Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 60481 |
| ensemblid | ENSG00000012660.14 |
| hgncid | 21308 |
| symbol | ELOVL5 |
| name | ELOVL fatty acid elongase 5 |
| refseq_nuc | NM_021814.5 |
| refseq_prot | NP_068586.1 |
| ensembl_nuc | ENST00000304434.11 |
| ensembl_prot | ENSP00000306640.6 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 53267404 |
| end | 53348950 |
| strand | - |
| ver | v1.2 |
| region | chr6:53267404-53348950 |
| region5000 | chr6:53262404-53353950 |
| regionname0 | ELOVL5_chr6_53267404_53348950 |
| regionname5000 | ELOVL5_chr6_53262404_53353950 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 299 | 319 | 76 | 74 | 126 | 15 | 26 | 98 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | MEHFD others(294): Show |
chr6 | 53262404 | 53353950 |
| a0002 | 0/0 | 299 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | MEHFD others(294): Show |
chr6 | 53262404 | 53353950 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 897 | 317 | 76 | 72 | 126 | 15 | 26 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | ATGGA others(892): Show |
chr6 | 53262404 | 53353950 | ||
| a0001c0002 | 0/0 | 897 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | ATGGA others(892): Show |
chr6 | 53262404 | 53353950 | ||
| a0002c0003 | 0/0 | 897 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | ATGGA others(892): Show |
chr6 | 53262404 | 53353950 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2765 | 270 | 55 | 64 | 113 | 12 | 24 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0002 | 0/0 | 2765 | 19 | 11 | 4 | 0 | 2 | 2 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0003 | 0/0 | 2765 | 5 | 0 | 0 | 5 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0004 | 0/0 | 2765 | 3 | 0 | 0 | 3 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0005 | 0/0 | 2765 | 3 | 0 | 3 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0006 | 0/0 | 2765 | 3 | 3 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0007 | 0/0 | 2765 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0008 | 0/0 | 2765 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0009 | 0/0 | 2765 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0010 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0011 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0012 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0013 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0014 | 0/0 | 2765 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0015 | 0/0 | 2765 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0016 | 0/0 | 2765 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0001t0017 | 0/0 | 2765 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0001c0002t0002 | 0/0 | 2765 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| a0002c0003t0004 | 0/0 | 2765 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | CTCTT others(2760): Show |
chr6 | 53262404 | 53353950 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0169 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0272 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0004g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0010g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0011g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0013g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0014g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0015g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0016g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0001t0017g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0002t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0001c0002t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| a0002c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | GBR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | GBR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | GBR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0294 | EUR | FIN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00323 | hp2 | a0002 | c0003 | t0004 | g0267 | EUR | FIN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0285 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00609 | hp2 | a0001 | c0001 | t0008 | g0153 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00639 | hp2 | a0001 | c0001 | t0015 | g0105 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0017 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0018 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0020 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0021 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0014 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | IBS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0271 | EUR | IBS | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02257 | hp1 | a0001 | c0001 | t0009 | g0303 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0013 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0304 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0302 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0305 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | STU | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | STU | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | STU | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | YRI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18612 | hp2 | a0001 | c0001 | t0016 | g0283 | EAS | CHB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | YRI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0289 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19010 | hp1 | a0001 | c0001 | t0008 | g0154 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19012 | hp1 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19088 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | YRI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA19240 | hp2 | a0001 | c0001 | t0013 | g0233 | AFR | YRI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0301 | AFR | ASW | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0192 | AFR | ASW | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | TSI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0158 | EUR | TSI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA20805 | hp1 | a0001 | c0001 | t0014 | g0107 | EUR | TSI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ACB | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | USA | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | USA | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA20300 | hp1 | a0001 | c0001 | t0012 | g0057 | AFR | USA | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | USA | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| NA21309 | hp2 | a0001 | c0001 | t0017 | g0300 | AFR | LWK | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0272 | REF | REF | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0169 | REF | REF | ELOVL5_chr6_53262404_53353950 | ELOVL5 | chr6 | 53262404 | 53353950 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:53269245 | C | T | 1 | a0002 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.782G>A | p.Arg261Gln | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 924/2765 | 782/900 | 261/299 | chr6 | 53269245 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:53269166 | C | A | 1 | a0001c0002 | 2 | HG01081.hp1 HG01168.hp1 |
synonymous_variant | LOW | c.861G>T | p.Leu287Leu | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 1003/2765 | 861/900 | 287/299 | chr6 | 53269166 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:53267467 | C | T | 1 | a0001c0001t0012 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1660G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 1660 | chr6 | 53267467 | ||||||
| chr6:53267482 | C | T | 1 | a0001c0001t0009 | 2 | HG02257.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1645G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 1645 | chr6 | 53267482 | ||||||
| chr6:53267492 | T | C | 1 | a0001c0001t0013 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1635A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 1635 | chr6 | 53267492 | ||||||
| chr6:53267677 | T | C | 1 | a0001c0001t0003 | 5 | HG02523.hp1 NA18942.hp1 NA18951.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1450A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 1450 | chr6 | 53267677 | ||||||
| chr6:53267947 | C | A | 1 | a0001c0001t0007 | 2 | NA19012.hp1 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1180G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 1180 | chr6 | 53267947 | ||||||
| chr6:53268048 | A | G | 1 | a0001c0001t0017 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1079T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 1079 | chr6 | 53268048 | ||||||
| chr6:53268090 | C | A | 1 | a0001c0001t0014 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1037G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 1037 | chr6 | 53268090 | ||||||
| chr6:53268164 | A | G | 1 | a0001c0001t0011 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*963T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 963 | chr6 | 53268164 | ||||||
| chr6:53268210 | G | A | 3 | a0001c0001t0002 a0001c0001t0005 a0001c0002t0002 |
24 | HG00140.hp1 HG00140.hp2 HG01081.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*917C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 917 | chr6 | 53268210 | ||||||
| chr6:53268436 | T | G | 1 | a0001c0001t0005 | 3 | HG01256.hp2 HG01257.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*691A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 691 | chr6 | 53268436 | ||||||
| chr6:53268678 | T | C | 2 | a0001c0001t0004 a0002c0003t0004 |
4 | HG00323.hp2 HG00423.hp2 NA18989.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*449A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 449 | chr6 | 53268678 | ||||||
| chr6:53268723 | T | C | 1 | a0001c0001t0015 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 404 | chr6 | 53268723 | ||||||
| chr6:53268910 | G | A | 1 | a0001c0001t0008 | 2 | HG00609.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*217C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 217 | chr6 | 53268910 | ||||||
| chr6:53269060 | T | C | 1 | a0001c0001t0016 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*67A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 8/8 | 67 | chr6 | 53269060 | ||||||
| chr6:53348822 | A | G | 1 | a0001c0001t0010 | 1 | HG02451.hp1 | 5_prime_UTR_variant | MODIFIER | c.-14T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/8 | 53123 | chr6 | 53348822 | ||||||
| chr6:53348930 | G | A | 3 | a0001c0001t0006 a0001c0001t0009 a0001c0001t0017 |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-122C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/8 | 53231 | chr6 | 53348930 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:53269306 | C | CACAG | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.757-40_757-37dupCT others(2): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269306 | |||||||
| chr6:53269314 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-44A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269314 | |||||||
| chr6:53269366 | C | CCTTTT | 172 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.757-97_757-96insAA others(3): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269366 | |||||||
| chr6:53269477 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.757-207C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269477 | |||||||
| chr6:53269503 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.757-233T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269503 | |||||||
| chr6:53269645 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-375G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269645 | |||||||
| chr6:53269678 | G | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.757-408C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269678 | |||||||
| chr6:53269755 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.757-485C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269755 | |||||||
| chr6:53269836 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.757-566G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269836 | |||||||
| chr6:53269872 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-602A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269872 | |||||||
| chr6:53269902 | C | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.757-632G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53269902 | |||||||
| chr6:53270200 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(168): Show |
180 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.756+393T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53270200 | |||||||
| chr6:53270339 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.756+254C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 7/7 | chr6 | 53270339 | |||||||
| chr6:53270739 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.622-12C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53270739 | |||||||
| chr6:53270770 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01255.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.622-43C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53270770 | |||||||
| chr6:53270773 | C | T | 1 | a0001c0001t0006g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.622-46G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53270773 | |||||||
| chr6:53270920 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.622-193A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53270920 | |||||||
| chr6:53270964 | C | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | HG01884.hp2 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-237G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53270964 | |||||||
| chr6:53271068 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.622-341C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271068 | |||||||
| chr6:53271069 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.622-342G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271069 | |||||||
| chr6:53271174 | C | T | 2 | a0001c0001t0002g0015 a0001c0001t0002g0028 |
2 | HG00140.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.622-447G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271174 | |||||||
| chr6:53271317 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.622-590G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271317 | |||||||
| chr6:53271318 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0070 |
2 | HG03492.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.622-591C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271318 | |||||||
| chr6:53271327 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.622-600C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271327 | |||||||
| chr6:53271453 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.622-726C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271453 | |||||||
| chr6:53271463 | T | C | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.622-736A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271463 | |||||||
| chr6:53271505 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0009g0303 a0001c0001t0009g0304 |
3 | HG02129.hp2 HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.622-778C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271505 | |||||||
| chr6:53271521 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.622-794C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271521 | |||||||
| chr6:53271718 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
129 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.622-991G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271718 | |||||||
| chr6:53271765 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.622-1038G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271765 | |||||||
| chr6:53271844 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.622-1117A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53271844 | |||||||
| chr6:53272223 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.621+997C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53272223 | |||||||
| chr6:53272265 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.621+955A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53272265 | |||||||
| chr6:53272577 | C | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.621+643G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53272577 | |||||||
| chr6:53272783 | A | G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(299): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.621+437T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53272783 | |||||||
| chr6:53272892 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.621+328C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53272892 | |||||||
| chr6:53272911 | CACACACA others(3): Show |
C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
129 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.621+299_621+308del others(10): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53272911 | |||||||
| chr6:53273161 | A | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0231 |
4 | HG00438.hp2 HG02523.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.621+59T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 6/7 | chr6 | 53273161 | |||||||
| chr6:53273402 | T | C | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.497-58A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53273402 | |||||||
| chr6:53273405 | TA | T | 168 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(165): Show |
177 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.497-62delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53273405 | |||||||
| chr6:53273405 | TAA | T | 6 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0075 others(3): Show |
6 | HG02055.hp1 HG02257.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.497-63_497-62delTT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53273405 | |||||||
| chr6:53273462 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.497-118C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53273462 | |||||||
| chr6:53273551 | C | T | 1 | a0001c0001t0009g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.497-207G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53273551 | |||||||
| chr6:53273645 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.497-301G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53273645 | |||||||
| chr6:53273698 | T | C | 2 | a0001c0002t0002g0017 a0001c0002t0002g0018 |
2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.497-354A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53273698 | |||||||
| chr6:53273726 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.497-382C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53273726 | |||||||
| chr6:53273755 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-411T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53273755 | |||||||
| chr6:53274063 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-719C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274063 | |||||||
| chr6:53274113 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.497-769C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274113 | |||||||
| chr6:53274114 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(65): Show |
73 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.497-770A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274114 | |||||||
| chr6:53274169 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.497-825G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274169 | |||||||
| chr6:53274244 | G | GAAGA | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
144 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.496+842_496+845dup others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274244 | |||||||
| chr6:53274278 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.496+812A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274278 | |||||||
| chr6:53274376 | G | A | 2 | a0001c0001t0008g0153 a0001c0001t0008g0154 |
2 | HG00609.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.496+714C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274376 | |||||||
| chr6:53274417 | A | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.496+673T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274417 | |||||||
| chr6:53274512 | T | A | 1 | a0001c0001t0001g0046 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.496+578A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274512 | |||||||
| chr6:53274524 | A | T | 1 | a0001c0001t0001g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.496+566T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274524 | |||||||
| chr6:53274566 | A | C | 1 | a0001c0001t0001g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.496+524T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274566 | |||||||
| chr6:53274621 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.496+469T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274621 | |||||||
| chr6:53274669 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.496+421A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274669 | |||||||
| chr6:53274788 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.496+302G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274788 | |||||||
| chr6:53274852 | T | C | 4 | a0001c0001t0001g0142 a0001c0001t0001g0296 a0001c0001t0001g0298 others(1): Show |
4 | HG02615.hp2 HG03225.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.496+238A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274852 | |||||||
| chr6:53274991 | C | A | 17 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(14): Show |
17 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.496+99G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53274991 | |||||||
| chr6:53275006 | A | C | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.496+84T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53275006 | |||||||
| chr6:53275026 | G | A | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
6 | HG01069.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.496+64C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 5/7 | chr6 | 53275026 | |||||||
| chr6:53275354 | T | C | 1 | a0001c0001t0002g0004 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.325-93A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53275354 | |||||||
| chr6:53275363 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.325-102C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53275363 | |||||||
| chr6:53275496 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.325-235T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53275496 | |||||||
| chr6:53275613 | GGAAAACC others(4): Show |
G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.325-363_325-353del others(11): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53275613 | |||||||
| chr6:53275631 | C | T | 1 | a0001c0001t0006g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.325-370G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53275631 | |||||||
| chr6:53275667 | C | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-406G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53275667 | |||||||
| chr6:53275684 | A | G | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.325-423T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53275684 | |||||||
| chr6:53275844 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.324+335T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53275844 | |||||||
| chr6:53275962 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.324+217C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53275962 | |||||||
| chr6:53276017 | C | A | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.324+162G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53276017 | |||||||
| chr6:53276130 | T | A | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.324+49A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53276130 | |||||||
| chr6:53276145 | T | TATA | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.324+31_324+33dupTA others(1): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53276145 | |||||||
| chr6:53276147 | T | C | 4 | a0001c0001t0001g0115 a0001c0001t0006g0301 a0001c0001t0006g0302 others(1): Show |
4 | HG02886.hp1 HG03098.hp1 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+32A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 4/7 | chr6 | 53276147 | |||||||
| chr6:53276406 | A | C | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-150T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53276406 | |||||||
| chr6:53276493 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.247-237A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53276493 | |||||||
| chr6:53276504 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-248G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53276504 | |||||||
| chr6:53276505 | G | A | 1 | a0001c0001t0001g0259 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.247-249C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53276505 | |||||||
| chr6:53276520 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.247-264T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53276520 | |||||||
| chr6:53276530 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.247-274G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53276530 | |||||||
| chr6:53276857 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.247-601A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53276857 | |||||||
| chr6:53276936 | T | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-680A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53276936 | |||||||
| chr6:53276995 | C | G | 1 | a0001c0001t0008g0154 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.247-739G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53276995 | |||||||
| chr6:53277030 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.247-774G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53277030 | |||||||
| chr6:53277059 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.247-803G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53277059 | |||||||
| chr6:53277089 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.247-833C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53277089 | |||||||
| chr6:53277192 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-936A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53277192 | |||||||
| chr6:53277393 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-1137A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53277393 | |||||||
| chr6:53277864 | T | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0115 a0001c0001t0001g0200 others(22): Show |
28 | HG00140.hp1 HG00438.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.247-1608A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53277864 | |||||||
| chr6:53277938 | G | T | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.247-1682C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53277938 | |||||||
| chr6:53278402 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.247-2146G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53278402 | |||||||
| chr6:53278607 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0163 |
3 | HG02280.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.247-2351G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53278607 | |||||||
| chr6:53278756 | T | C | 95 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
102 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.247-2500A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53278756 | |||||||
| chr6:53278973 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.247-2717G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53278973 | |||||||
| chr6:53279020 | C | CCGCT | 6 | a0001c0001t0001g0159 a0001c0001t0006g0301 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.247-2768_247-2765d others(6): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279020 | |||||||
| chr6:53279022 | G | A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0216 |
4 | HG02135.hp1 NA18945.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.247-2766C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279022 | |||||||
| chr6:53279204 | C | T | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.247-2948G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279204 | |||||||
| chr6:53279218 | T | C | 27 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(24): Show |
27 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.247-2962A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279218 | |||||||
| chr6:53279229 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.247-2973T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279229 | |||||||
| chr6:53279358 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-3102A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279358 | |||||||
| chr6:53279404 | C | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0050 others(27): Show |
32 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.247-3148G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279404 | |||||||
| chr6:53279556 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.247-3300C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279556 | |||||||
| chr6:53279571 | T | C | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG02056.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.247-3315A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279571 | |||||||
| chr6:53279667 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-3411T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279667 | |||||||
| chr6:53279777 | T | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-3521A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53279777 | |||||||
| chr6:53280192 | T | A | 1 | a0001c0001t0002g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.247-3936A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53280192 | |||||||
| chr6:53280205 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.247-3949C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53280205 | |||||||
| chr6:53280741 | C | T | 1 | a0001c0001t0002g0004 | 2 | HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.247-4485G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53280741 | |||||||
| chr6:53280753 | C | T | 2 | a0001c0001t0001g0189 a0001c0001t0017g0300 |
2 | NA19004.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.247-4497G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53280753 | |||||||
| chr6:53280904 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-4648A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53280904 | |||||||
| chr6:53281329 | T | C | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.247-5073A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53281329 | |||||||
| chr6:53281387 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0188 |
2 | HG00741.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.247-5131A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53281387 | |||||||
| chr6:53281605 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.247-5349T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53281605 | |||||||
| chr6:53281724 | G | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.247-5468C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53281724 | |||||||
| chr6:53281802 | C | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0036 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.247-5546G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53281802 | |||||||
| chr6:53281822 | G | GT | 192 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(189): Show |
202 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.247-5567dupA | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53281822 | |||||||
| chr6:53281894 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0157 |
3 | HG02040.hp1 NA18943.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.247-5638T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53281894 | |||||||
| chr6:53282096 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-5840T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53282096 | |||||||
| chr6:53282244 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-5988T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53282244 | |||||||
| chr6:53282278 | C | T | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.247-6022G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53282278 | |||||||
| chr6:53282294 | C | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.247-6038G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53282294 | |||||||
| chr6:53282493 | C | T | 1 | a0001c0001t0003g0121 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.247-6237G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53282493 | |||||||
| chr6:53282583 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247-6327T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53282583 | |||||||
| chr6:53282706 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247-6450G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53282706 | |||||||
| chr6:53282865 | G | A | 10 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0078 others(7): Show |
10 | HG01255.hp1 HG01358.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.247-6609C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53282865 | |||||||
| chr6:53283167 | G | A | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.247-6911C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283167 | |||||||
| chr6:53283172 | T | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.247-6916A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283172 | |||||||
| chr6:53283174 | G | A | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.247-6918C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283174 | |||||||
| chr6:53283221 | T | C | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.247-6965A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283221 | |||||||
| chr6:53283368 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.247-7112A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283368 | |||||||
| chr6:53283453 | T | C | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.247-7197A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283453 | |||||||
| chr6:53283522 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.247-7266C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283522 | |||||||
| chr6:53283772 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.247-7516A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283772 | |||||||
| chr6:53283838 | T | C | 1 | a0001c0001t0002g0038 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.247-7582A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283838 | |||||||
| chr6:53283926 | C | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.247-7670G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53283926 | |||||||
| chr6:53284005 | TA | T | 6 | a0001c0001t0001g0292 a0001c0001t0002g0030 a0001c0001t0004g0285 others(3): Show |
6 | HG00423.hp2 HG02257.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.247-7750delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284005 | |||||||
| chr6:53284043 | C | T | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.246+7733G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284043 | |||||||
| chr6:53284053 | C | T | 3 | a0001c0001t0002g0004 a0001c0001t0002g0037 a0001c0001t0002g0038 |
4 | HG02896.hp1 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+7723G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284053 | |||||||
| chr6:53284130 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.246+7646T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284130 | |||||||
| chr6:53284142 | C | CA | 11 | a0001c0001t0002g0015 a0001c0001t0002g0027 a0001c0001t0002g0028 others(8): Show |
11 | HG00140.hp2 HG01175.hp2 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.246+7633dupT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284142 | |||||||
| chr6:53284193 | CT | C | 5 | a0001c0001t0001g0235 a0001c0001t0001g0241 a0001c0001t0001g0278 others(2): Show |
5 | NA18941.hp2 NA18984.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+7582delA | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284193 | |||||||
| chr6:53284301 | CT | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(233): Show |
250 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.246+7474delA | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284301 | |||||||
| chr6:53284301 | CTT | C | 7 | a0001c0001t0001g0054 a0001c0001t0001g0084 a0001c0001t0001g0086 others(4): Show |
7 | HG01069.hp2 HG01884.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.246+7473_246+7474d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284301 | |||||||
| chr6:53284310 | T | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0114 a0001c0001t0001g0127 others(1): Show |
4 | HG02071.hp1 NA18975.hp1 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+7466A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284310 | |||||||
| chr6:53284311 | T | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
125 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.246+7465A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284311 | |||||||
| chr6:53284312 | T | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
178 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.246+7464A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284312 | |||||||
| chr6:53284313 | T | A | 170 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
179 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.246+7463A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284313 | |||||||
| chr6:53284314 | T | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(187): Show |
201 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.246+7462A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284314 | |||||||
| chr6:53284328 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+7448C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284328 | |||||||
| chr6:53284464 | T | C | 199 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.246+7312A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284464 | |||||||
| chr6:53284465 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+7311G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284465 | |||||||
| chr6:53284517 | A | C | 1 | a0001c0001t0001g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.246+7259T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284517 | |||||||
| chr6:53284528 | C | G | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.246+7248G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284528 | |||||||
| chr6:53284662 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01255.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.246+7114A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284662 | |||||||
| chr6:53284706 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+7070A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284706 | |||||||
| chr6:53284794 | A | AT | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+6981dupA | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284794 | |||||||
| chr6:53284838 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.246+6938A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53284838 | |||||||
| chr6:53285115 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+6661C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285115 | |||||||
| chr6:53285435 | T | A | 1 | a0001c0001t0001g0009 | 2 | NA18962.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.246+6341A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285435 | |||||||
| chr6:53285467 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.246+6309T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285467 | |||||||
| chr6:53285524 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+6252C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285524 | |||||||
| chr6:53285548 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+6228C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285548 | |||||||
| chr6:53285560 | AC | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+6215delG | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285560 | |||||||
| chr6:53285563 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+6213T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285563 | |||||||
| chr6:53285883 | G | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.246+5893C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285883 | |||||||
| chr6:53285884 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(133): Show |
144 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.246+5892T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285884 | |||||||
| chr6:53285894 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+5882A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53285894 | |||||||
| chr6:53286006 | C | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(188): Show |
200 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.246+5770G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53286006 | |||||||
| chr6:53286035 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.246+5741A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53286035 | |||||||
| chr6:53286369 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01255.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.246+5407A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53286369 | |||||||
| chr6:53286491 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.246+5285T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53286491 | |||||||
| chr6:53286599 | T | C | 5 | a0001c0001t0001g0115 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | NA19000.hp1 NA19007.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.246+5177A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53286599 | |||||||
| chr6:53286838 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.246+4938C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53286838 | |||||||
| chr6:53286909 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.246+4867C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53286909 | |||||||
| chr6:53287057 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.246+4719G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287057 | |||||||
| chr6:53287377 | A | G | 2 | a0001c0001t0001g0296 a0001c0001t0001g0298 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.246+4399T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287377 | |||||||
| chr6:53287542 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+4234G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287542 | |||||||
| chr6:53287669 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+4107G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287669 | |||||||
| chr6:53287687 | G | A | 2 | a0001c0001t0001g0286 a0001c0001t0001g0288 |
2 | HG01070.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.246+4089C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287687 | |||||||
| chr6:53287799 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+3977T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287799 | |||||||
| chr6:53287844 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+3932C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287844 | |||||||
| chr6:53287885 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.246+3891C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287885 | |||||||
| chr6:53287907 | G | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+3869C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287907 | |||||||
| chr6:53287913 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.246+3863C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287913 | |||||||
| chr6:53287960 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.246+3816T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53287960 | |||||||
| chr6:53288047 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+3729A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53288047 | |||||||
| chr6:53288197 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.246+3579C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53288197 | |||||||
| chr6:53288313 | T | G | 21 | a0001c0001t0001g0016 a0001c0001t0002g0004 a0001c0001t0002g0015 others(18): Show |
22 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.246+3463A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53288313 | |||||||
| chr6:53288430 | T | C | 2 | a0001c0001t0001g0061 a0001c0001t0001g0067 |
2 | HG01081.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.246+3346A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53288430 | |||||||
| chr6:53288448 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.246+3328C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53288448 | |||||||
| chr6:53288467 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+3309G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53288467 | |||||||
| chr6:53288832 | G | A | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.246+2944C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53288832 | |||||||
| chr6:53288916 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+2860G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53288916 | |||||||
| chr6:53288936 | T | C | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.246+2840A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53288936 | |||||||
| chr6:53289047 | C | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0231 |
2 | HG00438.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.246+2729G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53289047 | |||||||
| chr6:53289131 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.246+2645G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53289131 | |||||||
| chr6:53289156 | C | A | 166 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
174 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.246+2620G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53289156 | |||||||
| chr6:53289229 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0122 |
2 | HG02055.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.246+2547C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53289229 | |||||||
| chr6:53289412 | A | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+2364T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53289412 | |||||||
| chr6:53289446 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0231 |
4 | HG00438.hp2 HG02523.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.246+2330G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53289446 | |||||||
| chr6:53289699 | G | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0092 others(11): Show |
17 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.246+2077C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53289699 | |||||||
| chr6:53290220 | T | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0275 |
2 | NA18947.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.246+1556A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53290220 | |||||||
| chr6:53290313 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.246+1463C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53290313 | |||||||
| chr6:53290540 | A | G | 12 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0073 others(9): Show |
12 | HG01255.hp1 HG01358.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.246+1236T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53290540 | |||||||
| chr6:53290542 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.246+1234A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53290542 | |||||||
| chr6:53290797 | G | GA | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.246+978dupT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53290797 | |||||||
| chr6:53291013 | A | G | 1 | a0001c0001t0003g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.246+763T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53291013 | |||||||
| chr6:53291017 | T | C | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.246+759A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53291017 | |||||||
| chr6:53291192 | T | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0058 others(18): Show |
23 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.246+584A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53291192 | |||||||
| chr6:53291335 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.246+441A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53291335 | |||||||
| chr6:53291664 | C | T | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
6 | HG01069.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.246+112G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53291664 | |||||||
| chr6:53291666 | A | C | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.246+110T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 3/7 | chr6 | 53291666 | |||||||
| chr6:53292021 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.59-58C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292021 | |||||||
| chr6:53292087 | G | A | 3 | a0001c0001t0004g0256 a0001c0001t0004g0289 a0002c0003t0004g0267 |
3 | HG00323.hp2 NA18989.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.59-124C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292087 | |||||||
| chr6:53292132 | G | A | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.59-169C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292132 | |||||||
| chr6:53292297 | T | C | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-334A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292297 | |||||||
| chr6:53292416 | C | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
200 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.59-453G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292416 | |||||||
| chr6:53292681 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.59-718G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292681 | |||||||
| chr6:53292686 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-723C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292686 | |||||||
| chr6:53292911 | GC | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-949delG | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292911 | |||||||
| chr6:53292912 | C | T | 2 | a0001c0001t0001g0235 a0001c0001t0001g0241 |
2 | NA18984.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.59-949G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292912 | |||||||
| chr6:53292957 | T | C | 1 | a0001c0001t0001g0281 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.59-994A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292957 | |||||||
| chr6:53292957 | T | TA | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-995dupT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53292957 | |||||||
| chr6:53293004 | G | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.59-1041C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293004 | |||||||
| chr6:53293161 | T | C | 1 | a0001c0001t0010g0013 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.59-1198A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293161 | |||||||
| chr6:53293254 | G | A | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.59-1291C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293254 | |||||||
| chr6:53293356 | C | T | 9 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.59-1393G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293356 | |||||||
| chr6:53293379 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.59-1416C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293379 | |||||||
| chr6:53293387 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.59-1424T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293387 | |||||||
| chr6:53293397 | A | G | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-1434T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293397 | |||||||
| chr6:53293461 | A | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(136): Show |
147 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.59-1498T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293461 | |||||||
| chr6:53293480 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.59-1517C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293480 | |||||||
| chr6:53293537 | G | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(169): Show |
181 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.59-1574C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293537 | |||||||
| chr6:53293613 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0059 others(12): Show |
16 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.59-1650G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293613 | |||||||
| chr6:53293679 | C | T | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59-1716G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293679 | |||||||
| chr6:53293884 | G | A | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.58+1758C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293884 | |||||||
| chr6:53293904 | G | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+1738C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53293904 | |||||||
| chr6:53294133 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0232 |
2 | NA18951.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.58+1509G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294133 | |||||||
| chr6:53294165 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+1477A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294165 | |||||||
| chr6:53294195 | G | A | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.58+1447C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294195 | |||||||
| chr6:53294225 | A | C | 1 | a0001c0001t0001g0265 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.58+1417T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294225 | |||||||
| chr6:53294292 | G | T | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.58+1350C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294292 | |||||||
| chr6:53294435 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.58+1207C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294435 | |||||||
| chr6:53294599 | T | A | 1 | a0001c0001t0001g0048 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58+1043A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294599 | |||||||
| chr6:53294601 | T | C | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.58+1041A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294601 | |||||||
| chr6:53294749 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.58+893G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294749 | |||||||
| chr6:53294778 | T | C | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.58+864A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53294778 | |||||||
| chr6:53295435 | T | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0204 a0001c0001t0001g0205 others(14): Show |
19 | HG01167.hp1 HG01346.hp1 HG02135.hp1 others(16): Show |
intron_variant | MODIFIER | c.58+207A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53295435 | |||||||
| chr6:53295546 | C | T | 4 | a0001c0001t0002g0019 a0001c0001t0005g0014 a0001c0001t0005g0020 others(1): Show |
4 | HG01256.hp2 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+96G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53295546 | |||||||
| chr6:53295585 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.58+57C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 2/7 | chr6 | 53295585 | |||||||
| chr6:53296121 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8-414A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296121 | |||||||
| chr6:53296140 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(1): Show |
4 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-433C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296140 | |||||||
| chr6:53296240 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-533T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296240 | |||||||
| chr6:53296261 | C | G | 6 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-554G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296261 | |||||||
| chr6:53296727 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-1020A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296727 | |||||||
| chr6:53296744 | A | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(6): Show |
9 | HG01069.hp2 HG01346.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-1037T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296744 | |||||||
| chr6:53296804 | A | G | 18 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0058 others(15): Show |
20 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-1097T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296804 | |||||||
| chr6:53296824 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0099 |
2 | HG01099.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-8-1117C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296824 | |||||||
| chr6:53296825 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-1118A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296825 | |||||||
| chr6:53296832 | G | A | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-1125C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53296832 | |||||||
| chr6:53297287 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-1580G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297287 | |||||||
| chr6:53297309 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-8-1602T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297309 | |||||||
| chr6:53297349 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-1642A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297349 | |||||||
| chr6:53297405 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1698A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297405 | |||||||
| chr6:53297501 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-8-1794C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297501 | |||||||
| chr6:53297611 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1904G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297611 | |||||||
| chr6:53297632 | T | C | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG03017.hp1 HG03688.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-8-1925A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297632 | |||||||
| chr6:53297785 | A | AG | 6 | a0001c0001t0001g0050 a0001c0001t0001g0072 a0001c0001t0001g0238 others(3): Show |
6 | HG00621.hp2 HG02615.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-2079dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297785 | |||||||
| chr6:53297820 | A | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-2113T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297820 | |||||||
| chr6:53297853 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-8-2146A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297853 | |||||||
| chr6:53297938 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-8-2231A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297938 | |||||||
| chr6:53297978 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-8-2271T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53297978 | |||||||
| chr6:53298161 | G | A | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-2454C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298161 | |||||||
| chr6:53298253 | G | A | 1 | a0001c0001t0006g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-2546C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298253 | |||||||
| chr6:53298292 | G | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-8-2585C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298292 | |||||||
| chr6:53298377 | AACTT | A | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-2674_-8-2671del others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298377 | |||||||
| chr6:53298563 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-8-2856A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298563 | |||||||
| chr6:53298631 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-8-2924T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298631 | |||||||
| chr6:53298632 | T | C | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-2925A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298632 | |||||||
| chr6:53298872 | G | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-3165C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298872 | |||||||
| chr6:53298900 | C | CG | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
114 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.-8-3194dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298900 | |||||||
| chr6:53298900 | C | CGG | 53 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(50): Show |
53 | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.-8-3195_-8-3194dup others(2): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298900 | |||||||
| chr6:53298900 | C | CGGG | 20 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(17): Show |
20 | HG00738.hp1 HG00741.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-3196_-8-3194dup others(3): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53298900 | |||||||
| chr6:53299126 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-3419A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53299126 | |||||||
| chr6:53299140 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-3433G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53299140 | |||||||
| chr6:53299231 | AC | A | 3 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 |
3 | HG02615.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-8-3525delG | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53299231 | |||||||
| chr6:53299440 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-8-3733C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53299440 | |||||||
| chr6:53299544 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-3837T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53299544 | |||||||
| chr6:53299686 | A | G | 2 | a0001c0002t0002g0017 a0001c0002t0002g0018 |
2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-8-3979T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53299686 | |||||||
| chr6:53299792 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0230 |
2 | NA19000.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-8-4085C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53299792 | |||||||
| chr6:53300060 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01255.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-8-4353G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300060 | |||||||
| chr6:53300101 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-4394A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300101 | |||||||
| chr6:53300218 | A | G | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-8-4511T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300218 | |||||||
| chr6:53300284 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-8-4577T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300284 | |||||||
| chr6:53300342 | C | T | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-4635G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300342 | |||||||
| chr6:53300446 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-4739C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300446 | |||||||
| chr6:53300467 | C | CA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-4761dupT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300467 | |||||||
| chr6:53300532 | G | C | 1 | a0001c0001t0001g0290 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-8-4825C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300532 | |||||||
| chr6:53300744 | G | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-8-5037C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300744 | |||||||
| chr6:53300766 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-8-5059A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300766 | |||||||
| chr6:53300997 | T | A | 12 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0077 others(9): Show |
12 | HG01243.hp1 HG01255.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-8-5290A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53300997 | |||||||
| chr6:53301114 | A | G | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-5407T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301114 | |||||||
| chr6:53301468 | C | G | 2 | a0001c0001t0001g0284 a0001c0001t0016g0283 |
2 | HG02071.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-8-5761G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301468 | |||||||
| chr6:53301503 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-8-5796G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301503 | |||||||
| chr6:53301526 | G | T | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-8-5819C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301526 | |||||||
| chr6:53301604 | G | A | 1 | a0001c0002t0002g0018 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-8-5897C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301604 | |||||||
| chr6:53301700 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-8-5993C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301700 | |||||||
| chr6:53301739 | TA | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-6033delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301739 | |||||||
| chr6:53301834 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-6127A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301834 | |||||||
| chr6:53301989 | C | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0120 |
2 | NA18983.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-8-6282G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301989 | |||||||
| chr6:53301999 | C | G | 1 | a0001c0001t0009g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-8-6292G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53301999 | |||||||
| chr6:53302038 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-6331A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302038 | |||||||
| chr6:53302074 | TGGGCCTG others(13): Show |
T | 1 | a0001c0001t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-8-6387_-8-6368del others(20): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302074 | |||||||
| chr6:53302080 | TGAATTCG others(12): Show |
T | 1 | a0001c0001t0001g0148 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-8-6392_-8-6374del others(19): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302080 | |||||||
| chr6:53302172 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-6465G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302172 | |||||||
| chr6:53302195 | G | C | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-6488C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302195 | |||||||
| chr6:53302357 | G | GCAAATCA others(14): Show |
1 | a0001c0001t0002g0037 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-8-6671_-8-6651dup others(21): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302357 | |||||||
| chr6:53302501 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-8-6794C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302501 | |||||||
| chr6:53302542 | T | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-6835A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302542 | |||||||
| chr6:53302554 | G | C | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-6847C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302554 | |||||||
| chr6:53302582 | G | A | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-6875C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302582 | |||||||
| chr6:53302634 | T | A | 1 | a0001c0001t0001g0189 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-8-6927A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302634 | |||||||
| chr6:53302651 | G | A | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-6944C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302651 | |||||||
| chr6:53302665 | T | TAAGAATT others(293): Show |
4 | a0001c0001t0001g0177 a0001c0001t0001g0185 a0001c0001t0001g0186 others(1): Show |
4 | HG00639.hp1 HG01975.hp1 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-6959_-8-6958ins others(300): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302665 | |||||||
| chr6:53302665 | T | TAAGAATT others(294): Show |
14 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0168 others(11): Show |
14 | HG00323.hp1 HG00738.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-8-6959_-8-6958ins others(301): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302665 | |||||||
| chr6:53302665 | T | TAAGAATT others(295): Show |
11 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(8): Show |
11 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8-6959_-8-6958ins others(302): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302665 | |||||||
| chr6:53302665 | T | TAAGAATT others(296): Show |
1 | a0001c0001t0001g0183 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-8-6959_-8-6958ins others(303): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302665 | |||||||
| chr6:53302733 | G | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0120 |
2 | NA18983.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-8-7026C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302733 | |||||||
| chr6:53302784 | A | C | 2 | a0001c0001t0001g0225 a0001c0001t0013g0233 |
2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-8-7077T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302784 | |||||||
| chr6:53302885 | T | G | 1 | a0001c0001t0001g0208 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-8-7178A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302885 | |||||||
| chr6:53302965 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-7258T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53302965 | |||||||
| chr6:53303052 | G | T | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-7345C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303052 | |||||||
| chr6:53303225 | G | T | 1 | a0001c0001t0011g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-8-7518C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303225 | |||||||
| chr6:53303495 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-8-7788T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303495 | |||||||
| chr6:53303525 | A | T | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-7818T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303525 | |||||||
| chr6:53303535 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-7828G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303535 | |||||||
| chr6:53303536 | G | GAAGGCAA others(7): Show |
1 | a0001c0001t0001g0236 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-8-7843_-8-7830dup others(14): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303536 | |||||||
| chr6:53303641 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0231 |
4 | HG00438.hp2 HG02523.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-7934T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303641 | |||||||
| chr6:53303663 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(299): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-8-7956G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303663 | |||||||
| chr6:53303684 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-7977C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303684 | |||||||
| chr6:53303799 | TTTAACCA others(72): Show |
T | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-8171_-8-8093del others(79): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303799 | |||||||
| chr6:53303808 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-8101G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53303808 | |||||||
| chr6:53304147 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-8440T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304147 | |||||||
| chr6:53304175 | A | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-8468T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304175 | |||||||
| chr6:53304279 | G | A | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-8572C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304279 | |||||||
| chr6:53304371 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-8664A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304371 | |||||||
| chr6:53304380 | A | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-8673T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304380 | |||||||
| chr6:53304419 | CACAA | C | 21 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(18): Show |
21 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8-8716_-8-8713del others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304419 | |||||||
| chr6:53304435 | T | A | 1 | a0001c0001t0001g0145 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-8-8728A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304435 | |||||||
| chr6:53304436 | C | CTTTTA | 4 | a0001c0001t0001g0170 a0001c0001t0001g0236 a0001c0001t0001g0282 others(1): Show |
4 | HG01496.hp1 HG01934.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-8734_-8-8730dup others(5): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304436 | |||||||
| chr6:53304436 | C | CTTTTATT others(3): Show |
1 | a0001c0001t0002g0015 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-8-8739_-8-8730dup others(10): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304436 | |||||||
| chr6:53304436 | C | CTTTTATT others(8): Show |
2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-8-8744_-8-8730dup others(15): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304436 | |||||||
| chr6:53304436 | CTTTTA | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(156): Show |
166 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.-8-8734_-8-8730del others(5): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304436 | |||||||
| chr6:53304436 | CTTTTATT others(3): Show |
C | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-8739_-8-8730del others(10): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304436 | |||||||
| chr6:53304436 | CTTTTATT others(8): Show |
C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0073 others(5): Show |
10 | HG02257.hp2 HG02818.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-8744_-8-8730del others(15): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304436 | |||||||
| chr6:53304437 | T | A | 1 | a0001c0001t0001g0145 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-8-8730A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304437 | |||||||
| chr6:53304438 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-8-8731A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304438 | |||||||
| chr6:53304439 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-8-8732A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304439 | |||||||
| chr6:53304441 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-8-8734T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304441 | |||||||
| chr6:53304490 | G | A | 5 | a0001c0001t0001g0197 a0001c0001t0001g0250 a0001c0001t0001g0251 others(2): Show |
5 | HG01192.hp1 HG01496.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-8783C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304490 | |||||||
| chr6:53304638 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-8-8931T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304638 | |||||||
| chr6:53304674 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-8967A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304674 | |||||||
| chr6:53304699 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-8-8992G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304699 | |||||||
| chr6:53304716 | CAT | C | 4 | a0001c0001t0001g0208 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | NA18946.hp1 NA18978.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-9011_-8-9010del others(2): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304716 | |||||||
| chr6:53304808 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-8-9101T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304808 | |||||||
| chr6:53304836 | A | C | 1 | a0001c0001t0001g0286 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-8-9129T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304836 | |||||||
| chr6:53304837 | G | GA | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-9131_-8-9130ins others(1): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304837 | |||||||
| chr6:53304870 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-8-9163G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304870 | |||||||
| chr6:53304953 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-8-9246T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304953 | |||||||
| chr6:53304954 | C | CG | 19 | a0001c0001t0001g0060 a0001c0001t0001g0081 a0001c0001t0001g0093 others(16): Show |
19 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.-8-9248dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304954 | |||||||
| chr6:53304986 | T | C | 1 | a0001c0001t0006g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-8-9279A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53304986 | |||||||
| chr6:53305013 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0137 a0001c0001t0001g0160 others(1): Show |
5 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-9306G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305013 | |||||||
| chr6:53305058 | A | AC | 27 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0050 others(24): Show |
27 | HG01069.hp2 HG01192.hp1 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.-8-9352dupG | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305058 | |||||||
| chr6:53305068 | C | T | 6 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0099 others(3): Show |
6 | HG00733.hp1 HG00738.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-9361G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305068 | |||||||
| chr6:53305141 | G | A | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-8-9434C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305141 | |||||||
| chr6:53305142 | C | A | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-8-9435G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305142 | |||||||
| chr6:53305143 | C | T | 33 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 others(30): Show |
34 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-8-9436G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305143 | |||||||
| chr6:53305156 | G | A | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-8-9449C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305156 | |||||||
| chr6:53305159 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(119): Show |
129 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.-8-9452G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305159 | |||||||
| chr6:53305191 | C | A | 1 | a0001c0001t0004g0289 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-8-9484G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305191 | |||||||
| chr6:53305196 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-9489G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305196 | |||||||
| chr6:53305197 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-9490C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305197 | |||||||
| chr6:53305233 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01255.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-8-9526C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305233 | |||||||
| chr6:53305278 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-9571C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305278 | |||||||
| chr6:53305287 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-9580G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305287 | |||||||
| chr6:53305301 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-9594G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305301 | |||||||
| chr6:53305302 | G | A | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-9595C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305302 | |||||||
| chr6:53305332 | AC | A | 34 | a0001c0001t0001g0010 a0001c0001t0001g0063 a0001c0001t0001g0160 others(31): Show |
35 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.-8-9626delG | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305332 | |||||||
| chr6:53305333 | C | CCCCCCCA others(41): Show |
7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-9627_-8-9626ins others(48): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305333 | |||||||
| chr6:53305333 | C | CCCCCCCA others(314): Show |
2 | a0001c0001t0001g0163 a0001c0001t0001g0195 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-8-9627_-8-9626ins others(321): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305333 | |||||||
| chr6:53305333 | C | CCCCCCCA others(41): Show |
119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
126 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.-8-9627_-8-9626ins others(48): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305333 | |||||||
| chr6:53305341 | C | CCTCCCTC others(314): Show |
1 | a0001c0001t0001g0011 | 2 | HG02280.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-8-9635_-8-9634ins others(321): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305341 | |||||||
| chr6:53305353 | ACGGGGCG others(43): Show |
A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0275 |
2 | NA18947.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-8-9696_-8-9647del others(50): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305353 | |||||||
| chr6:53305364 | G | A | 36 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0160 others(33): Show |
38 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.-8-9657C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305364 | |||||||
| chr6:53305368 | T | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0114 a0001c0001t0001g0128 |
3 | HG02071.hp1 NA18975.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-8-9661A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305368 | |||||||
| chr6:53305380 | AC | A | 151 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(148): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-8-9674delG | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305380 | |||||||
| chr6:53305386 | C | CACCTCCC others(39): Show |
3 | a0001c0001t0001g0096 a0001c0001t0001g0114 a0001c0001t0001g0128 |
3 | HG02071.hp1 NA18975.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-8-9680_-8-9679ins others(46): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305386 | |||||||
| chr6:53305387 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-8-9680G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305387 | |||||||
| chr6:53305388 | C | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-9681G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305388 | |||||||
| chr6:53305389 | C | A | 2 | a0001c0001t0001g0225 a0001c0001t0013g0233 |
2 | HG01433.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-8-9682G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305389 | |||||||
| chr6:53305389 | CA | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-9683delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305389 | |||||||
| chr6:53305400 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-8-9693G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305400 | |||||||
| chr6:53305404 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-9697G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305404 | |||||||
| chr6:53305406 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0067 |
2 | HG01081.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.-8-9699C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305406 | |||||||
| chr6:53305417 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-9710C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305417 | |||||||
| chr6:53305444 | C | CG | 25 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0060 others(22): Show |
25 | HG00423.hp1 HG00544.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8-9738dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305444 | |||||||
| chr6:53305444 | C | T | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-8-9737G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305444 | |||||||
| chr6:53305457 | G | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-9750C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305457 | |||||||
| chr6:53305490 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(218): Show |
233 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.-8-9783T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305490 | |||||||
| chr6:53305561 | C | CG | 7 | a0001c0001t0001g0132 a0001c0001t0001g0183 a0001c0001t0001g0199 others(4): Show |
7 | HG00642.hp2 HG01192.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-9855dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305561 | |||||||
| chr6:53305564 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0001g0270 |
2 | NA18961.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-8-9857C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305564 | |||||||
| chr6:53305602 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8-9895C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305602 | |||||||
| chr6:53305608 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-9901G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305608 | |||||||
| chr6:53305609 | G | A | 6 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 others(3): Show |
6 | HG01884.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-9902C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305609 | |||||||
| chr6:53305648 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-9941G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305648 | |||||||
| chr6:53305688 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-9981G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305688 | |||||||
| chr6:53305729 | C | T | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG02056.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-8-10022G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305729 | |||||||
| chr6:53305735 | G | A | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-8-10028C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305735 | |||||||
| chr6:53305796 | C | CG | 21 | a0001c0001t0001g0050 a0001c0001t0001g0058 a0001c0001t0001g0095 others(18): Show |
21 | HG00544.hp1 HG01099.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8-10090dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305796 | |||||||
| chr6:53305834 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10127A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305834 | |||||||
| chr6:53305853 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10146C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305853 | |||||||
| chr6:53305909 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-10202C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305909 | |||||||
| chr6:53305959 | C | A | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-10252G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305959 | |||||||
| chr6:53305977 | G | A | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-8-10270C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53305977 | |||||||
| chr6:53306055 | C | G | 1 | a0001c0001t0001g0085 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-8-10348G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306055 | |||||||
| chr6:53306074 | C | T | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-10367G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306074 | |||||||
| chr6:53306077 | G | A | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-10370C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306077 | |||||||
| chr6:53306129 | G | A | 5 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0042 others(2): Show |
5 | HG02258.hp1 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-10422C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306129 | |||||||
| chr6:53306141 | C | T | 1 | a0001c0001t0001g0293 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-8-10434G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306141 | |||||||
| chr6:53306170 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-8-10463C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306170 | |||||||
| chr6:53306202 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-10495T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306202 | |||||||
| chr6:53306208 | A | AAGGGGAG others(40): Show |
1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-10502_-8-10501i others(49): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306208 | |||||||
| chr6:53306208 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-8-10501T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306208 | |||||||
| chr6:53306208 | AAGGGGAG | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0061 others(12): Show |
16 | HG00741.hp1 HG01081.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.-8-10508_-8-10502d others(9): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306208 | |||||||
| chr6:53306208 | AAGGGGAG others(54): Show |
A | 1 | a0001c0001t0001g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-8-10562_-8-10502d others(63): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306208 | |||||||
| chr6:53306208 | AAGGGGAG others(61): Show |
A | 1 | a0001c0001t0001g0099 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-8-10569_-8-10502d others(70): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306208 | |||||||
| chr6:53306208 | AAGGGGAG others(75): Show |
A | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-8-10583_-8-10502d others(84): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306208 | |||||||
| chr6:53306210 | G | GGGGAGAG others(40): Show |
1 | a0001c0001t0001g0277 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-8-10550_-8-10504d others(49): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306210 | |||||||
| chr6:53306212 | GGA | G | 29 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(26): Show |
29 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8-10507_-8-10506d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306212 | |||||||
| chr6:53306216 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-8-10509T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306216 | |||||||
| chr6:53306217 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-8-10510C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306217 | |||||||
| chr6:53306217 | G | GGGGAGAG others(6): Show |
1 | a0001c0001t0002g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-10523_-8-10511d others(15): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306217 | |||||||
| chr6:53306217 | GGGGAGAG others(33): Show |
G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0190 |
2 | HG01123.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-8-10550_-8-10511d others(42): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306217 | |||||||
| chr6:53306219 | G | A | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-10512C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306219 | |||||||
| chr6:53306220 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-8-10513C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306220 | |||||||
| chr6:53306222 | G | A | 29 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(26): Show |
29 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.-8-10515C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306222 | |||||||
| chr6:53306223 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-8-10516T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306223 | |||||||
| chr6:53306223 | AG | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10517delC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306223 | |||||||
| chr6:53306224 | G | A | 3 | a0001c0001t0001g0296 a0001c0001t0001g0298 a0001c0001t0001g0299 |
3 | HG02615.hp2 HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-8-10517C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306224 | |||||||
| chr6:53306224 | GGGGAGAG others(26): Show |
G | 1 | a0001c0001t0001g0108 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-8-10550_-8-10518d others(35): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306224 | |||||||
| chr6:53306224 | GGGGAGAG others(51): Show |
G | 1 | a0001c0001t0001g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-8-10575_-8-10518d others(60): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306224 | |||||||
| chr6:53306226 | G | A | 3 | a0001c0001t0001g0060 a0001c0001t0001g0132 a0001c0001t0001g0182 |
3 | HG01978.hp2 HG04204.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-8-10519C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306226 | |||||||
| chr6:53306228 | AGAGGGGA others(50): Show |
A | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8-10578_-8-10522d others(59): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306228 | |||||||
| chr6:53306230 | AG | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0137 a0001c0001t0001g0145 others(2): Show |
5 | HG01168.hp2 HG01884.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-10524delC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306230 | |||||||
| chr6:53306230 | AGGGGAGA others(34): Show |
A | 6 | a0001c0001t0001g0100 a0001c0001t0001g0109 a0001c0001t0001g0139 others(3): Show |
6 | HG00733.hp1 HG01361.hp1 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8-10564_-8-10524d others(43): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306230 | |||||||
| chr6:53306230 | AGGGGAGA others(41): Show |
A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0058 a0001c0001t0001g0089 others(14): Show |
18 | HG00423.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-10571_-8-10524d others(50): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306230 | |||||||
| chr6:53306230 | AGGGGAGA others(48): Show |
A | 36 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(33): Show |
40 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.-8-10578_-8-10524d others(57): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306230 | |||||||
| chr6:53306230 | AGGGGAGA others(55): Show |
A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0050 others(37): Show |
42 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.-8-10585_-8-10524d others(64): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306230 | |||||||
| chr6:53306230 | AGGGGAGA others(62): Show |
A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0059 others(2): Show |
5 | HG02135.hp2 HG02145.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-10592_-8-10524d others(71): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306230 | |||||||
| chr6:53306230 | AGGGGAGA others(82): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-8-10612_-8-10524d others(91): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306230 | |||||||
| chr6:53306231 | G | GGGAGAGG others(12): Show |
12 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0027 others(9): Show |
13 | HG00140.hp2 HG01175.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-10525_-8-10524i others(21): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306231 | |||||||
| chr6:53306231 | G | GGGAGAGG others(12): Show |
2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-8-10525_-8-10524i others(21): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306231 | |||||||
| chr6:53306231 | GGGGAGAG others(74): Show |
G | 1 | a0001c0001t0001g0045 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-10605_-8-10525d others(83): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306231 | |||||||
| chr6:53306232 | G | T | 1 | a0001c0001t0006g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-8-10525C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306232 | |||||||
| chr6:53306233 | G | GA | 9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-10527_-8-10526i others(3): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306233 | |||||||
| chr6:53306236 | G | C | 1 | a0001c0001t0002g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-10529C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306236 | |||||||
| chr6:53306236 | GA | G | 9 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(6): Show |
9 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-10530delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306236 | |||||||
| chr6:53306237 | A | AG | 26 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0040 others(23): Show |
28 | HG00140.hp2 HG01175.hp2 HG01496.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-10531dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306237 | |||||||
| chr6:53306237 | AGGGAGAG others(20): Show |
A | 1 | a0001c0001t0001g0286 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-8-10557_-8-10531d others(29): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306237 | |||||||
| chr6:53306238 | GGGAGAGG others(67): Show |
G | 5 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0137 others(2): Show |
5 | HG01993.hp1 HG02258.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-10605_-8-10532d others(76): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306238 | |||||||
| chr6:53306243 | AG | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10537delC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306243 | |||||||
| chr6:53306244 | GGGGAGAG others(6): Show |
G | 2 | a0001c0001t0001g0210 a0001c0001t0004g0285 |
2 | HG00423.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.-8-10550_-8-10538d others(15): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306244 | |||||||
| chr6:53306249 | G | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(4): Show |
7 | HG01081.hp1 HG01168.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-10542C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306249 | |||||||
| chr6:53306253 | G | GA | 10 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(7): Show |
10 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-10547_-8-10546i others(3): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306253 | |||||||
| chr6:53306256 | G | C | 5 | a0001c0001t0001g0016 a0001c0001t0002g0019 a0001c0001t0005g0014 others(2): Show |
5 | HG01256.hp2 HG01257.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-10549C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306256 | |||||||
| chr6:53306256 | GA | G | 10 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(7): Show |
10 | HG01081.hp1 HG01167.hp1 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-10550delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306256 | |||||||
| chr6:53306257 | A | AG | 20 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0023 others(17): Show |
21 | HG01081.hp2 HG01167.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-8-10551dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306257 | |||||||
| chr6:53306257 | A | AGGGAGAG others(6): Show |
1 | a0001c0001t0013g0233 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-8-10551_-8-10550i others(15): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306257 | |||||||
| chr6:53306257 | A | AGGGAGAG others(49): Show |
2 | a0001c0001t0001g0249 a0001c0001t0001g0275 |
2 | NA18947.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-8-10606_-8-10551d others(58): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306257 | |||||||
| chr6:53306258 | GGGAGAGG others(47): Show |
G | 1 | a0001c0001t0001g0086 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-8-10605_-8-10552d others(56): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306258 | |||||||
| chr6:53306271 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-8-10564C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306271 | |||||||
| chr6:53306271 | G | GGGGAGA | 9 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(6): Show |
9 | HG00323.hp1 HG00741.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-10570_-8-10565d others(8): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306271 | |||||||
| chr6:53306277 | AG | A | 16 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0023 others(13): Show |
17 | HG01081.hp1 HG01168.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-10571delC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306277 | |||||||
| chr6:53306277 | AGGGGAGA others(1): Show |
A | 19 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(16): Show |
19 | HG00639.hp1 HG00738.hp1 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8-10578_-8-10571d others(10): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306277 | |||||||
| chr6:53306280 | GGAGAGGG others(74): Show |
G | 1 | a0001c0001t0001g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-8-10654_-8-10574d others(83): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306280 | |||||||
| chr6:53306284 | AG | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0160 others(5): Show |
9 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-10578delC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306284 | |||||||
| chr6:53306291 | AG | A | 14 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0027 others(11): Show |
15 | HG00140.hp2 HG01175.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8-10585delC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306291 | |||||||
| chr6:53306292 | G | GGGGAGA | 8 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(5): Show |
8 | HG00323.hp1 HG01069.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.-8-10591_-8-10586d others(8): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306292 | |||||||
| chr6:53306294 | GGAGAGGG others(60): Show |
G | 1 | a0001c0001t0001g0061 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-8-10654_-8-10588d others(69): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306294 | |||||||
| chr6:53306299 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-10592C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306299 | |||||||
| chr6:53306301 | GGAGAGGG others(53): Show |
G | 1 | a0001c0001t0001g0042 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8-10654_-8-10595d others(62): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306301 | |||||||
| chr6:53306305 | AGGGGAGA others(7): Show |
A | 1 | a0001c0001t0001g0271 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-8-10612_-8-10599d others(16): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306305 | |||||||
| chr6:53306306 | GGGGAGAG others(19): Show |
G | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-10625_-8-10600d others(28): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306306 | |||||||
| chr6:53306306 | GGGGAGAG others(33): Show |
G | 1 | a0001c0001t0003g0121 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-8-10639_-8-10600d others(42): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306306 | |||||||
| chr6:53306308 | G | GA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
7 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-10602_-8-10601i others(3): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306308 | |||||||
| chr6:53306311 | GA | G | 6 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
7 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-10605delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306311 | |||||||
| chr6:53306312 | A | AG | 202 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.-8-10606dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306312 | |||||||
| chr6:53306312 | A | AGGGGAGA others(1): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0199 a0001c0001t0001g0205 others(5): Show |
10 | HG02027.hp1 HG02135.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-10606_-8-10605i others(10): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306312 | |||||||
| chr6:53306312 | A | AGGGGAGA others(8): Show |
5 | a0001c0001t0001g0204 a0001c0001t0001g0212 a0001c0001t0001g0215 others(2): Show |
5 | HG01952.hp1 HG01975.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-10606_-8-10605i others(17): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306312 | |||||||
| chr6:53306312 | AGGGAGAG | A | 36 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0176 others(33): Show |
36 | HG00099.hp2 HG00423.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.-8-10612_-8-10606d others(9): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306312 | |||||||
| chr6:53306314 | G | A | 1 | a0001c0001t0006g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-10607C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306314 | |||||||
| chr6:53306314 | GGAGAGGG others(38): Show |
G | 1 | a0001c0001t0001g0152 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-8-10652_-8-10608d others(47): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306314 | |||||||
| chr6:53306318 | AG | A | 64 | a0001c0001t0001g0115 a0001c0001t0001g0166 a0001c0001t0001g0167 others(61): Show |
67 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.-8-10612delC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306318 | |||||||
| chr6:53306319 | G | GGGGAGA | 29 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0199 others(26): Show |
32 | HG00438.hp2 HG01433.hp1 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.-8-10618_-8-10613d others(8): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306319 | |||||||
| chr6:53306319 | G | GGGGAGAG others(20): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0214 |
2 | HG03669.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.-8-10639_-8-10613d others(29): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306319 | |||||||
| chr6:53306321 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-8-10614C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306321 | |||||||
| chr6:53306321 | GGAGAGGG others(59): Show |
G | 3 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0067 |
3 | HG01358.hp2 HG02055.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-8-10680_-8-10615d others(68): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306321 | |||||||
| chr6:53306325 | AG | A | 5 | a0001c0001t0001g0207 a0001c0001t0001g0290 a0001c0001t0002g0028 others(2): Show |
5 | HG01167.hp1 HG01256.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-10619delC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306325 | |||||||
| chr6:53306325 | AGGGGAGA others(1): Show |
A | 4 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 others(1): Show |
5 | HG02280.hp2 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-10626_-8-10619d others(10): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306325 | |||||||
| chr6:53306326 | G | GGGAGAGG others(5): Show |
1 | a0001c0001t0001g0242 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-8-10620_-8-10619i others(14): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306326 | |||||||
| chr6:53306332 | AG | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 others(12): Show |
17 | HG00140.hp2 HG00741.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-10626delC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306332 | |||||||
| chr6:53306335 | G | A | 12 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0027 others(9): Show |
13 | HG00140.hp2 HG01175.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8-10628C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306335 | |||||||
| chr6:53306335 | G | GAGAGGGA others(6): Show |
1 | a0001c0001t0001g0179 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-8-10629_-8-10628i others(15): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306335 | |||||||
| chr6:53306335 | G | GAGAGGGA others(65): Show |
1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-10629_-8-10628i others(74): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306335 | |||||||
| chr6:53306335 | G | GAGAGGGG others(5): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0183 a0001c0001t0005g0020 others(1): Show |
4 | HG01256.hp2 HG02886.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-10629_-8-10628i others(14): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306335 | |||||||
| chr6:53306335 | G | GGAGAGGG others(12): Show |
3 | a0001c0001t0002g0019 a0001c0001t0005g0014 a0001c0001t0005g0021 |
3 | HG01257.hp2 HG01433.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-8-10629_-8-10628i others(21): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306335 | |||||||
| chr6:53306342 | GGAGAGGG others(38): Show |
G | 1 | a0001c0001t0006g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-10680_-8-10636d others(47): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306342 | |||||||
| chr6:53306346 | A | AG | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
121 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.-8-10640dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306346 | |||||||
| chr6:53306348 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10641C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306348 | |||||||
| chr6:53306349 | GAGAGGGG others(5): Show |
G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-10654_-8-10643d others(14): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306349 | |||||||
| chr6:53306355 | GGAGAGAG others(25): Show |
G | 1 | a0001c0001t0001g0041 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-8-10680_-8-10649d others(34): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306355 | |||||||
| chr6:53306359 | AGAGAGAG | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10659_-8-10653d others(9): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306359 | |||||||
| chr6:53306368 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8-10661C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306368 | |||||||
| chr6:53306372 | A | AG | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0003g0104 |
4 | HG02280.hp2 HG03579.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-10666dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306372 | |||||||
| chr6:53306381 | GGAGAGA | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
134 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-8-10680_-8-10675d others(8): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306381 | |||||||
| chr6:53306385 | A | AG | 27 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0159 others(24): Show |
29 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.-8-10679dupC | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306385 | |||||||
| chr6:53306387 | A | AGAGAGGG others(20): Show |
39 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(36): Show |
39 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-8-10681_-8-10680i others(29): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306387 | |||||||
| chr6:53306387 | A | G | 27 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0159 others(24): Show |
29 | HG00140.hp2 HG00741.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.-8-10680T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306387 | |||||||
| chr6:53306439 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-10732G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306439 | |||||||
| chr6:53306504 | T | TA | 198 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.-8-10798dupT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306504 | |||||||
| chr6:53306823 | C | T | 30 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(27): Show |
30 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-11116G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306823 | |||||||
| chr6:53306876 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8-11169A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306876 | |||||||
| chr6:53306908 | A | C | 1 | a0001c0001t0001g0261 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-8-11201T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53306908 | |||||||
| chr6:53307043 | C | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
128 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.-8-11336G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307043 | |||||||
| chr6:53307095 | G | A | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-8-11388C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307095 | |||||||
| chr6:53307145 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-11438C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307145 | |||||||
| chr6:53307146 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-11439G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307146 | |||||||
| chr6:53307204 | A | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-8-11497T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307204 | |||||||
| chr6:53307259 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-11552T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307259 | |||||||
| chr6:53307284 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0120 |
2 | NA18983.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.-8-11577C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307284 | |||||||
| chr6:53307340 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-11633C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307340 | |||||||
| chr6:53307405 | T | C | 1 | a0001c0001t0006g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-11698A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307405 | |||||||
| chr6:53307477 | A | C | 1 | a0001c0001t0001g0260 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-8-11770T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307477 | |||||||
| chr6:53307544 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-11837A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307544 | |||||||
| chr6:53307579 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-8-11872G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307579 | |||||||
| chr6:53307760 | G | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
125 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-8-12053C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307760 | |||||||
| chr6:53307788 | G | C | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-12081C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307788 | |||||||
| chr6:53307912 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-8-12205T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307912 | |||||||
| chr6:53307961 | C | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-12254G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307961 | |||||||
| chr6:53307989 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-12282A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53307989 | |||||||
| chr6:53308045 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-8-12338A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308045 | |||||||
| chr6:53308116 | T | TA | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
132 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-8-12410dupT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308116 | |||||||
| chr6:53308149 | G | GT | 4 | a0001c0001t0002g0019 a0001c0001t0005g0014 a0001c0001t0005g0020 others(1): Show |
4 | HG01256.hp2 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-12443dupA | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308149 | |||||||
| chr6:53308167 | A | G | 5 | a0001c0001t0001g0115 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | NA19000.hp1 NA19007.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-12460T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308167 | |||||||
| chr6:53308235 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-12528G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308235 | |||||||
| chr6:53308372 | G | A | 5 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(2): Show |
5 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-12665C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308372 | |||||||
| chr6:53308525 | T | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(127): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-8-12818A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308525 | |||||||
| chr6:53308614 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0231 |
4 | HG00438.hp2 HG02523.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-12907T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308614 | |||||||
| chr6:53308684 | C | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
204 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(201): Show |
intron_variant | MODIFIER | c.-8-12977G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308684 | |||||||
| chr6:53308871 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-13164C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308871 | |||||||
| chr6:53308872 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-13165T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308872 | |||||||
| chr6:53308880 | C | T | 5 | a0001c0001t0002g0004 a0001c0001t0002g0032 a0001c0001t0002g0033 others(2): Show |
6 | HG01884.hp1 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-13173G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308880 | |||||||
| chr6:53308891 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-8-13184G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308891 | |||||||
| chr6:53308891 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-8-13184G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308891 | |||||||
| chr6:53308895 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-8-13188C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308895 | |||||||
| chr6:53308906 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(299): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-8-13199G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308906 | |||||||
| chr6:53308913 | A | T | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-13206T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308913 | |||||||
| chr6:53308991 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-8-13284A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53308991 | |||||||
| chr6:53309134 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-13427G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53309134 | |||||||
| chr6:53309140 | G | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG02258.hp1 HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-8-13433C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53309140 | |||||||
| chr6:53309409 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-13702G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53309409 | |||||||
| chr6:53309461 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-8-13754A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53309461 | |||||||
| chr6:53309539 | G | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
124 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-8-13832C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53309539 | |||||||
| chr6:53309650 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(104): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-8-13943A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53309650 | |||||||
| chr6:53309664 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-13957A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53309664 | |||||||
| chr6:53309802 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-14095A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53309802 | |||||||
| chr6:53309861 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-8-14154C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53309861 | |||||||
| chr6:53310008 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
126 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.-8-14301A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310008 | |||||||
| chr6:53310019 | C | G | 1 | a0001c0001t0001g0132 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-8-14312G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310019 | |||||||
| chr6:53310137 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8-14430G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310137 | |||||||
| chr6:53310298 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-8-14591G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310298 | |||||||
| chr6:53310349 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-14642C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310349 | |||||||
| chr6:53310431 | G | GGGGA | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8-14728_-8-14725d others(6): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310431 | |||||||
| chr6:53310439 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(291): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-8-14732A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310439 | |||||||
| chr6:53310492 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-14785C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310492 | |||||||
| chr6:53310845 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-8-15138G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310845 | |||||||
| chr6:53310884 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-15177G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310884 | |||||||
| chr6:53310983 | A | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-8-15276T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53310983 | |||||||
| chr6:53311126 | G | C | 1 | a0001c0001t0006g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-15419C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311126 | |||||||
| chr6:53311171 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-8-15464C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311171 | |||||||
| chr6:53311334 | T | G | 1 | a0001c0001t0001g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-8-15627A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311334 | |||||||
| chr6:53311375 | T | C | 2 | a0001c0001t0003g0104 a0001c0001t0003g0121 |
2 | NA18942.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-8-15668A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311375 | |||||||
| chr6:53311569 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-8-15862A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311569 | |||||||
| chr6:53311594 | CTGAT | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-15891_-8-15888d others(6): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311594 | |||||||
| chr6:53311654 | AAAGG | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-15951_-8-15948d others(6): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311654 | |||||||
| chr6:53311739 | C | T | 34 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 others(31): Show |
35 | HG00323.hp1 HG00639.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.-8-16032G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311739 | |||||||
| chr6:53311757 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-8-16050A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311757 | |||||||
| chr6:53311829 | C | A | 1 | a0001c0001t0002g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-16122G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311829 | |||||||
| chr6:53311830 | C | A | 1 | a0001c0001t0002g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-8-16123G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311830 | |||||||
| chr6:53311967 | G | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
205 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.-8-16260C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53311967 | |||||||
| chr6:53312110 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-16403G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312110 | |||||||
| chr6:53312232 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-8-16525A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312232 | |||||||
| chr6:53312278 | G | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-16571C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312278 | |||||||
| chr6:53312640 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-8-16933A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312640 | |||||||
| chr6:53312684 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-16977C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312684 | |||||||
| chr6:53312742 | A | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-8-17035T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312742 | |||||||
| chr6:53312754 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-8-17047C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312754 | |||||||
| chr6:53312880 | C | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-8-17173G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312880 | |||||||
| chr6:53312929 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-17222G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312929 | |||||||
| chr6:53312938 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-8-17231T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312938 | |||||||
| chr6:53312959 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0231 |
4 | HG00438.hp2 HG02523.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-17252A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53312959 | |||||||
| chr6:53313021 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-17314C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313021 | |||||||
| chr6:53313060 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-8-17353C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313060 | |||||||
| chr6:53313079 | A | G | 1 | a0001c0001t0002g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-8-17372T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313079 | |||||||
| chr6:53313089 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-17382C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313089 | |||||||
| chr6:53313381 | GAT | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-17676_-8-17675d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313381 | |||||||
| chr6:53313413 | T | G | 1 | a0001c0001t0001g0214 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8-17706A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313413 | |||||||
| chr6:53313535 | A | C | 1 | a0001c0001t0001g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-8-17828T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313535 | |||||||
| chr6:53313689 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
77 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.-8-17982G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313689 | |||||||
| chr6:53313740 | C | CA | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-18034dupT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313740 | |||||||
| chr6:53313763 | T | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG01884.hp2 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-8-18056A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313763 | |||||||
| chr6:53313839 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-18132A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313839 | |||||||
| chr6:53313939 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-18232C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53313939 | |||||||
| chr6:53314177 | T | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0221 a0001c0001t0001g0231 |
4 | HG00438.hp2 HG02523.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-18470A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53314177 | |||||||
| chr6:53314231 | CTTCAT | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-18529_-8-18525d others(7): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53314231 | |||||||
| chr6:53314249 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(98): Show |
106 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.-8-18542G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53314249 | |||||||
| chr6:53314266 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-18559G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53314266 | |||||||
| chr6:53314267 | T | A | 4 | a0001c0001t0001g0198 a0001c0001t0001g0268 a0001c0001t0001g0269 others(1): Show |
4 | HG02074.hp1 NA18961.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-18560A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53314267 | |||||||
| chr6:53314648 | AC | A | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-8-18942delG | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53314648 | |||||||
| chr6:53314929 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-8-19222C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53314929 | |||||||
| chr6:53314981 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-19274A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53314981 | |||||||
| chr6:53315079 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-19372C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315079 | |||||||
| chr6:53315203 | T | C | 1 | a0001c0001t0004g0285 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-8-19496A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315203 | |||||||
| chr6:53315272 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-8-19565A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315272 | |||||||
| chr6:53315342 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8-19635G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315342 | |||||||
| chr6:53315369 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-19662A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315369 | |||||||
| chr6:53315370 | G | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-8-19663C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315370 | |||||||
| chr6:53315391 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02257.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-19684T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315391 | |||||||
| chr6:53315445 | A | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0043 |
2 | HG02055.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-8-19738T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315445 | |||||||
| chr6:53315601 | A | C | 1 | a0001c0001t0006g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-8-19894T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315601 | |||||||
| chr6:53315764 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8-20057C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315764 | |||||||
| chr6:53315801 | A | G | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-8-20094T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53315801 | |||||||
| chr6:53316390 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-8-20683C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53316390 | |||||||
| chr6:53316396 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-20689C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53316396 | |||||||
| chr6:53316409 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-8-20702T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53316409 | |||||||
| chr6:53316602 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-20895G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53316602 | |||||||
| chr6:53316657 | G | A | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8-20950C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53316657 | |||||||
| chr6:53316762 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-8-21055C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53316762 | |||||||
| chr6:53316907 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-8-21200A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53316907 | |||||||
| chr6:53316929 | T | C | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 |
3 | HG00733.hp1 HG00738.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.-8-21222A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53316929 | |||||||
| chr6:53317063 | C | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-8-21356G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317063 | |||||||
| chr6:53317083 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-8-21376G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317083 | |||||||
| chr6:53317160 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-8-21453C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317160 | |||||||
| chr6:53317396 | A | T | 1 | a0001c0001t0001g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-8-21689T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317396 | |||||||
| chr6:53317525 | C | A | 1 | a0001c0001t0001g0214 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-8-21818G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317525 | |||||||
| chr6:53317616 | G | A | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-21909C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317616 | |||||||
| chr6:53317835 | T | TA | 121 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(118): Show |
128 | HG00099.hp1 HG00423.hp1 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-8-22129dupT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317835 | |||||||
| chr6:53317835 | T | TAA | 5 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0001g0086 others(2): Show |
5 | HG01358.hp1 HG01358.hp2 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.-8-22130_-8-22129d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317835 | |||||||
| chr6:53317836 | A | T | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-8-22129T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317836 | |||||||
| chr6:53317839 | AAAAAT | A | 4 | a0001c0001t0001g0195 a0001c0001t0006g0301 a0001c0001t0006g0302 others(1): Show |
4 | HG02647.hp1 HG02886.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22137_-8-22133d others(7): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317839 | |||||||
| chr6:53317844 | T | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
135 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-8-22137A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317844 | |||||||
| chr6:53317967 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-8-22260A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53317967 | |||||||
| chr6:53318062 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-22355G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53318062 | |||||||
| chr6:53318324 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-8-22617C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53318324 | |||||||
| chr6:53318711 | G | C | 3 | a0001c0001t0001g0248 a0001c0001t0001g0257 a0001c0001t0001g0273 |
3 | HG01243.hp2 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-8-23004C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53318711 | |||||||
| chr6:53318856 | ATATC | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-23153_-8-23150d others(6): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53318856 | |||||||
| chr6:53318938 | A | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-23231T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53318938 | |||||||
| chr6:53318996 | T | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(131): Show |
140 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-8-23289A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53318996 | |||||||
| chr6:53319006 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-23299C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319006 | |||||||
| chr6:53319009 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-8-23302A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319009 | |||||||
| chr6:53319059 | A | G | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-23352T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319059 | |||||||
| chr6:53319270 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-8-23573_-8-23564d others(12): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CA | C | 7 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0180 others(4): Show |
7 | HG01109.hp2 HG01175.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-23564delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-23577_-8-23564d others(16): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(8): Show |
C | 3 | a0001c0001t0001g0043 a0001c0001t0006g0305 a0001c0001t0017g0300 |
3 | HG02055.hp1 HG03098.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-8-23578_-8-23564d others(17): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(9): Show |
C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0142 |
3 | HG02970.hp1 HG03486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-8-23579_-8-23564d others(18): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(10): Show |
C | 25 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0044 others(22): Show |
25 | HG00639.hp2 HG00733.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8-23580_-8-23564d others(19): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(11): Show |
C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(91): Show |
100 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-8-23581_-8-23564d others(20): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(12): Show |
C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0054 a0001c0001t0001g0061 others(6): Show |
10 | HG01069.hp2 HG01081.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8-23582_-8-23564d others(21): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(13): Show |
C | 2 | a0001c0001t0001g0137 a0001c0001t0006g0302 |
2 | HG02886.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-8-23583_-8-23564d others(22): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(16): Show |
C | 1 | a0001c0001t0006g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-23586_-8-23564d others(25): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(17): Show |
C | 5 | a0001c0001t0001g0159 a0001c0001t0001g0216 a0001c0001t0001g0230 others(2): Show |
5 | HG02135.hp1 HG02523.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-23587_-8-23564d others(26): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(18): Show |
C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(97): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.-8-23588_-8-23564d others(27): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(19): Show |
C | 16 | a0001c0001t0001g0258 a0001c0001t0001g0286 a0001c0001t0002g0004 others(13): Show |
17 | HG01070.hp2 HG01081.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.-8-23589_-8-23564d others(28): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319270 | CAAAAAAA others(20): Show |
C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(4): Show |
7 | HG01168.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8-23590_-8-23564d others(29): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319270 | |||||||
| chr6:53319300 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-8-23593T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319300 | |||||||
| chr6:53319311 | A | C | 22 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0165 others(19): Show |
22 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-8-23604T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319311 | |||||||
| chr6:53319313 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-8-23606T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319313 | |||||||
| chr6:53319470 | G | A | 14 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0092 others(11): Show |
17 | HG00544.hp1 HG02027.hp2 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8-23763C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319470 | |||||||
| chr6:53319524 | A | G | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-23817T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319524 | |||||||
| chr6:53319710 | T | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-8-24003A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319710 | |||||||
| chr6:53319809 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-8-24102A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319809 | |||||||
| chr6:53319822 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-8-24115G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319822 | |||||||
| chr6:53319897 | CAT | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-24192_-8-24191d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319897 | |||||||
| chr6:53319930 | A | C | 1 | a0001c0001t0001g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-8-24223T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53319930 | |||||||
| chr6:53320016 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-8-24309A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320016 | |||||||
| chr6:53320171 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-8-24464C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320171 | |||||||
| chr6:53320185 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(104): Show |
112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-8-24478A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320185 | |||||||
| chr6:53320263 | C | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-8-24556G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320263 | |||||||
| chr6:53320326 | A | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0159 others(105): Show |
113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.-8-24619T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320326 | |||||||
| chr6:53320347 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-8-24640G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320347 | |||||||
| chr6:53320361 | T | C | 2 | a0001c0001t0001g0249 a0001c0001t0001g0275 |
2 | NA18947.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-8-24654A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320361 | |||||||
| chr6:53320375 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-24668G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320375 | |||||||
| chr6:53320376 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-8-24669C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320376 | |||||||
| chr6:53320399 | C | G | 4 | a0001c0001t0001g0053 a0001c0001t0001g0086 a0001c0001t0001g0087 others(1): Show |
4 | HG01884.hp2 HG02451.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-24692G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320399 | |||||||
| chr6:53320461 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-8-24754C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320461 | |||||||
| chr6:53320473 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-8-24766G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320473 | |||||||
| chr6:53320481 | A | G | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-8-24774T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320481 | |||||||
| chr6:53320558 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-8-24851G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320558 | |||||||
| chr6:53320651 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(126): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.-8-24944A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320651 | |||||||
| chr6:53320655 | G | A | 1 | a0001c0001t0001g0276 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-8-24948C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320655 | |||||||
| chr6:53320811 | C | T | 1 | a0001c0001t0004g0285 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-8-25104G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320811 | |||||||
| chr6:53320981 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-25274C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53320981 | |||||||
| chr6:53321001 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0215 a0001c0001t0001g0216 |
5 | HG02135.hp1 NA18945.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-25294C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321001 | |||||||
| chr6:53321003 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-25296C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321003 | |||||||
| chr6:53321008 | A | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 |
3 | NA19002.hp1 NA19054.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-8-25301T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321008 | |||||||
| chr6:53321232 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-25525G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321232 | |||||||
| chr6:53321270 | G | T | 1 | a0001c0001t0001g0236 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-8-25563C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321270 | |||||||
| chr6:53321359 | T | C | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-8-25652A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321359 | |||||||
| chr6:53321405 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-8-25698G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321405 | |||||||
| chr6:53321406 | G | T | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-8-25699C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321406 | |||||||
| chr6:53321792 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-26085T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321792 | |||||||
| chr6:53321810 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-8-26103C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53321810 | |||||||
| chr6:53322357 | C | A | 2 | a0001c0002t0002g0017 a0001c0002t0002g0018 |
2 | HG01081.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.-9+26460G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53322357 | |||||||
| chr6:53322430 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-9+26387T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53322430 | |||||||
| chr6:53322480 | T | C | 4 | a0001c0001t0001g0096 a0001c0001t0001g0114 a0001c0001t0001g0128 others(1): Show |
4 | HG02071.hp1 NA18975.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+26337A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53322480 | |||||||
| chr6:53322496 | A | T | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+26321T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53322496 | |||||||
| chr6:53322786 | A | C | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+26031T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53322786 | |||||||
| chr6:53322885 | A | G | 20 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0019 others(17): Show |
21 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9+25932T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53322885 | |||||||
| chr6:53323169 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+25648A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323169 | |||||||
| chr6:53323291 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01255.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-9+25526C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323291 | |||||||
| chr6:53323321 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+25496A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323321 | |||||||
| chr6:53323339 | C | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-9+25478G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323339 | |||||||
| chr6:53323352 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-9+25465G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323352 | |||||||
| chr6:53323576 | C | CT | 136 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(133): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-9+25240dupA | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323576 | |||||||
| chr6:53323576 | C | CTT | 120 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
127 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.-9+25239_-9+25240d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323576 | |||||||
| chr6:53323576 | C | CTTT | 25 | a0001c0001t0001g0005 a0001c0001t0001g0041 a0001c0001t0001g0042 others(22): Show |
26 | HG00423.hp1 HG00544.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.-9+25238_-9+25240d others(5): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323576 | |||||||
| chr6:53323576 | CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+25231_-9+25240d others(12): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323576 | |||||||
| chr6:53323586 | T | TG | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+25230_-9+25231i others(3): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323586 | |||||||
| chr6:53323651 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-9+25166G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323651 | |||||||
| chr6:53323810 | C | T | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+25007G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323810 | |||||||
| chr6:53323938 | C | T | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(265): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-9+24879G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323938 | |||||||
| chr6:53323957 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(276): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.-9+24860C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53323957 | |||||||
| chr6:53324053 | G | C | 2 | a0001c0001t0001g0005 a0001c0001t0001g0157 |
3 | HG02040.hp1 NA18943.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-9+24764C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324053 | |||||||
| chr6:53324111 | G | A | 14 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0027 others(11): Show |
15 | HG00140.hp2 HG01175.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+24706C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324111 | |||||||
| chr6:53324239 | C | T | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+24578G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324239 | |||||||
| chr6:53324252 | CA | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(137): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.-9+24564delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324252 | |||||||
| chr6:53324252 | CAA | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
136 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.-9+24563_-9+24564d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324252 | |||||||
| chr6:53324270 | A | AG | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+24546_-9+24547i others(3): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324270 | |||||||
| chr6:53324270 | A | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(262): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-9+24547T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324270 | |||||||
| chr6:53324270 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02257.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+24547T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324270 | |||||||
| chr6:53324426 | A | G | 1 | a0001c0001t0004g0256 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-9+24391T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324426 | |||||||
| chr6:53324633 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+24184G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324633 | |||||||
| chr6:53324634 | C | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+24183G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324634 | |||||||
| chr6:53324661 | G | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(132): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-9+24156C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324661 | |||||||
| chr6:53324672 | C | CAAAAAAA | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01168.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.-9+24138_-9+24144d others(9): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324672 | |||||||
| chr6:53324672 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0006g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+24135_-9+24144d others(12): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324672 | |||||||
| chr6:53324672 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0041 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-9+24134_-9+24144d others(13): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324672 | |||||||
| chr6:53324672 | CAAAA | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(98): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.-9+24141_-9+24144d others(6): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324672 | |||||||
| chr6:53324691 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0147 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-9+24125_-9+24126i others(15): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324691 | |||||||
| chr6:53324691 | A | AAAAAAAA others(5): Show |
4 | a0001c0001t0001g0072 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG00621.hp1 HG02074.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+24125_-9+24126i others(14): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324691 | |||||||
| chr6:53324691 | A | AAAAAAAA others(4): Show |
47 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0048 others(44): Show |
49 | HG00735.hp2 HG01069.hp2 HG01123.hp2 others(46): Show |
intron_variant | MODIFIER | c.-9+24125_-9+24126i others(13): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324691 | |||||||
| chr6:53324691 | A | AAAAAAAA others(3): Show |
66 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
71 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.-9+24125_-9+24126i others(12): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324691 | |||||||
| chr6:53324691 | A | C | 2 | a0001c0001t0007g0131 a0001c0001t0007g0135 |
2 | NA19012.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-9+24126T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324691 | |||||||
| chr6:53324764 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-9+24053G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324764 | |||||||
| chr6:53324896 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-9+23921A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53324896 | |||||||
| chr6:53325132 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+23685T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325132 | |||||||
| chr6:53325232 | T | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
125 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.-9+23585A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325232 | |||||||
| chr6:53325336 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+23481T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325336 | |||||||
| chr6:53325370 | C | CG | 129 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(126): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.-9+23446_-9+23447i others(3): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325370 | |||||||
| chr6:53325371 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
151 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-9+23446T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325371 | |||||||
| chr6:53325371 | A | T | 129 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(126): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.-9+23446T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325371 | |||||||
| chr6:53325374 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+23443A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325374 | |||||||
| chr6:53325436 | C | T | 21 | a0001c0001t0001g0016 a0001c0001t0002g0004 a0001c0001t0002g0015 others(18): Show |
22 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-9+23381G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325436 | |||||||
| chr6:53325447 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+23370C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325447 | |||||||
| chr6:53325452 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+23365A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325452 | |||||||
| chr6:53325493 | T | C | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+23324A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325493 | |||||||
| chr6:53325494 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-9+23323C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325494 | |||||||
| chr6:53325759 | G | T | 1 | a0001c0002t0002g0018 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-9+23058C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325759 | |||||||
| chr6:53325786 | T | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+23031A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325786 | |||||||
| chr6:53325874 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-9+22943C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53325874 | |||||||
| chr6:53326016 | G | T | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-9+22801C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326016 | |||||||
| chr6:53326031 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+22786A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326031 | |||||||
| chr6:53326064 | G | A | 2 | a0001c0001t0008g0153 a0001c0001t0008g0154 |
2 | HG00609.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-9+22753C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326064 | |||||||
| chr6:53326344 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 |
3 | HG02258.hp1 HG02572.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-9+22473C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326344 | |||||||
| chr6:53326413 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+22404G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326413 | |||||||
| chr6:53326472 | C | T | 1 | a0001c0001t0006g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-9+22345G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326472 | |||||||
| chr6:53326483 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-9+22334C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326483 | |||||||
| chr6:53326552 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-9+22265G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326552 | |||||||
| chr6:53326608 | C | A | 2 | a0001c0001t0001g0239 a0001c0001t0001g0240 |
2 | HG02056.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-9+22209G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326608 | |||||||
| chr6:53326646 | C | A | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0255 |
3 | HG02056.hp1 NA18968.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-9+22171G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326646 | |||||||
| chr6:53326802 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9+22015C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326802 | |||||||
| chr6:53326805 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG00323.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-9+22012G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326805 | |||||||
| chr6:53326810 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-9+22007G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326810 | |||||||
| chr6:53326866 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+21951G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326866 | |||||||
| chr6:53326952 | CTG | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
6 | HG01069.hp2 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+21863_-9+21864d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53326952 | |||||||
| chr6:53327224 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-9+21593A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53327224 | |||||||
| chr6:53327254 | C | T | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+21563G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53327254 | |||||||
| chr6:53327262 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+21555C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53327262 | |||||||
| chr6:53327264 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+21553C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53327264 | |||||||
| chr6:53327408 | A | G | 1 | a0001c0001t0001g0022 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-9+21409T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53327408 | |||||||
| chr6:53327504 | C | CAGATG | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-9+21308_-9+21312d others(7): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53327504 | |||||||
| chr6:53327883 | G | C | 1 | a0001c0001t0004g0285 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9+20934C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53327883 | |||||||
| chr6:53327947 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+20870A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53327947 | |||||||
| chr6:53328197 | G | A | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+20620C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53328197 | |||||||
| chr6:53328208 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+20609A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53328208 | |||||||
| chr6:53328365 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-9+20452G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53328365 | |||||||
| chr6:53328704 | G | T | 3 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0001c0001t0001g0255 |
3 | HG02056.hp1 NA18968.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-9+20113C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53328704 | |||||||
| chr6:53328764 | TA | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-9+20052delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53328764 | |||||||
| chr6:53328846 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+19971C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53328846 | |||||||
| chr6:53328847 | G | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-9+19970C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53328847 | |||||||
| chr6:53329194 | ACTACTG | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+19617_-9+19622d others(8): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329194 | |||||||
| chr6:53329328 | T | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+19489A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329328 | |||||||
| chr6:53329476 | T | C | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+19341A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329476 | |||||||
| chr6:53329605 | C | T | 6 | a0001c0001t0001g0197 a0001c0001t0001g0250 a0001c0001t0001g0251 others(3): Show |
6 | HG01192.hp1 HG01496.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+19212G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329605 | |||||||
| chr6:53329642 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0074 |
3 | HG02257.hp2 HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-9+19175C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329642 | |||||||
| chr6:53329685 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+19132T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329685 | |||||||
| chr6:53329695 | G | A | 12 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0077 others(9): Show |
12 | HG01243.hp1 HG01255.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-9+19122C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329695 | |||||||
| chr6:53329747 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(265): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-9+19070A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329747 | |||||||
| chr6:53329857 | T | G | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-9+18960A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329857 | |||||||
| chr6:53329970 | T | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-9+18847A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53329970 | |||||||
| chr6:53330024 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+18793A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330024 | |||||||
| chr6:53330235 | TTG | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+18580_-9+18581d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330235 | |||||||
| chr6:53330483 | C | G | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+18334G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330483 | |||||||
| chr6:53330517 | C | CT | 21 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0058 others(18): Show |
21 | HG01243.hp1 HG01255.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.-9+18299dupA | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330517 | |||||||
| chr6:53330517 | C | CTT | 5 | a0001c0001t0001g0010 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
6 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+18298_-9+18299d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330517 | |||||||
| chr6:53330517 | C | CTTTT | 85 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(82): Show |
90 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.-9+18296_-9+18299d others(6): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330517 | |||||||
| chr6:53330517 | C | CTTTTT | 28 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(25): Show |
28 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.-9+18295_-9+18299d others(7): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330517 | |||||||
| chr6:53330517 | C | CTTTTTT | 6 | a0001c0001t0001g0022 a0001c0001t0001g0234 a0001c0001t0001g0235 others(3): Show |
6 | HG00438.hp1 HG00621.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+18294_-9+18299d others(8): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330517 | |||||||
| chr6:53330517 | CT | C | 7 | a0001c0001t0001g0076 a0001c0001t0001g0156 a0001c0001t0001g0175 others(4): Show |
7 | HG01069.hp1 HG02896.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+18299delA | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330517 | |||||||
| chr6:53330759 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+18058A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330759 | |||||||
| chr6:53330829 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(126): Show |
135 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.-9+17988A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330829 | |||||||
| chr6:53330857 | C | T | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-9+17960G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330857 | |||||||
| chr6:53330874 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-9+17943A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53330874 | |||||||
| chr6:53331021 | T | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+17796A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331021 | |||||||
| chr6:53331039 | CTT | C | 18 | a0001c0001t0001g0002 a0001c0001t0001g0204 a0001c0001t0001g0205 others(15): Show |
20 | HG01167.hp1 HG01346.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.-9+17776_-9+17777d others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331039 | |||||||
| chr6:53331108 | C | G | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-9+17709G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331108 | |||||||
| chr6:53331109 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA19064.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-9+17708A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331109 | |||||||
| chr6:53331345 | T | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+17472A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331345 | |||||||
| chr6:53331429 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0132 |
3 | NA18941.hp1 NA18984.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.-9+17388C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331429 | |||||||
| chr6:53331517 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-9+17300A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331517 | |||||||
| chr6:53331534 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9+17283G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331534 | |||||||
| chr6:53331598 | T | C | 1 | a0001c0001t0006g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-9+17219A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331598 | |||||||
| chr6:53331800 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-9+17017C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331800 | |||||||
| chr6:53331806 | T | C | 1 | a0001c0001t0013g0233 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-9+17011A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53331806 | |||||||
| chr6:53332115 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-9+16702C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332115 | |||||||
| chr6:53332254 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02257.hp2 HG02818.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+16563A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332254 | |||||||
| chr6:53332280 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-9+16537T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332280 | |||||||
| chr6:53332306 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+16511A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332306 | |||||||
| chr6:53332321 | T | C | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+16496A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332321 | |||||||
| chr6:53332483 | T | C | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9+16334A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332483 | |||||||
| chr6:53332551 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-9+16266G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332551 | |||||||
| chr6:53332583 | G | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0058 others(18): Show |
23 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.-9+16234C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332583 | |||||||
| chr6:53332947 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+15870C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332947 | |||||||
| chr6:53332987 | G | C | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-9+15830C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53332987 | |||||||
| chr6:53333139 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
140 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.-9+15678T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53333139 | |||||||
| chr6:53333374 | T | A | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9+15443A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53333374 | |||||||
| chr6:53333434 | T | C | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+15383A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53333434 | |||||||
| chr6:53333649 | C | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01255.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-9+15168G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53333649 | |||||||
| chr6:53333759 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+15058C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53333759 | |||||||
| chr6:53333887 | AAAC | A | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+14927_-9+14929d others(5): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53333887 | |||||||
| chr6:53333973 | T | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-9+14844A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53333973 | |||||||
| chr6:53333989 | C | T | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9+14828G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53333989 | |||||||
| chr6:53334025 | TCTC | T | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-9+14789_-9+14791d others(5): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53334025 | |||||||
| chr6:53334050 | A | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+14767T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53334050 | |||||||
| chr6:53334096 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+14721A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53334096 | |||||||
| chr6:53334402 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-9+14415A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53334402 | |||||||
| chr6:53334451 | A | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+14366T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53334451 | |||||||
| chr6:53334497 | AAATCATT others(13): Show |
A | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-9+14300_-9+14319d others(22): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53334497 | |||||||
| chr6:53335021 | T | A | 3 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 |
3 | NA18941.hp2 NA19003.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-9+13796A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335021 | |||||||
| chr6:53335048 | C | T | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+13769G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335048 | |||||||
| chr6:53335279 | G | A | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+13538C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335279 | |||||||
| chr6:53335289 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+13528T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335289 | |||||||
| chr6:53335320 | T | A | 21 | a0001c0001t0001g0016 a0001c0001t0002g0004 a0001c0001t0002g0015 others(18): Show |
22 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-9+13497A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335320 | |||||||
| chr6:53335475 | T | C | 1 | a0001c0001t0007g0135 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-9+13342A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335475 | |||||||
| chr6:53335501 | C | G | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+13316G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335501 | |||||||
| chr6:53335522 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
137 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-9+13295C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335522 | |||||||
| chr6:53335618 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+13199G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335618 | |||||||
| chr6:53335674 | C | A | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-9+13143G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335674 | |||||||
| chr6:53335815 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-9+13002A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53335815 | |||||||
| chr6:53336008 | C | T | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+12809G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336008 | |||||||
| chr6:53336058 | T | C | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+12759A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336058 | |||||||
| chr6:53336190 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+12627G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336190 | |||||||
| chr6:53336562 | G | A | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+12255C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336562 | |||||||
| chr6:53336598 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-9+12219C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336598 | |||||||
| chr6:53336643 | T | C | 1 | a0001c0001t0005g0014 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-9+12174A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336643 | |||||||
| chr6:53336684 | A | T | 1 | a0001c0001t0001g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-9+12133T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336684 | |||||||
| chr6:53336739 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+12078G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336739 | |||||||
| chr6:53336777 | A | C | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-9+12040T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336777 | |||||||
| chr6:53336803 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+12014C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336803 | |||||||
| chr6:53336885 | G | A | 11 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0077 others(8): Show |
11 | HG01255.hp1 HG01358.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-9+11932C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53336885 | |||||||
| chr6:53337221 | T | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0037 a0001c0001t0002g0038 |
4 | HG02896.hp1 HG02970.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+11596A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53337221 | |||||||
| chr6:53337237 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-9+11580A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53337237 | |||||||
| chr6:53337456 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-9+11361C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53337456 | |||||||
| chr6:53337808 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-9+11009A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53337808 | |||||||
| chr6:53338003 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-9+10814T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338003 | |||||||
| chr6:53338138 | T | C | 2 | a0001c0001t0001g0281 a0001c0001t0001g0282 |
2 | NA18959.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-9+10679A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338138 | |||||||
| chr6:53338209 | G | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(256): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-9+10608C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338209 | |||||||
| chr6:53338241 | C | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0136 a0001c0001t0001g0137 others(2): Show |
6 | NA18960.hp1 NA18961.hp2 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+10576G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338241 | |||||||
| chr6:53338291 | T | A | 3 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 |
3 | HG02886.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-9+10526A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338291 | |||||||
| chr6:53338296 | T | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-9+10521A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338296 | |||||||
| chr6:53338600 | A | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+10217T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338600 | |||||||
| chr6:53338759 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+10058C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338759 | |||||||
| chr6:53338766 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-9+10051C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338766 | |||||||
| chr6:53338779 | T | C | 57 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(54): Show |
57 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.-9+10038A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338779 | |||||||
| chr6:53338854 | T | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+9963A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338854 | |||||||
| chr6:53338957 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-9+9860G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53338957 | |||||||
| chr6:53339088 | G | C | 2 | a0001c0001t0001g0284 a0001c0001t0016g0283 |
2 | HG02071.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-9+9729C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339088 | |||||||
| chr6:53339184 | C | T | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-9+9633G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339184 | |||||||
| chr6:53339273 | C | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+9544G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339273 | |||||||
| chr6:53339377 | A | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0204 a0001c0001t0001g0205 others(16): Show |
21 | HG01167.hp1 HG01256.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.-9+9440T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339377 | |||||||
| chr6:53339411 | G | A | 1 | a0001c0001t0004g0285 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-9+9406C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339411 | |||||||
| chr6:53339608 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+9209G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339608 | |||||||
| chr6:53339628 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+9189A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339628 | |||||||
| chr6:53339655 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+9162A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339655 | |||||||
| chr6:53339747 | G | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-9+9070C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339747 | |||||||
| chr6:53339819 | T | C | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+8998A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339819 | |||||||
| chr6:53339886 | G | A | 21 | a0001c0001t0001g0016 a0001c0001t0002g0004 a0001c0001t0002g0015 others(18): Show |
22 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.-9+8931C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339886 | |||||||
| chr6:53339899 | T | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG01884.hp2 HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-9+8918A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339899 | |||||||
| chr6:53339929 | T | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(291): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.-9+8888A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53339929 | |||||||
| chr6:53340273 | T | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+8544A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53340273 | |||||||
| chr6:53340290 | G | A | 1 | a0001c0001t0011g0192 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-9+8527C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53340290 | |||||||
| chr6:53340437 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-9+8380T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53340437 | |||||||
| chr6:53340519 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+8298C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53340519 | |||||||
| chr6:53340709 | T | C | 3 | a0001c0001t0001g0286 a0001c0001t0001g0287 a0001c0001t0001g0288 |
3 | HG01070.hp2 HG01257.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-9+8108A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53340709 | |||||||
| chr6:53340790 | T | G | 1 | a0001c0001t0001g0140 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-9+8027A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53340790 | |||||||
| chr6:53340893 | C | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-9+7924G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53340893 | |||||||
| chr6:53340979 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+7838G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53340979 | |||||||
| chr6:53340995 | T | C | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+7822A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53340995 | |||||||
| chr6:53341010 | G | A | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-9+7807C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341010 | |||||||
| chr6:53341042 | G | T | 2 | a0001c0001t0001g0048 a0001c0001t0001g0049 |
2 | HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-9+7775C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341042 | |||||||
| chr6:53341124 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-9+7693C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341124 | |||||||
| chr6:53341149 | G | A | 128 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(125): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-9+7668C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341149 | |||||||
| chr6:53341182 | T | C | 1 | a0001c0001t0004g0289 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-9+7635A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341182 | |||||||
| chr6:53341245 | T | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+7572A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341245 | |||||||
| chr6:53341353 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
130 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.-9+7464T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341353 | |||||||
| chr6:53341410 | C | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(134): Show |
144 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.-9+7407G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341410 | |||||||
| chr6:53341701 | T | C | 72 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(69): Show |
77 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.-9+7116A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341701 | |||||||
| chr6:53341802 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-9+7015G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341802 | |||||||
| chr6:53341848 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-9+6969A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341848 | |||||||
| chr6:53341967 | C | T | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-9+6850G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53341967 | |||||||
| chr6:53342030 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+6787G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342030 | |||||||
| chr6:53342122 | C | CTTCTGCA others(19): Show |
3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+6694_-9+6695ins others(26): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342122 | |||||||
| chr6:53342124 | G | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+6693C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342124 | |||||||
| chr6:53342126 | A | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+6691T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342126 | |||||||
| chr6:53342191 | T | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-9+6626A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342191 | |||||||
| chr6:53342263 | A | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+6554T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342263 | |||||||
| chr6:53342279 | A | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG03017.hp1 HG03688.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-9+6538T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342279 | |||||||
| chr6:53342352 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-9+6465T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342352 | |||||||
| chr6:53342364 | T | G | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+6453A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342364 | |||||||
| chr6:53342585 | C | T | 3 | a0001c0001t0009g0303 a0001c0001t0009g0304 a0001c0001t0017g0300 |
3 | HG02257.hp1 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-9+6232G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342585 | |||||||
| chr6:53342652 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-9+6165T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342652 | |||||||
| chr6:53342775 | C | G | 1 | a0001c0001t0009g0303 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-9+6042G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342775 | |||||||
| chr6:53342927 | G | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-9+5890C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342927 | |||||||
| chr6:53342985 | A | T | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+5832T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53342985 | |||||||
| chr6:53343072 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+5745A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343072 | |||||||
| chr6:53343182 | A | C | 1 | a0001c0001t0002g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-9+5635T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343182 | |||||||
| chr6:53343218 | C | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-9+5599G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343218 | |||||||
| chr6:53343218 | CTTTA | C | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-9+5595_-9+5598del others(4): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343218 | |||||||
| chr6:53343222 | A | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(4): Show |
7 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+5595T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343222 | |||||||
| chr6:53343260 | C | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
132 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.-9+5557G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343260 | |||||||
| chr6:53343464 | T | C | 4 | a0001c0001t0002g0019 a0001c0001t0005g0014 a0001c0001t0005g0020 others(1): Show |
4 | HG01256.hp2 HG01257.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+5353A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343464 | |||||||
| chr6:53343473 | A | G | 1 | a0001c0001t0006g0301 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-9+5344T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343473 | |||||||
| chr6:53343508 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-9+5309G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343508 | |||||||
| chr6:53343648 | G | A | 14 | a0001c0001t0002g0004 a0001c0001t0002g0015 a0001c0001t0002g0027 others(11): Show |
15 | HG00140.hp2 HG01175.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.-9+5169C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343648 | |||||||
| chr6:53343882 | G | A | 103 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0194 others(100): Show |
108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.-9+4935C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343882 | |||||||
| chr6:53343902 | C | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+4915G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343902 | |||||||
| chr6:53343911 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-9+4906G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343911 | |||||||
| chr6:53343956 | C | T | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+4861G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343956 | |||||||
| chr6:53343990 | G | A | 1 | a0001c0001t0006g0302 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-9+4827C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53343990 | |||||||
| chr6:53344153 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-9+4664A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53344153 | |||||||
| chr6:53344201 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-9+4616T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53344201 | |||||||
| chr6:53344225 | T | C | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
3 | NA18946.hp1 NA18978.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-9+4592A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53344225 | |||||||
| chr6:53344322 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-9+4495A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53344322 | |||||||
| chr6:53344632 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-9+4185T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53344632 | |||||||
| chr6:53344709 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-9+4108G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53344709 | |||||||
| chr6:53344894 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-9+3923G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53344894 | |||||||
| chr6:53344925 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-9+3892G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53344925 | |||||||
| chr6:53344995 | T | G | 5 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(2): Show |
5 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+3822A>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53344995 | |||||||
| chr6:53345005 | C | T | 1 | a0001c0001t0017g0300 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-9+3812G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345005 | |||||||
| chr6:53345044 | T | C | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(269): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-9+3773A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345044 | |||||||
| chr6:53345125 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+3692T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345125 | |||||||
| chr6:53345262 | C | A | 1 | a0001c0001t0001g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-9+3555G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345262 | |||||||
| chr6:53345325 | A | G | 1 | a0001c0001t0001g0046 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-9+3492T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345325 | |||||||
| chr6:53345374 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-9+3443T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345374 | |||||||
| chr6:53345391 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+3426A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345391 | |||||||
| chr6:53345474 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-9+3343C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345474 | |||||||
| chr6:53345528 | C | CTCTGGAA others(129): Show |
102 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-9+3288_-9+3289ins others(136): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345528 | |||||||
| chr6:53345557 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-9+3260A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53345557 | |||||||
| chr6:53346131 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
6 | HG00621.hp1 HG02074.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+2686C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346131 | |||||||
| chr6:53346150 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG03492.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-9+2667C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346150 | |||||||
| chr6:53346153 | T | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(268): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.-9+2664A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346153 | |||||||
| chr6:53346236 | C | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-9+2581G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346236 | |||||||
| chr6:53346296 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02630.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+2521A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346296 | |||||||
| chr6:53346313 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0195 |
4 | HG02280.hp2 HG02647.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+2504T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346313 | |||||||
| chr6:53346353 | T | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-9+2464A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346353 | |||||||
| chr6:53346430 | C | A | 6 | a0001c0001t0006g0301 a0001c0001t0006g0302 a0001c0001t0006g0305 others(3): Show |
6 | HG02257.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+2387G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346430 | |||||||
| chr6:53346481 | A | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+2336T>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346481 | |||||||
| chr6:53346597 | A | G | 1 | a0001c0001t0001g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-9+2220T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346597 | |||||||
| chr6:53346822 | G | A | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+1995C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53346822 | |||||||
| chr6:53347046 | G | A | 2 | a0001c0001t0009g0303 a0001c0001t0009g0304 |
2 | HG02257.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-9+1771C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347046 | |||||||
| chr6:53347242 | GA | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-9+1574delT | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347242 | |||||||
| chr6:53347340 | T | A | 1 | a0001c0001t0006g0305 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-9+1477A>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347340 | |||||||
| chr6:53347401 | G | T | 1 | a0001c0001t0001g0162 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-9+1416C>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347401 | |||||||
| chr6:53347415 | C | A | 124 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
131 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.-9+1402G>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347415 | |||||||
| chr6:53347459 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-9+1358G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347459 | |||||||
| chr6:53347487 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-9+1330C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347487 | |||||||
| chr6:53347517 | A | T | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+1300T>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347517 | |||||||
| chr6:53347690 | A | G | 5 | a0001c0001t0002g0015 a0001c0001t0002g0027 a0001c0001t0002g0028 others(2): Show |
5 | HG00140.hp2 HG01175.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+1127T>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347690 | |||||||
| chr6:53347897 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-9+920A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53347897 | |||||||
| chr6:53348022 | G | GC | 107 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0022 others(104): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.-9+794dupG | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348022 | |||||||
| chr6:53348022 | G | GCCC | 13 | a0001c0001t0002g0004 a0001c0001t0002g0027 a0001c0001t0002g0028 others(10): Show |
14 | HG01175.hp2 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-9+792_-9+794dupGG others(1): Show |
ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348022 | |||||||
| chr6:53348200 | T | C | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
7 | HG00609.hp2 NA19002.hp1 NA19010.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+617A>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348200 | |||||||
| chr6:53348244 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-9+573C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348244 | |||||||
| chr6:53348304 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | HG00741.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+513G>C | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348304 | |||||||
| chr6:53348428 | G | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0197 others(99): Show |
107 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-9+389C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348428 | |||||||
| chr6:53348467 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-9+350C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348467 | |||||||
| chr6:53348640 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-9+177C>G | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348640 | |||||||
| chr6:53348643 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(128): Show |
138 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.-9+174G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348643 | |||||||
| chr6:53348654 | G | A | 4 | a0001c0001t0001g0296 a0001c0001t0001g0297 a0001c0001t0001g0298 others(1): Show |
4 | HG02615.hp2 HG03225.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-9+163C>T | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348654 | |||||||
| chr6:53348660 | C | T | 1 | a0001c0001t0005g0014 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-9+157G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348660 | |||||||
| chr6:53348681 | C | T | 26 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0023 others(23): Show |
27 | HG00140.hp2 HG01081.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.-9+136G>A | ELOVL5 | ENSG00000012660.14 | transcript | ENST00000304434.11 | protein_coding | 1/7 | chr6 | 53348681 |