| geneid | 6397 |
|---|---|
| ensemblid | ENSG00000129657.16 |
| hgncid | 10698 |
| symbol | SEC14L1 |
| name | SEC14 like lipid binding 1 |
| refseq_nuc | NM_001143998.2 |
| refseq_prot | NP_001137470.2 |
| ensembl_nuc | ENST00000436233.9 |
| ensembl_prot | ENSP00000390392.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 77140969 |
| end | 77217101 |
| strand | + |
| ver | v1.2 |
| region | chr17:77140969-77217101 |
| region5000 | chr17:77135969-77222101 |
| regionname0 | SEC14L1_chr17_77140969_77217101 |
| regionname5000 | SEC14L1_chr17_77135969_77222101 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 715 | 413 | 78 | 77 | 198 | 14 | 45 | 157 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0002 | 1/0 | 715 | 8 | 7 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0003 | 0/0 | 715 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0004 | 0/0 | 715 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0005 | 0/0 | 715 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0006 | 0/0 | 715 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0007 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0008 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0009 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2148 | 249 | 50 | 52 | 122 | 6 | 18 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0002 | 0/0 | 2148 | 127 | 21 | 25 | 55 | 7 | 19 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0003 | 0/0 | 2148 | 30 | 1 | 0 | 21 | 1 | 7 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0004 | 1/0 | 2148 | 8 | 7 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0005 | 0/0 | 2148 | 6 | 6 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0006 | 0/0 | 2148 | 2 | 0 | 0 | 0 | 0 | 2 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0007 | 0/0 | 2148 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0008 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0009 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0010 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0011 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0012 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| c0013 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3271 | 52 | 7 | 11 | 25 | 1 | 8 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0002 | 0/0 | 3418 | 49 | 5 | 2 | 41 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0003 | 0/1 | 3301 | 47 | 14 | 3 | 25 | 1 | 3 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0004 | 0/0 | 3353 | 43 | 1 | 10 | 21 | 3 | 8 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0005 | 0/0 | 3353 | 41 | 10 | 6 | 14 | 3 | 8 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0006 | 0/0 | 2810 | 36 | 3 | 11 | 18 | 0 | 4 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0007 | 0/0 | 3288 | 20 | 7 | 11 | 0 | 1 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0008 | 0/0 | 3314 | 16 | 0 | 0 | 13 | 0 | 3 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0009 | 0/0 | 3236 | 7 | 6 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0010 | 0/0 | 3259 | 6 | 0 | 5 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0011 | 0/0 | 3353 | 6 | 0 | 0 | 6 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0012 | 0/0 | 3340 | 5 | 5 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0013 | 1/0 | 3353 | 5 | 4 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0014 | 0/0 | 3327 | 4 | 1 | 1 | 0 | 2 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0015 | 0/0 | 3141 | 4 | 4 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0016 | 0/0 | 3418 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0017 | 0/0 | 3288 | 3 | 3 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0018 | 0/0 | 3340 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0019 | 0/0 | 3223 | 3 | 3 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0020 | 0/0 | 3258 | 3 | 0 | 0 | 0 | 0 | 3 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0021 | 0/0 | 3353 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0022 | 0/0 | 3377 | 3 | 0 | 0 | 0 | 0 | 3 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0023 | 0/0 | 3271 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0024 | 0/0 | 3353 | 2 | 1 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0025 | 0/0 | 3275 | 2 | 0 | 0 | 1 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0026 | 0/0 | 3288 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0027 | 0/0 | 3353 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0028 | 0/0 | 3340 | 2 | 0 | 0 | 1 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0029 | 0/0 | 3275 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0030 | 0/0 | 3418 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0031 | 0/0 | 3405 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0032 | 0/0 | 3288 | 2 | 1 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0033 | 0/0 | 3245 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0034 | 0/0 | 3310 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0035 | 0/0 | 3258 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0036 | 0/0 | 3145 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0037 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0038 | 0/0 | 3271 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0039 | 0/0 | 3327 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0040 | 0/0 | 3353 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0041 | 0/0 | 3206 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0042 | 0/0 | 3353 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0043 | 0/0 | 3340 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0044 | 0/0 | 3284 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0045 | 0/0 | 3301 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0046 | 0/0 | 3301 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0047 | 0/0 | 3340 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0048 | 0/0 | 3353 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0049 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0050 | 0/0 | 3301 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0051 | 0/0 | 3236 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0052 | 0/0 | 3340 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0053 | 0/0 | 3366 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0054 | 0/0 | 3366 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0055 | 0/0 | 3366 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0056 | 0/0 | 3395 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0057 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0058 | 0/0 | 3418 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0059 | 0/0 | 3275 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0060 | 0/0 | 3236 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0061 | 0/0 | 3392 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0062 | 0/0 | 3366 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0063 | 0/0 | 2810 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0064 | 0/0 | 3327 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0065 | 0/0 | 3288 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0066 | 0/0 | 3353 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0067 | 0/0 | 3271 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0068 | 0/0 | 3271 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0069 | 0/0 | 2797 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0070 | 0/0 | 2797 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0071 | 0/0 | 3271 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0072 | 0/0 | 3353 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0073 | 0/0 | 3340 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0074 | 0/0 | 3301 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0075 | 0/0 | 3340 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| t0076 | 0/0 | 3418 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0392 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0404 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0405 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0406 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2148 | 249 | 50 | 52 | 122 | 6 | 18 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002 | 0/0 | 2148 | 127 | 21 | 25 | 55 | 7 | 19 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0003 | 0/0 | 2148 | 30 | 1 | 0 | 21 | 1 | 7 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0005 | 0/0 | 2148 | 6 | 6 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0009 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0002c0004 | 1/0 | 2148 | 8 | 7 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0003c0007 | 0/0 | 2148 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0004c0006 | 0/0 | 2148 | 2 | 0 | 0 | 0 | 0 | 2 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0005c0008 | 0/0 | 2148 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0006c0013 | 0/0 | 2148 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0007c0010 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0008c0011 | 0/0 | 2148 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0009c0012 | 0/0 | 2148 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5418 | 30 | 6 | 11 | 9 | 0 | 4 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0002 | 0/0 | 5565 | 46 | 4 | 1 | 40 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0003 | 0/1 | 5448 | 47 | 14 | 3 | 25 | 1 | 3 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0005 | 0/0 | 5500 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0006 | 0/0 | 4957 | 35 | 3 | 10 | 18 | 0 | 4 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0007 | 0/0 | 5435 | 18 | 5 | 11 | 0 | 1 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0008 | 0/0 | 5461 | 16 | 0 | 0 | 13 | 0 | 3 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0009 | 0/0 | 5383 | 7 | 6 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0010 | 0/0 | 5406 | 6 | 0 | 5 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0016 | 0/0 | 5565 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0017 | 0/0 | 5435 | 3 | 3 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0019 | 0/0 | 5370 | 3 | 3 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0025 | 0/0 | 5422 | 2 | 0 | 0 | 1 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0026 | 0/0 | 5435 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0030 | 0/0 | 5565 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0031 | 0/0 | 5552 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0032 | 0/0 | 5435 | 2 | 1 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0033 | 0/0 | 5392 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0035 | 0/0 | 5405 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0039 | 0/0 | 5474 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0041 | 0/0 | 5353 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0044 | 0/0 | 5431 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0045 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0050 | 0/0 | 5448 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0056 | 0/0 | 5542 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0057 | 0/0 | 5565 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0058 | 0/0 | 5565 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0059 | 0/0 | 5422 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0061 | 0/0 | 5539 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0063 | 0/0 | 4957 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0064 | 0/0 | 5474 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0065 | 0/0 | 5435 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0067 | 0/0 | 5418 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0068 | 0/0 | 5418 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0069 | 0/0 | 4944 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0070 | 0/0 | 4944 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0071 | 0/0 | 5418 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0074 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0001t0076 | 0/0 | 5565 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0002 | 0/0 | 5565 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0004 | 0/0 | 5500 | 43 | 1 | 10 | 21 | 3 | 8 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0005 | 0/0 | 5500 | 38 | 10 | 6 | 13 | 2 | 7 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0006 | 0/0 | 4957 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0011 | 0/0 | 5500 | 6 | 0 | 0 | 6 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0012 | 0/0 | 5487 | 5 | 5 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0014 | 0/0 | 5474 | 4 | 1 | 1 | 0 | 2 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0018 | 0/0 | 5487 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0021 | 0/0 | 5500 | 3 | 0 | 0 | 3 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0024 | 0/0 | 5500 | 2 | 1 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0027 | 0/0 | 5500 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0028 | 0/0 | 5487 | 2 | 0 | 0 | 1 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0029 | 0/0 | 5422 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0040 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0042 | 0/0 | 5500 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0043 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0047 | 0/0 | 5487 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0048 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0049 | 0/0 | 5513 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0051 | 0/0 | 5383 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0052 | 0/0 | 5487 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0053 | 0/0 | 5513 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0054 | 0/0 | 5513 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0055 | 0/0 | 5513 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0066 | 0/0 | 5500 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0072 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0073 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0002t0075 | 0/0 | 5487 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0003t0001 | 0/0 | 5418 | 22 | 1 | 0 | 16 | 1 | 4 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0003t0020 | 0/0 | 5405 | 3 | 0 | 0 | 0 | 0 | 3 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0003t0023 | 0/0 | 5418 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0003t0034 | 0/0 | 5457 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0003t0038 | 0/0 | 5418 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0005t0015 | 0/0 | 5288 | 4 | 4 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0005t0036 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0005t0037 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0001c0009t0022 | 0/0 | 5524 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0002c0004t0013 | 1/0 | 5500 | 5 | 4 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0002c0004t0046 | 0/0 | 5448 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0002c0004t0060 | 0/0 | 5383 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0002c0004t0062 | 0/0 | 5513 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0003c0007t0007 | 0/0 | 5435 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0004c0006t0022 | 0/0 | 5524 | 2 | 0 | 0 | 0 | 0 | 2 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0005c0008t0002 | 0/0 | 5565 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0006c0013t0005 | 0/0 | 5500 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0007c0010t0002 | 0/0 | 5565 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0008c0011t0036 | 0/0 | 5292 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| a0009c0012t0005 | 0/0 | 5500 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | copy fasta | chr17 | 77135969 | 77222101 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0123 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0006g0391 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0401 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0404 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0405 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0406 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0410 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0008g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0009g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0009g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0010g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0010g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0010g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0010g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0016g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0016g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0016g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0017g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0017g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0017g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0019g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0019g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0019g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0025g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0025g0392 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0026g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0026g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0030g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0030g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0031g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0031g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0032g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0033g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0033g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0035g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0039g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0041g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0044g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0045g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0050g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0056g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0057g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0058g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0059g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0061g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0063g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0064g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0065g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0067g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0068g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0069g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0070g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0071g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0074g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0001t0076g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0013 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0342 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0347 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0351 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0379 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0380 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0382 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0004g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0385 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0005g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0006g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0011g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0011g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0011g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0011g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0011g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0012g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0012g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0012g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0012g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0012g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0014g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0014g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0014g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0014g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0018g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0018g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0018g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0021g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0021g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0021g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0024g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0024g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0027g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0027g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0028g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0028g0387 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0029g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0029g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0040g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0042g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0043g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0047g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0048g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0049g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0051g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0052g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0053g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0054g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0055g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0066g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0072g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0073g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0002t0075g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0020g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0020g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0020g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0023g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0023g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0034g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0034g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0003t0038g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0005t0015g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0005t0015g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0005t0015g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0005t0036g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0005t0037g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0001c0009t0022g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0002c0004t0013g0172 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0002c0004t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0002c0004t0013g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0002c0004t0013g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0002c0004t0013g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0002c0004t0046g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0002c0004t0060g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0002c0004t0062g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0003c0007t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0003c0007t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0004c0006t0022g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0004c0006t0022g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0005c0008t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0006c0013t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0007c0010t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0008c0011t0036g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| a0009c0012t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0025 | g0392 | EUR | GBR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0039 | EUR | GBR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0179 | EUR | GBR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00140 | hp2 | a0001 | c0002 | t0004 | g0342 | EUR | GBR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00323 | hp1 | a0001 | c0002 | t0005 | g0305 | EUR | FIN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00323 | hp2 | a0001 | c0001 | t0007 | g0037 | EUR | FIN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0234 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00408 | hp2 | a0001 | c0002 | t0004 | g0166 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00423 | hp1 | a0001 | c0002 | t0004 | g0131 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00423 | hp2 | a0001 | c0003 | t0034 | g0250 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00438 | hp1 | a0001 | c0002 | t0011 | g0015 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00544 | hp1 | a0001 | c0002 | t0005 | g0293 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00558 | hp1 | a0001 | c0002 | t0053 | g0339 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00558 | hp2 | a0001 | c0001 | t0031 | g0088 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00597 | hp1 | a0001 | c0002 | t0040 | g0366 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00597 | hp2 | a0001 | c0001 | t0006 | g0208 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00639 | hp1 | a0001 | c0002 | t0004 | g0334 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00639 | hp2 | a0001 | c0001 | t0032 | g0009 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0120 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00673 | hp2 | a0001 | c0002 | t0072 | g0365 | EAS | CHS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0042 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00735 | hp1 | a0001 | c0002 | t0004 | g0370 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00735 | hp2 | a0001 | c0001 | t0071 | g0244 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00738 | hp1 | a0001 | c0002 | t0004 | g0352 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0122 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0204 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG00741 | hp2 | a0001 | c0002 | t0004 | g0303 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0148 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01071 | hp1 | a0001 | c0002 | t0024 | g0318 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01071 | hp2 | a0001 | c0001 | t0007 | g0155 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01074 | hp1 | a0001 | c0002 | t0004 | g0382 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0156 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01081 | hp1 | a0001 | c0001 | t0007 | g0041 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01081 | hp2 | a0001 | c0002 | t0005 | g0300 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0036 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01109 | hp2 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01167 | hp1 | a0001 | c0001 | t0010 | g0114 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01167 | hp2 | a0001 | c0002 | t0004 | g0341 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01168 | hp1 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01169 | hp1 | a0001 | c0002 | t0004 | g0013 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01169 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01175 | hp1 | a0001 | c0002 | t0005 | g0310 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0044 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01192 | hp2 | a0001 | c0002 | t0014 | g0358 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01243 | hp1 | a0001 | c0002 | t0075 | g0302 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01243 | hp2 | a0001 | c0001 | t0007 | g0154 | AMR | PUR | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01255 | hp1 | a0001 | c0001 | t0009 | g0051 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0038 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01256 | hp1 | a0001 | c0002 | t0004 | g0336 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01256 | hp2 | a0001 | c0001 | t0035 | g0011 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01257 | hp1 | a0001 | c0002 | t0005 | g0388 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01258 | hp1 | a0001 | c0002 | t0005 | g0376 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01258 | hp2 | a0001 | c0001 | t0035 | g0011 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0027 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01346 | hp1 | a0001 | c0001 | t0068 | g0248 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01346 | hp2 | a0001 | c0002 | t0073 | g0372 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01358 | hp1 | a0001 | c0002 | t0005 | g0298 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01358 | hp2 | a0001 | c0001 | t0010 | g0006 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01361 | hp1 | a0001 | c0001 | t0007 | g0043 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01361 | hp2 | a0001 | c0002 | t0043 | g0316 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01433 | hp2 | a0001 | c0002 | t0027 | g0002 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01496 | hp1 | a0001 | c0001 | t0006 | g0209 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01496 | hp2 | a0001 | c0002 | t0005 | g0385 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01515 | hp1 | a0001 | c0002 | t0004 | g0347 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01516 | hp1 | a0001 | c0002 | t0014 | g0317 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01516 | hp2 | a0001 | c0001 | t0010 | g0121 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01517 | hp1 | a0001 | c0002 | t0004 | g0351 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01517 | hp2 | a0001 | c0002 | t0014 | g0314 | EUR | IBS | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01884 | hp1 | a0001 | c0002 | t0005 | g0371 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01884 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01891 | hp1 | a0001 | c0005 | t0037 | g0016 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01891 | hp2 | a0002 | c0004 | t0013 | g0174 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01928 | hp1 | a0001 | c0002 | t0054 | g0375 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01928 | hp2 | a0001 | c0001 | t0063 | g0001 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01934 | hp1 | a0001 | c0001 | t0065 | g0045 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0196 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01943 | hp2 | a0005 | c0008 | t0002 | g0073 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01978 | hp2 | a0001 | c0001 | t0006 | g0026 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01993 | hp2 | a0001 | c0001 | t0006 | g0001 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02004 | hp1 | a0001 | c0001 | t0056 | g0078 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0206 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02015 | hp1 | a0001 | c0001 | t0076 | g0084 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02015 | hp2 | a0001 | c0002 | t0004 | g0348 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0207 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0271 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02040 | hp2 | a0007 | c0010 | t0002 | g0194 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0236 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02055 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02056 | hp1 | a0001 | c0002 | t0004 | g0023 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02056 | hp2 | a0001 | c0003 | t0001 | g0269 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02071 | hp2 | a0001 | c0003 | t0034 | g0247 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02074 | hp1 | a0001 | c0002 | t0028 | g0296 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02074 | hp2 | a0001 | c0003 | t0001 | g0233 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02080 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02080 | hp2 | a0001 | c0003 | t0001 | g0239 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02129 | hp2 | a0001 | c0002 | t0005 | g0287 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02132 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02132 | hp2 | a0001 | c0002 | t0005 | g0286 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02135 | hp2 | a0001 | c0002 | t0011 | g0015 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02145 | hp1 | a0001 | c0001 | t0059 | g0390 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02145 | hp2 | a0001 | c0001 | t0006 | g0225 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02155 | hp1 | a0001 | c0003 | t0001 | g0257 | EAS | CDX | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02155 | hp2 | a0001 | c0003 | t0001 | g0270 | EAS | CDX | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02165 | hp1 | a0001 | c0002 | t0005 | g0313 | EAS | CDX | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | CDX | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02257 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02258 | hp1 | a0001 | c0002 | t0005 | g0304 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02258 | hp2 | a0001 | c0001 | t0017 | g0160 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02273 | hp1 | a0001 | c0001 | t0058 | g0071 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02273 | hp2 | a0001 | c0001 | t0026 | g0394 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02280 | hp1 | a0001 | c0002 | t0005 | g0198 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02293 | hp1 | a0001 | c0002 | t0055 | g0335 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02293 | hp2 | a0001 | c0001 | t0006 | g0205 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02300 | hp2 | a0001 | c0002 | t0006 | g0221 | AMR | PEL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02451 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02451 | hp2 | a0001 | c0001 | t0074 | g0192 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02523 | hp2 | a0001 | c0001 | t0016 | g0060 | EAS | KHV | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02602 | hp1 | a0001 | c0002 | t0047 | g0350 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0118 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02615 | hp1 | a0001 | c0002 | t0012 | g0323 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02615 | hp2 | a0002 | c0004 | t0013 | g0173 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02622 | hp2 | a0001 | c0002 | t0012 | g0325 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02630 | hp2 | a0001 | c0001 | t0006 | g0224 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02683 | hp1 | a0001 | c0002 | t0028 | g0387 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0404 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02698 | hp2 | a0001 | c0002 | t0005 | g0321 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02717 | hp1 | a0001 | c0005 | t0015 | g0008 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0103 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02723 | hp2 | a0001 | c0002 | t0014 | g0359 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02735 | hp1 | a0001 | c0003 | t0001 | g0282 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02735 | hp2 | a0001 | c0002 | t0004 | g0014 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0119 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02738 | hp2 | a0001 | c0003 | t0020 | g0029 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02886 | hp1 | a0002 | c0004 | t0046 | g0186 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0331 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02895 | hp2 | a0001 | c0002 | t0012 | g0377 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02896 | hp2 | a0001 | c0001 | t0045 | g0116 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0311 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02965 | hp1 | a0001 | c0005 | t0015 | g0008 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02965 | hp2 | a0001 | c0001 | t0019 | g0108 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02970 | hp1 | a0001 | c0005 | t0015 | g0171 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02970 | hp2 | a0001 | c0002 | t0005 | g0328 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0220 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03017 | hp2 | a0001 | c0002 | t0004 | g0380 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03098 | hp1 | a0003 | c0007 | t0007 | g0025 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0056 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03130 | hp1 | a0001 | c0002 | t0052 | g0357 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0111 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03139 | hp1 | a0001 | c0001 | t0019 | g0107 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03139 | hp2 | a0001 | c0002 | t0005 | g0327 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03195 | hp1 | a0002 | c0004 | t0062 | g0177 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03195 | hp2 | a0001 | c0001 | t0017 | g0161 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0297 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0054 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03239 | hp1 | a0001 | c0002 | t0004 | g0379 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03239 | hp2 | a0001 | c0003 | t0001 | g0268 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03453 | hp1 | a0002 | c0004 | t0013 | g0176 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03453 | hp2 | a0001 | c0001 | t0017 | g0159 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03486 | hp1 | a0001 | c0005 | t0015 | g0170 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03486 | hp2 | a0001 | c0002 | t0012 | g0326 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03490 | hp1 | a0001 | c0001 | t0006 | g0223 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0308 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03491 | hp1 | a0004 | c0006 | t0022 | g0190 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03491 | hp2 | a0001 | c0002 | t0004 | g0013 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03492 | hp1 | a0004 | c0006 | t0022 | g0189 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03492 | hp2 | a0001 | c0002 | t0005 | g0309 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03516 | hp1 | a0001 | c0002 | t0024 | g0319 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0110 | AFR | ESN | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03540 | hp2 | a0002 | c0004 | t0060 | g0187 | AFR | GWD | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0329 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0184 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03669 | hp1 | a0001 | c0001 | t0006 | g0218 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03688 | hp1 | a0001 | c0002 | t0004 | g0035 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0259 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03704 | hp2 | a0001 | c0002 | t0027 | g0349 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03710 | hp2 | a0001 | c0001 | t0026 | g0396 | SAS | PJL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0095 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0401 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03834 | hp1 | a0001 | c0002 | t0005 | g0307 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03834 | hp2 | a0001 | c0003 | t0001 | g0178 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03927 | hp1 | a0001 | c0003 | t0020 | g0028 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03927 | hp2 | a0001 | c0001 | t0008 | g0405 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03942 | hp1 | a0006 | c0013 | t0005 | g0292 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03942 | hp2 | a0001 | c0002 | t0042 | g0353 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04115 | hp1 | a0001 | c0003 | t0020 | g0264 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04115 | hp2 | a0001 | c0002 | t0005 | g0197 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04184 | hp1 | a0001 | c0001 | t0006 | g0391 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04184 | hp2 | a0001 | c0002 | t0004 | g0378 | SAS | BEB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04199 | hp1 | a0001 | c0002 | t0005 | g0306 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04199 | hp2 | a0001 | c0002 | t0004 | g0381 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04204 | hp1 | a0001 | c0002 | t0005 | g0315 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04204 | hp2 | a0001 | c0001 | t0070 | g0219 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04228 | hp1 | a0001 | c0009 | t0022 | g0191 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0129 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18522 | hp2 | a0001 | c0001 | t0009 | g0052 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18612 | hp1 | a0001 | c0002 | t0004 | g0383 | EAS | CHB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18612 | hp2 | a0001 | c0002 | t0004 | g0181 | EAS | CHB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18906 | hp1 | a0002 | c0004 | t0013 | g0175 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18906 | hp2 | a0001 | c0002 | t0005 | g0330 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18939 | hp2 | a0001 | c0002 | t0021 | g0386 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18940 | hp1 | a0001 | c0001 | t0008 | g0393 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18943 | hp1 | a0001 | c0002 | t0051 | g0367 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0389 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18945 | hp2 | a0001 | c0001 | t0030 | g0085 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18946 | hp1 | a0001 | c0001 | t0008 | g0402 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18946 | hp2 | a0001 | c0002 | t0004 | g0354 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18947 | hp1 | a0001 | c0001 | t0067 | g0246 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18948 | hp1 | a0001 | c0002 | t0004 | g0337 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18949 | hp1 | a0001 | c0002 | t0005 | g0374 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18949 | hp2 | a0001 | c0002 | t0021 | g0360 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18954 | hp1 | a0001 | c0001 | t0008 | g0399 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18954 | hp2 | a0001 | c0002 | t0021 | g0368 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18959 | hp1 | a0009 | c0012 | t0005 | g0320 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18959 | hp2 | a0001 | c0001 | t0033 | g0280 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18960 | hp1 | a0001 | c0003 | t0001 | g0266 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18960 | hp2 | a0001 | c0002 | t0018 | g0362 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18963 | hp1 | a0001 | c0002 | t0005 | g0295 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18963 | hp2 | a0001 | c0002 | t0018 | g0364 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18967 | hp2 | a0001 | c0002 | t0005 | g0284 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18969 | hp1 | a0001 | c0001 | t0006 | g0202 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18969 | hp2 | a0001 | c0002 | t0004 | g0356 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18970 | hp1 | a0001 | c0001 | t0008 | g0409 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18971 | hp1 | a0001 | c0003 | t0023 | g0267 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18971 | hp2 | a0001 | c0001 | t0006 | g0227 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18972 | hp1 | a0001 | c0002 | t0049 | g0373 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0127 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18974 | hp1 | a0001 | c0002 | t0005 | g0290 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18975 | hp2 | a0001 | c0002 | t0011 | g0363 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18977 | hp1 | a0001 | c0002 | t0004 | g0384 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18977 | hp2 | a0001 | c0001 | t0008 | g0403 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18978 | hp1 | a0001 | c0002 | t0004 | g0180 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18979 | hp2 | a0001 | c0001 | t0061 | g0089 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18981 | hp1 | a0001 | c0001 | t0008 | g0406 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18981 | hp2 | a0001 | c0003 | t0023 | g0030 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18982 | hp1 | a0001 | c0002 | t0029 | g0343 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18982 | hp2 | a0001 | c0001 | t0016 | g0069 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18983 | hp1 | a0001 | c0001 | t0016 | g0070 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18984 | hp1 | a0001 | c0001 | t0057 | g0072 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18985 | hp2 | a0001 | c0002 | t0005 | g0285 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0213 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0203 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18989 | hp2 | a0001 | c0001 | t0031 | g0090 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18990 | hp1 | a0001 | c0001 | t0008 | g0408 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18992 | hp2 | a0001 | c0002 | t0004 | g0182 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0251 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18998 | hp1 | a0001 | c0002 | t0004 | g0355 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18998 | hp2 | a0001 | c0001 | t0008 | g0411 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19000 | hp2 | a0001 | c0001 | t0069 | g0195 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19002 | hp2 | a0001 | c0001 | t0008 | g0398 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19003 | hp1 | a0001 | c0001 | t0006 | g0214 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19007 | hp1 | a0001 | c0002 | t0048 | g0288 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19010 | hp1 | a0001 | c0001 | t0033 | g0255 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19010 | hp2 | a0001 | c0002 | t0004 | g0369 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19011 | hp1 | a0001 | c0002 | t0005 | g0289 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19011 | hp2 | a0001 | c0002 | t0004 | g0193 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19012 | hp2 | a0001 | c0001 | t0008 | g0410 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | LWK | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19043 | hp2 | a0001 | c0001 | t0041 | g0109 | AFR | LWK | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19054 | hp2 | a0001 | c0002 | t0005 | g0291 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19055 | hp1 | a0001 | c0002 | t0005 | g0032 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19055 | hp2 | a0001 | c0001 | t0030 | g0093 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19056 | hp1 | a0001 | c0002 | t0011 | g0344 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19058 | hp1 | a0001 | c0002 | t0029 | g0002 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0407 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19062 | hp1 | a0001 | c0001 | t0008 | g0400 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19063 | hp1 | a0001 | c0002 | t0004 | g0034 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19064 | hp1 | a0001 | c0001 | t0006 | g0210 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19064 | hp2 | a0001 | c0002 | t0004 | g0338 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0201 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19066 | hp2 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19068 | hp1 | a0001 | c0001 | t0039 | g0412 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19068 | hp2 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19076 | hp1 | a0001 | c0003 | t0038 | g0228 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19079 | hp1 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19079 | hp2 | a0001 | c0001 | t0025 | g0199 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19080 | hp1 | a0001 | c0002 | t0004 | g0002 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19081 | hp1 | a0001 | c0002 | t0011 | g0345 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19082 | hp1 | a0001 | c0003 | t0001 | g0265 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19082 | hp2 | a0001 | c0002 | t0011 | g0294 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19083 | hp1 | a0001 | c0002 | t0018 | g0361 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19083 | hp2 | a0001 | c0001 | t0050 | g0395 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19084 | hp1 | a0001 | c0002 | t0004 | g0340 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19085 | hp2 | a0001 | c0003 | t0001 | g0261 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19086 | hp1 | a0001 | c0001 | t0006 | g0216 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19088 | hp2 | a0001 | c0001 | t0008 | g0397 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19089 | hp2 | a0001 | c0002 | t0004 | g0333 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19090 | hp2 | a0001 | c0002 | t0005 | g0033 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19091 | hp1 | a0001 | c0002 | t0004 | g0332 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA19240 | hp2 | a0001 | c0001 | t0009 | g0003 | AFR | YRI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA20752 | hp1 | a0001 | c0002 | t0005 | g0322 | EUR | TSI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA20752 | hp2 | a0001 | c0001 | t0044 | g0046 | EUR | TSI | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA20905 | hp1 | a0001 | c0002 | t0004 | g0346 | SAS | GIH | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0019 | SAS | GIH | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0047 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG01123 | hp2 | a0001 | c0002 | t0004 | g0014 | AMR | CLM | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02109 | hp1 | a0008 | c0011 | t0036 | g0018 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02109 | hp2 | a0001 | c0001 | t0019 | g0053 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02486 | hp1 | a0001 | c0005 | t0036 | g0017 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02486 | hp2 | a0001 | c0002 | t0004 | g0299 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02559 | hp1 | a0001 | c0001 | t0032 | g0009 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ACB | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03471 | hp1 | a0001 | c0001 | t0064 | g0055 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG03471 | hp2 | a0001 | c0002 | t0066 | g0301 | AFR | MSL | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG06807 | hp1 | a0001 | c0002 | t0005 | g0312 | AFR | USA | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | USA | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA18955 | hp2 | a0001 | c0001 | t0006 | g0102 | EAS | JPT | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0215 | AFR | USA | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA20300 | hp2 | a0003 | c0007 | t0007 | g0168 | AFR | USA | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | LWK | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| NA21309 | hp2 | a0001 | c0002 | t0012 | g0324 | AFR | LWK | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0123 | REF | REF | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| homoSapiens_grch38 | hp1 | a0002 | c0004 | t0013 | g0172 | REF | REF | SEC14L1_chr17_77135969_77222101 | SEC14L1 | chr17 | 77135969 | 77222101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:77191224
|
T | G | 1 | a0004 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.257T>G | p.Leu86Arg | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/17 | 531/5500 | 257/2148 | 86/715 | chr17 | 77191224 | ||
| chr17:77193467
|
G | A | 1 | a0005 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.392G>A | p.Ser131Asn | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/17 | 666/5500 | 392/2148 | 131/715 | chr17 | 77193467 | ||
| chr17:77194758
|
A | G | 1 | a0004 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.556A>G | p.Ile186Val | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/17 | 830/5500 | 556/2148 | 186/715 | chr17 | 77194758 | ||
| chr17:77194764
|
A | C | 8 | a0001a0003a0004others(5): Show | 422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
missense_variant | MODERATE | c.562A>C | p.Thr188Pro | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/17 | 836/5500 | 562/2148 | 188/715 | chr17 | 77194764 | ||
| chr17:77200626
|
A | C | 1 | a0006 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.962A>C | p.Gln321Pro | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/17 | 1236/5500 | 962/2148 | 321/715 | chr17 | 77200626 | ||
| chr17:77212016
|
A | G | 1 | a0009 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1678A>G | p.Ile560Val | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/17 | 1952/5500 | 1678/2148 | 560/715 | chr17 | 77212016 | ||
| chr17:77212079
|
G | T | 1 | a0003 | 2 | HG03098.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.1741G>T | p.Ala581Ser | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/17 | 2015/5500 | 1741/2148 | 581/715 | chr17 | 77212079 | ||
| chr17:77212145
|
C | T | 1 | a0007 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1807C>T | p.Arg603Cys | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/17 | 2081/5500 | 1807/2148 | 603/715 | chr17 | 77212145 | ||
| chr17:77213398
|
C | T | 1 | a0008 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.1948C>T | p.Pro650Ser | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/17 | 2222/5500 | 1948/2148 | 650/715 | chr17 | 77213398 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:77194880
|
C | T | 3 | a0001c0002a0006c0013a0009c0012 | 129 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
synonymous_variant | LOW | c.678C>T | p.Ser226Ser | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/17 | 952/5500 | 678/2148 | 226/715 | chr17 | 77194880 | ||
| chr17:77196230
|
A | G | 2 | a0001c0005a0008c0011 | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
synonymous_variant | LOW | c.738A>G | p.Arg246Arg | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/17 | 1012/5500 | 738/2148 | 246/715 | chr17 | 77196230 | ||
| chr17:77206305
|
C | A | 1 | a0001c0003 | 30 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(27): Show |
synonymous_variant | LOW | c.1246C>A | p.Arg416Arg | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/17 | 1520/5500 | 1246/2148 | 416/715 | chr17 | 77206305 | ||
| chr17:77213972
|
C | T | 2 | a0001c0009a0004c0006 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
synonymous_variant | LOW | c.2097C>T | p.Ala699Ala | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2371/5500 | 2097/2148 | 699/715 | chr17 | 77213972 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:77140982
|
C | T | 1 | a0001c0001t0076 | 1 | HG02015.hp1 | 5_prime_UTR_variant | MODIFIER | c.-261C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/17 | 2615 | chr17 | 77140982 | |||||
| chr17:77140995
|
A | G | 1 | a0001c0002t0075 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-248A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/17 | 2602 | chr17 | 77140995 | |||||
| chr17:77141074
|
C | G | 1 | a0001c0001t0074 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-169C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/17 | 2523 | chr17 | 77141074 | |||||
| chr17:77214030
|
G | A | 1 | a0001c0005t0037 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 7 | chr17 | 77214030 | |||||
| chr17:77214094
|
C | T | 1 | a0001c0002t0073 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 71 | chr17 | 77214094 | |||||
| chr17:77214140
|
A | G | 2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*117A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 117 | chr17 | 77214140 | |||||
| chr17:77214358
|
G | A | 1 | a0001c0003t0038 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*335G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 335 | chr17 | 77214358 | |||||
| chr17:77214360
|
A | G | 2 | a0001c0002t0021a0001c0002t0072 | 4 | HG00673.hp2 NA18939.hp2 NA18949.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*337A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 337 | chr17 | 77214360 | |||||
| chr17:77214461
|
C | T | 6 | a0001c0005t0015a0001c0005t0036a0001c0005t0037others(3): Show | 10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*438C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 438 | chr17 | 77214461 | |||||
| chr17:77214492
|
A | C | 14 | a0001c0001t0001a0001c0001t0006a0001c0001t0033others(11): Show | 103 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*469A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 469 | chr17 | 77214492 | |||||
| chr17:77214571
|
C | T | 1 | a0001c0001t0071 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*548C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 548 | chr17 | 77214571 | |||||
| chr17:77214936
|
A | G | 1 | a0001c0002t0066 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*913A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 913 | chr17 | 77214936 | |||||
| chr17:77214945
|
T | G | 1 | a0001c0001t0039 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*922T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 922 | chr17 | 77214945 | |||||
| chr17:77215018
|
T | G | 1 | a0001c0002t0040 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*995T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 995 | chr17 | 77215018 | |||||
| chr17:77215062
|
CGTGT | C | 12 | a0001c0001t0001a0001c0001t0033a0001c0001t0035others(9): Show | 68 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1049_*1052delTGTG | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1049 | INFO_REALIGN_3_PRIME | chr17 | 77215062 | ||||
| chr17:77215066
|
T | C | 1 | a0001c0001t0016 | 3 | HG02523.hp2 NA18982.hp2 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1043T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1043 | chr17 | 77215066 | |||||
| chr17:77215126
|
C | T | 3 | a0001c0001t0065a0001c0009t0022a0004c0006t0022 | 4 | HG01934.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1103C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1103 | chr17 | 77215126 | |||||
| chr17:77215202
|
T | C | 1 | a0001c0002t0042 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1179T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1179 | chr17 | 77215202 | |||||
| chr17:77215461
|
C | A | 2 | a0001c0002t0024a0001c0002t0043 | 3 | HG01071.hp1 HG01361.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1438C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1438 | chr17 | 77215461 | |||||
| chr17:77215526
|
G | A | 10 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(7): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1503G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1503 | chr17 | 77215526 | |||||
| chr17:77215714
|
G | A | 1 | a0001c0001t0067 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1691G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1691 | chr17 | 77215714 | |||||
| chr17:77215747
|
T | C | 1 | a0001c0001t0033 | 2 | NA18959.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1724T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1724 | chr17 | 77215747 | |||||
| chr17:77215760
|
CTAGTAGG others(58): Show |
C | 6 | a0001c0001t0059a0001c0005t0015a0001c0005t0036others(3): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1765_*1829delCGTA others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1765 | INFO_REALIGN_3_PRIME | chr17 | 77215760 | ||||
| chr17:77215762
|
AGTAGGTA others(19): Show |
A | 1 | a0001c0001t0033 | 2 | NA18959.hp2 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1750_*1775delCTAG others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1750 | INFO_REALIGN_3_PRIME | chr17 | 77215762 | ||||
| chr17:77215773
|
CTAGTAGG others(71): Show |
C | 1 | a0001c0001t0041 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1789_*1866delCTGG others(74): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1789 | INFO_REALIGN_3_PRIME | chr17 | 77215773 | ||||
| chr17:77215775
|
AGTAGGTA others(6): Show |
A | 1 | a0001c0003t0020 | 3 | HG02738.hp2 HG03927.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1776_*1788delTTCG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1776 | INFO_REALIGN_3_PRIME | chr17 | 77215775 | ||||
| chr17:77215786
|
T | C | 9 | a0001c0001t0001a0001c0001t0035a0001c0001t0067others(6): Show | 62 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*1763T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1763 | chr17 | 77215786 | |||||
| chr17:77215786
|
TTCGTAGG others(45): Show |
T | 1 | a0001c0001t0032 | 2 | HG00639.hp2 HG02559.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1765_*1816delCGTA others(48): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1765 | INFO_REALIGN_3_PRIME | chr17 | 77215786 | ||||
| chr17:77215788
|
C | A | 67 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(64): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*1765C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1765 | chr17 | 77215788 | |||||
| chr17:77215788
|
CGTAGGTA others(58): Show |
C | 1 | a0001c0001t0009 | 7 | HG01255.hp1 HG01884.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1789_*1853delCTGG others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1789 | INFO_REALIGN_3_PRIME | chr17 | 77215788 | ||||
| chr17:77215801
|
CGTAGGTA others(523): Show |
C | 3 | a0001c0001t0006a0001c0001t0063a0001c0002t0006 | 37 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1789_*2318del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1789 | INFO_REALIGN_3_PRIME | chr17 | 77215801 | ||||
| chr17:77215801
|
CGTAGGTA others(536): Show |
C | 1 | a0001c0001t0069 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1791_*2333del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1791 | INFO_REALIGN_3_PRIME | chr17 | 77215801 | ||||
| chr17:77215805
|
G | T | 1 | a0001c0001t0061 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1782G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1782 | chr17 | 77215805 | |||||
| chr17:77215812
|
C | T | 3 | a0001c0001t0019a0001c0001t0064a0001c0001t0070 | 5 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1789C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1789 | chr17 | 77215812 | |||||
| chr17:77215814
|
G | C | 3 | a0001c0001t0019a0001c0001t0064a0001c0001t0070 | 5 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1791G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1791 | chr17 | 77215814 | |||||
| chr17:77215825
|
T | C | 10 | a0001c0001t0003a0001c0001t0007a0001c0001t0017others(7): Show | 77 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1802T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1802 | chr17 | 77215825 | |||||
| chr17:77215825
|
TTAGTAGG others(536): Show |
T | 1 | a0001c0001t0070 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1828_*2370del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1828 | INFO_REALIGN_3_PRIME | chr17 | 77215825 | ||||
| chr17:77215827
|
A | AGTAGGTA others(58): Show |
9 | a0001c0001t0002a0001c0001t0016a0001c0001t0030others(6): Show | 58 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1869_*1933dupCGTA others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1934 | INFO_REALIGN_3_PRIME | chr17 | 77215827 | ||||
| chr17:77215827
|
A | C | 2 | a0001c0001t0019a0001c0001t0064 | 4 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1804A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1804 | chr17 | 77215827 | |||||
| chr17:77215827
|
AGTAGGTA others(32): Show |
A | 1 | a0001c0001t0010 | 6 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1815_*1853delCTAG others(35): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1815 | INFO_REALIGN_3_PRIME | chr17 | 77215827 | ||||
| chr17:77215853
|
A | C | 14 | a0001c0001t0003a0001c0001t0007a0001c0001t0017others(11): Show | 85 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*1830A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1830 | chr17 | 77215853 | |||||
| chr17:77215890
|
TTCGTAGG others(71): Show |
T | 1 | a0001c0001t0019 | 3 | HG02109.hp2 HG02965.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1869_*1946delCGTA others(74): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1869 | INFO_REALIGN_3_PRIME | chr17 | 77215890 | ||||
| chr17:77215892
|
CGTAGGTA others(6): Show |
C | 1 | a0001c0001t0035 | 2 | HG01256.hp2 HG01258.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1880_*1892delCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1880 | INFO_REALIGN_3_PRIME | chr17 | 77215892 | ||||
| chr17:77215902
|
GCTA | G | 1 | a0001c0001t0010 | 6 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1880_*1882delCTA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1880 | chr17 | 77215902 | |||||
| chr17:77215903
|
C | CTAGTAGG others(6): Show |
2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1895_*1907dupAGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1908 | INFO_REALIGN_3_PRIME | chr17 | 77215903 | ||||
| chr17:77215903
|
C | T | 1 | a0001c0001t0064 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1880C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1880 | chr17 | 77215903 | |||||
| chr17:77215903
|
CTAGTAGG others(6): Show |
C | 1 | a0001c0002t0043 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1895_*1907delAGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1895 | INFO_REALIGN_3_PRIME | chr17 | 77215903 | ||||
| chr17:77215905
|
A | C | 1 | a0001c0001t0064 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1882A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1882 | chr17 | 77215905 | |||||
| chr17:77215906
|
G | T | 1 | a0001c0001t0010 | 6 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1883G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1883 | chr17 | 77215906 | |||||
| chr17:77215918
|
A | AGTAGGTA others(58): Show |
1 | a0001c0001t0058 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1933_*1934insCGTA others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1934 | INFO_REALIGN_3_PRIME | chr17 | 77215918 | ||||
| chr17:77215918
|
A | C | 3 | a0001c0001t0009a0001c0001t0032a0001c0001t0041 | 10 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1895A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1895 | chr17 | 77215918 | |||||
| chr17:77215929
|
T | C | 2 | a0001c0001t0010a0001c0001t0064 | 7 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1906T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1906 | chr17 | 77215929 | |||||
| chr17:77215931
|
C | A | 2 | a0001c0001t0010a0001c0001t0064 | 7 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1908C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1908 | chr17 | 77215931 | |||||
| chr17:77215944
|
C | A | 1 | a0001c0001t0064 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1921C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1921 | chr17 | 77215944 | |||||
| chr17:77215955
|
T | TTCGTAGG others(22): Show |
1 | a0001c0001t0056 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1933_*1934insCGTA others(25): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1934 | INFO_REALIGN_3_PRIME | chr17 | 77215955 | ||||
| chr17:77215955
|
TTAGGTAG others(6): Show |
T | 1 | a0001c0001t0041 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1944_*1956delCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1944 | INFO_REALIGN_3_PRIME | chr17 | 77215955 | ||||
| chr17:77215955
|
TTAGGTAG others(136): Show |
T | 3 | a0001c0005t0036a0001c0005t0037a0008c0011t0036 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2061_*2203del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2061 | INFO_REALIGN_3_PRIME | chr17 | 77215955 | ||||
| chr17:77215965
|
T | C | 2 | a0001c0001t0061a0001c0001t0064 | 2 | HG03471.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1942T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1942 | chr17 | 77215965 | |||||
| chr17:77215967
|
C | A | 2 | a0001c0001t0061a0001c0001t0064 | 2 | HG03471.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1944C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1944 | chr17 | 77215967 | |||||
| chr17:77215967
|
CGTAGGTA others(6): Show |
C | 10 | a0001c0001t0001a0001c0001t0033a0001c0001t0035others(7): Show | 65 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1955_*1967delTTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1955 | INFO_REALIGN_3_PRIME | chr17 | 77215967 | ||||
| chr17:77215978
|
T | C | 2 | a0001c0002t0047a0001c0003t0034 | 3 | HG00423.hp2 HG02071.hp2 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1955T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1955 | chr17 | 77215978 | |||||
| chr17:77215980
|
A | C | 1 | a0001c0001t0056 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1957A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1957 | chr17 | 77215980 | |||||
| chr17:77215991
|
C | T | 2 | a0001c0001t0061a0001c0003t0034 | 3 | HG00423.hp2 HG02071.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1968C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1968 | chr17 | 77215991 | |||||
| chr17:77215993
|
A | C | 2 | a0001c0001t0061a0001c0003t0034 | 3 | HG00423.hp2 HG02071.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1970A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1970 | chr17 | 77215993 | |||||
| chr17:77215993
|
AGTAGGTA others(140): Show |
A | 1 | a0001c0005t0015 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1976_*2122del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1976 | INFO_REALIGN_3_PRIME | chr17 | 77215993 | ||||
| chr17:77215994
|
G | T | 1 | a0001c0001t0056 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1971G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1971 | chr17 | 77215994 | |||||
| chr17:77215999
|
T | C | 1 | a0001c0002t0048 | 1 | NA19007.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1976T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1976 | chr17 | 77215999 | |||||
| chr17:77216004
|
T | C | 1 | a0001c0001t0064 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1981T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1981 | chr17 | 77216004 | |||||
| chr17:77216006
|
C | A | 8 | a0001c0001t0009a0001c0001t0019a0001c0001t0041others(5): Show | 17 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1983C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1983 | chr17 | 77216006 | |||||
| chr17:77216008
|
T | TA | 2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1986dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1987 | INFO_REALIGN_3_PRIME | chr17 | 77216008 | ||||
| chr17:77216017
|
T | C | 1 | a0001c0003t0034 | 2 | HG00423.hp2 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1994T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1994 | chr17 | 77216017 | |||||
| chr17:77216019
|
C | A | 3 | a0001c0001t0056a0001c0001t0064a0001c0003t0034 | 4 | HG00423.hp2 HG02004.hp1 HG02071.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1996C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 1996 | chr17 | 77216019 | |||||
| chr17:77216019
|
C | CGTAGGTA others(6): Show |
1 | a0001c0002t0049 | 1 | NA18972.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2007_*2019dupCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2020 | INFO_REALIGN_3_PRIME | chr17 | 77216019 | ||||
| chr17:77216030
|
C | T | 3 | a0001c0001t0061a0001c0001t0064a0001c0003t0034 | 4 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2007C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2007 | chr17 | 77216030 | |||||
| chr17:77216032
|
A | C | 2 | a0001c0001t0061a0001c0003t0034 | 3 | HG00423.hp2 HG02071.hp2 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2009A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2009 | chr17 | 77216032 | |||||
| chr17:77216043
|
T | C | 1 | a0001c0001t0064 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2020T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2020 | chr17 | 77216043 | |||||
| chr17:77216045
|
A | C | 2 | a0001c0001t0056a0001c0003t0034 | 3 | HG00423.hp2 HG02004.hp1 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2022A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2022 | chr17 | 77216045 | |||||
| chr17:77216056
|
C | T | 5 | a0001c0001t0056a0001c0001t0061a0001c0001t0064others(2): Show | 6 | HG02004.hp1 HG03471.hp1 HG03491.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2033C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2033 | chr17 | 77216056 | |||||
| chr17:77216058
|
A | C | 4 | a0001c0001t0056a0001c0001t0064a0001c0009t0022others(1): Show | 5 | HG02004.hp1 HG03471.hp1 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2035A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2035 | chr17 | 77216058 | |||||
| chr17:77216069
|
C | CTAGTAGG others(6): Show |
2 | a0001c0001t0059a0001c0002t0055 | 2 | HG02145.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2059_*2071dupTTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2072 | INFO_REALIGN_3_PRIME | chr17 | 77216069 | ||||
| chr17:77216069
|
C | T | 5 | a0001c0001t0061a0001c0001t0064a0001c0003t0034others(2): Show | 7 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2046C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2046 | chr17 | 77216069 | |||||
| chr17:77216071
|
A | C | 4 | a0001c0001t0061a0001c0001t0064a0001c0009t0022others(1): Show | 5 | HG03471.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2048A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2048 | chr17 | 77216071 | |||||
| chr17:77216082
|
T | C | 2 | a0001c0001t0064a0001c0003t0034 | 3 | HG00423.hp2 HG02071.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2059T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2059 | chr17 | 77216082 | |||||
| chr17:77216084
|
A | AGGTAGGG others(3): Show |
2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2062_*2063insGTAG others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2063 | INFO_REALIGN_3_PRIME | chr17 | 77216084 | ||||
| chr17:77216084
|
A | C | 1 | a0001c0001t0061 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2061A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2061 | chr17 | 77216084 | |||||
| chr17:77216084
|
AGTAGGTA others(19): Show |
A | 4 | a0001c0001t0009a0001c0001t0019a0001c0001t0041others(1): Show | 12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2072_*2097delCTAG others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2072 | INFO_REALIGN_3_PRIME | chr17 | 77216084 | ||||
| chr17:77216095
|
C | T | 3 | a0001c0001t0064a0001c0009t0022a0004c0006t0022 | 4 | HG03471.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2072C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2072 | chr17 | 77216095 | |||||
| chr17:77216108
|
T | C | 5 | a0001c0001t0056a0001c0001t0059a0001c0001t0064others(2): Show | 6 | HG02004.hp1 HG02145.hp1 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2085T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2085 | chr17 | 77216108 | |||||
| chr17:77216110
|
C | A | 7 | a0001c0001t0056a0001c0001t0059a0001c0001t0061others(4): Show | 9 | HG00423.hp2 HG02004.hp1 HG02071.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2087C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2087 | chr17 | 77216110 | |||||
| chr17:77216121
|
T | C | 2 | a0001c0001t0064a0001c0003t0034 | 3 | HG00423.hp2 HG02071.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2098T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2098 | chr17 | 77216121 | |||||
| chr17:77216123
|
A | C | 2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2100A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2100 | chr17 | 77216123 | |||||
| chr17:77216134
|
C | T | 4 | a0001c0001t0064a0001c0003t0034a0001c0009t0022others(1): Show | 6 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2111C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2111 | chr17 | 77216134 | |||||
| chr17:77216136
|
A | C | 4 | a0001c0001t0064a0001c0003t0034a0001c0009t0022others(1): Show | 6 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2113A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2113 | chr17 | 77216136 | |||||
| chr17:77216147
|
T | C | 3 | a0001c0001t0061a0001c0009t0022a0004c0006t0022 | 4 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2124T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2124 | chr17 | 77216147 | |||||
| chr17:77216147
|
TTCGTAGG others(19): Show |
T | 9 | a0001c0001t0001a0001c0001t0033a0001c0001t0035others(6): Show | 63 | HG00140.hp1 HG00408.hp1 HG00642.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*2126_*2151delCGTA others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2126 | INFO_REALIGN_3_PRIME | chr17 | 77216147 | ||||
| chr17:77216149
|
C | A | 5 | a0001c0001t0061a0001c0001t0064a0001c0003t0034others(2): Show | 7 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2126C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2126 | chr17 | 77216149 | |||||
| chr17:77216149
|
C | T | 1 | a0001c0003t0023 | 2 | NA18971.hp1 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2126C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2126 | chr17 | 77216149 | |||||
| chr17:77216149
|
CGTAGGTA others(19): Show |
C | 1 | a0001c0001t0039 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2139_*2164delCGTA others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2139 | INFO_REALIGN_3_PRIME | chr17 | 77216149 | ||||
| chr17:77216150
|
G | A | 1 | a0001c0001t0059 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2127G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2127 | chr17 | 77216150 | |||||
| chr17:77216160
|
T | C | 3 | a0001c0001t0061a0001c0001t0064a0001c0003t0034 | 4 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2137T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2137 | chr17 | 77216160 | |||||
| chr17:77216160
|
TTCGTAGG others(32): Show |
T | 11 | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(8): Show | 96 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*2139_*2177delCGTA others(35): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2139 | INFO_REALIGN_3_PRIME | chr17 | 77216160 | ||||
| chr17:77216162
|
C | A | 11 | a0001c0001t0017a0001c0001t0026a0001c0001t0044others(8): Show | 16 | HG00423.hp2 HG02004.hp1 HG02071.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2139C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2139 | chr17 | 77216162 | |||||
| chr17:77216173
|
C | T | 3 | a0001c0001t0061a0001c0001t0064a0001c0003t0034 | 4 | HG00423.hp2 HG02071.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2150C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2150 | chr17 | 77216173 | |||||
| chr17:77216175
|
A | AGTAGGTA others(6): Show |
1 | a0001c0001t0056 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2164_*2165insCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2165 | INFO_REALIGN_3_PRIME | chr17 | 77216175 | ||||
| chr17:77216175
|
A | C | 2 | a0001c0001t0061a0001c0001t0064 | 2 | HG03471.hp1 NA18979.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2152A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2152 | chr17 | 77216175 | |||||
| chr17:77216175
|
A | T | 10 | a0001c0001t0001a0001c0001t0033a0001c0001t0035others(7): Show | 65 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2152A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2152 | chr17 | 77216175 | |||||
| chr17:77216175
|
AGTAGGTA others(36): Show |
A | 1 | a0001c0001t0044 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2158_*2200delTAGG others(39): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2158 | INFO_REALIGN_3_PRIME | chr17 | 77216175 | ||||
| chr17:77216175
|
AGTAGGTA others(45): Show |
A | 2 | a0001c0001t0017a0001c0001t0045 | 4 | HG02258.hp2 HG02896.hp2 HG03195.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2165_*2216delAGTA others(48): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2165 | INFO_REALIGN_3_PRIME | chr17 | 77216175 | ||||
| chr17:77216175
|
AGTAGGTA others(58): Show |
A | 2 | a0001c0001t0026a0003c0007t0007 | 3 | HG02273.hp2 HG03710.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2165_*2229delAGTA others(61): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2165 | INFO_REALIGN_3_PRIME | chr17 | 77216175 | ||||
| chr17:77216186
|
T | C | 2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2163T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2163 | chr17 | 77216186 | |||||
| chr17:77216186
|
T | TTAGTAGG others(6): Show |
1 | a0002c0004t0062 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2189_*2201dupCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2202 | INFO_REALIGN_3_PRIME | chr17 | 77216186 | ||||
| chr17:77216186
|
TTAGTAGG others(6): Show |
T | 10 | a0001c0001t0001a0001c0001t0033a0001c0001t0035others(7): Show | 65 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2189_*2201delCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2189 | INFO_REALIGN_3_PRIME | chr17 | 77216186 | ||||
| chr17:77216186
|
TTAGTAGG others(110): Show |
T | 1 | a0001c0002t0051 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2204_*2320del | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2204 | INFO_REALIGN_3_PRIME | chr17 | 77216186 | ||||
| chr17:77216188
|
A | C | 1 | a0001c0001t0056 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2165 | chr17 | 77216188 | |||||
| chr17:77216199
|
C | T | 2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2176C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2176 | chr17 | 77216199 | |||||
| chr17:77216212
|
C | A | 1 | a0001c0002t0040 | 1 | HG00597.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2189C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2189 | chr17 | 77216212 | |||||
| chr17:77216212
|
C | T | 3 | a0001c0001t0039a0001c0001t0061a0001c0001t0064 | 3 | HG03471.hp1 NA18979.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2189C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2189 | chr17 | 77216212 | |||||
| chr17:77216214
|
A | C | 2 | a0001c0001t0039a0001c0001t0061 | 2 | NA18979.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2191A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2191 | chr17 | 77216214 | |||||
| chr17:77216214
|
AGTAGGTA others(6): Show |
A | 1 | a0001c0002t0047 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2243_*2255delCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2243 | INFO_REALIGN_3_PRIME | chr17 | 77216214 | ||||
| chr17:77216219
|
G | A | 2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2196G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2196 | chr17 | 77216219 | |||||
| chr17:77216238
|
T | C | 2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2215T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2215 | chr17 | 77216238 | |||||
| chr17:77216240
|
C | A | 3 | a0001c0001t0039a0001c0009t0022a0004c0006t0022 | 4 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2217C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2217 | chr17 | 77216240 | |||||
| chr17:77216240
|
C | CGTAGGTA others(32): Show |
1 | a0001c0001t0061 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2227_*2228insCTAG others(35): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2228 | INFO_REALIGN_3_PRIME | chr17 | 77216240 | ||||
| chr17:77216242
|
T | C | 1 | a0001c0001t0039 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2219T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2219 | chr17 | 77216242 | |||||
| chr17:77216253
|
C | A | 56 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(53): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
3_prime_UTR_variant | MODIFIER | c.*2230C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2230 | chr17 | 77216253 | |||||
| chr17:77216255
|
T | C | 2 | a0001c0001t0008a0001c0001t0050 | 17 | HG02698.hp1 HG03831.hp2 HG03927.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2232T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2232 | chr17 | 77216255 | |||||
| chr17:77216266
|
C | A | 4 | a0001c0001t0039a0001c0001t0045a0001c0009t0022others(1): Show | 5 | HG02896.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2243C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2243 | chr17 | 77216266 | |||||
| chr17:77216266
|
C | CGTAGGTA others(6): Show |
1 | a0001c0002t0053 | 1 | HG00558.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2256_*2268dupAGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2269 | INFO_REALIGN_3_PRIME | chr17 | 77216266 | ||||
| chr17:77216266
|
CGTAGGTA others(6): Show |
C | 1 | a0001c0002t0018 | 3 | NA18960.hp2 NA18963.hp2 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2256_*2268delAGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2256 | INFO_REALIGN_3_PRIME | chr17 | 77216266 | ||||
| chr17:77216277
|
T | C | 2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2254T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2254 | chr17 | 77216277 | |||||
| chr17:77216279
|
A | C | 5 | a0001c0001t0039a0001c0002t0011a0001c0002t0021others(2): Show | 12 | HG00438.hp1 HG00597.hp1 HG00673.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2256A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2256 | chr17 | 77216279 | |||||
| chr17:77216281
|
T | C | 1 | a0001c0001t0026 | 2 | HG02273.hp2 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2258T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2258 | chr17 | 77216281 | |||||
| chr17:77216290
|
T | C | 1 | a0001c0001t0039 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2267T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2267 | chr17 | 77216290 | |||||
| chr17:77216292
|
C | A | 2 | a0001c0001t0039a0001c0001t0045 | 2 | HG02896.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2269C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2269 | chr17 | 77216292 | |||||
| chr17:77216292
|
CGTAGGTA others(6): Show |
C | 9 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(6): Show | 78 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2306_*2318delCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2306 | INFO_REALIGN_3_PRIME | chr17 | 77216292 | ||||
| chr17:77216303
|
C | T | 7 | a0001c0001t0026a0001c0001t0045a0001c0001t0061others(4): Show | 9 | HG01361.hp2 HG02273.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2280C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2280 | chr17 | 77216303 | |||||
| chr17:77216305
|
A | C | 4 | a0001c0001t0045a0001c0002t0043a0001c0009t0022others(1): Show | 5 | HG01361.hp2 HG02896.hp2 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2282A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2282 | chr17 | 77216305 | |||||
| chr17:77216312
|
A | C | 1 | a0001c0001t0057 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2289A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2289 | chr17 | 77216312 | |||||
| chr17:77216316
|
C | T | 5 | a0001c0001t0026a0001c0001t0061a0001c0009t0022others(2): Show | 7 | HG02273.hp2 HG03491.hp1 HG03492.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2293C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2293 | chr17 | 77216316 | |||||
| chr17:77216318
|
A | C | 2 | a0001c0001t0026a0003c0007t0007 | 3 | HG02273.hp2 HG03710.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2295A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2295 | chr17 | 77216318 | |||||
| chr17:77216329
|
C | T | 2 | a0001c0009t0022a0004c0006t0022 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2306C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2306 | chr17 | 77216329 | |||||
| chr17:77216329
|
CTAGTAGG others(6): Show |
C | 1 | a0001c0002t0073 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2319_*2331delTTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2319 | INFO_REALIGN_3_PRIME | chr17 | 77216329 | ||||
| chr17:77216331
|
AGTAGGTA others(71): Show |
A | 1 | a0001c0002t0029 | 2 | NA18982.hp1 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2321_*2398delAGTA others(74): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2321 | INFO_REALIGN_3_PRIME | chr17 | 77216331 | ||||
| chr17:77216342
|
T | C | 4 | a0001c0001t0061a0001c0001t0068a0001c0002t0027others(1): Show | 5 | HG01346.hp1 HG01433.hp2 HG03704.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2319T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2319 | chr17 | 77216342 | |||||
| chr17:77216342
|
TTAGTAGG others(6): Show |
T | 5 | a0001c0001t0008a0001c0001t0031a0001c0001t0050others(2): Show | 11 | HG00558.hp2 HG02074.hp1 HG02615.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2371_*2383delCTAG others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2371 | INFO_REALIGN_3_PRIME | chr17 | 77216342 | ||||
| chr17:77216344
|
A | C | 8 | a0001c0001t0006a0001c0001t0008a0001c0001t0026others(5): Show | 58 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2321A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2321 | chr17 | 77216344 | |||||
| chr17:77216355
|
C | T | 8 | a0001c0001t0006a0001c0001t0008a0001c0001t0026others(5): Show | 57 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2332C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2332 | chr17 | 77216355 | |||||
| chr17:77216357
|
A | C | 8 | a0001c0001t0006a0001c0001t0008a0001c0001t0026others(5): Show | 58 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2334A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2334 | chr17 | 77216357 | |||||
| chr17:77216368
|
C | T | 4 | a0001c0001t0008a0001c0001t0026a0001c0001t0039others(1): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2345C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2345 | chr17 | 77216368 | |||||
| chr17:77216370
|
A | C | 4 | a0001c0001t0008a0001c0001t0026a0001c0001t0050others(1): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2347A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2347 | chr17 | 77216370 | |||||
| chr17:77216381
|
C | T | 4 | a0001c0001t0008a0001c0001t0026a0001c0001t0039others(1): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2358C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2358 | chr17 | 77216381 | |||||
| chr17:77216383
|
A | C | 3 | a0001c0001t0008a0001c0001t0039a0001c0001t0050 | 3 | HG02698.hp1 NA19068.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2360A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2360 | chr17 | 77216383 | |||||
| chr17:77216383
|
AGTAGGTA others(19): Show |
A | 18 | a0001c0001t0001a0001c0001t0009a0001c0001t0019others(15): Show | 85 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*2371_*2396delCTAG others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2371 | INFO_REALIGN_3_PRIME | chr17 | 77216383 | ||||
| chr17:77216393
|
G | T | 11 | a0001c0001t0003a0001c0001t0007a0001c0001t0010others(8): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*2370G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2370 | chr17 | 77216393 | |||||
| chr17:77216394
|
C | T | 4 | a0001c0001t0008a0001c0001t0026a0001c0001t0039others(1): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2371C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2371 | chr17 | 77216394 | |||||
| chr17:77216396
|
A | AGTAGGTA others(6): Show |
2 | a0001c0001t0008a0001c0002t0054 | 2 | HG01928.hp1 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2412_*2424dupCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2425 | INFO_REALIGN_3_PRIME | chr17 | 77216396 | ||||
| chr17:77216396
|
A | C | 3 | a0001c0001t0008a0001c0001t0026a0001c0001t0039 | 18 | HG02273.hp2 HG03710.hp2 HG03831.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2373A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2373 | chr17 | 77216396 | |||||
| chr17:77216396
|
AGTAGGTA others(6): Show |
A | 13 | a0001c0001t0006a0001c0001t0007a0001c0001t0017others(10): Show | 67 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2412_*2424delCGTA others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2412 | INFO_REALIGN_3_PRIME | chr17 | 77216396 | ||||
| chr17:77216396
|
AGTAGGTA others(19): Show |
A | 1 | a0001c0001t0025 | 2 | HG00099.hp1 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2399_*2424delCGTA others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2399 | INFO_REALIGN_3_PRIME | chr17 | 77216396 | ||||
| chr17:77216406
|
G | T | 1 | a0003c0007t0007 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2383G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2383 | chr17 | 77216406 | |||||
| chr17:77216407
|
T | C | 1 | a0003c0007t0007 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2384T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2384 | chr17 | 77216407 | |||||
| chr17:77216409
|
C | A | 1 | a0003c0007t0007 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2386C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2386 | chr17 | 77216409 | |||||
| chr17:77216890
|
G | A | 1 | a0001c0001t0030 | 2 | NA18945.hp2 NA19055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2867G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 2867 | chr17 | 77216890 | |||||
| chr17:77217072
|
C | T | 1 | a0001c0002t0072 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3049C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 17/17 | 3049 | chr17 | 77217072 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:77141199
|
C | G | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+92C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141199 | ||||||
| chr17:77141227
|
C | T | 1 | a0001c0001t0025g0392 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-136+120C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141227 | ||||||
| chr17:77141234
|
C | G | 1 | a0001c0001t0006g0391 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-136+127C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141234 | ||||||
| chr17:77141238
|
C | G | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-136+131C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141238 | ||||||
| chr17:77141259
|
A | G | 1 | a0001c0001t0006g0389 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-136+152A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141259 | ||||||
| chr17:77141333
|
C | A | 3 | a0001c0005t0036g0017a0001c0005t0037g0016a0008c0011t0036g0018 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.-136+226C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141333 | ||||||
| chr17:77141336
|
T | TC | 18 | a0001c0001t0001g0031a0001c0001t0002g0020a0001c0001t0002g0022others(15): Show | 18 | HG01109.hp1 HG01261.hp2 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.-136+234dupC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77141336 | |||||
| chr17:77141369
|
C | T | 116 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(113): Show | 119 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.-136+262C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141369 | ||||||
| chr17:77141496
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-136+389C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141496 | ||||||
| chr17:77141534
|
C | T | 1 | a0001c0003t0001g0282 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-136+427C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141534 | ||||||
| chr17:77141560
|
C | T | 61 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(58): Show | 63 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.-136+453C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141560 | ||||||
| chr17:77141569
|
C | T | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.-136+462C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141569 | ||||||
| chr17:77141596
|
C | T | 1 | a0001c0001t0006g0227 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-136+489C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141596 | ||||||
| chr17:77141722
|
G | A | 10 | a0001c0002t0005g0032a0001c0002t0005g0033a0001c0002t0005g0284others(7): Show | 10 | HG02129.hp2 HG02132.hp2 NA18967.hp2 others(7): Show |
intron_variant | MODIFIER | c.-136+615G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141722 | ||||||
| chr17:77141738
|
C | G | 1 | a0001c0001t0003g0226 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-136+631C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141738 | ||||||
| chr17:77141800
|
G | A | 13 | a0001c0001t0005g0039a0001c0001t0007g0019a0001c0001t0007g0037others(10): Show | 13 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.-136+693G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141800 | ||||||
| chr17:77141812
|
A | C | 156 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(153): Show | 162 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.-136+705A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141812 | ||||||
| chr17:77141873
|
C | T | 1 | a0001c0002t0004g0193 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-136+766C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77141873 | ||||||
| chr17:77142060
|
A | C | 1 | a0001c0001t0074g0192 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-135-586A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142060 | ||||||
| chr17:77142296
|
C | T | 1 | a0001c0001t0025g0392 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-135-350C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142296 | ||||||
| chr17:77142300
|
C | T | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.-135-346C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142300 | ||||||
| chr17:77142324
|
T | A | 1 | a0001c0003t0001g0282 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-135-322T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142324 | ||||||
| chr17:77142557
|
C | CA | 65 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(62): Show | 67 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-135-68dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | |||||
| chr17:77142557
|
C | CAA | 12 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.-135-69_-135-68dup others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | |||||
| chr17:77142557
|
CA | C | 50 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(47): Show | 50 | HG00408.hp1 HG01074.hp1 HG01258.hp1 others(47): Show |
intron_variant | MODIFIER | c.-135-68delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | |||||
| chr17:77142557
|
CAA | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0237a0001c0001t0001g0238others(42): Show | 47 | HG00423.hp2 HG00642.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.-135-69_-135-68del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | |||||
| chr17:77142557
|
CAAA | C | 10 | a0001c0001t0001g0031a0001c0001t0001g0273a0001c0001t0001g0274others(7): Show | 10 | NA18952.hp2 NA18957.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.-135-70_-135-68del others(3): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142557 | |||||
| chr17:77142630
|
CT | C | 23 | a0001c0001t0006g0196a0001c0001t0008g0393a0001c0001t0008g0397others(20): Show | 23 | HG01943.hp1 HG02273.hp2 HG02698.hp1 others(20): Show |
splice_region_variant&intron_variant | LOW | c.-135-6delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr17 | 77142630 | |||||
| chr17:77142632
|
T | C | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.-135-14T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142632 | ||||||
| chr17:77142634
|
T | C | 1 | a0001c0001t0002g0048 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-135-12T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142634 | ||||||
| chr17:77142641
|
A | C | 1 | a0001c0001t0003g0183 | 1 | HG02818.hp2 | splice_region_variant&intron_variant | LOW | c.-135-5A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 1/16 | chr17 | 77142641 | ||||||
| chr17:77142870
|
A | G | 4 | a0001c0003t0001g0188a0001c0009t0022g0191a0004c0006t0022g0189others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+120A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77142870 | ||||||
| chr17:77142918
|
C | A | 2 | a0001c0001t0009g0051a0001c0001t0009g0052 | 2 | HG01255.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-31+168C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77142918 | ||||||
| chr17:77143037
|
T | C | 1 | a0001c0001t0003g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-31+287T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143037 | ||||||
| chr17:77143104
|
A | G | 1 | a0001c0001t0007g0047 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-31+354A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143104 | ||||||
| chr17:77143104
|
AT | A | 118 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(115): Show | 121 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.-31+361delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr17 | 77143104 | |||||
| chr17:77143248
|
G | C | 1 | a0001c0001t0010g0114 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-30-319G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143248 | ||||||
| chr17:77143347
|
C | T | 1 | a0001c0001t0003g0110 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-30-220C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143347 | ||||||
| chr17:77143423
|
A | C | 1 | a0001c0002t0073g0372 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-30-144A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143423 | ||||||
| chr17:77143531
|
T | C | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-30-36T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 2/16 | chr17 | 77143531 | ||||||
| chr17:77143757
|
C | T | 1 | a0001c0001t0006g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.63+98C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143757 | ||||||
| chr17:77143881
|
G | T | 1 | a0001c0001t0006g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.63+222G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143881 | ||||||
| chr17:77143915
|
C | T | 1 | a0001c0003t0001g0272 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.63+256C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143915 | ||||||
| chr17:77143942
|
C | G | 2 | a0002c0004t0046g0186a0002c0004t0060g0187 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.63+283C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143942 | ||||||
| chr17:77143948
|
G | T | 3 | a0001c0002t0004g0180a0001c0002t0004g0181a0001c0002t0004g0182 | 3 | NA18612.hp2 NA18978.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.63+289G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77143948 | ||||||
| chr17:77143956
|
CT | C | 87 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(84): Show | 89 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.63+304delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77143956 | |||||
| chr17:77144206
|
C | T | 1 | a0001c0001t0002g0105 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.63+547C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144206 | ||||||
| chr17:77144229
|
T | C | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.63+570T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144229 | ||||||
| chr17:77144241
|
T | A | 2 | a0001c0002t0005g0295a0001c0002t0005g0374 | 2 | NA18949.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.63+582T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144241 | ||||||
| chr17:77144325
|
C | T | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+666C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144325 | ||||||
| chr17:77144344
|
A | G | 1 | a0001c0002t0005g0371 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.63+685A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144344 | ||||||
| chr17:77144416
|
G | C | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+757G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144416 | ||||||
| chr17:77144827
|
G | A | 1 | a0001c0002t0028g0296 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.63+1168G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77144827 | ||||||
| chr17:77145002
|
C | T | 1 | a0001c0001t0002g0104 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.63+1343C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145002 | ||||||
| chr17:77145012
|
A | G | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+1353A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145012 | ||||||
| chr17:77145063
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+1404C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145063 | ||||||
| chr17:77145077
|
TTGTGTGT others(15): Show |
T | 91 | a0001c0002t0004g0002a0001c0002t0004g0013a0001c0002t0004g0014others(88): Show | 93 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.63+1436_63+1457del others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145077 | |||||
| chr17:77145077
|
TTGTGTGT others(17): Show |
T | 4 | a0001c0002t0004g0299a0001c0002t0005g0286a0001c0002t0005g0287others(1): Show | 4 | HG01928.hp1 HG02129.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1436_63+1459del others(24): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145077 | |||||
| chr17:77145077
|
TTGTGTGT others(21): Show |
T | 1 | a0001c0002t0005g0298 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.63+1436_63+1463del others(28): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145077 | |||||
| chr17:77145079
|
GTGTGTGT others(13): Show |
G | 21 | a0001c0002t0004g0036a0001c0002t0004g0193a0001c0002t0004g0369others(18): Show | 22 | HG00438.hp1 HG00597.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.63+1436_63+1455del others(20): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145079 | |||||
| chr17:77145081
|
GTGTGTGT others(11): Show |
G | 1 | a0001c0002t0004g0370 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.63+1436_63+1453del others(18): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145081 | |||||
| chr17:77145095
|
A | ATG | 4 | a0001c0003t0001g0188a0001c0003t0001g0268a0001c0003t0023g0030others(1): Show | 4 | HG03239.hp2 NA18941.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1438_63+1439dup others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145095 | |||||
| chr17:77145095
|
A | ATGTG | 6 | a0001c0003t0001g0233a0001c0003t0001g0234a0001c0003t0001g0269others(3): Show | 6 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.63+1439_63+1440ins others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145095 | |||||
| chr17:77145099
|
A | ATG | 11 | a0001c0001t0001g0031a0001c0001t0001g0229a0001c0001t0001g0238others(8): Show | 11 | HG01070.hp2 HG01106.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+1476_63+1477dup others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | |||||
| chr17:77145099
|
A | ATGTG | 28 | a0001c0001t0001g0012a0001c0001t0001g0230a0001c0001t0001g0231others(25): Show | 30 | HG00423.hp2 HG00642.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.63+1474_63+1477dup others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | |||||
| chr17:77145099
|
A | ATGTGTG | 10 | a0001c0001t0001g0258a0001c0001t0001g0263a0001c0003t0001g0179others(7): Show | 10 | HG00140.hp1 HG02155.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+1472_63+1477dup others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | |||||
| chr17:77145099
|
A | ATGTGTGT others(1): Show |
3 | a0001c0003t0001g0265a0001c0003t0001g0266a0001c0003t0020g0264 | 3 | HG04115.hp1 NA18960.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.63+1470_63+1477dup others(8): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | |||||
| chr17:77145099
|
A | G | 10 | a0001c0003t0001g0188a0001c0003t0001g0233a0001c0003t0001g0234others(7): Show | 10 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+1440A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145099 | ||||||
| chr17:77145099
|
ATG | A | 15 | a0001c0001t0006g0196a0001c0001t0006g0224a0001c0001t0006g0225others(12): Show | 16 | HG01255.hp1 HG01884.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.63+1476_63+1477del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | |||||
| chr17:77145099
|
ATGTG | A | 11 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0006g0391others(8): Show | 12 | HG02109.hp2 HG02145.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+1474_63+1477del others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | |||||
| chr17:77145099
|
ATGTGTG | A | 103 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(100): Show | 106 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.63+1472_63+1477del others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145099 | |||||
| chr17:77145125
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0002g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.63+1468_63+1479del others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145125 | |||||
| chr17:77145127
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0002g0058 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.63+1470_63+1479del others(10): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145127 | |||||
| chr17:77145129
|
GTGTGTGT others(1): Show |
G | 52 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(49): Show | 54 | HG00558.hp2 HG00673.hp1 HG01943.hp2 others(51): Show |
intron_variant | MODIFIER | c.63+1472_63+1479del others(8): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145129 | |||||
| chr17:77145131
|
G | A | 1 | a0001c0001t0006g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.63+1472G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145131 | ||||||
| chr17:77145131
|
GTGTGTA | G | 4 | a0001c0001t0002g0099a0001c0001t0002g0100a0001c0001t0002g0101others(1): Show | 4 | HG00544.hp2 NA18967.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+1474_63+1479del others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145131 | |||||
| chr17:77145133
|
G | A | 41 | a0001c0001t0001g0211a0001c0001t0003g0115a0001c0001t0003g0226others(38): Show | 46 | HG00597.hp2 HG00639.hp2 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.63+1474G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145133 | ||||||
| chr17:77145135
|
G | A | 248 | a0001c0001t0001g0211a0001c0001t0003g0007a0001c0001t0003g0021others(245): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.63+1476G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145135 | ||||||
| chr17:77145137
|
A | G | 3 | a0001c0001t0001g0012a0001c0001t0001g0240a0001c0001t0001g0256 | 4 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1478A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145137 | ||||||
| chr17:77145153
|
ATTTGT | A | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+1508_63+1512del others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77145153 | |||||
| chr17:77145239
|
C | T | 1 | a0007c0010t0002g0194 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+1580C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145239 | ||||||
| chr17:77145322
|
G | T | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+1663G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145322 | ||||||
| chr17:77145561
|
T | C | 37 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(34): Show | 40 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.63+1902T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145561 | ||||||
| chr17:77145596
|
C | T | 2 | a0001c0001t0003g0165a0001c0001t0003g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.63+1937C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145596 | ||||||
| chr17:77145723
|
G | A | 1 | a0001c0002t0066g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+2064G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145723 | ||||||
| chr17:77145828
|
G | T | 35 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+2169G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145828 | ||||||
| chr17:77145831
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0256 | 3 | HG00642.hp2 HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.63+2172G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145831 | ||||||
| chr17:77145832
|
G | T | 1 | a0001c0001t0041g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.63+2173G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145832 | ||||||
| chr17:77145869
|
C | T | 2 | a0001c0001t0002g0097a0001c0001t0002g0098 | 2 | NA18944.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.63+2210C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77145869 | ||||||
| chr17:77146022
|
A | C | 1 | a0001c0002t0052g0357 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.63+2363A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146022 | ||||||
| chr17:77146039
|
C | T | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+2380C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146039 | ||||||
| chr17:77146237
|
G | C | 1 | a0001c0001t0003g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.63+2578G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146237 | ||||||
| chr17:77146278
|
G | A | 8 | a0001c0001t0003g0118a0001c0001t0003g0119a0001c0001t0003g0123others(5): Show | 9 | HG00642.hp1 HG00738.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+2619G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146278 | ||||||
| chr17:77146713
|
A | C | 1 | a0001c0002t0073g0372 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.63+3054A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146713 | ||||||
| chr17:77146713
|
A | G | 11 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(8): Show | 12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+3054A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146713 | ||||||
| chr17:77146728
|
A | G | 409 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(406): Show | 424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.63+3069A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146728 | ||||||
| chr17:77146734
|
G | A | 1 | a0001c0001t0002g0059 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.63+3075G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146734 | ||||||
| chr17:77146993
|
A | G | 2 | a0002c0004t0046g0186a0002c0004t0060g0187 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.63+3334A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146993 | ||||||
| chr17:77146999
|
G | A | 1 | a0001c0003t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.63+3340G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77146999 | ||||||
| chr17:77147050
|
C | T | 61 | a0001c0002t0004g0002a0001c0002t0004g0013a0001c0002t0004g0014others(58): Show | 64 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.63+3391C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147050 | ||||||
| chr17:77147079
|
C | T | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+3420C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147079 | ||||||
| chr17:77147139
|
A | G | 11 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(8): Show | 12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+3480A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147139 | ||||||
| chr17:77147230
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+3571G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147230 | ||||||
| chr17:77147279
|
C | T | 1 | a0001c0001t0002g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.63+3620C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147279 | ||||||
| chr17:77147312
|
T | C | 4 | a0001c0003t0001g0188a0001c0009t0022g0191a0004c0006t0022g0189others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+3653T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147312 | ||||||
| chr17:77147373
|
T | TA | 48 | a0001c0001t0003g0106a0001c0001t0003g0124a0001c0001t0003g0125others(45): Show | 48 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.63+3724dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77147373 | |||||
| chr17:77147538
|
G | A | 12 | a0001c0002t0004g0034a0001c0002t0004g0035a0001c0002t0004g0332others(9): Show | 12 | HG00558.hp1 HG00639.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+3879G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147538 | ||||||
| chr17:77147601
|
G | T | 1 | a0001c0001t0007g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+3942G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147601 | ||||||
| chr17:77147680
|
A | C | 2 | a0001c0002t0004g0355a0001c0002t0004g0356 | 2 | NA18969.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.63+4021A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147680 | ||||||
| chr17:77147770
|
G | C | 6 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0128others(3): Show | 6 | HG03491.hp1 HG03492.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+4111G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147770 | ||||||
| chr17:77147949
|
C | G | 5 | a0001c0002t0005g0033a0001c0002t0005g0284a0001c0002t0005g0285others(2): Show | 5 | NA18967.hp2 NA18974.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+4290C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147949 | ||||||
| chr17:77147984
|
C | T | 1 | a0001c0002t0005g0322 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.63+4325C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77147984 | ||||||
| chr17:77148004
|
C | T | 1 | a0001c0001t0008g0411 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.63+4345C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148004 | ||||||
| chr17:77148047
|
G | A | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.63+4388G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148047 | ||||||
| chr17:77148058
|
AGT | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+4402_63+4403del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77148058 | |||||
| chr17:77148065
|
C | G | 1 | a0001c0002t0066g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+4406C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148065 | ||||||
| chr17:77148140
|
A | G | 1 | a0001c0002t0005g0321 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.63+4481A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148140 | ||||||
| chr17:77148190
|
G | C | 1 | a0001c0001t0007g0047 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.63+4531G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148190 | ||||||
| chr17:77148311
|
A | G | 62 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(59): Show | 64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.63+4652A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148311 | ||||||
| chr17:77148522
|
C | T | 119 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(116): Show | 122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+4863C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148522 | ||||||
| chr17:77148676
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+5017G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148676 | ||||||
| chr17:77148753
|
C | T | 62 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(59): Show | 64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.63+5094C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148753 | ||||||
| chr17:77148774
|
C | T | 1 | a0001c0001t0002g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.63+5115C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77148774 | ||||||
| chr17:77149015
|
T | C | 1 | a0001c0001t0016g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.63+5356T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149015 | ||||||
| chr17:77149139
|
C | T | 1 | a0001c0001t0008g0410 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.63+5480C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149139 | ||||||
| chr17:77149163
|
T | G | 1 | a0001c0001t0016g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.63+5504T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149163 | ||||||
| chr17:77149216
|
T | A | 1 | a0001c0001t0016g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.63+5557T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149216 | ||||||
| chr17:77149610
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.63+5951G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149610 | ||||||
| chr17:77149660
|
C | A | 1 | a0001c0001t0016g0060 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.63+6001C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149660 | ||||||
| chr17:77149856
|
GT | G | 12 | a0001c0001t0001g0230a0001c0001t0001g0258a0001c0001t0003g0130others(9): Show | 12 | HG01167.hp1 HG01168.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+6215delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77149856 | |||||
| chr17:77149864
|
T | G | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+6205T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77149864 | ||||||
| chr17:77150184
|
T | C | 35 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+6525T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150184 | ||||||
| chr17:77150287
|
G | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+6628G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150287 | ||||||
| chr17:77150351
|
G | A | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+6692G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150351 | ||||||
| chr17:77150594
|
AG | A | 5 | a0001c0002t0005g0033a0001c0002t0005g0284a0001c0002t0005g0285others(2): Show | 5 | NA18967.hp2 NA18974.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+6938delG | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77150594 | |||||
| chr17:77150719
|
T | C | 1 | a0001c0002t0066g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+7060T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150719 | ||||||
| chr17:77150808
|
C | T | 5 | a0001c0001t0006g0215a0001c0001t0006g0216a0001c0001t0006g0217others(2): Show | 5 | HG02300.hp2 NA19000.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+7149C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150808 | ||||||
| chr17:77150827
|
C | G | 69 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(66): Show | 72 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.63+7168C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77150827 | ||||||
| chr17:77151159
|
C | T | 2 | a0001c0003t0001g0235a0001c0003t0001g0236 | 2 | HG02055.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.63+7500C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151159 | ||||||
| chr17:77151238
|
C | CAATCAGT others(3): Show |
1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+7581_63+7590dup others(10): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77151238 | |||||
| chr17:77151242
|
C | G | 1 | a0002c0004t0062g0177 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.63+7583C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151242 | ||||||
| chr17:77151264
|
C | T | 1 | a0007c0010t0002g0194 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+7605C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151264 | ||||||
| chr17:77151419
|
G | C | 1 | a0001c0001t0006g0200 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.63+7760G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151419 | ||||||
| chr17:77151572
|
C | T | 1 | a0001c0002t0005g0331 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.63+7913C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151572 | ||||||
| chr17:77151591
|
GT | G | 408 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(405): Show | 423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.63+7937delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77151591 | |||||
| chr17:77151592
|
T | A | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+7933T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151592 | ||||||
| chr17:77151701
|
A | G | 18 | a0001c0001t0002g0005a0001c0001t0002g0020a0001c0001t0002g0082others(15): Show | 19 | HG00558.hp2 HG02015.hp1 HG03831.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+8042A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77151701 | ||||||
| chr17:77152074
|
C | T | 11 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(8): Show | 12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+8415C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152074 | ||||||
| chr17:77152147
|
T | C | 1 | a0001c0002t0054g0375 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.63+8488T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152147 | ||||||
| chr17:77152264
|
G | A | 4 | a0001c0002t0004g0378a0001c0002t0004g0379a0001c0002t0004g0380others(1): Show | 4 | HG03017.hp2 HG03239.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+8605G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152264 | ||||||
| chr17:77152307
|
G | A | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+8648G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152307 | ||||||
| chr17:77152315
|
C | T | 1 | a0001c0001t0045g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.63+8656C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152315 | ||||||
| chr17:77152436
|
T | C | 275 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(272): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.63+8777T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152436 | ||||||
| chr17:77152535
|
CA | C | 367 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(364): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.63+8895delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77152535 | |||||
| chr17:77152535
|
CAA | C | 9 | a0001c0001t0001g0281a0001c0001t0002g0105a0001c0001t0003g0164others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.63+8894_63+8895del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77152535 | |||||
| chr17:77152551
|
A | C | 1 | a0001c0002t0011g0294 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.63+8892A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152551 | ||||||
| chr17:77152659
|
G | A | 68 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(65): Show | 71 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.63+9000G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152659 | ||||||
| chr17:77152731
|
A | G | 36 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.63+9072A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152731 | ||||||
| chr17:77152913
|
C | T | 12 | a0001c0001t0005g0039a0001c0001t0007g0019a0001c0001t0007g0037others(9): Show | 12 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+9254C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152913 | ||||||
| chr17:77152964
|
C | A | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+9305C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77152964 | ||||||
| chr17:77153072
|
T | C | 1 | a0001c0002t0018g0361 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.63+9413T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153072 | ||||||
| chr17:77153199
|
C | T | 2 | a0001c0001t0003g0106a0001c0001t0003g0125 | 2 | NA19000.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.63+9540C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153199 | ||||||
| chr17:77153385
|
T | C | 1 | a0001c0001t0045g0116 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.63+9726T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153385 | ||||||
| chr17:77153420
|
A | G | 1 | a0001c0002t0004g0370 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.63+9761A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153420 | ||||||
| chr17:77153515
|
T | C | 1 | a0001c0002t0066g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+9856T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153515 | ||||||
| chr17:77153741
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.63+10082C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153741 | ||||||
| chr17:77153951
|
C | T | 1 | a0001c0001t0002g0095 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.63+10292C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77153951 | ||||||
| chr17:77154057
|
C | A | 1 | a0001c0002t0004g0333 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.63+10398C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154057 | ||||||
| chr17:77154094
|
A | G | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+10435A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154094 | ||||||
| chr17:77154115
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.63+10456A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154115 | ||||||
| chr17:77154241
|
C | T | 1 | a0001c0002t0053g0339 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.63+10582C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154241 | ||||||
| chr17:77154350
|
C | T | 7 | a0001c0001t0059g0390a0001c0005t0015g0008a0001c0005t0015g0170others(4): Show | 8 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.63+10691C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154350 | ||||||
| chr17:77154369
|
G | A | 87 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(84): Show | 89 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.63+10710G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154369 | ||||||
| chr17:77154405
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+10746G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154405 | ||||||
| chr17:77154475
|
A | G | 13 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0075others(10): Show | 14 | HG01943.hp2 HG02004.hp1 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.63+10816A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154475 | ||||||
| chr17:77154567
|
A | T | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.63+10908A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154567 | ||||||
| chr17:77154601
|
G | A | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.63+10942G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154601 | ||||||
| chr17:77154637
|
G | GT | 203 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(200): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.63+10987dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77154637 | |||||
| chr17:77154637
|
G | T | 2 | a0001c0001t0044g0046a0009c0012t0005g0320 | 2 | NA18959.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.63+10978G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154637 | ||||||
| chr17:77154647
|
G | T | 407 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(404): Show | 422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.63+10988G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154647 | ||||||
| chr17:77154648
|
G | T | 5 | a0001c0001t0006g0391a0001c0009t0022g0191a0004c0006t0022g0189others(2): Show | 5 | HG03491.hp1 HG03492.hp1 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+10989G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154648 | ||||||
| chr17:77154675
|
A | G | 57 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(54): Show | 60 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+11016A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154675 | ||||||
| chr17:77154946
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+11287G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154946 | ||||||
| chr17:77154963
|
C | G | 2 | a0001c0001t0002g0068a0001c0001t0002g0104 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.63+11304C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77154963 | ||||||
| chr17:77155277
|
T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0256 | 3 | HG00642.hp2 HG01099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.63+11618T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155277 | ||||||
| chr17:77155357
|
A | G | 37 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(34): Show | 40 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.63+11698A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155357 | ||||||
| chr17:77155361
|
A | G | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+11702A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155361 | ||||||
| chr17:77155390
|
C | T | 119 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(116): Show | 122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+11731C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155390 | ||||||
| chr17:77155422
|
G | A | 1 | a0001c0003t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.63+11763G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155422 | ||||||
| chr17:77155499
|
C | G | 1 | a0001c0003t0001g0282 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.63+11840C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155499 | ||||||
| chr17:77155504
|
A | T | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+11845A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155504 | ||||||
| chr17:77155635
|
G | T | 268 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(265): Show | 276 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.63+11976G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155635 | ||||||
| chr17:77155719
|
C | T | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+12060C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155719 | ||||||
| chr17:77155766
|
C | T | 3 | a0001c0001t0008g0407a0001c0001t0008g0408a0001c0001t0008g0409 | 3 | NA18970.hp1 NA18990.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.63+12107C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155766 | ||||||
| chr17:77155828
|
C | G | 37 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(34): Show | 40 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.63+12169C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155828 | ||||||
| chr17:77155935
|
T | G | 119 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(116): Show | 122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+12276T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77155935 | ||||||
| chr17:77156116
|
G | A | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.63+12457G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156116 | ||||||
| chr17:77156132
|
A | G | 2 | a0001c0001t0033g0255a0001c0001t0033g0280 | 2 | NA18959.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.63+12473A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156132 | ||||||
| chr17:77156156
|
C | A | 118 | a0001c0002t0004g0002a0001c0002t0004g0013a0001c0002t0004g0014others(115): Show | 121 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.63+12497C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156156 | ||||||
| chr17:77156175
|
C | A | 1 | a0001c0001t0002g0099 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.63+12516C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156175 | ||||||
| chr17:77156180
|
G | T | 1 | a0001c0001t0008g0409 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.63+12521G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156180 | ||||||
| chr17:77156298
|
G | A | 35 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+12639G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156298 | ||||||
| chr17:77156329
|
C | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+12670C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156329 | ||||||
| chr17:77156337
|
A | G | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+12678A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156337 | ||||||
| chr17:77156349
|
C | T | 145 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(142): Show | 149 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.63+12690C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156349 | ||||||
| chr17:77156431
|
T | C | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+12772T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156431 | ||||||
| chr17:77156561
|
C | T | 4 | a0001c0001t0025g0392a0001c0009t0022g0191a0004c0006t0022g0189others(1): Show | 4 | HG00099.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+12902C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156561 | ||||||
| chr17:77156574
|
TA | T | 15 | a0001c0001t0001g0229a0001c0001t0001g0281a0001c0001t0002g0067others(12): Show | 15 | HG01891.hp1 HG02109.hp1 HG03041.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+12931delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77156574 | |||||
| chr17:77156668
|
T | G | 1 | a0001c0002t0004g0182 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.63+13009T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156668 | ||||||
| chr17:77156669
|
G | T | 1 | a0001c0002t0004g0182 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.63+13010G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156669 | ||||||
| chr17:77156851
|
C | T | 1 | a0001c0001t0065g0045 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.63+13192C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156851 | ||||||
| chr17:77156995
|
T | C | 1 | a0001c0001t0069g0195 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.63+13336T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77156995 | ||||||
| chr17:77157118
|
T | C | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+13459T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157118 | ||||||
| chr17:77157169
|
T | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+13510T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157169 | ||||||
| chr17:77157340
|
C | T | 3 | a0001c0001t0003g0130a0001c0001t0003g0163a0001c0001t0003g0169 | 3 | HG01168.hp2 HG01515.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.63+13681C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157340 | ||||||
| chr17:77157389
|
G | A | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+13730G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157389 | ||||||
| chr17:77157530
|
C | CT | 72 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(69): Show | 76 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.63+13886dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77157530 | |||||
| chr17:77157546
|
G | A | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.63+13887G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157546 | ||||||
| chr17:77157559
|
G | A | 2 | a0002c0004t0046g0186a0002c0004t0060g0187 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.63+13900G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157559 | ||||||
| chr17:77157731
|
T | C | 2 | a0001c0001t0002g0005a0001c0001t0002g0105 | 3 | NA18961.hp2 NA18973.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.63+14072T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157731 | ||||||
| chr17:77157762
|
G | A | 62 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(59): Show | 64 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.63+14103G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157762 | ||||||
| chr17:77157767
|
G | C | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+14108G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157767 | ||||||
| chr17:77157812
|
C | T | 1 | a0001c0001t0003g0162 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.63+14153C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157812 | ||||||
| chr17:77157833
|
T | C | 1 | a0001c0001t0025g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.63+14174T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157833 | ||||||
| chr17:77157843
|
G | A | 2 | a0001c0001t0006g0215a0001c0002t0006g0221 | 2 | HG02300.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.63+14184G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157843 | ||||||
| chr17:77157893
|
T | C | 1 | a0001c0002t0005g0300 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.63+14234T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157893 | ||||||
| chr17:77157907
|
C | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0231 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.63+14248C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77157907 | ||||||
| chr17:77158032
|
C | T | 2 | a0001c0002t0024g0318a0001c0002t0024g0319 | 2 | HG01071.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.63+14373C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158032 | ||||||
| chr17:77158056
|
A | G | 3 | a0001c0001t0006g0216a0001c0001t0006g0217a0001c0001t0069g0195 | 3 | NA19000.hp2 NA19002.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.63+14397A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158056 | ||||||
| chr17:77158090
|
A | G | 1 | a0001c0001t0006g0391 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.63+14431A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158090 | ||||||
| chr17:77158119
|
A | G | 3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG02895.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.63+14460A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158119 | ||||||
| chr17:77158149
|
A | T | 3 | a0001c0001t0017g0159a0001c0001t0017g0160a0001c0001t0017g0161 | 3 | HG02258.hp2 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+14490A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158149 | ||||||
| chr17:77158469
|
T | TTAA | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+14810_63+14811i others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158469 | ||||||
| chr17:77158565
|
T | G | 125 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(122): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.63+14906T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158565 | ||||||
| chr17:77158619
|
CA | C | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+14961delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158619 | ||||||
| chr17:77158674
|
A | G | 1 | a0001c0002t0012g0326 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.63+15015A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158674 | ||||||
| chr17:77158691
|
C | T | 4 | a0001c0001t0002g0068a0001c0001t0002g0103a0001c0001t0002g0104others(1): Show | 4 | HG02717.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+15032C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158691 | ||||||
| chr17:77158714
|
T | C | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15055T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158714 | ||||||
| chr17:77158765
|
T | G | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+15106T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158765 | ||||||
| chr17:77158774
|
A | G | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+15115A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158774 | ||||||
| chr17:77158798
|
C | CT | 14 | a0001c0001t0003g0007a0001c0001t0003g0125a0001c0001t0003g0126others(11): Show | 15 | HG00544.hp1 HG01516.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+15172dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
C | CTT | 25 | a0001c0001t0003g0021a0001c0001t0003g0106a0001c0001t0003g0124others(22): Show | 25 | HG00438.hp2 HG01168.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+15171_63+15172d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
C | CTTT | 25 | a0001c0001t0003g0117a0001c0001t0003g0149a0001c0001t0003g0150others(22): Show | 25 | HG00099.hp1 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.63+15170_63+15172d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
C | CTTTT | 11 | a0001c0001t0003g0123a0001c0001t0003g0158a0001c0001t0003g0183others(8): Show | 11 | HG00738.hp2 HG01074.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+15169_63+15172d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
CT | C | 30 | a0001c0001t0001g0012a0001c0001t0001g0256a0001c0001t0059g0390others(27): Show | 31 | HG00323.hp1 HG00642.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.63+15172delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
CTT | C | 50 | a0001c0001t0001g0031a0001c0001t0001g0229a0001c0001t0001g0230others(47): Show | 51 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.63+15171_63+15172d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
CTTT | C | 149 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0001g0238others(146): Show | 154 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.63+15170_63+15172d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
CTTTT | C | 40 | a0001c0001t0001g0274a0001c0001t0002g0004a0001c0001t0002g0022others(37): Show | 42 | HG01074.hp1 HG01167.hp2 HG01943.hp2 others(39): Show |
intron_variant | MODIFIER | c.63+15169_63+15172d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
CTTTTTTT others(1): Show |
C | 39 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(36): Show | 42 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+15165_63+15172d others(10): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0002t0005g0376a0001c0002t0005g0388 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.63+15161_63+15172d others(14): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158798
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+15154_63+15172d others(21): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77158798 | |||||
| chr17:77158826
|
T | A | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15167T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158826 | ||||||
| chr17:77158827
|
T | C | 39 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(36): Show | 42 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+15168T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158827 | ||||||
| chr17:77158889
|
G | T | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15230G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158889 | ||||||
| chr17:77158890
|
C | G | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+15231C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158890 | ||||||
| chr17:77158916
|
A | C | 1 | a0001c0001t0009g0057 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.63+15257A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158916 | ||||||
| chr17:77158990
|
A | G | 414 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(411): Show | 429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.63+15331A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158990 | ||||||
| chr17:77158992
|
A | G | 414 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(411): Show | 429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.63+15333A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77158992 | ||||||
| chr17:77159030
|
G | A | 1 | a0001c0001t0002g0283 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.63+15371G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159030 | ||||||
| chr17:77159054
|
A | G | 414 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(411): Show | 429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.63+15395A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159054 | ||||||
| chr17:77159087
|
A | G | 414 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(411): Show | 429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.63+15428A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159087 | ||||||
| chr17:77159091
|
A | G | 414 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(411): Show | 429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.63+15432A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159091 | ||||||
| chr17:77159095
|
T | C | 414 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(411): Show | 429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.63+15436T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159095 | ||||||
| chr17:77159096
|
T | A | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+15437T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159096 | ||||||
| chr17:77159098
|
A | T | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+15439A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159098 | ||||||
| chr17:77159124
|
G | T | 414 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(411): Show | 429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.63+15465G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159124 | ||||||
| chr17:77159162
|
G | GT | 414 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(411): Show | 429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.63+15504dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77159162 | |||||
| chr17:77159221
|
AC | A | 414 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(411): Show | 429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.63+15564delC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77159221 | |||||
| chr17:77159264
|
G | T | 1 | a0001c0002t0066g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+15605G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159264 | ||||||
| chr17:77159338
|
G | A | 39 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(36): Show | 42 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+15679G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159338 | ||||||
| chr17:77159363
|
G | A | 7 | a0001c0003t0001g0234a0001c0003t0001g0269a0001c0003t0001g0270others(4): Show | 7 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.63+15704G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159363 | ||||||
| chr17:77159382
|
C | CT | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+15739dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77159382 | |||||
| chr17:77159385
|
T | C | 2 | a0001c0002t0004g0299a0001c0002t0004g0342 | 2 | HG00140.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.63+15726T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159385 | ||||||
| chr17:77159483
|
C | T | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.63+15824C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159483 | ||||||
| chr17:77159642
|
G | A | 1 | a0001c0001t0007g0156 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.63+15983G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159642 | ||||||
| chr17:77159694
|
T | C | 39 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(36): Show | 42 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.63+16035T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159694 | ||||||
| chr17:77159868
|
G | GACCC | 63 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(60): Show | 65 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.63+16212_63+16215d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77159868 | |||||
| chr17:77159899
|
G | T | 1 | a0001c0001t0001g0276 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.63+16240G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159899 | ||||||
| chr17:77159929
|
G | A | 2 | a0001c0001t0007g0132a0001c0001t0007g0157 | 2 | HG01099.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.63+16270G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159929 | ||||||
| chr17:77159956
|
T | C | 409 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(406): Show | 424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.63+16297T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77159956 | ||||||
| chr17:77160131
|
T | C | 3 | a0001c0001t0019g0053a0001c0001t0019g0107a0001c0001t0019g0108 | 3 | HG02109.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.63+16472T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160131 | ||||||
| chr17:77160323
|
C | T | 120 | a0001c0001t0001g0252a0001c0002t0002g0297a0001c0002t0004g0002others(117): Show | 123 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.63+16664C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160323 | ||||||
| chr17:77160331
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+16672G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160331 | ||||||
| chr17:77160362
|
A | G | 2 | a0001c0001t0003g0135a0001c0001t0003g0136 | 2 | NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.63+16703A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160362 | ||||||
| chr17:77160531
|
C | A | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.63+16872C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160531 | ||||||
| chr17:77160532
|
G | A | 409 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(406): Show | 424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.63+16873G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160532 | ||||||
| chr17:77160539
|
T | C | 12 | a0001c0002t0005g0327a0001c0002t0005g0328a0001c0002t0005g0329others(9): Show | 12 | HG01884.hp1 HG02615.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.63+16880T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160539 | ||||||
| chr17:77160663
|
C | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.63+17004C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160663 | ||||||
| chr17:77160721
|
T | C | 1 | a0001c0002t0004g0193 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.63+17062T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160721 | ||||||
| chr17:77160802
|
C | G | 2 | a0001c0001t0003g0165a0001c0001t0003g0185 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.63+17143C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160802 | ||||||
| chr17:77160810
|
T | TTTTTTTT others(3): Show |
3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+17151_63+17152i others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160810 | ||||||
| chr17:77160811
|
A | G | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+17152A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160811 | ||||||
| chr17:77160812
|
G | A | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+17153G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160812 | ||||||
| chr17:77160830
|
C | A | 14 | a0001c0001t0006g0200a0001c0001t0006g0201a0001c0001t0006g0202others(11): Show | 14 | HG02145.hp2 HG02630.hp2 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.63+17171C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160830 | ||||||
| chr17:77160855
|
T | C | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.63+17196T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77160855 | ||||||
| chr17:77161037
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.63+17378C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161037 | ||||||
| chr17:77161272
|
G | T | 61 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0229others(58): Show | 63 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.63+17613G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161272 | ||||||
| chr17:77161301
|
A | G | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+17642A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161301 | ||||||
| chr17:77161318
|
C | G | 3 | a0001c0001t0017g0159a0001c0001t0017g0160a0001c0001t0017g0161 | 3 | HG02258.hp2 HG03195.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.63+17659C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161318 | ||||||
| chr17:77161334
|
A | G | 5 | a0001c0001t0006g0215a0001c0001t0006g0216a0001c0001t0006g0217others(2): Show | 5 | HG02300.hp2 NA19000.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+17675A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161334 | ||||||
| chr17:77161458
|
A | G | 1 | a0001c0002t0066g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.63+17799A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161458 | ||||||
| chr17:77161475
|
G | A | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+17816G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161475 | ||||||
| chr17:77161557
|
G | C | 35 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.63+17898G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161557 | ||||||
| chr17:77161558
|
G | A | 15 | a0001c0001t0006g0102a0001c0001t0006g0200a0001c0001t0006g0201others(12): Show | 15 | HG02145.hp2 HG02630.hp2 HG03017.hp1 others(12): Show |
intron_variant | MODIFIER | c.63+17899G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161558 | ||||||
| chr17:77161624
|
A | G | 2 | a0002c0004t0013g0174a0002c0004t0013g0175 | 2 | HG01891.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.63+17965A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161624 | ||||||
| chr17:77161656
|
A | G | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+17997A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161656 | ||||||
| chr17:77161707
|
T | G | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+18048T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161707 | ||||||
| chr17:77161712
|
C | CT | 115 | a0001c0001t0001g0031a0001c0001t0001g0237a0001c0001t0001g0238others(112): Show | 120 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.63+18077dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | |||||
| chr17:77161712
|
C | CTT | 18 | a0001c0001t0002g0048a0001c0001t0002g0058a0001c0001t0002g0067others(15): Show | 19 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.63+18076_63+18077d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | |||||
| chr17:77161712
|
C | CTTT | 10 | a0001c0001t0006g0201a0001c0001t0006g0206a0001c0001t0006g0218others(7): Show | 10 | HG02004.hp2 HG02109.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+18075_63+18077d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | |||||
| chr17:77161712
|
C | CTTTT | 28 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(25): Show | 31 | HG00597.hp2 HG00741.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.63+18074_63+18077d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | |||||
| chr17:77161712
|
CT | C | 79 | a0001c0001t0001g0230a0001c0001t0003g0007a0001c0001t0003g0021others(76): Show | 80 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(77): Show |
intron_variant | MODIFIER | c.63+18077delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | |||||
| chr17:77161712
|
CTT | C | 9 | a0001c0001t0003g0130a0001c0001t0003g0169a0001c0001t0003g0183others(6): Show | 10 | HG00323.hp2 HG01070.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.63+18076_63+18077d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161712 | |||||
| chr17:77161736
|
T | A | 1 | a0001c0002t0018g0362 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.63+18077T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161736 | ||||||
| chr17:77161743
|
C | T | 1 | a0001c0002t0005g0329 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.63+18084C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161743 | ||||||
| chr17:77161784
|
T | A | 40 | a0001c0001t0001g0211a0001c0001t0006g0001a0001c0001t0006g0010others(37): Show | 43 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.63+18125T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161784 | ||||||
| chr17:77161818
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.63+18159C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161818 | ||||||
| chr17:77161852
|
C | T | 1 | a0001c0001t0006g0203 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.63+18193C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161852 | ||||||
| chr17:77161915
|
TTTCTTCT others(6): Show |
T | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+18266_63+18278d others(15): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77161915 | |||||
| chr17:77161937
|
T | C | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+18278T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161937 | ||||||
| chr17:77161978
|
C | T | 1 | a0001c0001t0044g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.63+18319C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161978 | ||||||
| chr17:77161980
|
A | G | 1 | a0001c0001t0006g0212 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.63+18321A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77161980 | ||||||
| chr17:77162022
|
C | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+18363C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162022 | ||||||
| chr17:77162036
|
G | T | 3 | a0001c0001t0003g0130a0001c0001t0003g0163a0001c0001t0003g0169 | 3 | HG01168.hp2 HG01515.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.63+18377G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162036 | ||||||
| chr17:77162131
|
T | G | 186 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(183): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.63+18472T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162131 | ||||||
| chr17:77162174
|
C | T | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+18515C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162174 | ||||||
| chr17:77162179
|
C | G | 290 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(287): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.63+18520C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162179 | ||||||
| chr17:77162189
|
A | G | 1 | a0001c0002t0028g0387 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.63+18530A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162189 | ||||||
| chr17:77162259
|
C | T | 1 | a0001c0001t0007g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.63+18600C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162259 | ||||||
| chr17:77162260
|
G | A | 1 | a0001c0001t0002g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.63+18601G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162260 | ||||||
| chr17:77162437
|
A | G | 148 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(145): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.63+18778A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162437 | ||||||
| chr17:77162625
|
G | A | 1 | a0001c0001t0003g0130 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.63+18966G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162625 | ||||||
| chr17:77162631
|
G | A | 1 | a0001c0002t0004g0383 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.63+18972G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162631 | ||||||
| chr17:77162644
|
C | T | 44 | a0001c0002t0004g0303a0001c0002t0005g0032a0001c0002t0005g0033others(41): Show | 44 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.63+18985C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162644 | ||||||
| chr17:77162729
|
T | C | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+19070T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162729 | ||||||
| chr17:77162761
|
T | C | 395 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(392): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.63+19102T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162761 | ||||||
| chr17:77162765
|
G | C | 1 | a0001c0002t0011g0294 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.63+19106G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162765 | ||||||
| chr17:77162825
|
T | G | 12 | a0001c0001t0005g0039a0001c0001t0007g0019a0001c0001t0007g0037others(9): Show | 12 | HG00099.hp2 HG00323.hp2 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.63+19166T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162825 | ||||||
| chr17:77162830
|
C | CAA | 158 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0022others(155): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.63+19182_63+19183d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77162830 | |||||
| chr17:77162830
|
C | CAAA | 10 | a0001c0001t0002g0020a0001c0001t0003g0021a0001c0001t0003g0149others(7): Show | 10 | HG00408.hp2 HG00423.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.63+19181_63+19183d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77162830 | |||||
| chr17:77162830
|
CA | C | 119 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(116): Show | 122 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.63+19183delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77162830 | |||||
| chr17:77162999
|
C | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+19340C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77162999 | ||||||
| chr17:77163017
|
G | A | 1 | a0001c0001t0006g0218 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.63+19358G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163017 | ||||||
| chr17:77163203
|
C | T | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+19544C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163203 | ||||||
| chr17:77163281
|
G | A | 1 | a0001c0001t0076g0084 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.63+19622G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163281 | ||||||
| chr17:77163391
|
T | TTTTTCTC others(18): Show |
407 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(404): Show | 422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.63+19733_63+19734i others(27): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77163391 | |||||
| chr17:77163459
|
C | T | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+19800C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163459 | ||||||
| chr17:77163632
|
T | A | 6 | a0001c0001t0003g0117a0001c0001t0003g0137a0001c0001t0003g0138others(3): Show | 6 | HG02622.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+19973T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163632 | ||||||
| chr17:77163859
|
T | C | 36 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.63+20200T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77163859 | ||||||
| chr17:77164028
|
T | G | 2 | a0001c0002t0005g0305a0001c0002t0075g0302 | 2 | HG00323.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.63+20369T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164028 | ||||||
| chr17:77164138
|
G | A | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.63+20479G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164138 | ||||||
| chr17:77164158
|
G | A | 1 | a0001c0002t0005g0321 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.63+20499G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164158 | ||||||
| chr17:77164175
|
C | T | 1 | a0001c0002t0012g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.63+20516C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164175 | ||||||
| chr17:77164555
|
G | A | 1 | a0001c0002t0075g0302 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.63+20896G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164555 | ||||||
| chr17:77164778
|
C | G | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+21119C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164778 | ||||||
| chr17:77164994
|
C | T | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.63+21335C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77164994 | ||||||
| chr17:77165070
|
A | AC | 5 | a0001c0001t0003g0118a0001c0001t0007g0047a0001c0002t0004g0034others(2): Show | 5 | HG01123.hp1 HG02602.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.63+21415dupC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77165070 | |||||
| chr17:77165096
|
A | T | 45 | a0001c0002t0004g0303a0001c0002t0005g0032a0001c0002t0005g0033others(42): Show | 45 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.63+21437A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165096 | ||||||
| chr17:77165208
|
A | G | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+21549A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165208 | ||||||
| chr17:77165403
|
A | G | 4 | a0001c0001t0019g0053a0001c0001t0019g0107a0001c0001t0019g0108others(1): Show | 4 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.63+21744A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165403 | ||||||
| chr17:77165476
|
A | T | 1 | a0001c0002t0005g0033 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.63+21817A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165476 | ||||||
| chr17:77165621
|
T | A | 1 | a0001c0001t0003g0110 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.63+21962T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165621 | ||||||
| chr17:77165873
|
A | G | 1 | a0001c0001t0009g0056 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.63+22214A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165873 | ||||||
| chr17:77165965
|
G | T | 3 | a0001c0002t0004g0303a0001c0002t0005g0322a0001c0002t0005g0385 | 3 | HG00741.hp2 HG01496.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.63+22306G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77165965 | ||||||
| chr17:77166076
|
A | G | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.63+22417A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166076 | ||||||
| chr17:77166124
|
T | C | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.63+22465T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166124 | ||||||
| chr17:77166140
|
T | G | 79 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(76): Show | 81 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(78): Show |
intron_variant | MODIFIER | c.63+22481T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166140 | ||||||
| chr17:77166189
|
C | T | 1 | a0001c0001t0003g0162 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.63+22530C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166189 | ||||||
| chr17:77166254
|
G | C | 83 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.63+22595G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166254 | ||||||
| chr17:77166304
|
A | G | 2 | a0002c0004t0046g0186a0002c0004t0060g0187 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.63+22645A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166304 | ||||||
| chr17:77166469
|
A | G | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.63+22810A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166469 | ||||||
| chr17:77166696
|
A | T | 1 | a0001c0001t0044g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.63+23037A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166696 | ||||||
| chr17:77166710
|
A | C | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.63+23051A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166710 | ||||||
| chr17:77166799
|
A | G | 5 | a0001c0002t0005g0198a0001c0002t0005g0308a0001c0002t0005g0309others(2): Show | 5 | HG01175.hp1 HG02280.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.63+23140A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166799 | ||||||
| chr17:77166882
|
A | C | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.63+23223A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77166882 | ||||||
| chr17:77167146
|
C | CT | 14 | a0001c0001t0001g0031a0001c0001t0001g0238a0001c0001t0006g0224others(11): Show | 15 | HG01070.hp2 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.63+23506dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77167146 | |||||
| chr17:77167146
|
CT | C | 73 | a0001c0001t0001g0230a0001c0001t0001g0278a0001c0001t0002g0004others(70): Show | 76 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.63+23506delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77167146 | |||||
| chr17:77167146
|
CTT | C | 17 | a0001c0001t0002g0020a0001c0001t0009g0051a0001c0001t0009g0052others(14): Show | 17 | HG01255.hp1 HG01884.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.63+23505_63+23506d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77167146 | |||||
| chr17:77167146
|
CTTTTT | C | 78 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(75): Show | 80 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.63+23502_63+23506d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77167146 | |||||
| chr17:77167283
|
C | T | 153 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(150): Show | 158 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.64-23520C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77167283 | ||||||
| chr17:77167885
|
T | G | 3 | a0001c0002t0004g0013a0001c0002t0004g0341a0001c0002t0004g0352 | 4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-22918T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77167885 | ||||||
| chr17:77167932
|
G | T | 69 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(66): Show | 72 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.64-22871G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77167932 | ||||||
| chr17:77167947
|
G | A | 286 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(283): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.64-22856G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77167947 | ||||||
| chr17:77168345
|
G | T | 67 | a0001c0002t0004g0002a0001c0002t0004g0013a0001c0002t0004g0014others(64): Show | 70 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.64-22458G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168345 | ||||||
| chr17:77168386
|
G | T | 63 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(60): Show | 65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.64-22417G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168386 | ||||||
| chr17:77168395
|
G | A | 14 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(11): Show | 15 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-22408G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168395 | ||||||
| chr17:77168730
|
G | T | 1 | a0001c0002t0004g0166 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.64-22073G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168730 | ||||||
| chr17:77168737
|
C | G | 1 | a0001c0001t0006g0225 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.64-22066C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168737 | ||||||
| chr17:77168804
|
A | G | 286 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(283): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.64-21999A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168804 | ||||||
| chr17:77168879
|
G | T | 14 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(11): Show | 15 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-21924G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168879 | ||||||
| chr17:77168996
|
G | A | 2 | a0002c0004t0046g0186a0002c0004t0060g0187 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.64-21807G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77168996 | ||||||
| chr17:77169007
|
C | CTTTTT | 8 | a0001c0001t0008g0402a0001c0001t0008g0407a0001c0001t0008g0408others(5): Show | 8 | NA18946.hp1 NA18970.hp1 NA18990.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-21770_64-21766d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CT | C | 104 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(101): Show | 107 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.64-21766delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CTT | C | 20 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(17): Show | 21 | HG00323.hp1 HG00423.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-21767_64-21766d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CTTT | C | 7 | a0001c0001t0006g0200a0001c0001t0006g0214a0001c0001t0006g0215others(4): Show | 7 | HG02145.hp2 NA18994.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-21768_64-21766d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CTTTT | C | 30 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(27): Show | 33 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(30): Show |
intron_variant | MODIFIER | c.64-21769_64-21766d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CTTTTTT | C | 7 | a0001c0001t0003g0115a0001c0001t0003g0125a0001c0001t0003g0126others(4): Show | 7 | HG01175.hp2 HG02280.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-21771_64-21766d others(8): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CTTTTTTT | C | 76 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(73): Show | 79 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(76): Show |
intron_variant | MODIFIER | c.64-21772_64-21766d others(9): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CTTTTTTT others(2): Show |
C | 5 | a0001c0001t0002g0048a0001c0001t0002g0094a0001c0005t0015g0008others(2): Show | 6 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-21774_64-21766d others(11): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CTTTTTTT others(3): Show |
C | 56 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(53): Show | 58 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.64-21775_64-21766d others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CTTTTTTT others(4): Show |
C | 64 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(61): Show | 66 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.64-21776_64-21766d others(13): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169007
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0256a0001c0001t0033g0280 | 2 | HG01192.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.64-21777_64-21766d others(14): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77169007 | |||||
| chr17:77169205
|
G | C | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-21598G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169205 | ||||||
| chr17:77169317
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.64-21486G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169317 | ||||||
| chr17:77169370
|
A | C | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-21433A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169370 | ||||||
| chr17:77169452
|
C | A | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-21351C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169452 | ||||||
| chr17:77169553
|
C | T | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-21250C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169553 | ||||||
| chr17:77169574
|
T | C | 3 | a0001c0001t0007g0156a0001c0003t0001g0178a0001c0003t0001g0179 | 3 | HG00140.hp1 HG01074.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.64-21229T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169574 | ||||||
| chr17:77169696
|
G | T | 1 | a0001c0001t0044g0046 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.64-21107G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169696 | ||||||
| chr17:77169705
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.64-21098G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169705 | ||||||
| chr17:77169760
|
A | G | 1 | a0001c0001t0001g0263 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.64-21043A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169760 | ||||||
| chr17:77169823
|
A | C | 1 | a0001c0001t0001g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.64-20980A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169823 | ||||||
| chr17:77169848
|
T | G | 3 | a0001c0005t0036g0017a0001c0005t0037g0016a0008c0011t0036g0018 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-20955T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77169848 | ||||||
| chr17:77170015
|
A | G | 81 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.64-20788A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170015 | ||||||
| chr17:77170268
|
C | T | 50 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(47): Show | 55 | HG00597.hp2 HG00639.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.64-20535C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170268 | ||||||
| chr17:77170314
|
G | T | 33 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(30): Show | 36 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.64-20489G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170314 | ||||||
| chr17:77170405
|
TC | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-20397delC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170405 | ||||||
| chr17:77170430
|
C | T | 1 | a0001c0001t0007g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.64-20373C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170430 | ||||||
| chr17:77170647
|
C | T | 5 | a0001c0001t0005g0039a0001c0001t0007g0038a0001c0001t0007g0043others(2): Show | 5 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-20156C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170647 | ||||||
| chr17:77170795
|
T | C | 1 | a0001c0001t0071g0244 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.64-20008T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170795 | ||||||
| chr17:77170860
|
A | G | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-19943A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170860 | ||||||
| chr17:77170882
|
A | G | 2 | a0001c0001t0001g0232a0001c0001t0001g0258 | 2 | HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.64-19921A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77170882 | ||||||
| chr17:77171079
|
T | C | 2 | a0001c0001t0006g0218a0001c0001t0070g0219 | 2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.64-19724T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171079 | ||||||
| chr17:77171117
|
T | G | 1 | a0001c0002t0005g0298 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64-19686T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171117 | ||||||
| chr17:77171182
|
A | G | 1 | a0001c0001t0025g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.64-19621A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171182 | ||||||
| chr17:77171185
|
A | T | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-19618A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171185 | ||||||
| chr17:77171191
|
G | A | 5 | a0001c0001t0002g0022a0001c0001t0002g0048a0001c0001t0002g0050others(2): Show | 5 | NA18972.hp2 NA18985.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-19612G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171191 | ||||||
| chr17:77171222
|
C | T | 1 | a0001c0002t0024g0318 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.64-19581C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171222 | ||||||
| chr17:77171233
|
T | C | 1 | a0001c0001t0007g0157 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.64-19570T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171233 | ||||||
| chr17:77171360
|
T | C | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-19443T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171360 | ||||||
| chr17:77171371
|
G | A | 1 | a0001c0002t0004g0303 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.64-19432G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171371 | ||||||
| chr17:77171525
|
A | G | 63 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(60): Show | 65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.64-19278A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171525 | ||||||
| chr17:77171590
|
G | A | 14 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(11): Show | 15 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-19213G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171590 | ||||||
| chr17:77171725
|
G | A | 3 | a0001c0002t0005g0295a0001c0002t0005g0313a0001c0002t0005g0374 | 3 | HG02165.hp1 NA18949.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.64-19078G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171725 | ||||||
| chr17:77171760
|
A | G | 41 | a0001c0002t0005g0032a0001c0002t0005g0033a0001c0002t0005g0197others(38): Show | 41 | HG00323.hp1 HG00544.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.64-19043A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171760 | ||||||
| chr17:77171768
|
C | T | 407 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(404): Show | 422 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(419): Show |
intron_variant | MODIFIER | c.64-19035C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171768 | ||||||
| chr17:77171778
|
T | C | 1 | a0001c0002t0028g0296 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64-19025T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171778 | ||||||
| chr17:77171919
|
G | A | 3 | a0001c0005t0036g0017a0001c0005t0037g0016a0008c0011t0036g0018 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-18884G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171919 | ||||||
| chr17:77171947
|
T | A | 14 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(11): Show | 15 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.64-18856T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77171947 | ||||||
| chr17:77172030
|
C | T | 81 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.64-18773C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172030 | ||||||
| chr17:77172041
|
T | C | 4 | a0001c0001t0010g0114a0001c0001t0010g0120a0001c0001t0010g0121others(1): Show | 4 | HG00642.hp1 HG00738.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-18762T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172041 | ||||||
| chr17:77172078
|
C | A | 12 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(9): Show | 13 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.64-18725C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172078 | ||||||
| chr17:77172082
|
C | G | 1 | a0001c0002t0051g0367 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.64-18721C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172082 | ||||||
| chr17:77172241
|
T | C | 1 | a0001c0001t0003g0128 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.64-18562T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172241 | ||||||
| chr17:77172547
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.64-18256C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172547 | ||||||
| chr17:77172548
|
G | A | 5 | a0001c0002t0012g0323a0001c0002t0012g0324a0001c0002t0012g0325others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-18255G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172548 | ||||||
| chr17:77172622
|
T | C | 1 | a0001c0001t0003g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.64-18181T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172622 | ||||||
| chr17:77172815
|
G | A | 82 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(79): Show | 84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.64-17988G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172815 | ||||||
| chr17:77172818
|
A | G | 281 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(278): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.64-17985A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172818 | ||||||
| chr17:77172846
|
C | G | 13 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(10): Show | 14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-17957C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172846 | ||||||
| chr17:77172919
|
A | C | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-17884A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77172919 | ||||||
| chr17:77173039
|
A | G | 3 | a0001c0001t0016g0060a0001c0001t0016g0069a0001c0001t0016g0070 | 3 | HG02523.hp2 NA18982.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.64-17764A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173039 | ||||||
| chr17:77173283
|
G | A | 4 | a0001c0001t0003g0149a0001c0001t0003g0150a0001c0001t0003g0184others(1): Show | 4 | HG02559.hp2 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-17520G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173283 | ||||||
| chr17:77173287
|
C | T | 1 | a0001c0003t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64-17516C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173287 | ||||||
| chr17:77173288
|
G | A | 1 | a0001c0001t0007g0040 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.64-17515G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173288 | ||||||
| chr17:77173368
|
G | A | 1 | a0001c0001t0006g0203 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.64-17435G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173368 | ||||||
| chr17:77173430
|
G | C | 2 | a0001c0001t0003g0151a0001c0001t0003g0158 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.64-17373G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173430 | ||||||
| chr17:77173477
|
G | A | 1 | a0001c0002t0004g0370 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-17326G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173477 | ||||||
| chr17:77173577
|
C | T | 13 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(10): Show | 14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-17226C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173577 | ||||||
| chr17:77173674
|
G | C | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-17129G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173674 | ||||||
| chr17:77173793
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-17010G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173793 | ||||||
| chr17:77173905
|
C | CT | 21 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(18): Show | 21 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(18): Show |
intron_variant | MODIFIER | c.64-16885dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77173905 | |||||
| chr17:77173971
|
G | A | 1 | a0001c0002t0024g0319 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.64-16832G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77173971 | ||||||
| chr17:77174005
|
A | C | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-16798A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174005 | ||||||
| chr17:77174040
|
A | G | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-16763A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174040 | ||||||
| chr17:77174095
|
T | G | 11 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(8): Show | 11 | NA18940.hp1 NA18946.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-16708T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174095 | ||||||
| chr17:77174194
|
C | T | 164 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(161): Show | 171 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.64-16609C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174194 | ||||||
| chr17:77174199
|
A | G | 94 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(91): Show | 98 | HG00544.hp2 HG00558.hp2 HG00639.hp2 others(95): Show |
intron_variant | MODIFIER | c.64-16604A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174199 | ||||||
| chr17:77174210
|
C | T | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-16593C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174210 | ||||||
| chr17:77174225
|
A | G | 1 | a0001c0003t0001g0239 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.64-16578A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174225 | ||||||
| chr17:77174291
|
CCTT | C | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-16509_64-16507d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77174291 | |||||
| chr17:77174392
|
T | C | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-16411T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174392 | ||||||
| chr17:77174421
|
C | T | 1 | a0001c0002t0012g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-16382C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174421 | ||||||
| chr17:77174591
|
C | T | 124 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(121): Show | 127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-16212C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174591 | ||||||
| chr17:77174625
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-16178G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174625 | ||||||
| chr17:77174652
|
C | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-16151C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174652 | ||||||
| chr17:77174677
|
C | T | 1 | a0001c0002t0043g0316 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.64-16126C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174677 | ||||||
| chr17:77174728
|
G | T | 1 | a0001c0001t0003g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-16075G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174728 | ||||||
| chr17:77174894
|
C | T | 1 | a0002c0004t0060g0187 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.64-15909C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174894 | ||||||
| chr17:77174906
|
C | T | 1 | a0001c0001t0016g0070 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.64-15897C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174906 | ||||||
| chr17:77174947
|
T | G | 55 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(52): Show | 58 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(55): Show |
intron_variant | MODIFIER | c.64-15856T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174947 | ||||||
| chr17:77174987
|
A | G | 2 | a0001c0002t0005g0197a0001c0002t0005g0198 | 2 | HG02280.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.64-15816A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77174987 | ||||||
| chr17:77175069
|
G | A | 1 | a0001c0002t0005g0284 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.64-15734G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175069 | ||||||
| chr17:77175096
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.64-15707A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175096 | ||||||
| chr17:77175142
|
G | C | 1 | a0001c0002t0005g0284 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.64-15661G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175142 | ||||||
| chr17:77175194
|
A | G | 1 | a0001c0001t0002g0061 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.64-15609A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175194 | ||||||
| chr17:77175253
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-15550G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175253 | ||||||
| chr17:77175351
|
C | T | 13 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(10): Show | 14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.64-15452C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175351 | ||||||
| chr17:77175354
|
A | G | 1 | a0001c0001t0003g0130 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.64-15449A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175354 | ||||||
| chr17:77175548
|
G | A | 409 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(406): Show | 424 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(421): Show |
intron_variant | MODIFIER | c.64-15255G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175548 | ||||||
| chr17:77175572
|
C | T | 3 | a0001c0001t0003g0113a0001c0001t0006g0224a0001c0001t0006g0225 | 3 | HG02135.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-15231C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175572 | ||||||
| chr17:77175631
|
G | A | 3 | a0001c0001t0059g0390a0002c0004t0046g0186a0002c0004t0060g0187 | 3 | HG02145.hp1 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.64-15172G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175631 | ||||||
| chr17:77175867
|
G | A | 1 | a0001c0002t0004g0378 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64-14936G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175867 | ||||||
| chr17:77175870
|
C | T | 1 | a0001c0002t0028g0296 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.64-14933C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77175870 | ||||||
| chr17:77176006
|
G | A | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-14797G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176006 | ||||||
| chr17:77176056
|
A | G | 408 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(405): Show | 423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.64-14747A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176056 | ||||||
| chr17:77176152
|
T | C | 66 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(63): Show | 68 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.64-14651T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176152 | ||||||
| chr17:77176191
|
G | A | 1 | a0001c0001t0008g0404 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.64-14612G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176191 | ||||||
| chr17:77176234
|
G | A | 1 | a0001c0001t0025g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.64-14569G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176234 | ||||||
| chr17:77176321
|
G | C | 32 | a0001c0001t0003g0134a0001c0001t0006g0001a0001c0001t0006g0010others(29): Show | 35 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.64-14482G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176321 | ||||||
| chr17:77176393
|
C | T | 124 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(121): Show | 127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-14410C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176393 | ||||||
| chr17:77176402
|
G | C | 38 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(35): Show | 43 | HG00597.hp2 HG00639.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.64-14401G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176402 | ||||||
| chr17:77176404
|
G | A | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-14399G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176404 | ||||||
| chr17:77176411
|
T | C | 2 | a0001c0001t0003g0151a0001c0001t0003g0158 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.64-14392T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176411 | ||||||
| chr17:77176550
|
C | T | 15 | a0001c0003t0001g0188a0001c0003t0001g0233a0001c0003t0001g0234others(12): Show | 15 | HG00408.hp1 HG02040.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.64-14253C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176550 | ||||||
| chr17:77176769
|
TA | T | 18 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(15): Show | 21 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.64-14033delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176769 | ||||||
| chr17:77176829
|
C | T | 1 | a0001c0003t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.64-13974C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176829 | ||||||
| chr17:77176866
|
C | T | 2 | a0001c0001t0003g0110a0001c0001t0074g0192 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.64-13937C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77176866 | ||||||
| chr17:77177100
|
A | G | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-13703A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177100 | ||||||
| chr17:77177138
|
C | T | 124 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(121): Show | 127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-13665C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177138 | ||||||
| chr17:77177142
|
A | G | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-13661A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177142 | ||||||
| chr17:77177167
|
CAT | C | 7 | a0001c0003t0001g0234a0001c0003t0001g0269a0001c0003t0001g0270others(4): Show | 7 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.64-13635_64-13634d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177167 | ||||||
| chr17:77177270
|
G | A | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-13533G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177270 | ||||||
| chr17:77177395
|
A | C | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-13408A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177395 | ||||||
| chr17:77177480
|
G | T | 1 | a0001c0002t0004g0036 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.64-13323G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177480 | ||||||
| chr17:77177766
|
T | G | 285 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(282): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.64-13037T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177766 | ||||||
| chr17:77177816
|
C | G | 5 | a0001c0001t0006g0200a0001c0001t0006g0201a0001c0001t0006g0202others(2): Show | 5 | NA18945.hp1 NA18969.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-12987C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177816 | ||||||
| chr17:77177833
|
A | G | 1 | a0001c0002t0011g0345 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.64-12970A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77177833 | ||||||
| chr17:77178055
|
T | TC | 37 | a0001c0001t0001g0232a0001c0001t0001g0237a0001c0001t0001g0245others(34): Show | 37 | HG00438.hp2 HG00735.hp1 HG01192.hp2 others(34): Show |
intron_variant | MODIFIER | c.64-12738dupC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77178055 | |||||
| chr17:77178055
|
TC | T | 15 | a0001c0001t0001g0278a0001c0001t0003g0126a0001c0001t0003g0127others(12): Show | 16 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.64-12738delC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77178055 | |||||
| chr17:77178065
|
C | CT | 6 | a0001c0001t0001g0263a0001c0001t0008g0400a0001c0002t0012g0323others(3): Show | 6 | HG02615.hp1 HG02622.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-12728dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77178065 | |||||
| chr17:77178065
|
C | T | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-12738C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178065 | ||||||
| chr17:77178093
|
A | G | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-12710A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178093 | ||||||
| chr17:77178207
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.64-12596G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178207 | ||||||
| chr17:77178258
|
C | T | 1 | a0001c0002t0004g0378 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.64-12545C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178258 | ||||||
| chr17:77178525
|
AGCAGTGG others(4): Show |
A | 1 | a0001c0001t0007g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.64-12277_64-12267d others(13): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178525 | ||||||
| chr17:77178613
|
C | T | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.64-12190C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178613 | ||||||
| chr17:77178661
|
C | T | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-12142C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77178661 | ||||||
| chr17:77179084
|
C | T | 1 | a0001c0001t0006g0217 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.64-11719C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179084 | ||||||
| chr17:77179135
|
G | GCAGA | 3 | a0001c0001t0016g0060a0001c0001t0016g0069a0001c0001t0016g0070 | 3 | HG02523.hp2 NA18982.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.64-11667_64-11664d others(6): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77179135 | |||||
| chr17:77179481
|
C | T | 1 | a0001c0001t0002g0086 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.64-11322C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179481 | ||||||
| chr17:77179497
|
C | A | 1 | a0001c0001t0003g0162 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.64-11306C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179497 | ||||||
| chr17:77179519
|
A | C | 5 | a0001c0002t0005g0033a0001c0002t0005g0284a0001c0002t0005g0285others(2): Show | 5 | NA18967.hp2 NA18974.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-11284A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179519 | ||||||
| chr17:77179719
|
G | A | 1 | a0002c0004t0046g0186 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.64-11084G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179719 | ||||||
| chr17:77179735
|
C | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-11068C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179735 | ||||||
| chr17:77179810
|
G | A | 124 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(121): Show | 127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-10993G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179810 | ||||||
| chr17:77179877
|
C | G | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.64-10926C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179877 | ||||||
| chr17:77179931
|
C | G | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-10872C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179931 | ||||||
| chr17:77179965
|
C | G | 1 | a0001c0002t0005g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.64-10838C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179965 | ||||||
| chr17:77179966
|
C | G | 2 | a0001c0001t0003g0151a0001c0001t0003g0158 | 2 | HG01106.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.64-10837C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179966 | ||||||
| chr17:77179968
|
C | T | 64 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(61): Show | 66 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.64-10835C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77179968 | ||||||
| chr17:77180036
|
ATGTTT | A | 10 | a0001c0001t0001g0273a0001c0001t0008g0399a0001c0001t0008g0406others(7): Show | 10 | HG01891.hp1 HG02273.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.64-10757_64-10753d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180036 | |||||
| chr17:77180041
|
TTGTTTTG others(3): Show |
T | 17 | a0001c0001t0001g0012a0001c0001t0001g0256a0001c0001t0001g0263others(14): Show | 18 | HG00642.hp2 HG01099.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.64-10757_64-10748d others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | |||||
| chr17:77180041
|
TTGTTTTG others(8): Show |
T | 55 | a0001c0001t0001g0031a0001c0001t0001g0211a0001c0001t0001g0232others(52): Show | 56 | HG00423.hp2 HG00733.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.64-10757_64-10743d others(17): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | |||||
| chr17:77180041
|
TTGTTTTG others(13): Show |
T | 39 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(36): Show | 42 | HG00408.hp1 HG00597.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.64-10757_64-10738d others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | |||||
| chr17:77180041
|
TTGTTTTG others(18): Show |
T | 6 | a0001c0001t0006g0224a0001c0001t0006g0225a0001c0001t0032g0009others(3): Show | 8 | HG00639.hp2 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-10757_64-10733d others(27): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | |||||
| chr17:77180041
|
TTGTTTTG others(28): Show |
T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-10757_64-10723d others(37): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180041 | |||||
| chr17:77180046
|
T | TTGTTA | 22 | a0001c0001t0003g0110a0001c0001t0003g0136a0001c0001t0003g0149others(19): Show | 22 | HG00423.hp1 HG01123.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.64-10706_64-10702d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | |||||
| chr17:77180046
|
TTGTTA | T | 114 | a0001c0001t0002g0005a0001c0001t0002g0066a0001c0001t0002g0068others(111): Show | 119 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.64-10706_64-10702d others(7): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | |||||
| chr17:77180046
|
TTGTTATG others(3): Show |
T | 59 | a0001c0001t0002g0004a0001c0001t0002g0020a0001c0001t0002g0022others(56): Show | 60 | HG00099.hp1 HG00323.hp2 HG00733.hp1 others(57): Show |
intron_variant | MODIFIER | c.64-10711_64-10702d others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | |||||
| chr17:77180046
|
TTGTTATG others(8): Show |
T | 5 | a0001c0001t0002g0048a0001c0001t0002g0050a0001c0001t0002g0067others(2): Show | 5 | NA18972.hp2 NA18994.hp2 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.64-10716_64-10702d others(17): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | |||||
| chr17:77180046
|
TTGTTATG others(13): Show |
T | 1 | a0001c0001t0002g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.64-10721_64-10702d others(22): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | |||||
| chr17:77180046
|
TTGTTATG others(23): Show |
T | 1 | a0001c0002t0004g0336 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.64-10731_64-10702d others(32): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77180046 | |||||
| chr17:77180051
|
A | T | 1 | a0001c0001t0002g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.64-10752A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180051 | ||||||
| chr17:77180056
|
A | T | 5 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0146others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.64-10747A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180056 | ||||||
| chr17:77180096
|
A | G | 1 | a0001c0001t0003g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.64-10707A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180096 | ||||||
| chr17:77180228
|
C | T | 1 | a0001c0001t0003g0123 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.64-10575C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180228 | ||||||
| chr17:77180463
|
G | A | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-10340G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180463 | ||||||
| chr17:77180718
|
T | C | 1 | a0001c0002t0066g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.64-10085T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180718 | ||||||
| chr17:77180760
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0232a0001c0001t0001g0237others(5): Show | 9 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.64-10043C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180760 | ||||||
| chr17:77180840
|
C | T | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-9963C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77180840 | ||||||
| chr17:77181002
|
C | G | 1 | a0001c0001t0003g0183 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.64-9801C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181002 | ||||||
| chr17:77181179
|
A | G | 103 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(100): Show | 109 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.64-9624A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181179 | ||||||
| chr17:77181233
|
T | C | 84 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.64-9570T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181233 | ||||||
| chr17:77181297
|
A | G | 84 | a0001c0001t0002g0082a0001c0001t0003g0007a0001c0001t0003g0021others(81): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(83): Show |
intron_variant | MODIFIER | c.64-9506A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181297 | ||||||
| chr17:77181356
|
G | T | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-9447G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181356 | ||||||
| chr17:77181453
|
T | C | 408 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(405): Show | 423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.64-9350T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181453 | ||||||
| chr17:77181488
|
C | G | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.64-9315C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181488 | ||||||
| chr17:77181815
|
T | G | 1 | a0001c0005t0037g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.64-8988T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181815 | ||||||
| chr17:77181897
|
C | T | 1 | a0001c0001t0030g0085 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.64-8906C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181897 | ||||||
| chr17:77181932
|
A | G | 4 | a0001c0001t0007g0156a0001c0001t0025g0199a0001c0003t0001g0178others(1): Show | 4 | HG00140.hp1 HG01074.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-8871A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77181932 | ||||||
| chr17:77182502
|
G | A | 1 | a0001c0001t0009g0054 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.64-8301G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77182502 | ||||||
| chr17:77182632
|
T | C | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-8171T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77182632 | ||||||
| chr17:77182647
|
C | G | 9 | a0001c0001t0006g0001a0001c0001t0006g0026a0001c0001t0006g0027others(6): Show | 11 | HG00741.hp1 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.64-8156C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77182647 | ||||||
| chr17:77182732
|
G | A | 1 | a0001c0002t0005g0298 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.64-8071G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77182732 | ||||||
| chr17:77183310
|
G | A | 1 | a0001c0001t0007g0024 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.64-7493G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183310 | ||||||
| chr17:77183328
|
T | C | 1 | a0001c0002t0028g0387 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.64-7475T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183328 | ||||||
| chr17:77183334
|
TTC | T | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-7465_64-7464del others(2): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77183334 | |||||
| chr17:77183412
|
A | G | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-7391A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183412 | ||||||
| chr17:77183560
|
G | A | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.64-7243G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183560 | ||||||
| chr17:77183669
|
T | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-7134T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183669 | ||||||
| chr17:77183708
|
G | A | 1 | a0001c0001t0035g0011 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.64-7095G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183708 | ||||||
| chr17:77183805
|
G | T | 285 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(282): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.64-6998G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183805 | ||||||
| chr17:77183833
|
A | AT | 81 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.64-6960dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77183833 | |||||
| chr17:77183853
|
G | A | 1 | a0001c0001t0002g0097 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.64-6950G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183853 | ||||||
| chr17:77183887
|
G | A | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-6916G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77183887 | ||||||
| chr17:77184185
|
T | C | 1 | a0001c0001t0067g0246 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.64-6618T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184185 | ||||||
| chr17:77184189
|
G | A | 1 | a0001c0001t0003g0021 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.64-6614G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184189 | ||||||
| chr17:77184193
|
T | G | 1 | a0001c0001t0007g0129 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.64-6610T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184193 | ||||||
| chr17:77184350
|
A | G | 272 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(269): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.64-6453A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184350 | ||||||
| chr17:77184505
|
G | A | 4 | a0001c0001t0007g0156a0001c0001t0025g0199a0001c0003t0001g0178others(1): Show | 4 | HG00140.hp1 HG01074.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.64-6298G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184505 | ||||||
| chr17:77184745
|
C | A | 44 | a0001c0002t0004g0303a0001c0002t0005g0032a0001c0002t0005g0033others(41): Show | 44 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.64-6058C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184745 | ||||||
| chr17:77184751
|
C | T | 1 | a0001c0002t0012g0377 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.64-6052C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184751 | ||||||
| chr17:77184805
|
A | G | 1 | a0007c0010t0002g0194 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.64-5998A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184805 | ||||||
| chr17:77184907
|
C | G | 1 | a0001c0005t0015g0171 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.64-5896C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184907 | ||||||
| chr17:77184935
|
G | A | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.64-5868G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77184935 | ||||||
| chr17:77185016
|
A | G | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-5787A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185016 | ||||||
| chr17:77185052
|
G | A | 6 | a0001c0002t0005g0327a0001c0002t0005g0328a0001c0002t0005g0330others(3): Show | 6 | HG01884.hp1 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-5751G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185052 | ||||||
| chr17:77185271
|
C | T | 124 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(121): Show | 127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.64-5532C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185271 | ||||||
| chr17:77185416
|
C | T | 1 | a0001c0001t0002g0081 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.64-5387C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185416 | ||||||
| chr17:77185447
|
G | A | 5 | a0001c0002t0005g0298a0001c0002t0005g0306a0001c0002t0005g0307others(2): Show | 5 | HG01358.hp1 HG03834.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.64-5356G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185447 | ||||||
| chr17:77185459
|
G | C | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-5344G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185459 | ||||||
| chr17:77185661
|
G | A | 1 | a0001c0001t0002g0076 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.64-5142G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185661 | ||||||
| chr17:77185799
|
G | C | 6 | a0001c0002t0005g0327a0001c0002t0005g0328a0001c0002t0005g0330others(3): Show | 6 | HG01884.hp1 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.64-5004G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77185799 | ||||||
| chr17:77186086
|
T | C | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.64-4717T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186086 | ||||||
| chr17:77186140
|
T | C | 408 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(405): Show | 423 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(420): Show |
intron_variant | MODIFIER | c.64-4663T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186140 | ||||||
| chr17:77186169
|
A | G | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.64-4634A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186169 | ||||||
| chr17:77186195
|
G | A | 2 | a0001c0001t0003g0149a0001c0001t0003g0150 | 2 | HG02559.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.64-4608G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186195 | ||||||
| chr17:77186195
|
G | T | 1 | a0001c0001t0026g0396 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.64-4608G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186195 | ||||||
| chr17:77186339
|
C | T | 1 | a0001c0001t0003g0162 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.64-4464C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186339 | ||||||
| chr17:77186341
|
C | G | 11 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(8): Show | 12 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.64-4462C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186341 | ||||||
| chr17:77186496
|
A | C | 3 | a0001c0001t0002g0068a0001c0001t0002g0104a0001c0001t0002g0111 | 3 | HG02818.hp1 HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.64-4307A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186496 | ||||||
| chr17:77186591
|
A | G | 2 | a0001c0002t0004g0333a0001c0002t0004g0337 | 2 | NA18948.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.64-4212A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186591 | ||||||
| chr17:77186605
|
C | T | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-4198C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186605 | ||||||
| chr17:77186649
|
A | G | 3 | a0001c0005t0036g0017a0001c0005t0037g0016a0008c0011t0036g0018 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.64-4154A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186649 | ||||||
| chr17:77186729
|
T | C | 56 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(53): Show | 59 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.64-4074T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186729 | ||||||
| chr17:77186737
|
C | G | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.64-4066C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77186737 | ||||||
| chr17:77187040
|
A | G | 27 | a0001c0001t0005g0039a0001c0001t0007g0019a0001c0001t0007g0037others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(24): Show |
intron_variant | MODIFIER | c.64-3763A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187040 | ||||||
| chr17:77187109
|
T | C | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-3694T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187109 | ||||||
| chr17:77187128
|
C | T | 1 | a0001c0001t0002g0283 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.64-3675C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187128 | ||||||
| chr17:77187379
|
C | A | 78 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(75): Show | 81 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.64-3424C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187379 | ||||||
| chr17:77187437
|
G | A | 1 | a0001c0001t0006g0026 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.64-3366G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187437 | ||||||
| chr17:77187456
|
C | T | 1 | a0001c0001t0002g0020 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.64-3347C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187456 | ||||||
| chr17:77187696
|
A | G | 1 | a0001c0002t0021g0368 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.64-3107A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187696 | ||||||
| chr17:77187737
|
A | AT | 116 | a0001c0001t0001g0232a0001c0001t0001g0281a0001c0001t0002g0062others(113): Show | 121 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(118): Show |
intron_variant | MODIFIER | c.64-3048dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77187737 | |||||
| chr17:77187737
|
AT | A | 18 | a0001c0001t0001g0243a0001c0001t0002g0020a0001c0001t0002g0077others(15): Show | 19 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.64-3048delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77187737 | |||||
| chr17:77187830
|
C | T | 64 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(61): Show | 66 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.64-2973C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187830 | ||||||
| chr17:77187870
|
G | T | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.64-2933G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77187870 | ||||||
| chr17:77188299
|
T | C | 37 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(34): Show | 41 | HG00597.hp2 HG00639.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.64-2504T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188299 | ||||||
| chr17:77188412
|
CT | C | 377 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(374): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.64-2377delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77188412 | |||||
| chr17:77188494
|
T | A | 1 | a0001c0001t0001g0240 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.64-2309T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188494 | ||||||
| chr17:77188494
|
T | G | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.64-2309T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188494 | ||||||
| chr17:77188510
|
G | A | 1 | a0001c0001t0003g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.64-2293G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188510 | ||||||
| chr17:77188533
|
A | G | 1 | a0001c0002t0004g0370 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.64-2270A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188533 | ||||||
| chr17:77188550
|
A | AAGGACAT others(5): Show |
1 | a0001c0002t0004g0333 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.64-2250_64-2239dup others(12): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77188550 | |||||
| chr17:77188561
|
G | A | 36 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-2242G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188561 | ||||||
| chr17:77188591
|
C | T | 124 | a0001c0001t0032g0009a0001c0002t0002g0297a0001c0002t0004g0002others(121): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.64-2212C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188591 | ||||||
| chr17:77188626
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-2177G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188626 | ||||||
| chr17:77188789
|
C | T | 395 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(392): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.64-2014C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188789 | ||||||
| chr17:77188899
|
G | A | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.64-1904G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77188899 | ||||||
| chr17:77188994
|
G | GT | 11 | a0001c0001t0001g0031a0001c0001t0003g0119a0001c0001t0006g0102others(8): Show | 11 | HG00423.hp2 HG02738.hp1 HG03017.hp1 others(8): Show |
intron_variant | MODIFIER | c.64-1797dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77188994 | |||||
| chr17:77189006
|
T | TA | 31 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(28): Show | 34 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.64-1795dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77189006 | |||||
| chr17:77189042
|
A | G | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-1761A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189042 | ||||||
| chr17:77189266
|
G | C | 1 | a0001c0002t0028g0387 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.64-1537G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189266 | ||||||
| chr17:77189322
|
C | T | 35 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.64-1481C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189322 | ||||||
| chr17:77189345
|
G | T | 1 | a0005c0008t0002g0073 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.64-1458G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189345 | ||||||
| chr17:77189595
|
T | G | 1 | a0001c0002t0024g0318 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.64-1208T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189595 | ||||||
| chr17:77189626
|
G | GGTTTT | 36 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-1160_64-1156dup others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr17 | 77189626 | |||||
| chr17:77189690
|
G | T | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.64-1113G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189690 | ||||||
| chr17:77189715
|
G | T | 36 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.64-1088G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189715 | ||||||
| chr17:77189764
|
A | G | 63 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(60): Show | 65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.64-1039A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189764 | ||||||
| chr17:77189778
|
G | A | 1 | a0001c0002t0028g0387 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.64-1025G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189778 | ||||||
| chr17:77189818
|
C | T | 8 | a0001c0001t0007g0129a0001c0001t0007g0153a0001c0001t0007g0154others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.64-985C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189818 | ||||||
| chr17:77189919
|
C | T | 3 | a0001c0002t0004g0013a0001c0002t0004g0341a0001c0002t0004g0352 | 4 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.64-884C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189919 | ||||||
| chr17:77189994
|
C | G | 1 | a0001c0001t0070g0219 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.64-809C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189994 | ||||||
| chr17:77189998
|
T | C | 1 | a0001c0003t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.64-805T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77189998 | ||||||
| chr17:77190017
|
C | G | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-786C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77190017 | ||||||
| chr17:77190072
|
C | T | 395 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(392): Show | 409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.64-731C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77190072 | ||||||
| chr17:77190271
|
C | T | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.64-532C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77190271 | ||||||
| chr17:77190447
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.64-356G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 3/16 | chr17 | 77190447 | ||||||
| chr17:77190961
|
C | T | 9 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.213+9C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | chr17 | 77190961 | ||||||
| chr17:77190962
|
G | A | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.213+10G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | chr17 | 77190962 | ||||||
| chr17:77190983
|
AAGGGCGT others(11): Show |
A | 1 | a0001c0001t0002g0081 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.213+62_213+79delTG others(16): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr17 | 77190983 | |||||
| chr17:77191043
|
A | ATCCTGGA others(11): Show |
4 | a0001c0001t0003g0110a0001c0001t0003g0151a0001c0001t0003g0158others(1): Show | 4 | HG01106.hp1 HG02451.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.214-109_214-92dupA others(17): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr17 | 77191043 | |||||
| chr17:77191155
|
C | T | 1 | a0001c0001t0006g0203 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.214-26C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 4/16 | chr17 | 77191155 | ||||||
| chr17:77191321
|
T | C | 7 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(4): Show | 8 | HG01255.hp1 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.345+9T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191321 | ||||||
| chr17:77191331
|
G | A | 9 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.345+19G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191331 | ||||||
| chr17:77191334
|
G | A | 1 | a0001c0003t0001g0265 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.345+22G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191334 | ||||||
| chr17:77191355
|
T | C | 3 | a0001c0002t0004g0036a0001c0002t0004g0370a0001c0002t0073g0372 | 3 | HG00735.hp1 HG01109.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.345+43T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191355 | ||||||
| chr17:77191641
|
C | T | 2 | a0001c0003t0001g0235a0001c0003t0001g0236 | 2 | HG02055.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.345+329C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191641 | ||||||
| chr17:77191652
|
C | G | 124 | a0001c0002t0004g0002a0001c0002t0004g0013a0001c0002t0004g0014others(121): Show | 127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.345+340C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191652 | ||||||
| chr17:77191666
|
C | T | 36 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.345+354C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191666 | ||||||
| chr17:77191763
|
G | C | 81 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(80): Show |
intron_variant | MODIFIER | c.345+451G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191763 | ||||||
| chr17:77191774
|
C | T | 82 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(79): Show | 84 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.345+462C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191774 | ||||||
| chr17:77191778
|
C | T | 1 | a0001c0003t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.345+466C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191778 | ||||||
| chr17:77191957
|
C | T | 36 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.345+645C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77191957 | ||||||
| chr17:77192158
|
A | G | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.345+846A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192158 | ||||||
| chr17:77192247
|
A | G | 2 | a0001c0001t0002g0081a0001c0001t0002g0101 | 2 | NA18956.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.345+935A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192247 | ||||||
| chr17:77192269
|
A | T | 1 | a0001c0001t0041g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.345+957A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192269 | ||||||
| chr17:77192291
|
G | C | 3 | a0001c0001t0003g0130a0001c0001t0003g0163a0001c0001t0003g0169 | 3 | HG01168.hp2 HG01515.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.345+979G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192291 | ||||||
| chr17:77192538
|
G | C | 78 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(75): Show | 80 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.346-883G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192538 | ||||||
| chr17:77192600
|
A | G | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.346-821A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192600 | ||||||
| chr17:77192618
|
C | T | 63 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(60): Show | 65 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.346-803C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192618 | ||||||
| chr17:77192663
|
C | CT | 10 | a0001c0001t0007g0129a0001c0001t0007g0132a0001c0001t0007g0153others(7): Show | 10 | HG01099.hp2 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.346-746dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr17 | 77192663 | |||||
| chr17:77192777
|
C | T | 81 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.346-644C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192777 | ||||||
| chr17:77192970
|
T | C | 12 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(9): Show | 12 | NA18940.hp1 NA18946.hp1 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.346-451T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77192970 | ||||||
| chr17:77193158
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.346-263G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77193158 | ||||||
| chr17:77193418
|
C | T | 1 | a0001c0001t0003g0167 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.346-3C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 5/16 | chr17 | 77193418 | ||||||
| chr17:77193995
|
A | G | 2 | a0001c0002t0005g0286a0001c0002t0005g0287 | 2 | HG02129.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.474+446A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77193995 | ||||||
| chr17:77193999
|
G | A | 1 | a0001c0002t0005g0371 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.474+450G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77193999 | ||||||
| chr17:77194030
|
C | T | 34 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(31): Show | 37 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.474+481C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194030 | ||||||
| chr17:77194176
|
G | T | 1 | a0002c0004t0013g0176 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.475-501G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194176 | ||||||
| chr17:77194280
|
C | T | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.475-397C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194280 | ||||||
| chr17:77194352
|
C | T | 3 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0128 | 3 | NA18940.hp2 NA18973.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.475-325C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194352 | ||||||
| chr17:77194540
|
A | G | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.475-137A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | chr17 | 77194540 | ||||||
| chr17:77194551
|
C | CA | 22 | a0001c0001t0002g0067a0001c0001t0006g0203a0001c0001t0008g0393others(19): Show | 22 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(19): Show |
intron_variant | MODIFIER | c.475-113dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr17 | 77194551 | |||||
| chr17:77194937
|
G | A | 1 | a0001c0002t0066g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.709+26G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77194937 | ||||||
| chr17:77194961
|
G | A | 3 | a0001c0003t0020g0028a0001c0003t0020g0029a0001c0003t0020g0264 | 3 | HG02738.hp2 HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.709+50G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77194961 | ||||||
| chr17:77194967
|
G | T | 1 | a0001c0002t0004g0383 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.709+56G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77194967 | ||||||
| chr17:77195160
|
G | GTGTT | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.709+263_709+266dup others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr17 | 77195160 | |||||
| chr17:77195243
|
G | A | 1 | a0001c0001t0006g0204 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.709+332G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195243 | ||||||
| chr17:77195304
|
G | T | 219 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(216): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.709+393G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195304 | ||||||
| chr17:77195306
|
G | GT | 67 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(64): Show | 69 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.709+404dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr17 | 77195306 | |||||
| chr17:77195315
|
TG | T | 3 | a0001c0001t0006g0213a0001c0001t0006g0224a0001c0001t0006g0225 | 3 | HG02145.hp2 HG02630.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.709+405delG | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195315 | ||||||
| chr17:77195316
|
G | T | 386 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(383): Show | 399 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(396): Show |
intron_variant | MODIFIER | c.709+405G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195316 | ||||||
| chr17:77195318
|
T | C | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.709+407T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195318 | ||||||
| chr17:77195320
|
G | T | 1 | a0001c0001t0007g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.709+409G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195320 | ||||||
| chr17:77195475
|
C | T | 7 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(4): Show | 8 | HG01255.hp1 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.709+564C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195475 | ||||||
| chr17:77195510
|
A | G | 54 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(51): Show | 57 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(54): Show |
intron_variant | MODIFIER | c.709+599A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195510 | ||||||
| chr17:77195514
|
A | G | 4 | a0001c0001t0006g0220a0001c0001t0006g0222a0001c0001t0006g0227others(1): Show | 4 | HG03017.hp1 HG04184.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+603A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195514 | ||||||
| chr17:77195629
|
A | G | 4 | a0001c0001t0019g0053a0001c0001t0019g0107a0001c0001t0019g0108others(1): Show | 4 | HG02109.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.710-573A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195629 | ||||||
| chr17:77195663
|
T | G | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.710-539T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195663 | ||||||
| chr17:77195736
|
C | T | 1 | a0001c0001t0003g0167 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.710-466C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195736 | ||||||
| chr17:77195837
|
C | CT | 21 | a0001c0001t0006g0203a0001c0001t0008g0393a0001c0001t0008g0397others(18): Show | 21 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(18): Show |
intron_variant | MODIFIER | c.710-355dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr17 | 77195837 | |||||
| chr17:77195853
|
A | G | 1 | a0001c0002t0004g0166 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.710-349A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195853 | ||||||
| chr17:77195929
|
A | T | 1 | a0001c0001t0003g0130 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.710-273A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77195929 | ||||||
| chr17:77196071
|
A | G | 26 | a0001c0001t0003g0183a0001c0001t0005g0039a0001c0001t0007g0019others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-131A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77196071 | ||||||
| chr17:77196082
|
C | T | 82 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(79): Show | 84 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.710-120C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77196082 | ||||||
| chr17:77196155
|
A | G | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.710-47A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 7/16 | chr17 | 77196155 | ||||||
| chr17:77196692
|
AG | A | 13 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(10): Show | 14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.819+383delG | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77196692 | |||||
| chr17:77196816
|
T | C | 65 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(62): Show | 67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.819+505T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77196816 | ||||||
| chr17:77196825
|
G | A | 79 | a0001c0002t0004g0002a0001c0002t0004g0013a0001c0002t0004g0014others(76): Show | 82 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.819+514G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77196825 | ||||||
| chr17:77196940
|
G | C | 1 | a0001c0002t0005g0298 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.819+629G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77196940 | ||||||
| chr17:77197080
|
A | G | 1 | a0001c0009t0022g0191 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.819+769A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197080 | ||||||
| chr17:77197162
|
G | A | 1 | a0001c0001t0003g0169 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.819+851G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197162 | ||||||
| chr17:77197193
|
G | A | 5 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0146others(2): Show | 6 | HG01070.hp1 HG01071.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.819+882G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197193 | ||||||
| chr17:77197218
|
C | G | 122 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(119): Show | 125 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.819+907C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197218 | ||||||
| chr17:77197313
|
A | G | 1 | a0001c0001t0002g0283 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.819+1002A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197313 | ||||||
| chr17:77197317
|
C | T | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.819+1006C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197317 | ||||||
| chr17:77197572
|
C | G | 2 | a0002c0004t0046g0186a0002c0004t0060g0187 | 2 | HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.819+1261C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197572 | ||||||
| chr17:77197637
|
G | A | 123 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(120): Show | 129 | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.819+1326G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197637 | ||||||
| chr17:77197656
|
G | A | 1 | a0001c0001t0003g0117 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.819+1345G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197656 | ||||||
| chr17:77197714
|
A | G | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.819+1403A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197714 | ||||||
| chr17:77197808
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.819+1497G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197808 | ||||||
| chr17:77197881
|
C | T | 65 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(62): Show | 67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.819+1570C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197881 | ||||||
| chr17:77197886
|
G | A | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.819+1575G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197886 | ||||||
| chr17:77197907
|
C | T | 2 | a0001c0002t0011g0344a0001c0002t0011g0345 | 2 | NA19056.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.819+1596C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197907 | ||||||
| chr17:77197956
|
G | T | 2 | a0001c0001t0003g0118a0001c0001t0003g0119 | 2 | HG02602.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.819+1645G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77197956 | ||||||
| chr17:77198164
|
G | A | 1 | a0001c0001t0003g0147 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.819+1853G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198164 | ||||||
| chr17:77198170
|
G | A | 1 | a0001c0002t0005g0328 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.819+1859G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198170 | ||||||
| chr17:77198197
|
C | A | 35 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.819+1886C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198197 | ||||||
| chr17:77198305
|
T | C | 270 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(267): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.819+1994T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198305 | ||||||
| chr17:77198327
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.819+2016A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198327 | ||||||
| chr17:77198368
|
C | T | 1 | a0001c0001t0007g0019 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.819+2057C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198368 | ||||||
| chr17:77198372
|
CT | C | 4 | a0001c0002t0005g0306a0001c0002t0005g0307a0001c0002t0005g0315others(1): Show | 4 | HG03834.hp1 HG03942.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.819+2064delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77198372 | |||||
| chr17:77198421
|
G | C | 83 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.820-2063G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198421 | ||||||
| chr17:77198576
|
C | CT | 6 | a0001c0001t0002g0004a0001c0001t0006g0207a0001c0001t0006g0208others(3): Show | 7 | HG00597.hp2 HG00733.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.820-1892dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77198576 | |||||
| chr17:77198598
|
G | A | 1 | a0001c0001t0003g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.820-1886G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198598 | ||||||
| chr17:77198614
|
G | A | 83 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.820-1870G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198614 | ||||||
| chr17:77198648
|
C | T | 1 | a0001c0001t0002g0100 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.820-1836C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198648 | ||||||
| chr17:77198731
|
G | T | 1 | a0001c0001t0041g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.820-1753G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198731 | ||||||
| chr17:77198785
|
G | C | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.820-1699G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198785 | ||||||
| chr17:77198819
|
G | A | 34 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(31): Show | 37 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.820-1665G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198819 | ||||||
| chr17:77198824
|
G | A | 83 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(80): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.820-1660G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198824 | ||||||
| chr17:77198862
|
G | A | 1 | a0009c0012t0005g0320 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.820-1622G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198862 | ||||||
| chr17:77198863
|
C | T | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.820-1621C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198863 | ||||||
| chr17:77198864
|
G | T | 124 | a0001c0002t0004g0002a0001c0002t0004g0013a0001c0002t0004g0014others(121): Show | 127 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.820-1620G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198864 | ||||||
| chr17:77198867
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.820-1617C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198867 | ||||||
| chr17:77198879
|
C | G | 1 | a0001c0002t0066g0301 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.820-1605C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77198879 | ||||||
| chr17:77199005
|
C | CG | 33 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(30): Show | 36 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.820-1479_820-1478i others(3): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199005 | ||||||
| chr17:77199005
|
C | CT | 139 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(136): Show | 143 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.820-1462dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77199005 | |||||
| chr17:77199005
|
CT | C | 6 | a0001c0001t0019g0108a0001c0002t0005g0198a0001c0002t0005g0308others(3): Show | 6 | HG02280.hp1 HG02965.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.820-1462delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77199005 | |||||
| chr17:77199006
|
T | G | 1 | a0001c0001t0006g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.820-1478T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199006 | ||||||
| chr17:77199022
|
T | G | 1 | a0001c0001t0006g0210 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.820-1462T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199022 | ||||||
| chr17:77199147
|
G | GGC | 12 | a0001c0002t0004g0034a0001c0002t0004g0035a0001c0002t0004g0332others(9): Show | 12 | HG00558.hp1 HG00639.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.820-1335_820-1334d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr17 | 77199147 | |||||
| chr17:77199161
|
C | T | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1323C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199161 | ||||||
| chr17:77199185
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.820-1299G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199185 | ||||||
| chr17:77199273
|
G | A | 1 | a0001c0002t0005g0298 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.820-1211G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199273 | ||||||
| chr17:77199356
|
C | G | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.820-1128C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199356 | ||||||
| chr17:77199393
|
G | A | 284 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(281): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.820-1091G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199393 | ||||||
| chr17:77199432
|
C | T | 13 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(10): Show | 14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.820-1052C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199432 | ||||||
| chr17:77199441
|
G | A | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.820-1043G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199441 | ||||||
| chr17:77199445
|
G | C | 1 | a0001c0003t0001g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.820-1039G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199445 | ||||||
| chr17:77199457
|
A | G | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.820-1027A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199457 | ||||||
| chr17:77199552
|
C | T | 1 | a0001c0002t0004g0014 | 2 | HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.820-932C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199552 | ||||||
| chr17:77199573
|
G | A | 1 | a0001c0001t0031g0088 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.820-911G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199573 | ||||||
| chr17:77199675
|
A | G | 1 | a0001c0003t0001g0239 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.820-809A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199675 | ||||||
| chr17:77199683
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.820-801G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199683 | ||||||
| chr17:77199695
|
G | A | 5 | a0001c0003t0001g0259a0001c0003t0001g0282a0001c0003t0020g0028others(2): Show | 5 | HG02735.hp1 HG02738.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.820-789G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199695 | ||||||
| chr17:77199781
|
G | A | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.820-703G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199781 | ||||||
| chr17:77199963
|
G | A | 1 | a0001c0002t0047g0350 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.820-521G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199963 | ||||||
| chr17:77199971
|
C | G | 1 | a0001c0002t0004g0182 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.820-513C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77199971 | ||||||
| chr17:77200034
|
C | T | 125 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(122): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.820-450C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200034 | ||||||
| chr17:77200059
|
A | T | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.820-425A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200059 | ||||||
| chr17:77200173
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.820-311G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200173 | ||||||
| chr17:77200177
|
A | G | 1 | a0001c0001t0008g0403 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.820-307A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200177 | ||||||
| chr17:77200356
|
A | T | 1 | a0001c0002t0012g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.820-128A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 8/16 | chr17 | 77200356 | ||||||
| chr17:77200678
|
C | T | 1 | a0001c0001t0006g0220 | 1 | HG03017.hp1 | splice_region_variant&intron_variant | LOW | c.1009+5C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200678 | ||||||
| chr17:77200679
|
G | A | 3 | a0001c0005t0036g0017a0001c0005t0037g0016a0008c0011t0036g0018 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
splice_region_variant&intron_variant | LOW | c.1009+6G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200679 | ||||||
| chr17:77200753
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1009+80G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200753 | ||||||
| chr17:77200920
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1009+247C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200920 | ||||||
| chr17:77200969
|
C | T | 1 | a0001c0002t0002g0297 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1009+296C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200969 | ||||||
| chr17:77200983
|
G | A | 1 | a0001c0002t0012g0324 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1009+310G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77200983 | ||||||
| chr17:77201315
|
A | T | 1 | a0001c0002t0005g0307 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1009+642A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201315 | ||||||
| chr17:77201376
|
C | T | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1009+703C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201376 | ||||||
| chr17:77201452
|
C | CT | 122 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(119): Show | 127 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.1009+795dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77201452 | |||||
| chr17:77201550
|
A | G | 65 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(62): Show | 67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1009+877A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201550 | ||||||
| chr17:77201773
|
T | C | 3 | a0001c0001t0003g0126a0001c0001t0003g0127a0001c0001t0003g0128 | 3 | NA18940.hp2 NA18973.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.1009+1100T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201773 | ||||||
| chr17:77201942
|
C | T | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1009+1269C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77201942 | ||||||
| chr17:77202072
|
G | A | 1 | a0001c0001t0041g0109 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1009+1399G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202072 | ||||||
| chr17:77202078
|
A | G | 1 | a0001c0003t0001g0251 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1009+1405A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202078 | ||||||
| chr17:77202141
|
T | C | 3 | a0001c0001t0001g0232a0001c0001t0001g0242a0001c0001t0001g0258 | 3 | HG01257.hp2 HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1010-1429T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202141 | ||||||
| chr17:77202154
|
C | T | 1 | a0001c0001t0009g0052 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1010-1416C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202154 | ||||||
| chr17:77202164
|
G | A | 1 | a0001c0001t0006g0010 | 2 | HG02071.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1010-1406G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202164 | ||||||
| chr17:77202324
|
TAAAA | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0273a0001c0001t0001g0274others(4): Show | 7 | NA18952.hp2 NA18957.hp1 NA19005.hp2 others(4): Show |
intron_variant | MODIFIER | c.1010-1240_1010-123 others(8): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77202324 | |||||
| chr17:77202347
|
G | A | 3 | a0001c0002t0005g0306a0001c0002t0005g0307a0006c0013t0005g0292 | 3 | HG03834.hp1 HG03942.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1010-1223G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202347 | ||||||
| chr17:77202447
|
C | T | 6 | a0001c0001t0006g0206a0001c0002t0012g0323a0001c0002t0012g0324others(3): Show | 6 | HG02004.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1010-1123C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202447 | ||||||
| chr17:77202658
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1010-912G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202658 | ||||||
| chr17:77202662
|
A | G | 1 | a0007c0010t0002g0194 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1010-908A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202662 | ||||||
| chr17:77202748
|
T | A | 1 | a0001c0003t0001g0188 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1010-822T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202748 | ||||||
| chr17:77202781
|
A | G | 269 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(266): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1010-789A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202781 | ||||||
| chr17:77202849
|
G | T | 3 | a0001c0001t0019g0053a0001c0001t0019g0107a0001c0001t0019g0108 | 3 | HG02109.hp2 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1010-721G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202849 | ||||||
| chr17:77202858
|
G | T | 81 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1010-712G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202858 | ||||||
| chr17:77202863
|
G | A | 35 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1010-707G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202863 | ||||||
| chr17:77202873
|
C | T | 1 | a0001c0001t0003g0139 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1010-697C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202873 | ||||||
| chr17:77202874
|
G | A | 1 | a0001c0002t0005g0321 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1010-696G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202874 | ||||||
| chr17:77202928
|
T | A | 3 | a0001c0005t0036g0017a0001c0005t0037g0016a0008c0011t0036g0018 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1010-642T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202928 | ||||||
| chr17:77202928
|
T | TA | 4 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0100others(1): Show | 4 | HG03831.hp1 NA18967.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.1010-635dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77202928 | |||||
| chr17:77202935
|
AT | A | 3 | a0001c0001t0002g0086a0001c0001t0058g0071a0007c0010t0002g0194 | 3 | HG02040.hp2 HG02273.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1010-634delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202935 | ||||||
| chr17:77202936
|
T | A | 58 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(55): Show | 60 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1010-634T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202936 | ||||||
| chr17:77202936
|
T | TA | 14 | a0001c0001t0008g0410a0001c0001t0009g0003a0001c0001t0009g0051others(11): Show | 16 | HG00639.hp2 HG01255.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.1010-618dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77202936 | |||||
| chr17:77202936
|
TA | T | 168 | a0001c0001t0001g0275a0001c0001t0003g0115a0001c0001t0003g0163others(165): Show | 175 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.1010-618delA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chr17 | 77202936 | |||||
| chr17:77202939
|
A | T | 3 | a0001c0001t0008g0407a0001c0001t0008g0408a0001c0001t0008g0409 | 3 | NA18970.hp1 NA18990.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1010-631A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202939 | ||||||
| chr17:77202941
|
A | T | 1 | a0001c0003t0001g0271 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1010-629A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202941 | ||||||
| chr17:77202942
|
A | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0232a0001c0001t0001g0237others(5): Show | 9 | HG00642.hp2 HG01099.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.1010-628A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77202942 | ||||||
| chr17:77203267
|
T | C | 1 | a0001c0002t0004g0014 | 2 | HG01123.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1010-303T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203267 | ||||||
| chr17:77203267
|
T | G | 1 | a0001c0001t0003g0144 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1010-303T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203267 | ||||||
| chr17:77203310
|
C | T | 34 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(31): Show | 35 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(32): Show |
intron_variant | MODIFIER | c.1010-260C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203310 | ||||||
| chr17:77203319
|
C | T | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1010-251C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203319 | ||||||
| chr17:77203456
|
T | A | 1 | a0001c0001t0009g0051 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1010-114T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203456 | ||||||
| chr17:77203473
|
C | G | 1 | a0001c0002t0004g0383 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1010-97C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203473 | ||||||
| chr17:77203494
|
G | A | 2 | a0001c0002t0018g0361a0001c0002t0018g0364 | 2 | NA18963.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1010-76G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203494 | ||||||
| chr17:77203498
|
A | G | 65 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(62): Show | 67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1010-72A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 9/16 | chr17 | 77203498 | ||||||
| chr17:77203667
|
G | A | 1 | a0001c0001t0008g0410 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1098+9G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203667 | ||||||
| chr17:77203787
|
T | C | 1 | a0001c0002t0005g0311 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1098+129T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203787 | ||||||
| chr17:77203791
|
A | C | 3 | a0001c0005t0036g0017a0001c0005t0037g0016a0008c0011t0036g0018 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1098+133A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203791 | ||||||
| chr17:77203796
|
C | T | 14 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(11): Show | 14 | HG02145.hp1 HG03540.hp2 NA18940.hp1 others(11): Show |
intron_variant | MODIFIER | c.1098+138C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203796 | ||||||
| chr17:77203821
|
CAG | C | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+165_1098+166d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77203821 | |||||
| chr17:77203872
|
G | T | 35 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1098+214G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203872 | ||||||
| chr17:77203950
|
C | T | 44 | a0001c0002t0004g0303a0001c0002t0005g0032a0001c0002t0005g0033others(41): Show | 44 | HG00323.hp1 HG00544.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.1098+292C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203950 | ||||||
| chr17:77203997
|
C | T | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1098+339C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77203997 | ||||||
| chr17:77204074
|
A | G | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1098+416A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204074 | ||||||
| chr17:77204199
|
T | TA | 65 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(62): Show | 67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1098+542dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204199 | |||||
| chr17:77204300
|
C | T | 1 | a0001c0001t0001g0249 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1098+642C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204300 | ||||||
| chr17:77204344
|
A | C | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1098+686A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204344 | ||||||
| chr17:77204466
|
C | T | 9 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1098+808C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204466 | ||||||
| chr17:77204479
|
C | T | 66 | a0001c0002t0004g0002a0001c0002t0004g0013a0001c0002t0004g0014others(63): Show | 69 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.1099-797C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204479 | ||||||
| chr17:77204521
|
G | GC | 34 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(31): Show | 36 | HG00438.hp2 HG00738.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1099-754dupC | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204521 | |||||
| chr17:77204522
|
C | CA | 24 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(21): Show | 27 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.1099-754_1099-753i others(3): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204522 | ||||||
| chr17:77204522
|
C | CAT | 6 | a0001c0001t0006g0203a0001c0001t0006g0218a0001c0001t0006g0222others(3): Show | 6 | HG03669.hp1 HG04184.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-754_1099-753i others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204522 | ||||||
| chr17:77204522
|
C | CT | 127 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(124): Show | 131 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.1099-727dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204522 | |||||
| chr17:77204522
|
C | CTT | 15 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0068others(12): Show | 16 | HG01256.hp2 HG01258.hp2 HG02155.hp1 others(13): Show |
intron_variant | MODIFIER | c.1099-728_1099-727d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204522 | |||||
| chr17:77204522
|
CT | C | 65 | a0001c0001t0003g0110a0001c0001t0003g0130a0001c0001t0006g0224others(62): Show | 65 | HG00323.hp1 HG00597.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1099-727delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204522 | |||||
| chr17:77204522
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0006g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1099-737_1099-727d others(13): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr17 | 77204522 | |||||
| chr17:77204523
|
T | A | 2 | a0001c0001t0006g0209a0001c0001t0006g0223 | 2 | HG01496.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1099-753T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204523 | ||||||
| chr17:77204523
|
T | C | 32 | a0001c0001t0003g0115a0001c0001t0003g0117a0001c0001t0003g0137others(29): Show | 32 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.1099-753T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204523 | ||||||
| chr17:77204524
|
T | A | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1099-752T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204524 | ||||||
| chr17:77204524
|
T | C | 14 | a0001c0001t0003g0110a0001c0001t0003g0130a0001c0001t0007g0038others(11): Show | 14 | HG01081.hp1 HG01168.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1099-752T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204524 | ||||||
| chr17:77204526
|
T | A | 3 | a0001c0005t0036g0017a0001c0005t0037g0016a0008c0011t0036g0018 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1099-750T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204526 | ||||||
| chr17:77204527
|
T | A | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1099-749T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204527 | ||||||
| chr17:77204529
|
T | A | 2 | a0001c0009t0022g0191a0004c0006t0022g0189 | 2 | HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1099-747T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204529 | ||||||
| chr17:77204530
|
T | A | 1 | a0004c0006t0022g0190 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1099-746T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204530 | ||||||
| chr17:77204534
|
T | A | 1 | a0001c0001t0006g0220 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1099-742T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204534 | ||||||
| chr17:77204662
|
C | G | 1 | a0001c0001t0067g0246 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1099-614C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204662 | ||||||
| chr17:77204764
|
A | G | 4 | a0001c0001t0003g0110a0001c0001t0003g0151a0001c0001t0003g0158others(1): Show | 4 | HG01106.hp1 HG02451.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1099-512A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204764 | ||||||
| chr17:77204766
|
G | A | 13 | a0001c0001t0009g0003a0001c0001t0009g0051a0001c0001t0009g0052others(10): Show | 14 | HG01255.hp1 HG01884.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1099-510G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204766 | ||||||
| chr17:77204862
|
C | A | 9 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(6): Show | 10 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1099-414C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204862 | ||||||
| chr17:77204888
|
C | T | 2 | a0001c0001t0006g0218a0001c0001t0070g0219 | 2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1099-388C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204888 | ||||||
| chr17:77204935
|
C | T | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1099-341C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77204935 | ||||||
| chr17:77205048
|
G | A | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.1099-228G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77205048 | ||||||
| chr17:77205070
|
G | C | 1 | a0001c0001t0001g0232 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1099-206G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77205070 | ||||||
| chr17:77205246
|
T | C | 3 | a0001c0003t0001g0251a0001c0003t0034g0247a0001c0003t0034g0250 | 3 | HG00423.hp2 HG02071.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1099-30T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77205246 | ||||||
| chr17:77205270
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA18970.hp2 | splice_region_variant&intron_variant | LOW | c.1099-6A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 10/16 | chr17 | 77205270 | ||||||
| chr17:77205447
|
G | C | 34 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(31): Show | 37 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.1169+101G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205447 | ||||||
| chr17:77205560
|
C | T | 3 | a0001c0001t0008g0407a0001c0001t0008g0408a0001c0001t0008g0409 | 3 | NA18970.hp1 NA18990.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1169+214C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205560 | ||||||
| chr17:77205668
|
A | G | 2 | a0001c0001t0019g0107a0001c0001t0019g0108 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1169+322A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205668 | ||||||
| chr17:77205861
|
T | C | 396 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(393): Show | 410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.1170-368T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205861 | ||||||
| chr17:77205931
|
G | A | 1 | a0001c0003t0001g0188 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1170-298G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205931 | ||||||
| chr17:77205963
|
A | G | 9 | a0001c0003t0001g0188a0001c0003t0001g0233a0001c0003t0001g0234others(6): Show | 9 | HG00408.hp1 HG02040.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1170-266A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77205963 | ||||||
| chr17:77206146
|
A | C | 1 | a0009c0012t0005g0320 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1170-83A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 11/16 | chr17 | 77206146 | ||||||
| chr17:77206428
|
T | C | 2 | a0001c0003t0001g0260a0001c0003t0001g0272 | 2 | NA19057.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1341+28T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/16 | chr17 | 77206428 | ||||||
| chr17:77206502
|
A | G | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1341+102A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/16 | chr17 | 77206502 | ||||||
| chr17:77206586
|
A | G | 2 | a0001c0001t0007g0153a0001c0001t0007g0154 | 2 | HG01243.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1342-142A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/16 | chr17 | 77206586 | ||||||
| chr17:77206636
|
C | A | 5 | a0001c0001t0007g0129a0001c0001t0007g0153a0001c0001t0007g0154others(2): Show | 5 | HG01243.hp2 HG02630.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1342-92C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 12/16 | chr17 | 77206636 | ||||||
| chr17:77206895
|
C | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1476+33C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77206895 | ||||||
| chr17:77206925
|
G | A | 2 | a0004c0006t0022g0189a0004c0006t0022g0190 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1476+63G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77206925 | ||||||
| chr17:77206982
|
G | T | 1 | a0001c0002t0004g0333 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1476+120G>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77206982 | ||||||
| chr17:77207010
|
C | T | 81 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(78): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.1476+148C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207010 | ||||||
| chr17:77207088
|
C | G | 125 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(122): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1476+226C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207088 | ||||||
| chr17:77207089
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1476+227G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207089 | ||||||
| chr17:77207256
|
CAG | C | 125 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(122): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1476+395_1476+396d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207256 | ||||||
| chr17:77207319
|
T | TTGG | 65 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(62): Show | 67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1476+461_1476+463d others(5): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr17 | 77207319 | |||||
| chr17:77207377
|
T | C | 1 | a0001c0001t0003g0126 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1476+515T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207377 | ||||||
| chr17:77207429
|
C | T | 10 | a0001c0001t0007g0129a0001c0001t0007g0132a0001c0001t0007g0153others(7): Show | 10 | HG01099.hp2 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1476+567C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207429 | ||||||
| chr17:77207461
|
T | C | 7 | a0001c0002t0005g0327a0001c0002t0005g0328a0001c0002t0005g0329others(4): Show | 7 | HG01884.hp1 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1476+599T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207461 | ||||||
| chr17:77207601
|
G | A | 35 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1476+739G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207601 | ||||||
| chr17:77207628
|
T | A | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1476+766T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207628 | ||||||
| chr17:77207783
|
G | A | 2 | a0001c0001t0026g0394a0001c0001t0026g0396 | 2 | HG02273.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1476+921G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77207783 | ||||||
| chr17:77208069
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1476+1207C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208069 | ||||||
| chr17:77208261
|
C | T | 1 | a0001c0003t0001g0266 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1477-1081C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208261 | ||||||
| chr17:77208466
|
C | T | 125 | a0001c0002t0002g0297a0001c0002t0004g0002a0001c0002t0004g0013others(122): Show | 128 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1477-876C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208466 | ||||||
| chr17:77208658
|
A | G | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1477-684A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208658 | ||||||
| chr17:77208805
|
T | C | 65 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(62): Show | 67 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1477-537T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77208805 | ||||||
| chr17:77208992
|
CTT | C | 13 | a0001c0001t0005g0039a0001c0001t0007g0019a0001c0001t0007g0037others(10): Show | 13 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(10): Show |
intron_variant | MODIFIER | c.1477-347_1477-346d others(4): Show |
SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr17 | 77208992 | |||||
| chr17:77209063
|
A | G | 36 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.1477-279A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77209063 | ||||||
| chr17:77209086
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1477-256G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77209086 | ||||||
| chr17:77209202
|
T | G | 1 | a0001c0002t0005g0305 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1477-140T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 13/16 | chr17 | 77209202 | ||||||
| chr17:77209480
|
C | T | 36 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
splice_region_variant&intron_variant | LOW | c.1611+4C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209480 | ||||||
| chr17:77209536
|
C | T | 6 | a0001c0002t0005g0198a0001c0002t0005g0300a0001c0002t0005g0308others(3): Show | 6 | HG01081.hp2 HG01175.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1611+60C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209536 | ||||||
| chr17:77209577
|
C | T | 3 | a0001c0005t0036g0017a0001c0005t0037g0016a0008c0011t0036g0018 | 3 | HG01891.hp1 HG02109.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1611+101C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209577 | ||||||
| chr17:77209641
|
A | G | 1 | a0001c0001t0003g0162 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1611+165A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209641 | ||||||
| chr17:77209848
|
C | CT | 66 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(63): Show | 68 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1611+383dupT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr17 | 77209848 | |||||
| chr17:77209848
|
CT | C | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1611+383delT | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr17 | 77209848 | |||||
| chr17:77209979
|
A | G | 3 | a0001c0001t0003g0115a0001c0001t0003g0226a0001c0001t0045g0116 | 3 | HG02280.hp2 HG02896.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1611+503A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77209979 | ||||||
| chr17:77210000
|
G | A | 5 | a0001c0001t0006g0215a0001c0001t0006g0216a0001c0001t0006g0217others(2): Show | 5 | HG02300.hp2 NA19000.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.1611+524G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210000 | ||||||
| chr17:77210069
|
C | G | 35 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(32): Show | 38 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1611+593C>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210069 | ||||||
| chr17:77210097
|
C | T | 80 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(77): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1611+621C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210097 | ||||||
| chr17:77210142
|
C | T | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1611+666C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210142 | ||||||
| chr17:77210519
|
G | C | 1 | a0001c0001t0032g0009 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1611+1043G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210519 | ||||||
| chr17:77210569
|
C | T | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1611+1093C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77210569 | ||||||
| chr17:77211148
|
A | G | 283 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(280): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.1612-802A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211148 | ||||||
| chr17:77211162
|
C | T | 3 | a0001c0001t0003g0113a0001c0001t0006g0224a0001c0001t0006g0225 | 3 | HG02135.hp1 HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1612-788C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211162 | ||||||
| chr17:77211229
|
G | A | 1 | a0001c0001t0003g0183 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1612-721G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211229 | ||||||
| chr17:77211238
|
G | A | 1 | a0001c0001t0006g0207 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1612-712G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211238 | ||||||
| chr17:77211261
|
T | G | 10 | a0001c0001t0007g0129a0001c0001t0007g0132a0001c0001t0007g0153others(7): Show | 10 | HG01099.hp2 HG01243.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1612-689T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211261 | ||||||
| chr17:77211264
|
C | A | 1 | a0001c0001t0003g0139 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1612-686C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211264 | ||||||
| chr17:77211271
|
A | G | 1 | a0001c0002t0004g0131 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1612-679A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211271 | ||||||
| chr17:77211341
|
C | T | 3 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171 | 4 | HG02717.hp1 HG02965.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1612-609C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211341 | ||||||
| chr17:77211449
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1612-501G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211449 | ||||||
| chr17:77211463
|
G | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(61): Show | 66 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1612-487G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211463 | ||||||
| chr17:77211500
|
C | T | 2 | a0001c0001t0006g0224a0001c0001t0006g0225 | 2 | HG02145.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1612-450C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211500 | ||||||
| chr17:77211504
|
T | G | 64 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(61): Show | 66 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1612-446T>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211504 | ||||||
| chr17:77211541
|
C | T | 5 | a0001c0003t0001g0234a0001c0003t0001g0270a0001c0003t0023g0030others(2): Show | 5 | HG00408.hp1 HG02155.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1612-409C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211541 | ||||||
| chr17:77211771
|
A | C | 64 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(61): Show | 66 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1612-179A>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211771 | ||||||
| chr17:77211866
|
G | A | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1612-84G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211866 | ||||||
| chr17:77211882
|
C | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1612-68C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211882 | ||||||
| chr17:77211884
|
A | G | 281 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(278): Show | 293 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.1612-66A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211884 | ||||||
| chr17:77211891
|
C | T | 1 | a0001c0002t0004g0369 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1612-59C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 14/16 | chr17 | 77211891 | ||||||
| chr17:77212331
|
G | A | 20 | a0001c0001t0008g0393a0001c0001t0008g0397a0001c0001t0008g0398others(17): Show | 20 | HG02273.hp2 HG02698.hp1 HG03710.hp2 others(17): Show |
intron_variant | MODIFIER | c.1863+130G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212331 | ||||||
| chr17:77212392
|
A | G | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1863+191A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212392 | ||||||
| chr17:77212440
|
A | G | 1 | a0001c0001t0008g0399 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1863+239A>G | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212440 | ||||||
| chr17:77212482
|
T | A | 10 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0079others(7): Show | 11 | HG01943.hp2 HG02004.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.1863+281T>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212482 | ||||||
| chr17:77212498
|
C | T | 80 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(77): Show | 82 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1863+297C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212498 | ||||||
| chr17:77212501
|
C | A | 1 | a0001c0001t0002g0283 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1863+300C>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212501 | ||||||
| chr17:77212519
|
G | A | 81 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(78): Show | 83 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.1863+318G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212519 | ||||||
| chr17:77212556
|
G | A | 93 | a0001c0001t0003g0007a0001c0001t0003g0021a0001c0001t0003g0106others(90): Show | 96 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.1863+355G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212556 | ||||||
| chr17:77212684
|
C | T | 61 | a0001c0001t0001g0012a0001c0001t0001g0031a0001c0001t0001g0211others(58): Show | 63 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1863+483C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212684 | ||||||
| chr17:77212716
|
T | C | 1 | a0001c0003t0001g0268 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1863+515T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212716 | ||||||
| chr17:77212912
|
G | A | 7 | a0001c0002t0005g0327a0001c0002t0005g0328a0001c0002t0005g0329others(4): Show | 7 | HG01884.hp1 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1864-402G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212912 | ||||||
| chr17:77212925
|
C | T | 3 | a0001c0002t0005g0295a0001c0002t0005g0313a0001c0002t0005g0374 | 3 | HG02165.hp1 NA18949.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.1864-389C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212925 | ||||||
| chr17:77212967
|
C | T | 1 | a0001c0002t0004g0131 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1864-347C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77212967 | ||||||
| chr17:77213307
|
G | C | 1 | a0001c0003t0001g0266 | 1 | NA18960.hp1 | splice_region_variant&intron_variant | LOW | c.1864-7G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 15/16 | chr17 | 77213307 | ||||||
| chr17:77213496
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG02976.hp2 | splice_region_variant&intron_variant | LOW | c.2042+4C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213496 | ||||||
| chr17:77213575
|
A | T | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2042+83A>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213575 | ||||||
| chr17:77213621
|
G | GA | 36 | a0001c0001t0006g0001a0001c0001t0006g0010a0001c0001t0006g0026others(33): Show | 39 | HG00597.hp2 HG00741.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.2042+130dupA | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr17 | 77213621 | |||||
| chr17:77213727
|
C | T | 1 | a0001c0001t0059g0390 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2043-191C>T | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213727 | ||||||
| chr17:77213734
|
G | C | 59 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0020others(56): Show | 61 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.2043-184G>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213734 | ||||||
| chr17:77213855
|
T | C | 6 | a0001c0005t0015g0008a0001c0005t0015g0170a0001c0005t0015g0171others(3): Show | 7 | HG01891.hp1 HG02109.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2043-63T>C | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213855 | ||||||
| chr17:77213860
|
G | A | 4 | a0001c0002t0005g0327a0001c0002t0005g0328a0001c0002t0005g0329others(1): Show | 4 | HG02970.hp2 HG03139.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2043-58G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213860 | ||||||
| chr17:77213863
|
G | A | 3 | a0001c0009t0022g0191a0004c0006t0022g0189a0004c0006t0022g0190 | 3 | HG03491.hp1 HG03492.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2043-55G>A | SEC14L1 | ENSG00000129657.16 | transcript | ENST00000436233.9 | protein_coding | 16/16 | chr17 | 77213863 |