02080.hp1 HG02486.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.808+93_808+102dupG others(9): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899523 | G | GGTGTGTG others(5): Show |
1 | a0001c0002t0002g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.808+91_808+102dupG others(11): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899523 | G | GGTGTGTG others(9): Show |
1 | a0001c0002t0002g0126 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.808+87_808+102dupG others(15): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899523 | G | T | 22 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(19): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.808+62G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128899523 | |||||||
| chr3:128899523 | GGT | G | 15 | a0001c0001t0001g0010a0001c0001t0001g0165a0001c0001t0001g0167others(12): Show | 18 | HG00323.hp2 HG01255.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.808+101_808+102del others(2): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899523 | GGTGT | G | 4 | a0001c0001t0001g0218a0001c0001t0001g0243a0001c0001t0001g0248others(1): Show | 4 | HG02273.hp1 HG02647.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.808+99_808+102delG others(3): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899523 | GGTGTGTG others(5): Show |
G | 5 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(2): Show | 7 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.808+91_808+102delG others(11): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128899523 | ||||||
| chr3:128899860 | G | T | 1 | a0001c0002t0002g0152 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.808+399G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128899860 | |||||||
| chr3:128899928 | A | G | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.808+467A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128899928 | |||||||
| chr3:128900044 | G | A | 1 | a0001c0003t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.808+583G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900044 | |||||||
| chr3:128900072 | C | G | 2 | a0001c0007t0001g0256a0001c0007t0002g0187 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.808+611C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900072 | |||||||
| chr3:128900114 | T | TAGAGATG others(21): Show |
1 | a0001c0001t0001g0238 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.808+655_808+682dup others(28): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128900114 | ||||||
| chr3:128900221 | C | A | 4 | a0001c0004t0004g0023a0001c0004t0004g0056a0001c0004t0004g0057others(1): Show | 4 | HG02056.hp2 NA19063.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.808+760C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900221 | |||||||
| chr3:128900260 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.808+799C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900260 | |||||||
| chr3:128900300 | C | T | 1 | a0001c0015t0002g0087 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.808+839C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900300 | |||||||
| chr3:128900323 | C | T | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.808+862C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900323 | |||||||
| chr3:128900377 | A | G | 1 | a0001c0002t0002g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.809-899A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900377 | |||||||
| chr3:128900394 | C | T | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-882C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900394 | |||||||
| chr3:128900398 | C | T | 1 | a0001c0003t0003g0253 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.809-878C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900398 | |||||||
| chr3:128900413 | A | G | 1 | a0003c0006t0001g0229 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.809-863A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900413 | |||||||
| chr3:128900481 | G | A | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.809-795G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900481 | |||||||
| chr3:128900514 | C | T | 130 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(127): Show | 183 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.809-762C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900514 | |||||||
| chr3:128900515 | G | A | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.809-761G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900515 | |||||||
| chr3:128900524 | C | CT | 26 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(23): Show | 30 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.809-735dupT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128900524 | ||||||
| chr3:128900524 | C | CTT | 7 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(4): Show | 8 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.809-736_809-735dup others(2): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128900524 | ||||||
| chr3:128900524 | CT | C | 13 | a0001c0001t0001g0185a0001c0001t0001g0207a0001c0001t0001g0214others(10): Show | 14 | HG01167.hp1 HG02698.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.809-735delT | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128900524 | ||||||
| chr3:128900641 | G | T | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.809-635G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900641 | |||||||
| chr3:128900662 | T | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.809-614T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900662 | |||||||
| chr3:128900700 | G | A | 2 | a0001c0007t0001g0256a0001c0007t0002g0187 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.809-576G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900700 | |||||||
| chr3:128900840 | G | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(27): Show | 48 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.809-436G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900840 | |||||||
| chr3:128900892 | C | T | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(27): Show | 48 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.809-384C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128900892 | |||||||
| chr3:128901161 | C | T | 4 | a0001c0002t0002g0006a0001c0002t0002g0013a0001c0002t0002g0112others(1): Show | 11 | HG02080.hp2 HG03490.hp1 HG03492.hp2 others(8): Show |
intron_variant | MODIFIER | c.809-115C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | chr3 | 128901161 | |||||||
| chr3:128901172 | T | TTGGATGG others(5): Show |
7 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(4): Show | 8 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.809-85_809-74dupGA others(10): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128901172 | ||||||
| chr3:128901172 | T | TTGGATGG others(9): Show |
22 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(19): Show | 24 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.809-89_809-74dupGA others(14): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 128901172 | ||||||
| chr3:128901424 | TC | T | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.882+78delC | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 128901424 | ||||||
| chr3:128901545 | T | C | 85 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(82): Show | 127 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.882+196T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128901545 | |||||||
| chr3:128901547 | A | G | 163 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(160): Show | 219 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.882+198A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128901547 | |||||||
| chr3:128901563 | C | T | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.882+214C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128901563 | |||||||
| chr3:128901768 | T | A | 1 | a0001c0002t0002g0145 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.882+419T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128901768 | |||||||
| chr3:128901883 | G | T | 6 | a0001c0003t0003g0028a0001c0003t0003g0081a0001c0003t0003g0082others(3): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.882+534G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128901883 | |||||||
| chr3:128901912 | T | C | 5 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(2): Show | 6 | HG02258.hp2 HG02622.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+563T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128901912 | |||||||
| chr3:128902015 | C | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0221a0007c0010t0001g0203 | 3 | HG02074.hp2 NA19010.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.883-538C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128902015 | |||||||
| chr3:128902109 | C | G | 1 | a0001c0002t0002g0122 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.883-444C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128902109 | |||||||
| chr3:128902197 | C | T | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.883-356C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128902197 | |||||||
| chr3:128902520 | A | G | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.883-33A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 8/17 | chr3 | 128902520 | |||||||
| chr3:128902683 | C | T | 1 | a0001c0004t0004g0059 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.958+55C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128902683 | |||||||
| chr3:128902710 | G | A | 1 | a0001c0002t0002g0120 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.958+82G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128902710 | |||||||
| chr3:128902721 | G | A | 2 | a0001c0002t0002g0112a0001c0002t0002g0129 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.958+93G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128902721 | |||||||
| chr3:128902797 | G | A | 2 | a0001c0007t0001g0256a0001c0007t0002g0187 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.958+169G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128902797 | |||||||
| chr3:128902803 | G | C | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.958+175G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128902803 | |||||||
| chr3:128902844 | C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0175 | 2 | NA19007.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.958+216C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128902844 | |||||||
| chr3:128902859 | G | C | 1 | a0001c0002t0002g0160 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.958+231G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128902859 | |||||||
| chr3:128902895 | T | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.958+267T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128902895 | |||||||
| chr3:128903363 | A | G | 1 | a0001c0002t0007g0159 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.959-699A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128903363 | |||||||
| chr3:128903435 | T | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.959-627T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128903435 | |||||||
| chr3:128903516 | C | T | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0041others(2): Show | 8 | HG00140.hp2 HG00280.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.959-546C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128903516 | |||||||
| chr3:128903762 | G | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(27): Show | 48 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.959-300G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128903762 | |||||||
| chr3:128903899 | G | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(27): Show | 48 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.959-163G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128903899 | |||||||
| chr3:128903917 | G | T | 90 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(87): Show | 132 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.959-145G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128903917 | |||||||
| chr3:128903930 | G | C | 2 | a0001c0003t0006g0045a0001c0003t0006g0255 | 3 | HG00639.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.959-132G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128903930 | |||||||
| chr3:128903952 | C | T | 1 | a0001c0002t0002g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.959-110C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 9/17 | chr3 | 128903952 | |||||||
| chr3:128904218 | C | A | 1 | a0004c0013t0004g0259 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1029+86C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 10/17 | chr3 | 128904218 | |||||||
| chr3:128904556 | C | T | 2 | a0001c0007t0001g0256a0001c0007t0002g0187 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1149+51C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904556 | |||||||
| chr3:128904562 | C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0233 | 2 | HG00741.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1149+57C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904562 | |||||||
| chr3:128904624 | T | C | 1 | a0001c0001t0001g0034 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1149+119T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904624 | |||||||
| chr3:128904713 | G | A | 1 | a0001c0014t0005g0190 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1149+208G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904713 | |||||||
| chr3:128904746 | T | C | 1 | a0001c0003t0003g0079 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1149+241T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904746 | |||||||
| chr3:128904802 | C | T | 1 | a0007c0010t0001g0203 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1149+297C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904802 | |||||||
| chr3:128904891 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1149+386T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904891 | |||||||
| chr3:128904914 | G | T | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.1149+409G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904914 | |||||||
| chr3:128904921 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1149+416G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904921 | |||||||
| chr3:128904942 | C | T | 38 | a0001c0003t0001g0017a0001c0003t0001g0212a0001c0003t0001g0237others(35): Show | 49 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(46): Show |
intron_variant | MODIFIER | c.1149+437C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128904942 | |||||||
| chr3:128905059 | T | C | 2 | a0001c0003t0002g0088a0001c0003t0002g0089 | 2 | HG00642.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.1149+554T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905059 | |||||||
| chr3:128905092 | G | A | 1 | a0001c0003t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1149+587G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905092 | |||||||
| chr3:128905123 | A | G | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1149+618A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905123 | |||||||
| chr3:128905164 | AC | A | 21 | a0001c0002t0002g0002a0001c0002t0002g0014a0001c0002t0002g0029others(18): Show | 34 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.1149+660delC | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905164 | |||||||
| chr3:128905165 | C | A | 1 | a0001c0002t0002g0147 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1149+660C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905165 | |||||||
| chr3:128905173 | A | G | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1149+668A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905173 | |||||||
| chr3:128905263 | T | C | 1 | a0001c0002t0002g0106 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1149+758T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905263 | |||||||
| chr3:128905427 | C | T | 1 | a0001c0003t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1150-694C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905427 | |||||||
| chr3:128905460 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1150-661G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905460 | |||||||
| chr3:128905501 | C | T | 1 | a0001c0007t0002g0187 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1150-620C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905501 | |||||||
| chr3:128905511 | G | C | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1150-610G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905511 | |||||||
| chr3:128905661 | G | A | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-460G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905661 | |||||||
| chr3:128905697 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1150-424T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905697 | |||||||
| chr3:128905706 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1150-415G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905706 | |||||||
| chr3:128905732 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1150-389G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905732 | |||||||
| chr3:128905929 | T | C | 91 | a0001c0001t0001g0225a0001c0002t0002g0002a0001c0002t0002g0003others(88): Show | 133 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1150-192T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905929 | |||||||
| chr3:128905967 | C | T | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1150-154C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128905967 | |||||||
| chr3:128906016 | C | T | 1 | a0001c0002t0002g0119 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1150-105C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128906016 | |||||||
| chr3:128906035 | C | T | 2 | a0001c0002t0002g0111a0001c0002t0002g0121 | 2 | NA18942.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.1150-86C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128906035 | |||||||
| chr3:128906036 | G | A | 2 | a0001c0007t0001g0256a0001c0007t0002g0187 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1150-85G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128906036 | |||||||
| chr3:128906037 | T | G | 163 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(160): Show | 219 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.1150-84T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 11/17 | chr3 | 128906037 | |||||||
| chr3:128906345 | A | G | 1 | a0007c0010t0001g0203 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1278+96A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906345 | |||||||
| chr3:128906356 | G | A | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1278+107G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906356 | |||||||
| chr3:128906399 | C | T | 17 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0035others(14): Show | 22 | HG00323.hp2 HG00423.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1278+150C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906399 | |||||||
| chr3:128906402 | C | T | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1278+153C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906402 | |||||||
| chr3:128906423 | C | T | 4 | a0001c0004t0004g0023a0001c0004t0004g0056a0001c0004t0004g0057others(1): Show | 4 | HG02056.hp2 NA19063.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.1278+174C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906423 | |||||||
| chr3:128906475 | C | T | 161 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(158): Show | 217 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(214): Show |
intron_variant | MODIFIER | c.1278+226C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906475 | |||||||
| chr3:128906650 | C | T | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1278+401C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906650 | |||||||
| chr3:128906785 | G | A | 1 | a0001c0002t0002g0126 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1278+536G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906785 | |||||||
| chr3:128906832 | A | G | 1 | a0001c0002t0002g0143 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1278+583A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906832 | |||||||
| chr3:128906947 | G | T | 190 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(187): Show | 262 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.1278+698G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128906947 | |||||||
| chr3:128907003 | G | A | 1 | a0001c0002t0002g0136 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1278+754G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907003 | |||||||
| chr3:128907010 | G | T | 93 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(90): Show | 135 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1278+761G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907010 | |||||||
| chr3:128907080 | G | T | 22 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(19): Show | 25 | HG02040.hp2 HG02056.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.1278+831G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907080 | |||||||
| chr3:128907134 | G | A | 1 | a0001c0002t0002g0108 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1278+885G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907134 | |||||||
| chr3:128907147 | T | C | 1 | a0007c0010t0001g0203 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1278+898T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907147 | |||||||
| chr3:128907301 | C | T | 3 | a0001c0001t0001g0177a0001c0007t0001g0256a0001c0007t0002g0187 | 3 | HG01978.hp2 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1279-884C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907301 | |||||||
| chr3:128907324 | C | T | 1 | a0001c0003t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1279-861C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907324 | |||||||
| chr3:128907465 | T | G | 2 | a0001c0001t0001g0210a0001c0001t0001g0216 | 2 | HG00323.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1279-720T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907465 | |||||||
| chr3:128907605 | A | G | 32 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(29): Show | 35 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(32): Show |
intron_variant | MODIFIER | c.1279-580A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907605 | |||||||
| chr3:128907702 | T | C | 2 | a0001c0002t0002g0086a0001c0002t0002g0114 | 2 | HG01243.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1279-483T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907702 | |||||||
| chr3:128907879 | C | T | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1279-306C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907879 | |||||||
| chr3:128907975 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1279-210A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128907975 | |||||||
| chr3:128908004 | CCCT | C | 1 | a0001c0001t0001g0011 | 4 | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279-176_1279-174d others(5): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr3 | 128908004 | ||||||
| chr3:128908106 | G | A | 1 | a0001c0002t0002g0093 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1279-79G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128908106 | |||||||
| chr3:128908109 | T | C | 160 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(157): Show | 214 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.1279-76T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128908109 | |||||||
| chr3:128908148 | G | A | 1 | a0001c0003t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1279-37G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128908148 | |||||||
| chr3:128908178 | A | G | 160 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(157): Show | 214 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(211): Show |
splice_region_variant&intron_variant | LOW | c.1279-7A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 12/17 | chr3 | 128908178 | |||||||
| chr3:128908326 | A | G | 1 | a0001c0003t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1358+62A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908326 | |||||||
| chr3:128908345 | G | A | 1 | a0002c0005t0001g0220 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1358+81G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908345 | |||||||
| chr3:128908401 | C | G | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1358+137C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908401 | |||||||
| chr3:128908416 | T | C | 17 | a0001c0001t0001g0016a0001c0001t0001g0034a0001c0001t0001g0035others(14): Show | 22 | HG00323.hp2 HG00423.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1358+152T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908416 | |||||||
| chr3:128908462 | G | A | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1358+198G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908462 | |||||||
| chr3:128908468 | G | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1358+204G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908468 | |||||||
| chr3:128908532 | G | T | 1 | a0001c0001t0001g0221 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1358+268G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908532 | |||||||
| chr3:128908544 | C | T | 1 | a0001c0002t0002g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1358+280C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908544 | |||||||
| chr3:128908631 | A | G | 1 | a0001c0003t0003g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1359-342A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908631 | |||||||
| chr3:128908671 | A | G | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1359-302A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908671 | |||||||
| chr3:128908777 | T | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1359-196T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908777 | |||||||
| chr3:128908780 | G | A | 92 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(89): Show | 134 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1359-193G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908780 | |||||||
| chr3:128908846 | AGCCAGGG others(15): Show |
A | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1359-121_1359-100d others(24): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 128908846 | ||||||
| chr3:128908910 | T | C | 160 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(157): Show | 214 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.1359-63T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 13/17 | chr3 | 128908910 | |||||||
| chr3:128909124 | C | A | 1 | a0001c0003t0003g0085 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1485+25C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 14/17 | chr3 | 128909124 | |||||||
| chr3:128909156 | T | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1485+57T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 14/17 | chr3 | 128909156 | |||||||
| chr3:128909550 | T | G | 22 | a0001c0003t0003g0007a0001c0003t0003g0027a0001c0003t0003g0044others(19): Show | 28 | HG00639.hp2 HG01069.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.1563+129T>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 15/17 | chr3 | 128909550 | |||||||
| chr3:128909633 | G | A | 2 | a0001c0007t0001g0256a0001c0007t0002g0187 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1563+212G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 15/17 | chr3 | 128909633 | |||||||
| chr3:128909635 | AGT | A | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1563+217_1563+218d others(4): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 128909635 | ||||||
| chr3:128909658 | G | C | 23 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(20): Show | 25 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.1563+237G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 15/17 | chr3 | 128909658 | |||||||
| chr3:128909783 | C | T | 1 | a0001c0004t0004g0056 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1564-238C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 15/17 | chr3 | 128909783 | |||||||
| chr3:128909880 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1564-141A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 15/17 | chr3 | 128909880 | |||||||
| chr3:128909966 | A | G | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1564-55A>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 15/17 | chr3 | 128909966 | |||||||
| chr3:128909970 | G | A | 1 | a0001c0002t0002g0149 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1564-51G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 15/17 | chr3 | 128909970 | |||||||
| chr3:128910196 | CCTG | C | 3 | a0001c0002t0002g0026a0001c0002t0002g0031a0001c0002t0002g0142 | 5 | HG00642.hp2 HG00733.hp1 HG01192.hp2 others(2): Show |
intron_variant | MODIFIER | c.1692+52_1692+54del others(3): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 128910196 | ||||||
| chr3:128910273 | G | A | 6 | a0001c0003t0003g0028a0001c0003t0003g0081a0001c0003t0003g0082others(3): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1692+124G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/17 | chr3 | 128910273 | |||||||
| chr3:128910294 | G | C | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1692+145G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/17 | chr3 | 128910294 | |||||||
| chr3:128910434 | C | T | 1 | a0001c0001t0001g0034 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1692+285C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/17 | chr3 | 128910434 | |||||||
| chr3:128910485 | T | C | 1 | a0001c0002t0002g0149 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1693-256T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/17 | chr3 | 128910485 | |||||||
| chr3:128910489 | G | A | 30 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0016others(27): Show | 48 | HG00323.hp2 HG00423.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.1693-252G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/17 | chr3 | 128910489 | |||||||
| chr3:128910575 | G | C | 1 | a0001c0002t0002g0150 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1693-166G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/17 | chr3 | 128910575 | |||||||
| chr3:128910662 | C | CTGAT | 93 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(90): Show | 135 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1693-78_1693-75dup others(4): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 128910662 | ||||||
| chr3:128910891 | T | C | 2 | a0001c0002t0002g0124a0001c0002t0002g0125 | 2 | HG02056.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1765+78T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128910891 | |||||||
| chr3:128910918 | C | A | 1 | a0001c0004t0004g0055 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1765+105C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128910918 | |||||||
| chr3:128910939 | C | T | 1 | a0001c0003t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1765+126C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128910939 | |||||||
| chr3:128911045 | G | GTGTA | 2 | a0001c0001t0001g0208a0001c0003t0006g0045 | 3 | HG01516.hp1 HG01517.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1765+250_1765+253d others(6): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 128911045 | ||||||
| chr3:128911050 | T | A | 2 | a0001c0007t0001g0256a0001c0007t0002g0187 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1765+237T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911050 | |||||||
| chr3:128911118 | G | A | 1 | a0001c0015t0002g0087 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1765+305G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911118 | |||||||
| chr3:128911202 | G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0195a0001c0001t0001g0201others(1): Show | 5 | NA18952.hp1 NA18965.hp2 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765+389G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911202 | |||||||
| chr3:128911206 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1765+393G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911206 | |||||||
| chr3:128911214 | G | A | 7 | a0001c0001t0001g0011a0001c0001t0001g0174a0001c0001t0001g0179others(4): Show | 10 | HG00735.hp2 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1765+401G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911214 | |||||||
| chr3:128911217 | C | T | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1765+404C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911217 | |||||||
| chr3:128911275 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1765+462C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911275 | |||||||
| chr3:128911278 | C | G | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1765+465C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911278 | |||||||
| chr3:128911342 | G | A | 29 | a0001c0003t0004g0050a0001c0003t0004g0054a0001c0003t0004g0061others(26): Show | 32 | HG02040.hp2 HG02055.hp2 HG02056.hp2 others(29): Show |
intron_variant | MODIFIER | c.1765+529G>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911342 | |||||||
| chr3:128911458 | T | C | 4 | a0001c0004t0004g0024a0001c0004t0004g0059a0001c0004t0004g0062others(1): Show | 4 | HG02922.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1765+645T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911458 | |||||||
| chr3:128911586 | C | T | 1 | a0001c0002t0002g0116 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1765+773C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911586 | |||||||
| chr3:128911654 | C | G | 3 | a0001c0002t0002g0030a0001c0002t0002g0092a0001c0002t0002g0093 | 4 | HG02647.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1765+841C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911654 | |||||||
| chr3:128911667 | CCT | C | 4 | a0001c0003t0006g0045a0001c0003t0006g0046a0001c0003t0006g0254others(1): Show | 6 | HG00639.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1766-839_1766-838d others(4): Show |
ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911667 | |||||||
| chr3:128911691 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1766-816C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911691 | |||||||
| chr3:128911736 | C | A | 1 | a0001c0003t0002g0193 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1766-771C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911736 | |||||||
| chr3:128911736 | C | G | 6 | a0001c0003t0003g0028a0001c0003t0003g0081a0001c0003t0003g0082others(3): Show | 7 | HG01123.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1766-771C>G | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911736 | |||||||
| chr3:128911792 | T | C | 163 | a0001c0002t0002g0002a0001c0002t0002g0003a0001c0002t0002g0005others(160): Show | 219 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(216): Show |
intron_variant | MODIFIER | c.1766-715T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911792 | |||||||
| chr3:128911966 | C | T | 1 | a0001c0002t0002g0118 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1766-541C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911966 | |||||||
| chr3:128911983 | G | T | 2 | a0001c0003t0003g0251a0001c0003t0003g0252 | 2 | HG01261.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1766-524G>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128911983 | |||||||
| chr3:128912023 | C | T | 1 | a0001c0002t0002g0144 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1766-484C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128912023 | |||||||
| chr3:128912119 | T | A | 2 | a0001c0007t0001g0256a0001c0007t0002g0187 | 2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1766-388T>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128912119 | |||||||
| chr3:128912251 | C | A | 1 | a0001c0003t0003g0044 | 2 | HG01109.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1766-256C>A | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128912251 | |||||||
| chr3:128912303 | G | C | 3 | a0001c0003t0002g0088a0001c0003t0002g0089a0001c0003t0002g0186 | 3 | HG00642.hp1 HG01891.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1766-204G>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128912303 | |||||||
| chr3:128912334 | C | T | 6 | a0001c0003t0005g0037a0001c0003t0005g0188a0001c0003t0005g0189others(3): Show | 7 | HG02258.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1766-173C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128912334 | |||||||
| chr3:128912344 | C | T | 1 | a0001c0002t0002g0142 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1766-163C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128912344 | |||||||
| chr3:128912448 | C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0207 | 2 | NA18974.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1766-59C>T | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128912448 | |||||||
| chr3:128912467 | T | C | 1 | a0001c0003t0003g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1766-40T>C | ACAD9 | ENSG00000177646.20 | transcript | ENST00000308982.12 | protein_coding | 17/17 | chr3 | 128912467 |