Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 146691 |
|---|---|
| ensemblid | ENSG00000175662.18 |
| hgncid | 11984 |
| symbol | TOM1L2 |
| name | target of myb1 like 2 membrane trafficking protein |
| refseq_nuc | NM_001082968.2 |
| refseq_prot | NP_001076437.1 |
| ensembl_nuc | ENST00000379504.8 |
| ensembl_prot | ENSP00000368818.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 17843511 |
| end | 17972400 |
| strand | - |
| ver | v1.2 |
| region | chr17:17843511-17972400 |
| region5000 | chr17:17838511-17977400 |
| regionname0 | TOM1L2_chr17_17843511_17972400 |
| regionname5000 | TOM1L2_chr17_17838511_17977400 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 507 | 238 | 83 | 56 | 74 | 8 | 15 | 52 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0002 | 0/0 | 507 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0003 | 0/0 | 507 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1524 | 235 | 82 | 55 | 73 | 8 | 15 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| c0002 | 0/0 | 1524 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| c0003 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| c0004 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| c0005 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4212 | 82 | 19 | 19 | 30 | 4 | 8 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0002 | 0/0 | 4212 | 53 | 11 | 23 | 8 | 3 | 8 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0003 | 0/0 | 4212 | 16 | 1 | 4 | 11 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0004 | 0/0 | 4212 | 14 | 13 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0005 | 0/0 | 4212 | 13 | 0 | 0 | 13 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0006 | 0/0 | 4210 | 7 | 5 | 0 | 2 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0007 | 0/0 | 4210 | 6 | 6 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0008 | 0/0 | 4212 | 5 | 2 | 0 | 3 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0009 | 0/0 | 4212 | 5 | 4 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0010 | 0/0 | 4212 | 4 | 3 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0011 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0012 | 0/0 | 4212 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0013 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0014 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0015 | 0/0 | 4212 | 2 | 0 | 2 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0016 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0017 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0018 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0019 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0020 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0021 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0022 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0023 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0024 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0025 | 0/0 | 4212 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0026 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0027 | 0/0 | 4210 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0028 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0029 | 0/0 | 4210 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0030 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0031 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0032 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0033 | 0/0 | 4212 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0034 | 0/0 | 4212 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0035 | 0/0 | 4212 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0036 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0037 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0038 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0039 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| t0040 | 0/0 | 4212 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1524 | 235 | 82 | 55 | 73 | 8 | 15 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0002 | 0/0 | 1524 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0005 | 0/0 | 1524 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0002c0004 | 0/0 | 1524 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0003c0003 | 0/0 | 1524 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5735 | 82 | 19 | 19 | 30 | 4 | 8 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0002 | 0/0 | 5735 | 52 | 11 | 23 | 8 | 3 | 7 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0003 | 0/0 | 5735 | 16 | 1 | 4 | 11 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0004 | 0/0 | 5735 | 13 | 12 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0005 | 0/0 | 5735 | 13 | 0 | 0 | 13 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0006 | 0/0 | 5733 | 7 | 5 | 0 | 2 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0007 | 0/0 | 5733 | 6 | 6 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0008 | 0/0 | 5735 | 5 | 2 | 0 | 3 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0009 | 0/0 | 5735 | 5 | 4 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0010 | 0/0 | 5735 | 4 | 3 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0011 | 0/0 | 5735 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0013 | 0/0 | 5735 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0014 | 0/0 | 5735 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0015 | 0/0 | 5735 | 2 | 0 | 2 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0016 | 0/0 | 5735 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0017 | 0/0 | 5735 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0018 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0019 | 0/0 | 5735 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0020 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0021 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0022 | 0/0 | 5735 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0023 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0024 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0025 | 0/0 | 5735 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0027 | 0/0 | 5733 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0028 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0029 | 0/0 | 5733 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0030 | 0/0 | 5735 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0031 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0032 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0033 | 0/0 | 5735 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0034 | 0/0 | 5735 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0035 | 0/0 | 5735 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0036 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0037 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0038 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0039 | 0/0 | 5735 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0001t0040 | 0/0 | 5735 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0002t0012 | 0/0 | 5735 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0001c0005t0026 | 0/0 | 5735 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0002c0004t0004 | 0/0 | 5735 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| a0003c0003t0002 | 0/0 | 5735 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | copy fasta | chr17 | 17838511 | 17977400 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0118 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0197 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0006g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0006g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0007g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0008g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0008g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0008g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0009g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0009g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0010g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0010g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0010g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0013g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0013g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0014g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0014g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0015g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0015g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0016g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0017g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0018g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0019g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0021g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0022g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0023g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0024g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0025g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0027g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0028g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0029g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0030g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0031g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0032g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0033g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0034g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0035g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0036g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0037g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0038g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0039g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0001t0040g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0002t0012g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0002t0012g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0001c0005t0026g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0002c0004t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| a0003c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | GBR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0168 | EUR | GBR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0218 | EUR | FIN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00438 | hp1 | a0001 | c0001 | t0022 | g0145 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0012 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00642 | hp1 | a0001 | c0001 | t0033 | g0207 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00733 | hp1 | a0001 | c0001 | t0025 | g0044 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00733 | hp2 | a0001 | c0001 | t0015 | g0190 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01070 | hp1 | a0001 | c0001 | t0009 | g0223 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01109 | hp1 | a0001 | c0001 | t0015 | g0188 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01243 | hp2 | a0001 | c0002 | t0012 | g0153 | AMR | PUR | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0151 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01516 | hp1 | a0001 | c0001 | t0035 | g0208 | EUR | IBS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0149 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01978 | hp2 | a0001 | c0001 | t0040 | g0235 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01993 | hp1 | a0001 | c0001 | t0034 | g0004 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02015 | hp1 | a0001 | c0001 | t0016 | g0224 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02056 | hp1 | a0001 | c0001 | t0005 | g0011 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02129 | hp2 | a0001 | c0001 | t0006 | g0231 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02135 | hp1 | a0001 | c0005 | t0026 | g0073 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | KHV | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02145 | hp1 | a0001 | c0001 | t0021 | g0119 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0173 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0199 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02258 | hp1 | a0001 | c0001 | t0037 | g0147 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02615 | hp1 | a0001 | c0001 | t0024 | g0111 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0127 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02717 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02723 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0135 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0220 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02818 | hp1 | a0001 | c0001 | t0027 | g0120 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02896 | hp1 | a0001 | c0001 | t0009 | g0236 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0116 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0117 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02897 | hp2 | a0001 | c0001 | t0009 | g0221 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02970 | hp1 | a0001 | c0001 | t0013 | g0008 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02970 | hp2 | a0001 | c0001 | t0036 | g0006 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02976 | hp2 | a0001 | c0001 | t0006 | g0234 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03041 | hp1 | a0001 | c0001 | t0028 | g0157 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0172 | AFR | GWD | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03098 | hp2 | a0001 | c0001 | t0038 | g0132 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03130 | hp2 | a0001 | c0001 | t0029 | g0228 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03139 | hp1 | a0001 | c0001 | t0014 | g0194 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03195 | hp1 | a0001 | c0001 | t0031 | g0171 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03195 | hp2 | a0001 | c0001 | t0018 | g0155 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0010 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03225 | hp1 | a0001 | c0001 | t0023 | g0110 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0148 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03516 | hp2 | a0001 | c0002 | t0012 | g0154 | AFR | ESN | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03704 | hp2 | a0003 | c0003 | t0002 | g0195 | SAS | PJL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | STU | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | YRI | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18522 | hp2 | a0002 | c0004 | t0004 | g0133 | AFR | YRI | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18906 | hp1 | a0001 | c0001 | t0007 | g0161 | AFR | YRI | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18906 | hp2 | a0001 | c0001 | t0020 | g0054 | AFR | YRI | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0015 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18964 | hp2 | a0001 | c0001 | t0008 | g0174 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18980 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18982 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18984 | hp1 | a0001 | c0001 | t0008 | g0176 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18986 | hp1 | a0001 | c0001 | t0006 | g0232 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18988 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA18998 | hp2 | a0001 | c0001 | t0008 | g0175 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19004 | hp1 | a0001 | c0001 | t0019 | g0023 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19011 | hp2 | a0001 | c0001 | t0030 | g0091 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19054 | hp2 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19060 | hp2 | a0001 | c0001 | t0017 | g0121 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19068 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19081 | hp2 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19088 | hp1 | a0001 | c0001 | t0005 | g0016 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19090 | hp1 | a0001 | c0001 | t0039 | g0186 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0131 | AFR | YRI | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0150 | AFR | YRI | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0088 | AFR | ASW | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA20129 | hp2 | a0001 | c0001 | t0007 | g0162 | AFR | ASW | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0225 | EUR | TSI | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | TSI | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0163 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02486 | hp1 | a0001 | c0001 | t0009 | g0159 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0160 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02559 | hp1 | a0001 | c0001 | t0032 | g0222 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | ACB | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0226 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0140 | AFR | MSL | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | USA | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| HG06807 | hp2 | a0001 | c0001 | t0013 | g0007 | AFR | USA | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | USA | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | USA | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0118 | REF | REF | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0197 | REF | REF | TOM1L2_chr17_17838511_17977400 | TOM1L2 | chr17 | 17838511 | 17977400 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17879688
|
G | T | 1 | a0003 | 1 | HG03704.hp2 | missense_variant | MODERATE | c.716C>A | p.Ser239Tyr | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/15 | 803/5735 | 716/1524 | 239/507 | chr17 | 17879688 | ||
| chr17:17882781
|
G | A | 1 | a0002 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.584C>T | p.Pro195Leu | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/15 | 671/5735 | 584/1524 | 195/507 | chr17 | 17882781 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17869402
|
C | T | 1 | a0001c0002 | 2 | HG01243.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.849G>A | p.Glu283Glu | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/15 | 936/5735 | 849/1524 | 283/507 | chr17 | 17869402 | ||
| chr17:17898635
|
G | A | 1 | a0001c0005 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.177C>T | p.Asn59Asn | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/15 | 264/5735 | 177/1524 | 59/507 | chr17 | 17898635 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17843664
|
CAT | C | 4 | a0001c0001t0006a0001c0001t0007a0001c0001t0027others(1): Show | 15 | HG02109.hp1 HG02129.hp2 HG02486.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3969_*3970delAT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3969 | chr17 | 17843664 | |||||
| chr17:17843666
|
T | C | 1 | a0001c0005t0026 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3969A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3969 | chr17 | 17843666 | |||||
| chr17:17843713
|
G | A | 1 | a0001c0001t0028 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3922C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3922 | chr17 | 17843713 | |||||
| chr17:17843813
|
C | T | 1 | a0001c0001t0025 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3822G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3822 | chr17 | 17843813 | |||||
| chr17:17843878
|
A | G | 1 | a0001c0001t0024 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3757T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3757 | chr17 | 17843878 | |||||
| chr17:17843937
|
C | T | 2 | a0001c0001t0011a0001c0001t0023 | 3 | HG02896.hp2 HG02897.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3698G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3698 | chr17 | 17843937 | |||||
| chr17:17843954
|
G | A | 1 | a0001c0001t0035 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3681C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3681 | chr17 | 17843954 | |||||
| chr17:17843975
|
A | G | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(22): Show | 114 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*3660T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3660 | chr17 | 17843975 | |||||
| chr17:17844052
|
A | C | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(22): Show | 114 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*3583T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3583 | chr17 | 17844052 | |||||
| chr17:17844171
|
C | T | 1 | a0001c0001t0034 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3464G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3464 | chr17 | 17844171 | |||||
| chr17:17844200
|
C | T | 20 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(17): Show | 97 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*3435G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3435 | chr17 | 17844200 | |||||
| chr17:17844233
|
T | C | 4 | a0001c0001t0006a0001c0001t0007a0001c0001t0029others(1): Show | 15 | HG02109.hp1 HG02129.hp2 HG02486.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3402A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3402 | chr17 | 17844233 | |||||
| chr17:17844485
|
C | T | 1 | a0001c0001t0011 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3150G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3150 | chr17 | 17844485 | |||||
| chr17:17844512
|
G | A | 4 | a0001c0001t0010a0001c0001t0013a0001c0001t0036others(1): Show | 8 | HG01433.hp2 HG01891.hp1 HG02258.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3123C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3123 | chr17 | 17844512 | |||||
| chr17:17844595
|
G | A | 4 | a0001c0001t0004a0001c0001t0014a0001c0001t0038others(1): Show | 17 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3040C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 3040 | chr17 | 17844595 | |||||
| chr17:17844686
|
G | A | 1 | a0001c0001t0029 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2949C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2949 | chr17 | 17844686 | |||||
| chr17:17844699
|
A | G | 26 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(23): Show | 115 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*2936T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2936 | chr17 | 17844699 | |||||
| chr17:17844814
|
C | T | 1 | a0001c0001t0021 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2821G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2821 | chr17 | 17844814 | |||||
| chr17:17845048
|
G | C | 1 | a0001c0001t0037 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2587C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2587 | chr17 | 17845048 | |||||
| chr17:17845065
|
G | A | 1 | a0001c0001t0007 | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2570C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2570 | chr17 | 17845065 | |||||
| chr17:17845113
|
G | A | 1 | a0001c0001t0038 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2522C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2522 | chr17 | 17845113 | |||||
| chr17:17845261
|
T | C | 4 | a0001c0001t0004a0001c0001t0014a0001c0001t0038others(1): Show | 17 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2374A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2374 | chr17 | 17845261 | |||||
| chr17:17845331
|
T | C | 19 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(16): Show | 92 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2304A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2304 | chr17 | 17845331 | |||||
| chr17:17845466
|
T | C | 2 | a0001c0001t0039a0001c0002t0012 | 3 | HG01243.hp2 HG03516.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2169A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2169 | chr17 | 17845466 | |||||
| chr17:17845601
|
C | T | 1 | a0001c0001t0020 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2034G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 2034 | chr17 | 17845601 | |||||
| chr17:17845641
|
G | C | 1 | a0001c0001t0033 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1994C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1994 | chr17 | 17845641 | |||||
| chr17:17845690
|
G | A | 1 | a0001c0001t0040 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1945C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1945 | chr17 | 17845690 | |||||
| chr17:17845742
|
A | G | 25 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(22): Show | 114 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*1893T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1893 | chr17 | 17845742 | |||||
| chr17:17846127
|
C | T | 1 | a0001c0001t0030 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1508G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1508 | chr17 | 17846127 | |||||
| chr17:17846208
|
C | T | 1 | a0001c0001t0033 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1427G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1427 | chr17 | 17846208 | |||||
| chr17:17846227
|
G | A | 1 | a0001c0001t0029 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1408C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1408 | chr17 | 17846227 | |||||
| chr17:17846242
|
C | G | 1 | a0001c0001t0019 | 1 | NA19004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1393G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1393 | chr17 | 17846242 | |||||
| chr17:17846306
|
G | A | 1 | a0001c0002t0012 | 2 | HG01243.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1329C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1329 | chr17 | 17846306 | |||||
| chr17:17846472
|
C | T | 2 | a0001c0001t0005a0001c0001t0019 | 14 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1163G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1163 | chr17 | 17846472 | |||||
| chr17:17846508
|
G | A | 21 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(18): Show | 98 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1127C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1127 | chr17 | 17846508 | |||||
| chr17:17846558
|
G | C | 1 | a0001c0001t0015 | 2 | HG00733.hp2 HG01109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1077C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 1077 | chr17 | 17846558 | |||||
| chr17:17846711
|
C | T | 1 | a0001c0001t0014 | 2 | HG03139.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*924G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 924 | chr17 | 17846711 | |||||
| chr17:17846794
|
T | C | 3 | a0001c0001t0003a0001c0001t0017a0001c0001t0030 | 18 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*841A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 841 | chr17 | 17846794 | |||||
| chr17:17846916
|
G | C | 2 | a0001c0001t0009a0001c0001t0032 | 6 | HG01070.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*719C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 719 | chr17 | 17846916 | |||||
| chr17:17847033
|
A | G | 1 | a0001c0001t0018 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*602T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 602 | chr17 | 17847033 | |||||
| chr17:17847105
|
A | G | 21 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(18): Show | 98 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*530T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 530 | chr17 | 17847105 | |||||
| chr17:17847244
|
G | A | 20 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(17): Show | 94 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*391C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 391 | chr17 | 17847244 | |||||
| chr17:17847267
|
C | T | 1 | a0001c0001t0013 | 2 | HG02970.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*368G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 368 | chr17 | 17847267 | |||||
| chr17:17847498
|
A | G | 1 | a0001c0001t0017 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*137T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 137 | chr17 | 17847498 | |||||
| chr17:17847593
|
G | A | 18 | a0001c0001t0002a0001c0001t0004a0001c0001t0008others(15): Show | 92 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*42C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 42 | chr17 | 17847593 | |||||
| chr17:17847596
|
C | T | 1 | a0001c0001t0016 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*39G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 15/15 | 39 | chr17 | 17847596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:17847936
|
G | GT | 6 | a0001c0001t0009g0159a0001c0001t0009g0220a0001c0001t0009g0221others(3): Show | 6 | HG01070.hp1 HG02258.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1376-154dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17847936 | ||||||
| chr17:17847938
|
G | C | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1376-155C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17847938 | ||||||
| chr17:17848026
|
A | ACCATTTT others(22): Show |
1 | a0001c0001t0002g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1376-272_1376-244d others(31): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17848026 | ||||||
| chr17:17848164
|
A | G | 131 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0057others(128): Show | 134 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1376-381T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17848164 | ||||||
| chr17:17848192
|
T | C | 25 | a0001c0001t0001g0152a0001c0001t0002g0074a0001c0001t0002g0134others(22): Show | 27 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.1376-409A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17848192 | ||||||
| chr17:17848298
|
C | T | 28 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(25): Show | 30 | HG00609.hp1 HG01243.hp2 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.1376-515G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17848298 | ||||||
| chr17:17848321
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1375+502G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17848321 | ||||||
| chr17:17848493
|
T | G | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1375+330A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17848493 | ||||||
| chr17:17848688
|
G | A | 14 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(11): Show | 14 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1375+135C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17848688 | ||||||
| chr17:17848734
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1375+89G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 14/14 | chr17 | 17848734 | ||||||
| chr17:17848880
|
A | G | 1 | a0001c0001t0001g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1339-21T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17848880 | ||||||
| chr17:17849018
|
A | T | 1 | a0001c0001t0001g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1339-159T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17849018 | ||||||
| chr17:17849078
|
T | C | 28 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(25): Show | 30 | HG00609.hp1 HG02056.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1339-219A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17849078 | ||||||
| chr17:17849172
|
C | T | 13 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0231others(10): Show | 15 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1339-313G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17849172 | ||||||
| chr17:17849244
|
G | A | 1 | a0001c0001t0002g0196 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1339-385C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17849244 | ||||||
| chr17:17849495
|
T | C | 175 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(172): Show | 178 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.1339-636A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17849495 | ||||||
| chr17:17849536
|
C | T | 28 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(25): Show | 30 | HG00609.hp1 HG02056.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1339-677G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17849536 | ||||||
| chr17:17849652
|
G | A | 2 | a0001c0001t0001g0034a0001c0001t0001g0052 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1339-793C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17849652 | ||||||
| chr17:17849930
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1338+963A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17849930 | ||||||
| chr17:17850028
|
C | G | 1 | a0001c0001t0001g0027 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1338+865G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850028 | ||||||
| chr17:17850168
|
G | A | 13 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0231others(10): Show | 15 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1338+725C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850168 | ||||||
| chr17:17850203
|
G | A | 1 | a0001c0001t0002g0198 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1338+690C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850203 | ||||||
| chr17:17850280
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0078 | 2 | HG01346.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1338+613G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850280 | ||||||
| chr17:17850419
|
A | T | 13 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0231others(10): Show | 15 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.1338+474T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850419 | ||||||
| chr17:17850467
|
T | A | 1 | a0001c0001t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1338+426A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850467 | ||||||
| chr17:17850514
|
C | A | 106 | a0001c0001t0001g0152a0001c0001t0002g0041a0001c0001t0002g0074others(103): Show | 108 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.1338+379G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850514 | ||||||
| chr17:17850532
|
A | T | 124 | a0001c0001t0001g0152a0001c0001t0002g0041a0001c0001t0002g0074others(121): Show | 127 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.1338+361T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850532 | ||||||
| chr17:17850692
|
G | A | 14 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(11): Show | 14 | HG00609.hp1 HG02056.hp1 HG03098.hp1 others(11): Show |
intron_variant | MODIFIER | c.1338+201C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850692 | ||||||
| chr17:17850748
|
G | A | 1 | a0001c0001t0020g0054 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1338+145C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850748 | ||||||
| chr17:17850852
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1338+41C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 13/14 | chr17 | 17850852 | ||||||
| chr17:17851319
|
C | T | 108 | a0001c0001t0001g0152a0001c0001t0002g0041a0001c0001t0002g0074others(105): Show | 110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1279-367G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17851319 | ||||||
| chr17:17851776
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1279-824T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17851776 | ||||||
| chr17:17851846
|
G | C | 1 | a0001c0001t0038g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1279-894C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17851846 | ||||||
| chr17:17851945
|
A | G | 108 | a0001c0001t0001g0152a0001c0001t0002g0041a0001c0001t0002g0074others(105): Show | 110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.1279-993T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17851945 | ||||||
| chr17:17851968
|
C | G | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1279-1016G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17851968 | ||||||
| chr17:17852117
|
GCT | G | 70 | a0001c0001t0002g0041a0001c0001t0002g0074a0001c0001t0002g0093others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1279-1167_1279-116 others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852117 | ||||||
| chr17:17852229
|
C | T | 2 | a0001c0001t0002g0191a0001c0001t0002g0214 | 2 | HG01952.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1279-1277G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852229 | ||||||
| chr17:17852230
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1279-1278C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852230 | ||||||
| chr17:17852328
|
G | A | 1 | a0001c0001t0018g0155 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1279-1376C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852328 | ||||||
| chr17:17852376
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1279-1424G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852376 | ||||||
| chr17:17852535
|
G | T | 4 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0019others(1): Show | 4 | HG00609.hp1 NA18982.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279-1583C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852535 | ||||||
| chr17:17852864
|
T | TA | 20 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0053others(17): Show | 20 | HG00438.hp2 HG01070.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1279-1913dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852864 | ||||||
| chr17:17852864
|
T | TAAA | 6 | a0001c0001t0010g0148a0001c0001t0010g0150a0001c0001t0013g0007others(3): Show | 6 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-1915_1279-191 others(7): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852864 | ||||||
| chr17:17852864
|
TA | T | 34 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0112others(31): Show | 36 | HG00609.hp1 HG01070.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1279-1913delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852864 | ||||||
| chr17:17852932
|
G | C | 1 | a0001c0001t0001g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1279-1980C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852932 | ||||||
| chr17:17852971
|
T | TG | 4 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0234others(1): Show | 6 | HG02717.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-2020dupC | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17852971 | ||||||
| chr17:17853005
|
G | A | 12 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(9): Show | 14 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.1279-2053C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853005 | ||||||
| chr17:17853025
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1279-2073C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853025 | ||||||
| chr17:17853089
|
G | A | 4 | a0001c0001t0001g0049a0001c0001t0001g0058a0001c0001t0001g0063others(1): Show | 4 | HG00438.hp1 HG02129.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279-2137C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853089 | ||||||
| chr17:17853157
|
A | C | 1 | a0001c0001t0016g0224 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1279-2205T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853157 | ||||||
| chr17:17853301
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1279-2349A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853301 | ||||||
| chr17:17853377
|
G | A | 4 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0234others(1): Show | 6 | HG02717.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-2425C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853377 | ||||||
| chr17:17853495
|
G | A | 1 | a0001c0001t0001g0030 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1279-2543C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853495 | ||||||
| chr17:17853558
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1279-2606G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853558 | ||||||
| chr17:17853614
|
A | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1279-2662T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853614 | ||||||
| chr17:17853768
|
G | A | 6 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(3): Show | 6 | HG01070.hp1 HG01243.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1279-2816C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17853768 | ||||||
| chr17:17854088
|
G | C | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1279-3136C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854088 | ||||||
| chr17:17854129
|
T | C | 1 | a0001c0001t0021g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1279-3177A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854129 | ||||||
| chr17:17854188
|
G | A | 3 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0236 | 3 | HG02809.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1279-3236C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854188 | ||||||
| chr17:17854414
|
A | G | 125 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.1279-3462T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854414 | ||||||
| chr17:17854434
|
G | A | 2 | a0001c0001t0013g0007a0001c0001t0013g0008 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1279-3482C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854434 | ||||||
| chr17:17854484
|
GTTTTATT others(5): Show |
G | 1 | a0001c0001t0002g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1279-3544_1279-353 others(16): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854484 | ||||||
| chr17:17854532
|
T | C | 1 | a0001c0001t0004g0135 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1279-3580A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854532 | ||||||
| chr17:17854533
|
A | T | 29 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(26): Show | 31 | HG00609.hp1 HG02056.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1279-3581T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854533 | ||||||
| chr17:17854669
|
C | T | 1 | a0001c0001t0025g0044 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1279-3717G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854669 | ||||||
| chr17:17854691
|
A | AT | 17 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0144others(14): Show | 19 | HG00597.hp2 HG01433.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1279-3740dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854691 | ||||||
| chr17:17854691
|
AT | A | 17 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(14): Show | 17 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.1279-3740delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17854691 | ||||||
| chr17:17855072
|
C | A | 7 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(4): Show | 9 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1279-4120G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17855072 | ||||||
| chr17:17855108
|
T | G | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1279-4156A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17855108 | ||||||
| chr17:17855277
|
C | A | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1279-4325G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17855277 | ||||||
| chr17:17855433
|
C | T | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1279-4481G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17855433 | ||||||
| chr17:17855657
|
G | C | 3 | a0001c0001t0004g0135a0001c0001t0004g0137a0001c0001t0004g0138 | 3 | HG02109.hp2 HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1279-4705C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17855657 | ||||||
| chr17:17855731
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1279-4779T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17855731 | ||||||
| chr17:17855852
|
C | G | 5 | a0001c0001t0007g0160a0001c0001t0007g0161a0001c0001t0007g0162others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1279-4900G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17855852 | ||||||
| chr17:17855962
|
G | GA | 9 | a0001c0001t0001g0229a0001c0001t0003g0143a0001c0001t0004g0003others(6): Show | 12 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1279-5011dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17855962 | ||||||
| chr17:17855962
|
GA | G | 62 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0093others(59): Show | 62 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1279-5011delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17855962 | ||||||
| chr17:17856357
|
C | T | 1 | a0001c0001t0021g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1278+5119G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17856357 | ||||||
| chr17:17856867
|
A | G | 1 | a0001c0001t0006g0231 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1278+4609T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17856867 | ||||||
| chr17:17856933
|
T | C | 1 | a0001c0001t0032g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1278+4543A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17856933 | ||||||
| chr17:17856955
|
T | C | 19 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 19 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1278+4521A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17856955 | ||||||
| chr17:17857140
|
A | G | 33 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(30): Show | 35 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1278+4336T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857140 | ||||||
| chr17:17857238
|
C | T | 1 | a0001c0001t0007g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1278+4238G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857238 | ||||||
| chr17:17857311
|
A | G | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+4165T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857311 | ||||||
| chr17:17857317
|
T | TAAAAATC others(324): Show |
1 | a0001c0001t0030g0091 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1278+4158_1278+415 others(335): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857317 | ||||||
| chr17:17857362
|
C | T | 5 | a0001c0001t0007g0160a0001c0001t0007g0161a0001c0001t0007g0162others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+4114G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857362 | ||||||
| chr17:17857382
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1278+4094A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857382 | ||||||
| chr17:17857398
|
G | A | 1 | a0001c0001t0005g0015 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1278+4078C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857398 | ||||||
| chr17:17857475
|
T | C | 125 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.1278+4001A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857475 | ||||||
| chr17:17857593
|
A | G | 1 | a0001c0001t0017g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1278+3883T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857593 | ||||||
| chr17:17857766
|
C | T | 1 | a0001c0001t0001g0101 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1278+3710G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17857766 | ||||||
| chr17:17858165
|
G | C | 7 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(4): Show | 9 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1278+3311C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858165 | ||||||
| chr17:17858187
|
G | A | 2 | a0001c0001t0002g0209a0001c0001t0035g0208 | 2 | HG01167.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1278+3289C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858187 | ||||||
| chr17:17858196
|
A | T | 16 | a0001c0001t0002g0129a0001c0001t0004g0003a0001c0001t0004g0126others(13): Show | 17 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1278+3280T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858196 | ||||||
| chr17:17858226
|
A | AT | 26 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0042others(23): Show | 27 | HG00099.hp1 HG01070.hp2 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.1278+3249dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858226 | ||||||
| chr17:17858226
|
A | ATT | 168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.1278+3248_1278+324 others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858226 | ||||||
| chr17:17858226
|
A | ATTTTTTC others(2): Show |
13 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(10): Show | 15 | HG02109.hp1 HG02129.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1278+3249_1278+325 others(13): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858226 | ||||||
| chr17:17858226
|
A | ATTTTTTC others(3): Show |
22 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(19): Show | 22 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.1278+3249_1278+325 others(14): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858226 | ||||||
| chr17:17858321
|
T | G | 1 | a0001c0001t0027g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1278+3155A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858321 | ||||||
| chr17:17858344
|
C | T | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+3132G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858344 | ||||||
| chr17:17858480
|
G | A | 19 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 19 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1278+2996C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858480 | ||||||
| chr17:17858615
|
G | A | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+2861C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858615 | ||||||
| chr17:17858732
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1278+2744C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858732 | ||||||
| chr17:17858933
|
T | G | 109 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(106): Show | 111 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1278+2543A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858933 | ||||||
| chr17:17858991
|
G | A | 1 | a0001c0001t0037g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1278+2485C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17858991 | ||||||
| chr17:17859143
|
G | C | 125 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.1278+2333C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859143 | ||||||
| chr17:17859322
|
G | A | 1 | a0001c0001t0013g0007 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1278+2154C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859322 | ||||||
| chr17:17859327
|
G | A | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1278+2149C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859327 | ||||||
| chr17:17859422
|
A | T | 2 | a0001c0001t0003g0082a0001c0001t0003g0083 | 2 | HG02040.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1278+2054T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859422 | ||||||
| chr17:17859426
|
C | T | 2 | a0001c0001t0003g0082a0001c0001t0003g0083 | 2 | HG02040.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1278+2050G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859426 | ||||||
| chr17:17859435
|
C | T | 2 | a0001c0001t0001g0034a0001c0001t0001g0052 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1278+2041G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859435 | ||||||
| chr17:17859652
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1278+1824C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859652 | ||||||
| chr17:17859656
|
A | G | 221 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0024others(218): Show | 225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.1278+1820T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859656 | ||||||
| chr17:17859733
|
T | C | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1278+1743A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859733 | ||||||
| chr17:17859737
|
C | T | 1 | a0001c0001t0013g0007 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1278+1739G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859737 | ||||||
| chr17:17859772
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1278+1704A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859772 | ||||||
| chr17:17859812
|
G | T | 35 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(32): Show | 37 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.1278+1664C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859812 | ||||||
| chr17:17859985
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1278+1491C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17859985 | ||||||
| chr17:17860493
|
G | A | 1 | a0001c0001t0003g0082 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1278+983C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17860493 | ||||||
| chr17:17860747
|
C | G | 109 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(106): Show | 111 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1278+729G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17860747 | ||||||
| chr17:17860857
|
C | G | 1 | a0001c0001t0002g0210 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1278+619G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17860857 | ||||||
| chr17:17861188
|
A | G | 125 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.1278+288T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 12/14 | chr17 | 17861188 | ||||||
| chr17:17861798
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1203-247A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 11/14 | chr17 | 17861798 | ||||||
| chr17:17861862
|
G | T | 1 | a0001c0001t0014g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1203-311C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 11/14 | chr17 | 17861862 | ||||||
| chr17:17862082
|
T | C | 1 | a0001c0001t0001g0035 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1203-531A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 11/14 | chr17 | 17862082 | ||||||
| chr17:17862341
|
C | T | 64 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.1202+390G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 11/14 | chr17 | 17862341 | ||||||
| chr17:17862352
|
A | G | 14 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(11): Show | 14 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1202+379T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 11/14 | chr17 | 17862352 | ||||||
| chr17:17862424
|
G | A | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1202+307C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 11/14 | chr17 | 17862424 | ||||||
| chr17:17862922
|
C | T | 1 | a0001c0005t0026g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1085-74G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17862922 | ||||||
| chr17:17862939
|
T | C | 35 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(32): Show | 37 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.1085-91A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17862939 | ||||||
| chr17:17862969
|
G | A | 2 | a0001c0001t0008g0173a0001c0001t0036g0006 | 2 | HG02145.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1085-121C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17862969 | ||||||
| chr17:17862998
|
A | C | 1 | a0001c0001t0001g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1085-150T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17862998 | ||||||
| chr17:17863122
|
C | A | 19 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 19 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1085-274G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17863122 | ||||||
| chr17:17863159
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1085-311G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17863159 | ||||||
| chr17:17863358
|
G | C | 1 | a0001c0001t0001g0108 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1085-510C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17863358 | ||||||
| chr17:17863558
|
C | G | 19 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 19 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1085-710G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17863558 | ||||||
| chr17:17863563
|
CT | C | 109 | a0001c0001t0001g0032a0001c0001t0001g0063a0001c0001t0001g0122others(106): Show | 112 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(109): Show |
intron_variant | MODIFIER | c.1085-716delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17863563 | ||||||
| chr17:17863563
|
CTT | C | 9 | a0001c0001t0002g0206a0001c0001t0005g0013a0001c0001t0007g0158others(6): Show | 9 | HG01070.hp1 HG01257.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1085-717_1085-716d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17863563 | ||||||
| chr17:17863583
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1085-735A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17863583 | ||||||
| chr17:17863642
|
C | T | 14 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(11): Show | 14 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1085-794G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17863642 | ||||||
| chr17:17863851
|
C | T | 52 | a0001c0001t0002g0141a0001c0001t0002g0177a0001c0001t0002g0178others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.1085-1003G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17863851 | ||||||
| chr17:17864212
|
A | AT | 70 | a0001c0001t0001g0024a0001c0001t0001g0035a0001c0001t0001g0036others(67): Show | 70 | HG00099.hp2 HG00280.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1085-1365dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864212 | ||||||
| chr17:17864219
|
T | C | 1 | a0001c0001t0003g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1085-1371A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864219 | ||||||
| chr17:17864298
|
C | G | 1 | a0001c0001t0028g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1085-1450G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864298 | ||||||
| chr17:17864311
|
C | T | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1085-1463G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864311 | ||||||
| chr17:17864314
|
C | T | 6 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1085-1466G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864314 | ||||||
| chr17:17864453
|
A | G | 109 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(106): Show | 111 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.1085-1605T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864453 | ||||||
| chr17:17864456
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1085-1608G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864456 | ||||||
| chr17:17864505
|
C | T | 71 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0093others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.1085-1657G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864505 | ||||||
| chr17:17864581
|
G | A | 5 | a0001c0001t0007g0160a0001c0001t0007g0161a0001c0001t0007g0162others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1084+1715C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864581 | ||||||
| chr17:17864655
|
G | A | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084+1641C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864655 | ||||||
| chr17:17864787
|
C | G | 1 | a0001c0001t0002g0204 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1084+1509G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864787 | ||||||
| chr17:17864819
|
T | C | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084+1477A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17864819 | ||||||
| chr17:17865525
|
C | T | 33 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(30): Show | 35 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.1084+771G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17865525 | ||||||
| chr17:17865655
|
G | A | 1 | a0001c0001t0002g0041 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1084+641C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17865655 | ||||||
| chr17:17865703
|
A | G | 2 | a0001c0001t0002g0164a0001c0001t0002g0165 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1084+593T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17865703 | ||||||
| chr17:17865727
|
T | C | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1084+569A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17865727 | ||||||
| chr17:17865737
|
C | A | 1 | a0001c0001t0001g0063 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1084+559G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17865737 | ||||||
| chr17:17865742
|
CT | C | 83 | a0001c0001t0001g0071a0001c0001t0001g0124a0001c0001t0001g0229others(80): Show | 85 | HG00280.hp2 HG00609.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.1084+553delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17865742 | ||||||
| chr17:17865742
|
CTT | C | 5 | a0001c0001t0002g0206a0001c0001t0002g0209a0001c0001t0002g0225others(2): Show | 5 | HG01167.hp2 HG01257.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1084+552_1084+553d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17865742 | ||||||
| chr17:17865748
|
T | C | 1 | a0001c0001t0004g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1084+548A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17865748 | ||||||
| chr17:17865805
|
T | C | 35 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(32): Show | 37 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.1084+491A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17865805 | ||||||
| chr17:17866138
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.1084+158T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 10/14 | chr17 | 17866138 | ||||||
| chr17:17867041
|
G | A | 73 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.912-117C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17867041 | ||||||
| chr17:17867077
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.912-153G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17867077 | ||||||
| chr17:17867214
|
G | GCCCAGAG others(12): Show |
33 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(30): Show | 35 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.912-291_912-290ins others(19): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17867214 | ||||||
| chr17:17867388
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.912-464A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17867388 | ||||||
| chr17:17867627
|
C | T | 11 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0028others(8): Show | 12 | HG01978.hp1 HG01981.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.912-703G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17867627 | ||||||
| chr17:17867651
|
T | C | 74 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0093others(71): Show | 74 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.912-727A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17867651 | ||||||
| chr17:17867905
|
G | C | 19 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 19 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.912-981C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17867905 | ||||||
| chr17:17868007
|
A | AC | 3 | a0001c0001t0002g0193a0001c0001t0002g0196a0001c0001t0034g0004 | 3 | HG01261.hp1 HG01358.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.912-1084_912-1083i others(3): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17868007 | ||||||
| chr17:17868053
|
A | T | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.912-1129T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17868053 | ||||||
| chr17:17868101
|
A | T | 23 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0118others(20): Show | 23 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.912-1177T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17868101 | ||||||
| chr17:17868318
|
G | A | 1 | a0001c0001t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.911+1022C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17868318 | ||||||
| chr17:17869115
|
C | A | 7 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(4): Show | 9 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.911+225G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17869115 | ||||||
| chr17:17869308
|
G | GA | 73 | a0001c0001t0001g0125a0001c0001t0001g0166a0001c0001t0002g0074others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.911+31dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17869308 | ||||||
| chr17:17869308
|
GAAAAAAA | G | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.911+25_911+31delTT others(5): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 8/14 | chr17 | 17869308 | ||||||
| chr17:17869593
|
A | G | 6 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-120T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17869593 | ||||||
| chr17:17869655
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.778-182C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17869655 | ||||||
| chr17:17869689
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.778-216C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17869689 | ||||||
| chr17:17869808
|
A | G | 1 | a0001c0001t0009g0223 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.778-335T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17869808 | ||||||
| chr17:17869861
|
G | A | 7 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.778-388C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17869861 | ||||||
| chr17:17870096
|
G | C | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.778-623C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17870096 | ||||||
| chr17:17870212
|
G | A | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.778-739C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17870212 | ||||||
| chr17:17870459
|
C | G | 1 | a0001c0001t0002g0196 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.778-986G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17870459 | ||||||
| chr17:17870552
|
C | T | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.778-1079G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17870552 | ||||||
| chr17:17870804
|
C | T | 124 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(121): Show | 127 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.778-1331G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17870804 | ||||||
| chr17:17871044
|
C | A | 2 | a0001c0001t0011g0116a0001c0001t0011g0117 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.778-1571G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871044 | ||||||
| chr17:17871055
|
A | G | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-1582T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871055 | ||||||
| chr17:17871108
|
C | T | 108 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(105): Show | 110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.778-1635G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871108 | ||||||
| chr17:17871137
|
G | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0068 | 2 | HG01934.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.778-1664C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871137 | ||||||
| chr17:17871142
|
G | A | 1 | a0001c0001t0006g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.778-1669C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871142 | ||||||
| chr17:17871198
|
GTC | G | 12 | a0001c0001t0002g0129a0001c0001t0004g0126a0001c0001t0004g0127others(9): Show | 12 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.778-1727_778-1726d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871198 | ||||||
| chr17:17871254
|
C | T | 73 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.778-1781G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871254 | ||||||
| chr17:17871288
|
G | A | 3 | a0001c0001t0001g0097a0001c0001t0001g0108a0001c0001t0001g0113 | 3 | HG02027.hp2 HG02738.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.778-1815C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871288 | ||||||
| chr17:17871354
|
G | C | 1 | a0001c0001t0001g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.778-1881C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871354 | ||||||
| chr17:17871397
|
C | T | 1 | a0001c0001t0039g0186 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.778-1924G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871397 | ||||||
| chr17:17871442
|
G | A | 6 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-1969C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871442 | ||||||
| chr17:17871460
|
A | G | 1 | a0001c0001t0007g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.778-1987T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871460 | ||||||
| chr17:17871960
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.778-2487G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17871960 | ||||||
| chr17:17872014
|
C | T | 4 | a0001c0001t0002g0182a0001c0001t0002g0185a0001c0001t0002g0189others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-2541G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17872014 | ||||||
| chr17:17872102
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.778-2629G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17872102 | ||||||
| chr17:17872132
|
A | G | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.778-2659T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17872132 | ||||||
| chr17:17872146
|
A | C | 8 | a0001c0001t0004g0130a0001c0001t0004g0131a0001c0001t0004g0135others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.778-2673T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17872146 | ||||||
| chr17:17872392
|
C | T | 28 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0026others(25): Show | 29 | HG00280.hp1 HG00438.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.778-2919G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17872392 | ||||||
| chr17:17872418
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.778-2945G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17872418 | ||||||
| chr17:17872615
|
G | A | 1 | a0001c0001t0014g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.778-3142C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17872615 | ||||||
| chr17:17873075
|
C | T | 108 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(105): Show | 110 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.778-3602G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17873075 | ||||||
| chr17:17873134
|
C | T | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.778-3661G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17873134 | ||||||
| chr17:17873521
|
C | T | 4 | a0001c0001t0002g0182a0001c0001t0002g0185a0001c0001t0002g0189others(1): Show | 4 | HG02055.hp2 HG03139.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-4048G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17873521 | ||||||
| chr17:17873769
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.778-4296T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17873769 | ||||||
| chr17:17873802
|
G | T | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.778-4329C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17873802 | ||||||
| chr17:17873919
|
G | C | 6 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.778-4446C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17873919 | ||||||
| chr17:17873931
|
A | G | 69 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.778-4458T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17873931 | ||||||
| chr17:17873958
|
AT | A | 21 | a0001c0001t0001g0152a0001c0001t0002g0041a0001c0001t0005g0011others(18): Show | 21 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.778-4486delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17873958 | ||||||
| chr17:17874042
|
G | A | 1 | a0001c0001t0038g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.778-4569C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17874042 | ||||||
| chr17:17874258
|
C | T | 15 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(12): Show | 15 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.778-4785G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17874258 | ||||||
| chr17:17874354
|
T | A | 19 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 19 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.778-4881A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17874354 | ||||||
| chr17:17874712
|
T | C | 1 | a0001c0001t0002g0184 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.777+4915A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17874712 | ||||||
| chr17:17874983
|
G | A | 14 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(11): Show | 14 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.777+4644C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17874983 | ||||||
| chr17:17875269
|
GA | G | 73 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(70): Show | 73 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.777+4357delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17875269 | ||||||
| chr17:17875545
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.777+4082G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17875545 | ||||||
| chr17:17875626
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.777+4001G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17875626 | ||||||
| chr17:17876123
|
G | C | 1 | a0001c0001t0003g0082 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.777+3504C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876123 | ||||||
| chr17:17876144
|
C | T | 64 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.777+3483G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876144 | ||||||
| chr17:17876230
|
G | C | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.777+3397C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876230 | ||||||
| chr17:17876237
|
G | A | 1 | a0001c0001t0004g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+3390C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876237 | ||||||
| chr17:17876310
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.777+3317C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876310 | ||||||
| chr17:17876390
|
C | G | 64 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.777+3237G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876390 | ||||||
| chr17:17876483
|
T | A | 7 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+3144A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876483 | ||||||
| chr17:17876510
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.777+3117C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876510 | ||||||
| chr17:17876872
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.777+2755C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876872 | ||||||
| chr17:17876958
|
A | G | 1 | a0001c0001t0002g0214 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.777+2669T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876958 | ||||||
| chr17:17876981
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.777+2646C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17876981 | ||||||
| chr17:17877044
|
C | T | 4 | a0001c0001t0002g0129a0001c0001t0004g0126a0001c0001t0004g0127others(1): Show | 4 | HG01934.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+2583G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17877044 | ||||||
| chr17:17877294
|
C | G | 1 | a0001c0001t0002g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.777+2333G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17877294 | ||||||
| chr17:17877520
|
C | T | 1 | a0001c0001t0004g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.777+2107G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17877520 | ||||||
| chr17:17877640
|
G | A | 1 | a0001c0001t0025g0044 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.777+1987C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17877640 | ||||||
| chr17:17877658
|
C | T | 1 | a0003c0003t0002g0195 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.777+1969G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17877658 | ||||||
| chr17:17877743
|
C | G | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.777+1884G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17877743 | ||||||
| chr17:17877899
|
A | C | 4 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0234others(1): Show | 6 | HG02717.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.777+1728T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17877899 | ||||||
| chr17:17877913
|
C | A | 1 | a0001c0001t0002g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.777+1714G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17877913 | ||||||
| chr17:17878014
|
C | G | 1 | a0001c0001t0009g0223 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.777+1613G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17878014 | ||||||
| chr17:17878509
|
GC | G | 33 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(30): Show | 35 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.777+1117delG | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17878509 | ||||||
| chr17:17878773
|
G | A | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.777+854C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17878773 | ||||||
| chr17:17879090
|
G | A | 64 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.777+537C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17879090 | ||||||
| chr17:17879170
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.777+457G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17879170 | ||||||
| chr17:17879335
|
A | G | 52 | a0001c0001t0002g0141a0001c0001t0002g0177a0001c0001t0002g0178others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.777+292T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17879335 | ||||||
| chr17:17879405
|
A | C | 16 | a0001c0001t0002g0129a0001c0001t0004g0003a0001c0001t0004g0126others(13): Show | 17 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.777+222T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17879405 | ||||||
| chr17:17879407
|
G | GA | 124 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(121): Show | 127 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(124): Show |
intron_variant | MODIFIER | c.777+219dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17879407 | ||||||
| chr17:17879533
|
C | T | 7 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+94G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 7/14 | chr17 | 17879533 | ||||||
| chr17:17879984
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.661-241G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17879984 | ||||||
| chr17:17880334
|
A | G | 6 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.661-591T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17880334 | ||||||
| chr17:17880434
|
A | G | 69 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.661-691T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17880434 | ||||||
| chr17:17880440
|
C | T | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.661-697G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17880440 | ||||||
| chr17:17880542
|
C | T | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.661-799G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17880542 | ||||||
| chr17:17880814
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.661-1071C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17880814 | ||||||
| chr17:17880852
|
G | A | 3 | a0001c0001t0008g0172a0001c0001t0008g0173a0001c0001t0031g0171 | 3 | HG02145.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.661-1109C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17880852 | ||||||
| chr17:17880879
|
C | T | 4 | a0001c0001t0011g0116a0001c0001t0011g0117a0001c0001t0023g0110others(1): Show | 4 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.661-1136G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17880879 | ||||||
| chr17:17880907
|
G | C | 1 | a0001c0002t0012g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.661-1164C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17880907 | ||||||
| chr17:17881060
|
T | C | 69 | a0001c0001t0001g0166a0001c0001t0002g0074a0001c0001t0002g0134others(66): Show | 69 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.661-1317A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17881060 | ||||||
| chr17:17881159
|
T | C | 35 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(32): Show | 37 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.661-1416A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17881159 | ||||||
| chr17:17881278
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.660+1427G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17881278 | ||||||
| chr17:17881603
|
T | C | 1 | a0001c0001t0039g0186 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.660+1102A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17881603 | ||||||
| chr17:17881683
|
G | A | 2 | a0001c0001t0013g0007a0001c0001t0013g0008 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.660+1022C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17881683 | ||||||
| chr17:17881845
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.660+860G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17881845 | ||||||
| chr17:17881870
|
A | G | 3 | a0001c0001t0008g0174a0001c0001t0008g0175a0001c0001t0008g0176 | 3 | NA18964.hp2 NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.660+835T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17881870 | ||||||
| chr17:17881979
|
T | C | 1 | a0001c0001t0019g0023 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.660+726A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17881979 | ||||||
| chr17:17882254
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.660+451C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17882254 | ||||||
| chr17:17882316
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.660+389C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17882316 | ||||||
| chr17:17882438
|
C | T | 23 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0118others(20): Show | 23 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.660+267G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17882438 | ||||||
| chr17:17882455
|
G | A | 23 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0118others(20): Show | 23 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.660+250C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 6/14 | chr17 | 17882455 | ||||||
| chr17:17883029
|
G | C | 1 | a0001c0001t0002g0184 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.502-166C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17883029 | ||||||
| chr17:17883255
|
C | T | 1 | a0001c0001t0032g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.502-392G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17883255 | ||||||
| chr17:17883419
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.502-556C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17883419 | ||||||
| chr17:17883501
|
G | A | 1 | a0001c0001t0003g0085 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.502-638C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17883501 | ||||||
| chr17:17883666
|
G | A | 23 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0118others(20): Show | 23 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.502-803C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17883666 | ||||||
| chr17:17883858
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.501+776A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17883858 | ||||||
| chr17:17883902
|
C | T | 1 | a0001c0001t0003g0087 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.501+732G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17883902 | ||||||
| chr17:17884050
|
G | A | 16 | a0001c0001t0002g0129a0001c0001t0004g0003a0001c0001t0004g0126others(13): Show | 17 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.501+584C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17884050 | ||||||
| chr17:17884069
|
G | C | 1 | a0001c0005t0026g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.501+565C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17884069 | ||||||
| chr17:17884103
|
G | A | 1 | a0001c0001t0038g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.501+531C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17884103 | ||||||
| chr17:17884128
|
A | G | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.501+506T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17884128 | ||||||
| chr17:17884458
|
A | G | 1 | a0001c0001t0001g0052 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.501+176T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17884458 | ||||||
| chr17:17884533
|
A | C | 1 | a0001c0001t0018g0155 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.501+101T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17884533 | ||||||
| chr17:17884566
|
T | C | 19 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 19 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.501+68A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 5/14 | chr17 | 17884566 | ||||||
| chr17:17885030
|
C | T | 14 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(11): Show | 14 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.367-262G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885030 | ||||||
| chr17:17885344
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.367-576C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885344 | ||||||
| chr17:17885393
|
T | C | 1 | a0001c0001t0001g0118 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.367-625A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885393 | ||||||
| chr17:17885473
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.367-705G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885473 | ||||||
| chr17:17885491
|
C | T | 1 | a0001c0001t0003g0082 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.367-723G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885491 | ||||||
| chr17:17885576
|
G | C | 7 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(4): Show | 9 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.367-808C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885576 | ||||||
| chr17:17885722
|
A | G | 16 | a0001c0001t0002g0129a0001c0001t0004g0003a0001c0001t0004g0126others(13): Show | 17 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.367-954T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885722 | ||||||
| chr17:17885917
|
T | G | 1 | a0001c0001t0002g0216 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.367-1149A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885917 | ||||||
| chr17:17885924
|
C | CA | 87 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0043others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.367-1157dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885924 | ||||||
| chr17:17885924
|
C | CAA | 16 | a0001c0001t0002g0081a0001c0001t0002g0183a0001c0001t0002g0184others(13): Show | 16 | HG00280.hp2 HG00621.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.367-1158_367-1157d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885924 | ||||||
| chr17:17885924
|
CA | C | 19 | a0001c0001t0001g0033a0001c0001t0001g0096a0001c0001t0001g0098others(16): Show | 19 | HG00609.hp1 HG01243.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.367-1157delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885924 | ||||||
| chr17:17885924
|
CAA | C | 19 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0006g0001others(16): Show | 21 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.367-1158_367-1157d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17885924 | ||||||
| chr17:17886172
|
ACT | A | 16 | a0001c0001t0002g0129a0001c0001t0004g0003a0001c0001t0004g0126others(13): Show | 17 | HG01891.hp2 HG01934.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.367-1406_367-1405d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17886172 | ||||||
| chr17:17886227
|
C | T | 1 | a0001c0001t0032g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.367-1459G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17886227 | ||||||
| chr17:17886442
|
C | T | 1 | a0001c0001t0002g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.367-1674G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17886442 | ||||||
| chr17:17886481
|
T | C | 1 | a0001c0001t0002g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.367-1713A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17886481 | ||||||
| chr17:17886820
|
T | A | 4 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(1): Show | 4 | HG01070.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.367-2052A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17886820 | ||||||
| chr17:17886834
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0071 | 2 | NA18982.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.367-2066G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17886834 | ||||||
| chr17:17886872
|
T | C | 35 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(32): Show | 37 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.367-2104A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17886872 | ||||||
| chr17:17887005
|
C | A | 68 | a0001c0001t0001g0166a0001c0001t0002g0134a0001c0001t0002g0141others(65): Show | 68 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.367-2237G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887005 | ||||||
| chr17:17887102
|
C | T | 1 | a0001c0001t0007g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.367-2334G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887102 | ||||||
| chr17:17887274
|
C | T | 51 | a0001c0001t0002g0141a0001c0001t0002g0177a0001c0001t0002g0178others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.367-2506G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887274 | ||||||
| chr17:17887439
|
C | T | 1 | a0001c0001t0003g0088 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.367-2671G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887439 | ||||||
| chr17:17887535
|
G | A | 1 | a0001c0002t0012g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.367-2767C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887535 | ||||||
| chr17:17887568
|
C | T | 63 | a0001c0001t0001g0166a0001c0001t0002g0134a0001c0001t0002g0141others(60): Show | 63 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.367-2800G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887568 | ||||||
| chr17:17887580
|
A | T | 35 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(32): Show | 37 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.367-2812T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887580 | ||||||
| chr17:17887648
|
G | T | 1 | a0001c0001t0002g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.367-2880C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887648 | ||||||
| chr17:17887815
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.367-3047C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887815 | ||||||
| chr17:17887975
|
AAGGCTGA others(10): Show |
A | 1 | a0001c0001t0002g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.367-3224_367-3208d others(19): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17887975 | ||||||
| chr17:17888369
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.367-3601G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17888369 | ||||||
| chr17:17888485
|
G | A | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.367-3717C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17888485 | ||||||
| chr17:17889000
|
C | T | 1 | a0001c0001t0003g0086 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.367-4232G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17889000 | ||||||
| chr17:17889093
|
G | A | 1 | a0001c0001t0001g0052 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.367-4325C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17889093 | ||||||
| chr17:17889530
|
T | C | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+4131A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17889530 | ||||||
| chr17:17889579
|
C | T | 1 | a0001c0001t0025g0044 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.366+4082G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17889579 | ||||||
| chr17:17889719
|
C | T | 1 | a0001c0001t0007g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.366+3942G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17889719 | ||||||
| chr17:17889807
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.366+3854G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17889807 | ||||||
| chr17:17889894
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.366+3767G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17889894 | ||||||
| chr17:17890063
|
C | G | 8 | a0001c0001t0004g0130a0001c0001t0004g0131a0001c0001t0004g0135others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.366+3598G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17890063 | ||||||
| chr17:17890610
|
A | G | 3 | a0001c0001t0002g0193a0001c0001t0002g0196a0001c0001t0034g0004 | 3 | HG01261.hp1 HG01358.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.366+3051T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17890610 | ||||||
| chr17:17890787
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.366+2874C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17890787 | ||||||
| chr17:17891001
|
A | T | 1 | a0001c0001t0023g0110 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.366+2660T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891001 | ||||||
| chr17:17891130
|
T | C | 123 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(120): Show | 126 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.366+2531A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891130 | ||||||
| chr17:17891495
|
G | A | 1 | a0001c0001t0005g0012 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.366+2166C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891495 | ||||||
| chr17:17891784
|
C | CGT | 80 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(77): Show | 81 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.366+1875_366+1876d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
C | CGTGT | 27 | a0001c0001t0001g0025a0001c0001t0001g0038a0001c0001t0001g0050others(24): Show | 27 | HG00280.hp1 HG01167.hp1 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.366+1873_366+1876d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
C | CGTGTGT | 16 | a0001c0001t0001g0059a0001c0001t0001g0156a0001c0001t0001g0229others(13): Show | 16 | HG00609.hp2 HG00642.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.366+1871_366+1876d others(8): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
C | CGTGTGTG others(1): Show |
8 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0006g0001others(5): Show | 10 | HG00099.hp2 HG00639.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.366+1869_366+1876d others(10): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
C | CGTGTGTG others(3): Show |
3 | a0001c0001t0005g0011a0001c0001t0005g0022a0001c0001t0006g0231 | 3 | HG02056.hp1 HG02129.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.366+1867_366+1876d others(12): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
C | CGTGTGTG others(5): Show |
6 | a0001c0001t0005g0016a0001c0001t0005g0017a0001c0001t0005g0018others(3): Show | 6 | HG02135.hp2 HG02976.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.366+1865_366+1876d others(14): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
C | CGTGTGTG others(7): Show |
2 | a0001c0001t0005g0019a0001c0001t0005g0020 | 2 | NA18982.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.366+1863_366+1876d others(16): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
C | CGTGTGTG others(9): Show |
3 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0021 | 3 | HG00609.hp1 NA18988.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.366+1861_366+1876d others(18): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
C | CGTGTGTG others(11): Show |
2 | a0001c0001t0005g0014a0001c0001t0005g0076 | 2 | NA18994.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.366+1859_366+1876d others(20): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
C | CGTGTGTG others(13): Show |
1 | a0001c0001t0005g0015 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.366+1857_366+1876d others(22): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
CGT | C | 12 | a0001c0001t0001g0122a0001c0001t0002g0129a0001c0001t0002g0204others(9): Show | 12 | HG01256.hp1 HG01346.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.366+1875_366+1876d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17891784
|
CGTGT | C | 8 | a0001c0001t0001g0152a0001c0001t0004g0003a0001c0001t0004g0135others(5): Show | 9 | HG01891.hp2 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.366+1873_366+1876d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17891784 | ||||||
| chr17:17892018
|
T | C | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+1643A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17892018 | ||||||
| chr17:17892034
|
A | T | 1 | a0001c0001t0027g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.366+1627T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17892034 | ||||||
| chr17:17892169
|
T | A | 4 | a0001c0001t0011g0116a0001c0001t0011g0117a0001c0001t0023g0110others(1): Show | 4 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.366+1492A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17892169 | ||||||
| chr17:17892301
|
C | T | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.366+1360G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17892301 | ||||||
| chr17:17892413
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.366+1248G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17892413 | ||||||
| chr17:17892742
|
G | A | 1 | a0001c0001t0004g0130 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.366+919C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17892742 | ||||||
| chr17:17893031
|
A | T | 1 | a0001c0001t0004g0128 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.366+630T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17893031 | ||||||
| chr17:17893144
|
G | C | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.366+517C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17893144 | ||||||
| chr17:17893371
|
T | C | 14 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(11): Show | 14 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.366+290A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17893371 | ||||||
| chr17:17893386
|
AG | A | 6 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.366+274delC | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17893386 | ||||||
| chr17:17893512
|
AT | A | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.366+148delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17893512 | ||||||
| chr17:17893632
|
C | A | 1 | a0001c0001t0001g0107 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.366+29G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 4/14 | chr17 | 17893632 | ||||||
| chr17:17894306
|
T | A | 1 | a0001c0001t0004g0003 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.217-496A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894306 | ||||||
| chr17:17894311
|
C | A | 1 | a0001c0001t0004g0003 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.217-501G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894311 | ||||||
| chr17:17894574
|
A | C | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.217-764T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894574 | ||||||
| chr17:17894732
|
A | C | 39 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0002g0129others(36): Show | 41 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(38): Show |
intron_variant | MODIFIER | c.217-922T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894732 | ||||||
| chr17:17894776
|
C | T | 3 | a0001c0001t0008g0172a0001c0001t0008g0173a0001c0001t0031g0171 | 3 | HG02145.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.217-966G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894776 | ||||||
| chr17:17894854
|
C | T | 1 | a0001c0001t0002g0201 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.217-1044G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894854 | ||||||
| chr17:17894932
|
A | C | 1 | a0001c0001t0003g0084 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.217-1122T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894932 | ||||||
| chr17:17894934
|
A | AACAT | 23 | a0001c0001t0001g0046a0001c0001t0001g0094a0001c0001t0001g0095others(20): Show | 23 | HG00642.hp2 HG00735.hp1 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.217-1128_217-1125d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894934 | ||||||
| chr17:17894934
|
A | AACATACA others(1): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0045a0001c0001t0001g0047others(3): Show | 6 | HG01516.hp2 HG02055.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.217-1132_217-1125d others(10): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894934 | ||||||
| chr17:17894934
|
A | T | 1 | a0001c0001t0003g0084 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.217-1124T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894934 | ||||||
| chr17:17894934
|
AACAT | A | 24 | a0001c0001t0001g0002a0001c0001t0001g0051a0001c0001t0001g0055others(21): Show | 25 | HG00558.hp2 HG00597.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.217-1128_217-1125d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894934 | ||||||
| chr17:17894934
|
AACATACA others(1): Show |
A | 7 | a0001c0001t0002g0167a0001c0001t0009g0220a0001c0001t0009g0221others(4): Show | 7 | HG00639.hp1 HG01070.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.217-1132_217-1125d others(10): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894934 | ||||||
| chr17:17894934
|
AACATACA others(5): Show |
A | 10 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(7): Show | 10 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.217-1136_217-1125d others(14): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894934 | ||||||
| chr17:17894934
|
AACATACA others(9): Show |
A | 22 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(19): Show | 24 | HG00609.hp1 HG02056.hp1 HG02129.hp2 others(21): Show |
intron_variant | MODIFIER | c.217-1140_217-1125d others(18): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894934 | ||||||
| chr17:17894940
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.217-1130G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894940 | ||||||
| chr17:17894975
|
A | ACATACAT others(5): Show |
1 | a0001c0001t0004g0130 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.217-1166_217-1165i others(14): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894975 | ||||||
| chr17:17894975
|
A | ACATACAT others(1): Show |
4 | a0001c0001t0004g0131a0001c0001t0004g0135a0001c0001t0004g0138others(1): Show | 4 | HG02451.hp1 HG02809.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.217-1166_217-1165i others(10): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894975 | ||||||
| chr17:17894975
|
A | ACATG | 32 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0152others(29): Show | 34 | HG00558.hp2 HG00609.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.217-1169_217-1166d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894975 | ||||||
| chr17:17894975
|
A | ACATGCAT others(1): Show |
64 | a0001c0001t0002g0134a0001c0001t0002g0141a0001c0001t0002g0164others(61): Show | 64 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.217-1173_217-1166d others(10): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894975 | ||||||
| chr17:17894975
|
A | ACATGCAT others(5): Show |
4 | a0001c0001t0002g0170a0001c0001t0002g0187a0001c0001t0002g0215others(1): Show | 4 | HG01981.hp1 HG02027.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.217-1177_217-1166d others(14): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894975 | ||||||
| chr17:17894975
|
A | G | 13 | a0001c0001t0004g0003a0001c0001t0004g0139a0001c0001t0004g0140others(10): Show | 14 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.217-1165T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17894975 | ||||||
| chr17:17895099
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.217-1289C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17895099 | ||||||
| chr17:17895319
|
A | G | 122 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(119): Show | 125 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.217-1509T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17895319 | ||||||
| chr17:17895444
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.217-1634C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17895444 | ||||||
| chr17:17895461
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.217-1651C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17895461 | ||||||
| chr17:17895506
|
G | A | 1 | a0001c0001t0032g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.217-1696C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17895506 | ||||||
| chr17:17895706
|
C | G | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.217-1896G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17895706 | ||||||
| chr17:17896268
|
G | A | 1 | a0001c0001t0002g0179 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.216+2328C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17896268 | ||||||
| chr17:17896295
|
T | C | 1 | a0001c0001t0002g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.216+2301A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17896295 | ||||||
| chr17:17896299
|
A | G | 11 | a0001c0001t0001g0166a0001c0001t0002g0134a0001c0001t0002g0164others(8): Show | 11 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.216+2297T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17896299 | ||||||
| chr17:17896420
|
G | A | 4 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(1): Show | 4 | HG01070.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.216+2176C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17896420 | ||||||
| chr17:17896510
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.216+2086A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17896510 | ||||||
| chr17:17896587
|
G | C | 1 | a0001c0001t0037g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.216+2009C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17896587 | ||||||
| chr17:17897061
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.216+1535G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17897061 | ||||||
| chr17:17897376
|
G | A | 1 | a0001c0001t0033g0207 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.216+1220C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17897376 | ||||||
| chr17:17897503
|
T | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0047 | 2 | HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.216+1093A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17897503 | ||||||
| chr17:17897809
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.216+787G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17897809 | ||||||
| chr17:17897810
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.216+786C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17897810 | ||||||
| chr17:17897922
|
CT | C | 8 | a0001c0001t0001g0034a0001c0001t0001g0052a0001c0001t0001g0101others(5): Show | 8 | HG01255.hp2 HG02615.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.216+673delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17897922 | ||||||
| chr17:17898161
|
A | T | 32 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(29): Show | 34 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.216+435T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17898161 | ||||||
| chr17:17898220
|
G | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0053a0001c0001t0001g0057 | 3 | HG01255.hp1 HG01358.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.216+376C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17898220 | ||||||
| chr17:17898248
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.216+348T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17898248 | ||||||
| chr17:17898254
|
A | G | 1 | a0001c0001t0003g0084 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.216+342T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17898254 | ||||||
| chr17:17898268
|
T | C | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.216+328A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17898268 | ||||||
| chr17:17898431
|
A | T | 8 | a0001c0001t0001g0166a0001c0001t0002g0134a0001c0001t0002g0164others(5): Show | 8 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.216+165T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17898431 | ||||||
| chr17:17898446
|
C | T | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+150G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17898446 | ||||||
| chr17:17898557
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.216+39G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 3/14 | chr17 | 17898557 | ||||||
| chr17:17898900
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.138-226A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17898900 | ||||||
| chr17:17899112
|
C | T | 5 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG01123.hp2 HG02027.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-438G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899112 | ||||||
| chr17:17899164
|
T | C | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.138-490A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899164 | ||||||
| chr17:17899355
|
G | A | 32 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(29): Show | 34 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.138-681C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899355 | ||||||
| chr17:17899460
|
T | C | 1 | a0001c0001t0007g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.138-786A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899460 | ||||||
| chr17:17899465
|
C | T | 106 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(103): Show | 108 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.138-791G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899465 | ||||||
| chr17:17899689
|
C | T | 34 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(31): Show | 36 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.138-1015G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899689 | ||||||
| chr17:17899904
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.138-1230T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899904 | ||||||
| chr17:17899948
|
CA | C | 106 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(103): Show | 108 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.138-1275delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899948 | ||||||
| chr17:17899983
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.138-1309T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899983 | ||||||
| chr17:17899993
|
C | T | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.138-1319G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17899993 | ||||||
| chr17:17900086
|
G | T | 4 | a0001c0001t0002g0129a0001c0001t0004g0126a0001c0001t0004g0127others(1): Show | 4 | HG01934.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-1412C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17900086 | ||||||
| chr17:17900102
|
G | A | 122 | a0001c0001t0001g0152a0001c0001t0001g0166a0001c0001t0001g0229others(119): Show | 125 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.138-1428C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17900102 | ||||||
| chr17:17900306
|
G | A | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.138-1632C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17900306 | ||||||
| chr17:17900498
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.138-1824C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17900498 | ||||||
| chr17:17900521
|
C | CA | 51 | a0001c0001t0001g0229a0001c0001t0002g0070a0001c0001t0002g0129others(48): Show | 54 | HG00609.hp1 HG00733.hp1 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.138-1848dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17900521 | ||||||
| chr17:17900546
|
A | G | 1 | a0001c0002t0012g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.138-1872T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17900546 | ||||||
| chr17:17901411
|
C | T | 71 | a0001c0001t0001g0166a0001c0001t0002g0141a0001c0001t0002g0164others(68): Show | 71 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.138-2737G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901411 | ||||||
| chr17:17901570
|
C | T | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.138-2896G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901570 | ||||||
| chr17:17901606
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.138-2932T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901606 | ||||||
| chr17:17901642
|
C | T | 4 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(1): Show | 4 | HG01070.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.138-2968G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901642 | ||||||
| chr17:17901643
|
A | C | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.138-2969T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901643 | ||||||
| chr17:17901690
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.138-3016G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901690 | ||||||
| chr17:17901815
|
C | T | 3 | a0001c0001t0008g0172a0001c0001t0008g0173a0001c0001t0031g0171 | 3 | HG02145.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.138-3141G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901815 | ||||||
| chr17:17901865
|
G | A | 12 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(9): Show | 12 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.138-3191C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901865 | ||||||
| chr17:17901892
|
A | C | 1 | a0001c0001t0004g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.138-3218T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901892 | ||||||
| chr17:17901902
|
A | G | 1 | a0001c0001t0032g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.138-3228T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17901902 | ||||||
| chr17:17902178
|
AAAAT | A | 19 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0006g0001others(16): Show | 21 | HG01433.hp2 HG01891.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.138-3508_138-3505d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17902178 | ||||||
| chr17:17902464
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.138-3790G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17902464 | ||||||
| chr17:17902632
|
G | A | 2 | a0001c0001t0001g0025a0001c0001t0001g0078 | 2 | HG04228.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.138-3958C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17902632 | ||||||
| chr17:17902938
|
G | GAAGT | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.138-4268_138-4265d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17902938 | ||||||
| chr17:17903080
|
C | T | 1 | a0001c0001t0016g0224 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.137+4367G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903080 | ||||||
| chr17:17903141
|
C | G | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+4306G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903141 | ||||||
| chr17:17903283
|
T | G | 6 | a0001c0001t0001g0166a0001c0001t0002g0164a0001c0001t0002g0165others(3): Show | 6 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+4164A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903283 | ||||||
| chr17:17903311
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.137+4136G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903311 | ||||||
| chr17:17903403
|
C | T | 32 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(29): Show | 34 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.137+4044G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903403 | ||||||
| chr17:17903405
|
C | G | 4 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0234others(1): Show | 6 | HG02717.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+4042G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903405 | ||||||
| chr17:17903469
|
T | C | 235 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.137+3978A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903469 | ||||||
| chr17:17903499
|
G | A | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+3948C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903499 | ||||||
| chr17:17903580
|
T | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0058others(2): Show | 5 | HG00438.hp1 HG02129.hp1 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+3867A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903580 | ||||||
| chr17:17903592
|
G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.137+3855C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903592 | ||||||
| chr17:17903600
|
G | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.137+3847C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903600 | ||||||
| chr17:17903612
|
C | CA | 9 | a0001c0001t0001g0002a0001c0001t0001g0045a0001c0001t0001g0057others(6): Show | 10 | HG00438.hp1 HG01243.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.137+3834dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903612 | ||||||
| chr17:17903631
|
T | A | 36 | a0001c0001t0002g0141a0001c0001t0002g0177a0001c0001t0002g0178others(33): Show | 36 | HG00639.hp2 HG00642.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+3816A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903631 | ||||||
| chr17:17903631
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.137+3816A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903631 | ||||||
| chr17:17903636
|
G | A | 34 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(31): Show | 36 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+3811C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903636 | ||||||
| chr17:17903872
|
A | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(161): Show | 168 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.137+3575T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903872 | ||||||
| chr17:17903911
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.137+3536G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903911 | ||||||
| chr17:17903912
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.137+3535A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903912 | ||||||
| chr17:17903921
|
G | T | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.137+3526C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903921 | ||||||
| chr17:17903990
|
G | GATTATT | 19 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(16): Show | 19 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.137+3451_137+3456d others(8): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903990 | ||||||
| chr17:17903990
|
G | GATTATTA others(2): Show |
6 | a0001c0001t0005g0018a0001c0001t0007g0160a0001c0001t0007g0161others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+3448_137+3456d others(11): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903990 | ||||||
| chr17:17903990
|
G | GATTATTA others(5): Show |
2 | a0001c0001t0007g0158a0001c0001t0009g0159 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.137+3445_137+3456d others(14): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903990 | ||||||
| chr17:17903990
|
G | GATTATTA others(8): Show |
6 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0231others(3): Show | 8 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.137+3442_137+3456d others(17): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903990 | ||||||
| chr17:17903990
|
G | GATTATTA others(11): Show |
1 | a0001c0001t0006g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.137+3439_137+3456d others(20): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17903990 | ||||||
| chr17:17904091
|
C | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.137+3356G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904091 | ||||||
| chr17:17904204
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+3243G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904204 | ||||||
| chr17:17904275
|
T | A | 1 | a0002c0004t0004g0133 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.137+3172A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904275 | ||||||
| chr17:17904443
|
C | G | 4 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0234others(1): Show | 6 | HG02717.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.137+3004G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904443 | ||||||
| chr17:17904544
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0024others(163): Show | 170 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.137+2903C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904544 | ||||||
| chr17:17904608
|
G | A | 1 | a0002c0004t0004g0133 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.137+2839C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904608 | ||||||
| chr17:17904649
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.137+2798C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904649 | ||||||
| chr17:17904684
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+2763C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904684 | ||||||
| chr17:17904735
|
C | T | 4 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(1): Show | 4 | HG01070.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.137+2712G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904735 | ||||||
| chr17:17904757
|
C | G | 6 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(3): Show | 6 | HG01243.hp2 HG02258.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.137+2690G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904757 | ||||||
| chr17:17904812
|
G | GC | 34 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(31): Show | 36 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.137+2634dupG | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904812 | ||||||
| chr17:17904830
|
C | T | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.137+2617G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904830 | ||||||
| chr17:17904850
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+2597G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904850 | ||||||
| chr17:17904928
|
C | G | 1 | a0001c0001t0002g0227 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.137+2519G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904928 | ||||||
| chr17:17904946
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.137+2501C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17904946 | ||||||
| chr17:17905124
|
C | T | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.137+2323G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17905124 | ||||||
| chr17:17905234
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.137+2213G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17905234 | ||||||
| chr17:17905297
|
C | T | 1 | a0001c0001t0038g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.137+2150G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17905297 | ||||||
| chr17:17905687
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.137+1760G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17905687 | ||||||
| chr17:17905998
|
G | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 5 | HG02055.hp1 HG02572.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.137+1449C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17905998 | ||||||
| chr17:17906052
|
CT | C | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.137+1394delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17906052 | ||||||
| chr17:17906105
|
T | C | 3 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006 | 3 | HG02970.hp1 HG02970.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.137+1342A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17906105 | ||||||
| chr17:17906131
|
CA | C | 169 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(166): Show | 173 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(170): Show |
intron_variant | MODIFIER | c.137+1315delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17906131 | ||||||
| chr17:17906132
|
A | C | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.137+1315T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17906132 | ||||||
| chr17:17906132
|
A | T | 1 | a0001c0001t0002g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.137+1315T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17906132 | ||||||
| chr17:17906816
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.137+631A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17906816 | ||||||
| chr17:17907327
|
C | T | 2 | a0001c0001t0002g0164a0001c0001t0002g0165 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.137+120G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 2/14 | chr17 | 17907327 | ||||||
| chr17:17907740
|
C | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0058 | 2 | HG02129.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.53-209G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17907740 | ||||||
| chr17:17907937
|
C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.53-406G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17907937 | ||||||
| chr17:17908151
|
C | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(161): Show | 168 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.53-620G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908151 | ||||||
| chr17:17908548
|
T | C | 1 | a0001c0001t0006g0231 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.53-1017A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908548 | ||||||
| chr17:17908563
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-1032G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908563 | ||||||
| chr17:17908615
|
A | T | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-1084T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908615 | ||||||
| chr17:17908640
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.53-1109T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908640 | ||||||
| chr17:17908683
|
A | G | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-1152T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908683 | ||||||
| chr17:17908754
|
T | C | 1 | a0001c0001t0032g0222 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.53-1223A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908754 | ||||||
| chr17:17908873
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-1342C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908873 | ||||||
| chr17:17908876
|
C | T | 6 | a0001c0001t0002g0134a0001c0001t0004g0135a0001c0001t0004g0136others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-1345G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908876 | ||||||
| chr17:17908911
|
G | A | 1 | a0001c0001t0002g0214 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.53-1380C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908911 | ||||||
| chr17:17908945
|
G | A | 1 | a0001c0001t0002g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.53-1414C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17908945 | ||||||
| chr17:17909009
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-1478C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17909009 | ||||||
| chr17:17909077
|
A | T | 5 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(2): Show | 5 | HG01070.hp1 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-1546T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17909077 | ||||||
| chr17:17909349
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-1818A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17909349 | ||||||
| chr17:17909621
|
T | C | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-2090A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17909621 | ||||||
| chr17:17909805
|
G | A | 11 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0099others(8): Show | 11 | HG01109.hp2 HG02280.hp1 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.53-2274C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17909805 | ||||||
| chr17:17909842
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.53-2311T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17909842 | ||||||
| chr17:17910008
|
A | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(231): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.53-2477T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910008 | ||||||
| chr17:17910096
|
C | T | 2 | a0001c0001t0015g0188a0001c0001t0015g0190 | 2 | HG00733.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.53-2565G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910096 | ||||||
| chr17:17910156
|
G | T | 1 | a0001c0001t0001g0098 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.53-2625C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910156 | ||||||
| chr17:17910213
|
G | A | 7 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(4): Show | 9 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-2682C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910213 | ||||||
| chr17:17910248
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-2717G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910248 | ||||||
| chr17:17910249
|
G | A | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-2718C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910249 | ||||||
| chr17:17910416
|
T | C | 7 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(4): Show | 9 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-2885A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910416 | ||||||
| chr17:17910487
|
G | A | 1 | a0001c0001t0021g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-2956C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910487 | ||||||
| chr17:17910723
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53-3192G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910723 | ||||||
| chr17:17910873
|
C | A | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-3342G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17910873 | ||||||
| chr17:17911086
|
T | G | 1 | a0001c0001t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.53-3555A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17911086 | ||||||
| chr17:17911103
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.53-3572A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17911103 | ||||||
| chr17:17911295
|
GCCTGC | G | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-3769_53-3765del others(5): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17911295 | ||||||
| chr17:17911384
|
A | G | 6 | a0001c0001t0002g0134a0001c0001t0004g0135a0001c0001t0004g0136others(3): Show | 6 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-3853T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17911384 | ||||||
| chr17:17911513
|
G | A | 1 | a0001c0001t0002g0211 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.53-3982C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17911513 | ||||||
| chr17:17911584
|
T | C | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-4053A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17911584 | ||||||
| chr17:17911663
|
T | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-4132A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17911663 | ||||||
| chr17:17911667
|
A | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-4136T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17911667 | ||||||
| chr17:17911680
|
C | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-4149G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17911680 | ||||||
| chr17:17912021
|
C | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(161): Show | 168 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.53-4490G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912021 | ||||||
| chr17:17912109
|
C | T | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-4578G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912109 | ||||||
| chr17:17912265
|
CGGCTGGC others(42): Show |
C | 1 | a0001c0001t0001g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.53-4783_53-4735del others(49): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912265 | ||||||
| chr17:17912288
|
C | G | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-4757G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912288 | ||||||
| chr17:17912325
|
C | T | 7 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(4): Show | 9 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-4794G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912325 | ||||||
| chr17:17912366
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-4835C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912366 | ||||||
| chr17:17912470
|
G | A | 1 | a0001c0001t0003g0092 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.53-4939C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912470 | ||||||
| chr17:17912566
|
G | A | 13 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0126others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.53-5035C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912566 | ||||||
| chr17:17912598
|
C | G | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-5067G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912598 | ||||||
| chr17:17912700
|
G | C | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.53-5169C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912700 | ||||||
| chr17:17912729
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.53-5198T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912729 | ||||||
| chr17:17912778
|
C | CG | 10 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0036others(7): Show | 10 | HG00621.hp2 HG00735.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-5248dupC | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912778 | ||||||
| chr17:17912844
|
T | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(170): Show | 177 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.53-5313A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912844 | ||||||
| chr17:17912870
|
T | C | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-5339A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912870 | ||||||
| chr17:17912946
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-5415C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912946 | ||||||
| chr17:17912976
|
G | T | 7 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-5445C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912976 | ||||||
| chr17:17912977
|
A | T | 7 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-5446T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912977 | ||||||
| chr17:17912988
|
G | C | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-5457C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17912988 | ||||||
| chr17:17913033
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(110): Show | 114 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.53-5502C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913033 | ||||||
| chr17:17913064
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.53-5533C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913064 | ||||||
| chr17:17913074
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-5543C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913074 | ||||||
| chr17:17913174
|
G | A | 1 | a0001c0001t0017g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.53-5643C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913174 | ||||||
| chr17:17913181
|
C | CAGAGGGA others(23): Show |
62 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0024others(59): Show | 63 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.53-5680_53-5651dup others(30): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913181 | ||||||
| chr17:17913199
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-5668C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913199 | ||||||
| chr17:17913239
|
G | GGGAGAGG others(14): Show |
1 | a0001c0001t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.53-5709_53-5708ins others(21): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913239 | ||||||
| chr17:17913248
|
C | G | 1 | a0001c0001t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.53-5717G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913248 | ||||||
| chr17:17913249
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.53-5718C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913249 | ||||||
| chr17:17913258
|
C | CGGGAGA | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-5733_53-5728dup others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913258 | ||||||
| chr17:17913258
|
C | CGGGAGAG others(5): Show |
13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-5739_53-5728dup others(12): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913258 | ||||||
| chr17:17913258
|
C | CGGGAGAG others(11): Show |
17 | a0001c0001t0002g0134a0001c0001t0004g0126a0001c0001t0004g0127others(14): Show | 17 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.53-5745_53-5728dup others(18): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913258 | ||||||
| chr17:17913258
|
C | CGGGAGAG others(17): Show |
1 | a0001c0001t0004g0003 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.53-5751_53-5728dup others(24): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913258 | ||||||
| chr17:17913258
|
C | CGGGAGAG others(23): Show |
1 | a0001c0001t0002g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.53-5728_53-5727ins others(30): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913258 | ||||||
| chr17:17913415
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.53-5884C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913415 | ||||||
| chr17:17913511
|
G | A | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-5980C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913511 | ||||||
| chr17:17913768
|
A | G | 1 | a0001c0001t0006g0232 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.53-6237T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913768 | ||||||
| chr17:17913929
|
G | T | 1 | a0001c0001t0005g0017 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.53-6398C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17913929 | ||||||
| chr17:17914149
|
G | A | 1 | a0001c0001t0005g0021 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.53-6618C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17914149 | ||||||
| chr17:17914292
|
T | C | 7 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-6761A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17914292 | ||||||
| chr17:17914600
|
T | C | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-7069A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17914600 | ||||||
| chr17:17915046
|
C | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0066a0001c0001t0001g0067 | 4 | NA18964.hp1 NA18966.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-7515G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915046 | ||||||
| chr17:17915046
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.53-7515G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915046 | ||||||
| chr17:17915352
|
A | G | 2 | a0001c0001t0008g0172a0001c0001t0031g0171 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.53-7821T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915352 | ||||||
| chr17:17915481
|
G | A | 1 | a0001c0001t0005g0011 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.53-7950C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915481 | ||||||
| chr17:17915503
|
G | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.53-7972C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915503 | ||||||
| chr17:17915515
|
C | CT | 4 | a0001c0001t0002g0129a0001c0001t0004g0126a0001c0001t0004g0127others(1): Show | 4 | HG01934.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-7985dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915515 | ||||||
| chr17:17915533
|
G | T | 1 | a0001c0001t0037g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.53-8002C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915533 | ||||||
| chr17:17915682
|
A | C | 2 | a0001c0001t0013g0007a0001c0001t0013g0008 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.53-8151T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915682 | ||||||
| chr17:17915780
|
C | G | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-8249G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915780 | ||||||
| chr17:17915787
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(129): Show | 134 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.53-8256T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915787 | ||||||
| chr17:17915841
|
GT | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(156): Show | 163 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.53-8311delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915841 | ||||||
| chr17:17915874
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(129): Show | 134 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.53-8343T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915874 | ||||||
| chr17:17915944
|
T | C | 1 | a0001c0001t0015g0190 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.53-8413A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17915944 | ||||||
| chr17:17916021
|
C | T | 173 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(170): Show | 177 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.53-8490G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17916021 | ||||||
| chr17:17916074
|
A | AT | 10 | a0001c0001t0001g0038a0001c0001t0001g0113a0001c0001t0001g0152others(7): Show | 10 | HG01109.hp1 HG01891.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-8544dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17916074 | ||||||
| chr17:17916129
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.53-8598T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17916129 | ||||||
| chr17:17916167
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.53-8636C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17916167 | ||||||
| chr17:17916321
|
C | T | 63 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(60): Show | 64 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.53-8790G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17916321 | ||||||
| chr17:17916343
|
G | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-8812C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17916343 | ||||||
| chr17:17916629
|
G | T | 1 | a0001c0001t0004g0003 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.53-9098C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17916629 | ||||||
| chr17:17916860
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.53-9329A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17916860 | ||||||
| chr17:17916883
|
C | T | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-9352G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17916883 | ||||||
| chr17:17917173
|
A | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(129): Show | 134 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.53-9642T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917173 | ||||||
| chr17:17917201
|
G | A | 1 | a0001c0001t0002g0215 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.53-9670C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917201 | ||||||
| chr17:17917383
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.53-9852C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917383 | ||||||
| chr17:17917450
|
CT | C | 41 | a0001c0001t0001g0166a0001c0001t0002g0141a0001c0001t0002g0164others(38): Show | 41 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.53-9920delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917450 | ||||||
| chr17:17917450
|
CTT | C | 15 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0178others(12): Show | 15 | HG00280.hp2 HG01070.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-9921_53-9920del others(2): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917450 | ||||||
| chr17:17917450
|
CTTT | C | 15 | a0001c0001t0001g0152a0001c0001t0005g0012a0001c0001t0005g0013others(12): Show | 15 | HG00609.hp1 HG02135.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.53-9922_53-9920del others(3): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917450 | ||||||
| chr17:17917450
|
CTTTT | C | 25 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0034others(22): Show | 27 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.53-9923_53-9920del others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917450 | ||||||
| chr17:17917450
|
CTTTTT | C | 102 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(99): Show | 104 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.53-9924_53-9920del others(5): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917450 | ||||||
| chr17:17917450
|
CTTTTTT | C | 17 | a0001c0001t0001g0046a0001c0001t0001g0063a0001c0001t0001g0072others(14): Show | 17 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.53-9925_53-9920del others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917450 | ||||||
| chr17:17917450
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0013g0007a0001c0001t0013g0008 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.53-9931_53-9920del others(12): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917450 | ||||||
| chr17:17917450
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0002g0205a0001c0001t0036g0006a0001c0001t0037g0147 | 3 | HG01069.hp1 HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.53-9932_53-9920del others(13): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917450 | ||||||
| chr17:17917480
|
T | C | 35 | a0001c0001t0001g0075a0001c0001t0001g0144a0001c0001t0001g0152others(32): Show | 37 | HG00597.hp2 HG00609.hp1 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.53-9949A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917480 | ||||||
| chr17:17917684
|
C | CAGGCATG others(2): Show |
168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.53-10154_53-10153i others(11): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917684 | ||||||
| chr17:17917693
|
C | T | 2 | a0001c0001t0002g0206a0001c0001t0002g0210 | 2 | HG01257.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.53-10162G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917693 | ||||||
| chr17:17917799
|
T | A | 6 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-10268A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17917799 | ||||||
| chr17:17918007
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.53-10476C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17918007 | ||||||
| chr17:17918256
|
T | C | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-10725A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17918256 | ||||||
| chr17:17918547
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53-11016G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17918547 | ||||||
| chr17:17918558
|
A | C | 4 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0234others(1): Show | 6 | HG02717.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-11027T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17918558 | ||||||
| chr17:17919065
|
G | C | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-11534C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17919065 | ||||||
| chr17:17919166
|
C | T | 168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.53-11635G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17919166 | ||||||
| chr17:17919321
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.53-11790G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17919321 | ||||||
| chr17:17919334
|
C | A | 1 | a0001c0001t0002g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.53-11803G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17919334 | ||||||
| chr17:17919615
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.53-12084G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17919615 | ||||||
| chr17:17919722
|
T | C | 1 | a0001c0001t0004g0131 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.53-12191A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17919722 | ||||||
| chr17:17919861
|
G | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-12330C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17919861 | ||||||
| chr17:17919863
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.53-12332G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17919863 | ||||||
| chr17:17920077
|
A | G | 1 | a0001c0001t0001g0026 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53-12546T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17920077 | ||||||
| chr17:17920217
|
CT | C | 29 | a0001c0001t0001g0229a0001c0001t0002g0227a0001c0001t0005g0011others(26): Show | 31 | HG00609.hp1 HG02056.hp1 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.53-12687delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17920217 | ||||||
| chr17:17920335
|
A | AT | 35 | a0001c0001t0001g0024a0001c0001t0001g0050a0001c0001t0001g0071others(32): Show | 37 | HG01243.hp1 HG01433.hp2 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.53-12805dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17920335 | ||||||
| chr17:17920335
|
A | ATT | 6 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0014others(3): Show | 6 | HG00609.hp1 HG01243.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-12806_53-12805d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17920335 | ||||||
| chr17:17920335
|
AT | A | 12 | a0001c0001t0001g0072a0001c0001t0001g0108a0001c0001t0002g0170others(9): Show | 12 | HG01070.hp1 HG02809.hp1 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.53-12805delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17920335 | ||||||
| chr17:17920430
|
TCC | T | 4 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(1): Show | 4 | HG01070.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-12901_53-12900d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17920430 | ||||||
| chr17:17920872
|
G | A | 5 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(2): Show | 5 | HG02055.hp1 HG02572.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-13341C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17920872 | ||||||
| chr17:17921260
|
A | C | 17 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0099others(14): Show | 17 | HG01109.hp2 HG02280.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.53-13729T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17921260 | ||||||
| chr17:17921325
|
C | T | 2 | a0001c0001t0004g0139a0001c0001t0004g0140 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.53-13794G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17921325 | ||||||
| chr17:17921443
|
G | A | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-13912C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17921443 | ||||||
| chr17:17921447
|
T | C | 1 | a0001c0001t0002g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.53-13916A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17921447 | ||||||
| chr17:17921664
|
G | T | 164 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(161): Show | 168 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.53-14133C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17921664 | ||||||
| chr17:17921751
|
C | T | 1 | a0001c0001t0005g0012 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.53-14220G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17921751 | ||||||
| chr17:17921874
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0233 | 2 | NA18994.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.53-14343G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17921874 | ||||||
| chr17:17921952
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-14421G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17921952 | ||||||
| chr17:17921953
|
C | CT | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-14423dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17921953 | ||||||
| chr17:17922531
|
G | T | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53-15000C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17922531 | ||||||
| chr17:17922706
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(129): Show | 134 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.53-15175T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17922706 | ||||||
| chr17:17922850
|
A | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.53-15319T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17922850 | ||||||
| chr17:17922850
|
A | T | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-15319T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17922850 | ||||||
| chr17:17922987
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.53-15456G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17922987 | ||||||
| chr17:17923079
|
G | GGCTCATA others(8): Show |
1 | a0001c0001t0039g0186 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.53-15563_53-15549d others(17): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923079 | ||||||
| chr17:17923093
|
G | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.53-15562C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923093 | ||||||
| chr17:17923177
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.53-15646G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923177 | ||||||
| chr17:17923214
|
T | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-15683A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923214 | ||||||
| chr17:17923235
|
C | A | 7 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(4): Show | 9 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-15704G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923235 | ||||||
| chr17:17923261
|
C | T | 1 | a0001c0001t0027g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.53-15730G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923261 | ||||||
| chr17:17923356
|
G | A | 6 | a0001c0001t0001g0166a0001c0001t0002g0164a0001c0001t0002g0165others(3): Show | 6 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-15825C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923356 | ||||||
| chr17:17923380
|
G | A | 3 | a0001c0001t0004g0139a0001c0001t0004g0140a0001c0001t0019g0023 | 3 | HG03471.hp2 HG03579.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.53-15849C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923380 | ||||||
| chr17:17923434
|
C | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(161): Show | 168 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.53-15903G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923434 | ||||||
| chr17:17923621
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-16090A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923621 | ||||||
| chr17:17923675
|
G | A | 34 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(31): Show | 36 | HG00609.hp1 HG01243.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.53-16144C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923675 | ||||||
| chr17:17923745
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.53-16214T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923745 | ||||||
| chr17:17923864
|
G | A | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-16333C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17923864 | ||||||
| chr17:17924039
|
G | T | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-16508C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17924039 | ||||||
| chr17:17924136
|
CAAACAA | C | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-16611_53-16606d others(8): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17924136 | ||||||
| chr17:17924173
|
A | G | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-16642T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17924173 | ||||||
| chr17:17924182
|
T | C | 2 | a0001c0001t0008g0172a0001c0001t0031g0171 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.53-16651A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17924182 | ||||||
| chr17:17924207
|
T | C | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-16676A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17924207 | ||||||
| chr17:17924335
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-16804G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17924335 | ||||||
| chr17:17924365
|
A | T | 1 | a0001c0001t0004g0127 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.53-16834T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17924365 | ||||||
| chr17:17924469
|
G | A | 1 | a0001c0001t0025g0044 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.53-16938C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17924469 | ||||||
| chr17:17924517
|
T | A | 1 | a0001c0001t0037g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.53-16986A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17924517 | ||||||
| chr17:17925136
|
T | C | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-17605A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925136 | ||||||
| chr17:17925138
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.53-17607G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925138 | ||||||
| chr17:17925149
|
A | G | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53-17618T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925149 | ||||||
| chr17:17925431
|
T | C | 1 | a0001c0001t0027g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.53-17900A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925431 | ||||||
| chr17:17925486
|
A | G | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-17955T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925486 | ||||||
| chr17:17925495
|
G | A | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-17964C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925495 | ||||||
| chr17:17925659
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-18128A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925659 | ||||||
| chr17:17925682
|
C | CA | 21 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0002g0183others(18): Show | 23 | HG01257.hp2 HG01258.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.53-18152dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925682 | ||||||
| chr17:17925682
|
CA | C | 20 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0031others(17): Show | 20 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.53-18152delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925682 | ||||||
| chr17:17925854
|
CA | C | 19 | a0001c0001t0001g0229a0001c0001t0002g0206a0001c0001t0004g0137others(16): Show | 21 | HG01257.hp1 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.53-18324delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17925854 | ||||||
| chr17:17926089
|
T | A | 1 | a0001c0001t0002g0211 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.53-18558A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926089 | ||||||
| chr17:17926109
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(164): Show | 171 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(168): Show |
intron_variant | MODIFIER | c.53-18578G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926109 | ||||||
| chr17:17926120
|
G | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(161): Show | 168 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.53-18589C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926120 | ||||||
| chr17:17926176
|
G | GA | 8 | a0001c0001t0001g0125a0001c0001t0002g0185a0001c0001t0010g0148others(5): Show | 8 | HG01433.hp2 HG01891.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.53-18646dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926176 | ||||||
| chr17:17926176
|
GA | G | 10 | a0001c0001t0002g0093a0001c0001t0002g0134a0001c0001t0004g0130others(7): Show | 10 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.53-18646delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926176 | ||||||
| chr17:17926181
|
A | G | 3 | a0001c0001t0001g0166a0001c0001t0002g0167a0001c0001t0002g0168 | 3 | HG00099.hp2 HG00639.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.53-18650T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926181 | ||||||
| chr17:17926260
|
CT | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-18730delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926260 | ||||||
| chr17:17926262
|
T | C | 113 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(110): Show | 114 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.53-18731A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926262 | ||||||
| chr17:17926320
|
C | T | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-18789G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926320 | ||||||
| chr17:17926368
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-18837G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926368 | ||||||
| chr17:17926471
|
A | G | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-18940T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926471 | ||||||
| chr17:17926589
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53-19058C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926589 | ||||||
| chr17:17926661
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.53-19130T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926661 | ||||||
| chr17:17926886
|
G | T | 32 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0005g0011others(29): Show | 34 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.53-19355C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17926886 | ||||||
| chr17:17927069
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-19538C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927069 | ||||||
| chr17:17927153
|
G | A | 7 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.53-19622C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927153 | ||||||
| chr17:17927195
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.53-19664C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927195 | ||||||
| chr17:17927239
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-19708G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927239 | ||||||
| chr17:17927381
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.53-19850A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927381 | ||||||
| chr17:17927443
|
G | A | 1 | a0001c0002t0012g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.53-19912C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927443 | ||||||
| chr17:17927663
|
CT | C | 23 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0002g0179others(20): Show | 24 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.53-20133delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927663 | ||||||
| chr17:17927862
|
A | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(1): Show | 4 | HG02572.hp2 HG03486.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-20331T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927862 | ||||||
| chr17:17927935
|
A | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.53-20404T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927935 | ||||||
| chr17:17927935
|
A | T | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53-20404T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927935 | ||||||
| chr17:17927941
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.53-20410T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927941 | ||||||
| chr17:17927971
|
G | A | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-20440C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17927971 | ||||||
| chr17:17928156
|
C | CA | 132 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(129): Show | 134 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.53-20626dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17928156 | ||||||
| chr17:17928159
|
C | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.53-20628G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17928159 | ||||||
| chr17:17928171
|
G | C | 1 | a0001c0001t0002g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.53-20640C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17928171 | ||||||
| chr17:17928171
|
GT | G | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-20641delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17928171 | ||||||
| chr17:17928289
|
T | A | 1 | a0001c0001t0002g0205 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.53-20758A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17928289 | ||||||
| chr17:17928402
|
G | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-20871C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17928402 | ||||||
| chr17:17928538
|
T | G | 1 | a0001c0001t0007g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.53-21007A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17928538 | ||||||
| chr17:17928581
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-21050C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17928581 | ||||||
| chr17:17928928
|
G | A | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-21397C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17928928 | ||||||
| chr17:17929076
|
G | A | 1 | a0001c0001t0002g0169 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.53-21545C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17929076 | ||||||
| chr17:17929146
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.53-21615T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17929146 | ||||||
| chr17:17929294
|
G | A | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.53-21763C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17929294 | ||||||
| chr17:17929297
|
T | G | 1 | a0001c0001t0002g0204 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.53-21766A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17929297 | ||||||
| chr17:17929317
|
G | T | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-21786C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17929317 | ||||||
| chr17:17929531
|
C | T | 1 | a0001c0001t0003g0084 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.53-22000G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17929531 | ||||||
| chr17:17929556
|
G | A | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-22025C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17929556 | ||||||
| chr17:17930007
|
T | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(2): Show | 6 | NA18942.hp1 NA18964.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-22476A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17930007 | ||||||
| chr17:17930247
|
G | C | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-22716C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17930247 | ||||||
| chr17:17930330
|
A | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-22799T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17930330 | ||||||
| chr17:17930371
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.53-22840C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17930371 | ||||||
| chr17:17930444
|
A | C | 2 | a0001c0001t0008g0172a0001c0001t0031g0171 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.53-22913T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17930444 | ||||||
| chr17:17930679
|
T | G | 1 | a0001c0001t0037g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.53-23148A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17930679 | ||||||
| chr17:17930804
|
C | T | 1 | a0001c0001t0027g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.53-23273G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17930804 | ||||||
| chr17:17930805
|
A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-23274T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17930805 | ||||||
| chr17:17931033
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53-23502C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931033 | ||||||
| chr17:17931159
|
G | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0037others(2): Show | 6 | NA18942.hp1 NA18964.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-23628C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931159 | ||||||
| chr17:17931193
|
C | T | 5 | a0001c0001t0001g0039a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.53-23662G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931193 | ||||||
| chr17:17931249
|
T | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-23718A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931249 | ||||||
| chr17:17931377
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(129): Show | 134 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.53-23846T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931377 | ||||||
| chr17:17931457
|
T | C | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-23926A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931457 | ||||||
| chr17:17931517
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.53-23986C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931517 | ||||||
| chr17:17931597
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.53-24066G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931597 | ||||||
| chr17:17931642
|
C | T | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.53-24111G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931642 | ||||||
| chr17:17931697
|
G | A | 9 | a0001c0001t0002g0134a0001c0001t0004g0130a0001c0001t0004g0131others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.53-24166C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931697 | ||||||
| chr17:17931743
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.53-24212C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17931743 | ||||||
| chr17:17932465
|
C | T | 1 | a0001c0001t0002g0203 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.53-24934G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17932465 | ||||||
| chr17:17933463
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.53-25932C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17933463 | ||||||
| chr17:17933594
|
C | T | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.53-26063G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17933594 | ||||||
| chr17:17933674
|
G | C | 1 | a0001c0001t0021g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.53-26143C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17933674 | ||||||
| chr17:17933842
|
T | C | 1 | a0001c0001t0017g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.53-26311A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17933842 | ||||||
| chr17:17934040
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.53-26509G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17934040 | ||||||
| chr17:17934096
|
G | A | 4 | a0001c0001t0002g0179a0001c0001t0002g0192a0001c0001t0002g0212others(1): Show | 4 | HG01243.hp1 HG02280.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.53-26565C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17934096 | ||||||
| chr17:17934367
|
A | G | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.53-26836T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17934367 | ||||||
| chr17:17934491
|
A | C | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-26960T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17934491 | ||||||
| chr17:17934537
|
T | G | 1 | a0001c0001t0001g0068 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.53-27006A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17934537 | ||||||
| chr17:17934608
|
A | T | 1 | a0001c0001t0001g0034 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.53-27077T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17934608 | ||||||
| chr17:17934951
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.53-27420C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17934951 | ||||||
| chr17:17935710
|
C | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(170): Show | 177 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(174): Show |
intron_variant | MODIFIER | c.53-28179G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935710 | ||||||
| chr17:17935873
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28342G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935873 | ||||||
| chr17:17935874
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28343A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935874 | ||||||
| chr17:17935877
|
G | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28346C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935877 | ||||||
| chr17:17935878
|
G | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28347C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935878 | ||||||
| chr17:17935881
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28350A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935881 | ||||||
| chr17:17935882
|
G | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28351C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935882 | ||||||
| chr17:17935883
|
A | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28352T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935883 | ||||||
| chr17:17935884
|
C | T | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28353G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935884 | ||||||
| chr17:17935885
|
T | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28354A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935885 | ||||||
| chr17:17935886
|
C | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0032 | 2 | HG01070.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.53-28355G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935886 | ||||||
| chr17:17935983
|
G | C | 1 | a0001c0001t0005g0021 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.53-28452C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17935983 | ||||||
| chr17:17936167
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.53-28636G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17936167 | ||||||
| chr17:17936453
|
A | G | 1 | a0001c0001t0004g0003 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.53-28922T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17936453 | ||||||
| chr17:17936515
|
T | C | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-28984A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17936515 | ||||||
| chr17:17936669
|
A | T | 1 | a0001c0002t0012g0153 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.53-29138T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17936669 | ||||||
| chr17:17936756
|
A | G | 3 | a0001c0001t0003g0082a0001c0001t0003g0083a0001c0001t0003g0090 | 3 | HG00621.hp1 HG02040.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.53-29225T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17936756 | ||||||
| chr17:17937133
|
G | A | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-29602C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937133 | ||||||
| chr17:17937141
|
T | C | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.53-29610A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937141 | ||||||
| chr17:17937216
|
C | T | 4 | a0001c0001t0006g0001a0001c0001t0006g0230a0001c0001t0006g0234others(1): Show | 6 | HG02717.hp2 HG02723.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-29685G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937216 | ||||||
| chr17:17937259
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.53-29728C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937259 | ||||||
| chr17:17937304
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.53-29773C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937304 | ||||||
| chr17:17937358
|
G | A | 4 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(1): Show | 4 | HG01070.hp1 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.53-29827C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937358 | ||||||
| chr17:17937462
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0114 | 2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.53-29931C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937462 | ||||||
| chr17:17937509
|
G | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(109): Show | 113 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.53-29978C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937509 | ||||||
| chr17:17937769
|
T | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(117): Show | 122 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.53-30238A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937769 | ||||||
| chr17:17937958
|
C | G | 1 | a0001c0001t0001g0229 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.53-30427G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937958 | ||||||
| chr17:17937975
|
G | A | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-30444C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17937975 | ||||||
| chr17:17938021
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.53-30490G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17938021 | ||||||
| chr17:17938142
|
A | G | 165 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(162): Show | 169 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.53-30611T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17938142 | ||||||
| chr17:17938234
|
T | A | 1 | a0001c0001t0001g0109 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.53-30703A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17938234 | ||||||
| chr17:17938451
|
C | G | 1 | a0001c0001t0004g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.53-30920G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17938451 | ||||||
| chr17:17938461
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.53-30930A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17938461 | ||||||
| chr17:17938545
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0166a0001c0001t0002g0164others(3): Show | 6 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-31014G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17938545 | ||||||
| chr17:17938766
|
G | GT | 125 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(122): Show | 127 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.53-31236dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17938766 | ||||||
| chr17:17938766
|
G | GTT | 6 | a0001c0001t0001g0097a0001c0001t0001g0107a0001c0001t0001g0108others(3): Show | 6 | HG01123.hp2 HG02027.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.53-31237_53-31236d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17938766 | ||||||
| chr17:17938771
|
T | G | 1 | a0001c0001t0002g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.53-31240A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17938771 | ||||||
| chr17:17939044
|
C | G | 6 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(3): Show | 6 | HG02109.hp1 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.53-31513G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17939044 | ||||||
| chr17:17939413
|
T | C | 1 | a0001c0001t0001g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.53-31882A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17939413 | ||||||
| chr17:17939469
|
T | C | 1 | a0001c0001t0002g0129 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.53-31938A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17939469 | ||||||
| chr17:17939473
|
G | C | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.53-31942C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17939473 | ||||||
| chr17:17939856
|
T | C | 1 | a0001c0001t0003g0089 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.53-32325A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17939856 | ||||||
| chr17:17939898
|
A | G | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+32364T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17939898 | ||||||
| chr17:17940044
|
C | T | 163 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(160): Show | 167 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(164): Show |
intron_variant | MODIFIER | c.52+32218G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940044 | ||||||
| chr17:17940064
|
G | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+32198C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940064 | ||||||
| chr17:17940082
|
G | A | 183 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.52+32180C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940082 | ||||||
| chr17:17940192
|
C | CA | 33 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0046others(30): Show | 33 | HG00621.hp1 HG01109.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.52+32069dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940192 | ||||||
| chr17:17940192
|
C | CAA | 18 | a0001c0001t0001g0099a0001c0001t0001g0113a0001c0001t0006g0001others(15): Show | 20 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.52+32068_52+32069d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940192 | ||||||
| chr17:17940192
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.52+32059_52+32069d others(13): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940192 | ||||||
| chr17:17940192
|
CA | C | 19 | a0001c0001t0001g0094a0001c0001t0002g0070a0001c0001t0002g0134others(16): Show | 20 | HG01256.hp2 HG01257.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.52+32069delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940192 | ||||||
| chr17:17940192
|
CAAAAAAA others(1): Show |
C | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.52+32062_52+32069d others(10): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940192 | ||||||
| chr17:17940420
|
G | A | 7 | a0001c0001t0007g0158a0001c0001t0007g0160a0001c0001t0007g0161others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.52+31842C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940420 | ||||||
| chr17:17940512
|
A | G | 14 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(11): Show | 16 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.52+31750T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940512 | ||||||
| chr17:17940580
|
A | G | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52+31682T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940580 | ||||||
| chr17:17940662
|
G | T | 2 | a0001c0001t0011g0116a0001c0001t0011g0117 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.52+31600C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940662 | ||||||
| chr17:17940758
|
G | A | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+31504C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940758 | ||||||
| chr17:17940907
|
G | A | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.52+31355C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17940907 | ||||||
| chr17:17941504
|
C | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0166a0001c0001t0002g0164others(5): Show | 8 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.52+30758G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17941504 | ||||||
| chr17:17941555
|
C | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.52+30707G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17941555 | ||||||
| chr17:17941556
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+30706C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17941556 | ||||||
| chr17:17941812
|
C | G | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.52+30450G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17941812 | ||||||
| chr17:17941939
|
C | T | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.52+30323G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17941939 | ||||||
| chr17:17942296
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+29966G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942296 | ||||||
| chr17:17942343
|
C | T | 2 | a0001c0001t0013g0007a0001c0001t0013g0008 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.52+29919G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942343 | ||||||
| chr17:17942422
|
T | A | 1 | a0001c0001t0001g0037 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.52+29840A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942422 | ||||||
| chr17:17942453
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.52+29809C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942453 | ||||||
| chr17:17942486
|
A | T | 183 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.52+29776T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942486 | ||||||
| chr17:17942522
|
T | C | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.52+29740A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942522 | ||||||
| chr17:17942766
|
C | A | 1 | a0001c0001t0025g0044 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.52+29496G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942766 | ||||||
| chr17:17942777
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.52+29485C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942777 | ||||||
| chr17:17942908
|
G | A | 1 | a0001c0001t0005g0016 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.52+29354C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942908 | ||||||
| chr17:17942930
|
T | C | 3 | a0001c0001t0001g0229a0001c0001t0006g0231a0001c0001t0006g0232 | 3 | HG02129.hp2 NA18986.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.52+29332A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942930 | ||||||
| chr17:17942999
|
T | C | 3 | a0001c0001t0005g0011a0001c0001t0005g0016a0001c0001t0005g0018 | 3 | HG02056.hp1 NA18980.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.52+29263A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17942999 | ||||||
| chr17:17943211
|
C | G | 7 | a0001c0001t0001g0229a0001c0001t0006g0001a0001c0001t0006g0230others(4): Show | 9 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+29051G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17943211 | ||||||
| chr17:17943375
|
T | C | 1 | a0001c0001t0002g0201 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.52+28887A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17943375 | ||||||
| chr17:17943490
|
G | C | 1 | a0001c0001t0001g0069 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.52+28772C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17943490 | ||||||
| chr17:17943613
|
G | C | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+28649C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17943613 | ||||||
| chr17:17943798
|
T | C | 1 | a0001c0001t0030g0091 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.52+28464A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17943798 | ||||||
| chr17:17943849
|
G | A | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.52+28413C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17943849 | ||||||
| chr17:17943854
|
C | A | 5 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(2): Show | 5 | HG01070.hp1 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+28408G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17943854 | ||||||
| chr17:17944034
|
G | A | 2 | a0001c0001t0008g0172a0001c0001t0031g0171 | 2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.52+28228C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944034 | ||||||
| chr17:17944148
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.52+28114C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944148 | ||||||
| chr17:17944452
|
C | G | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.52+27810G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944452 | ||||||
| chr17:17944506
|
A | G | 1 | a0001c0001t0001g0005 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.52+27756T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944506 | ||||||
| chr17:17944507
|
G | C | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.52+27755C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944507 | ||||||
| chr17:17944622
|
G | A | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 130 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.52+27640C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944622 | ||||||
| chr17:17944680
|
T | C | 1 | a0001c0001t0008g0176 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.52+27582A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944680 | ||||||
| chr17:17944797
|
A | G | 1 | a0002c0004t0004g0133 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.52+27465T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944797 | ||||||
| chr17:17944929
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.52+27333C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944929 | ||||||
| chr17:17944947
|
T | C | 3 | a0001c0001t0002g0074a0001c0002t0012g0153a0001c0002t0012g0154 | 3 | HG01243.hp2 HG02055.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.52+27315A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944947 | ||||||
| chr17:17944972
|
G | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(175): Show | 182 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(179): Show |
intron_variant | MODIFIER | c.52+27290C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17944972 | ||||||
| chr17:17945267
|
T | TAC | 16 | a0001c0001t0001g0025a0001c0001t0001g0166a0001c0001t0002g0164others(13): Show | 16 | HG00099.hp2 HG00609.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.52+26993_52+26994d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945267 | ||||||
| chr17:17945267
|
T | TACAC | 6 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0019others(3): Show | 6 | NA18949.hp2 NA18981.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+26991_52+26994d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945267 | ||||||
| chr17:17945267
|
TACAC | T | 4 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0030g0091others(1): Show | 4 | HG03098.hp2 HG03209.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+26991_52+26994d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945267 | ||||||
| chr17:17945267
|
TACACAC | T | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+26989_52+26994d others(8): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945267 | ||||||
| chr17:17945286
|
A | ACT | 4 | a0001c0001t0001g0036a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG00621.hp2 HG02572.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+26975_52+26976i others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945286 | ||||||
| chr17:17945286
|
A | T | 2 | a0001c0001t0001g0026a0001c0001t0002g0074 | 2 | HG01346.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.52+26976T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945286 | ||||||
| chr17:17945288
|
A | T | 126 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(123): Show | 128 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.52+26974T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945288 | ||||||
| chr17:17945290
|
A | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 130 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.52+26972T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945290 | ||||||
| chr17:17945292
|
T | A | 21 | a0001c0001t0002g0141a0001c0001t0002g0184a0001c0001t0002g0187others(18): Show | 21 | HG00609.hp1 HG01978.hp2 HG02015.hp1 others(18): Show |
intron_variant | MODIFIER | c.52+26970A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945292 | ||||||
| chr17:17945837
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.52+26425G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945837 | ||||||
| chr17:17945901
|
C | T | 1 | a0001c0001t0021g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.52+26361G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17945901 | ||||||
| chr17:17946026
|
G | A | 4 | a0001c0001t0002g0129a0001c0001t0004g0126a0001c0001t0004g0127others(1): Show | 4 | HG01934.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+26236C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946026 | ||||||
| chr17:17946136
|
C | T | 114 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(111): Show | 115 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.52+26126G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946136 | ||||||
| chr17:17946248
|
G | A | 3 | a0001c0001t0008g0174a0001c0001t0008g0175a0001c0001t0008g0176 | 3 | NA18964.hp2 NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.52+26014C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946248 | ||||||
| chr17:17946277
|
TCA | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(124): Show | 129 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.52+25983_52+25984d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946277 | ||||||
| chr17:17946357
|
C | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(124): Show | 129 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.52+25905G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946357 | ||||||
| chr17:17946461
|
C | T | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+25801G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946461 | ||||||
| chr17:17946669
|
T | C | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+25593A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946669 | ||||||
| chr17:17946685
|
T | C | 16 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(13): Show | 17 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+25577A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946685 | ||||||
| chr17:17946764
|
G | A | 15 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(12): Show | 15 | HG00609.hp1 HG01243.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.52+25498C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946764 | ||||||
| chr17:17946781
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.52+25481T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17946781 | ||||||
| chr17:17947210
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.52+25052C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17947210 | ||||||
| chr17:17947211
|
G | C | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.52+25051C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17947211 | ||||||
| chr17:17947578
|
A | C | 1 | a0001c0001t0001g0099 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.52+24684T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17947578 | ||||||
| chr17:17947848
|
C | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 130 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.52+24414G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17947848 | ||||||
| chr17:17947910
|
T | A | 7 | a0001c0001t0001g0098a0001c0001t0001g0102a0001c0001t0001g0103others(4): Show | 7 | HG02280.hp1 HG03130.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+24352A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17947910 | ||||||
| chr17:17948063
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 130 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.52+24199A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17948063 | ||||||
| chr17:17948162
|
T | A | 1 | a0001c0001t0002g0201 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.52+24100A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17948162 | ||||||
| chr17:17948253
|
G | A | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.52+24009C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17948253 | ||||||
| chr17:17948651
|
C | CAAAAAAA others(309): Show |
1 | a0001c0001t0031g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.52+23610_52+23611i others(318): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17948651 | ||||||
| chr17:17948651
|
C | CAAAAAAA others(326): Show |
1 | a0001c0001t0008g0172 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.52+23610_52+23611i others(335): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17948651 | ||||||
| chr17:17948651
|
C | CAAAAAAA others(328): Show |
1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52+23610_52+23611i others(337): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17948651 | ||||||
| chr17:17948790
|
G | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(108): Show | 112 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.52+23472C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17948790 | ||||||
| chr17:17948952
|
T | C | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+23310A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17948952 | ||||||
| chr17:17948962
|
C | G | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+23300G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17948962 | ||||||
| chr17:17949016
|
A | G | 164 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(161): Show | 168 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.52+23246T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949016 | ||||||
| chr17:17949034
|
A | T | 1 | a0001c0001t0002g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.52+23228T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949034 | ||||||
| chr17:17949132
|
G | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(127): Show | 132 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.52+23130C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949132 | ||||||
| chr17:17949175
|
G | A | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+23087C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949175 | ||||||
| chr17:17949263
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.52+22999G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949263 | ||||||
| chr17:17949381
|
G | A | 1 | a0001c0001t0002g0081 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.52+22881C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949381 | ||||||
| chr17:17949472
|
A | C | 2 | a0001c0001t0001g0034a0001c0001t0001g0052 | 2 | NA18980.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.52+22790T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949472 | ||||||
| chr17:17949617
|
T | C | 1 | a0001c0001t0001g0026 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.52+22645A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949617 | ||||||
| chr17:17949672
|
G | A | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52+22590C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949672 | ||||||
| chr17:17949693
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.52+22569C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949693 | ||||||
| chr17:17949834
|
TTCTC | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(115): Show | 119 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.52+22424_52+22427d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949834 | ||||||
| chr17:17949859
|
A | T | 1 | a0001c0001t0002g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.52+22403T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949859 | ||||||
| chr17:17949865
|
T | A | 1 | a0001c0001t0007g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.52+22397A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949865 | ||||||
| chr17:17949866
|
A | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(128): Show | 133 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.52+22396T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949866 | ||||||
| chr17:17949964
|
G | A | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+22298C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17949964 | ||||||
| chr17:17950140
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(128): Show | 133 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.52+22122A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17950140 | ||||||
| chr17:17950281
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(108): Show | 112 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.52+21981G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17950281 | ||||||
| chr17:17950409
|
T | C | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.52+21853A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17950409 | ||||||
| chr17:17950468
|
T | C | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 130 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.52+21794A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17950468 | ||||||
| chr17:17950507
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.52+21755G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17950507 | ||||||
| chr17:17950586
|
T | C | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.52+21676A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17950586 | ||||||
| chr17:17950644
|
T | C | 1 | a0001c0001t0022g0145 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.52+21618A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17950644 | ||||||
| chr17:17950693
|
G | C | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+21569C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17950693 | ||||||
| chr17:17950851
|
A | G | 8 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(5): Show | 10 | HG02129.hp2 HG02717.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+21411T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17950851 | ||||||
| chr17:17951212
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.52+21050C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17951212 | ||||||
| chr17:17951266
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.52+20996C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17951266 | ||||||
| chr17:17951381
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.52+20881G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17951381 | ||||||
| chr17:17951433
|
A | C | 1 | a0001c0001t0002g0081 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.52+20829T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17951433 | ||||||
| chr17:17951631
|
C | T | 18 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(15): Show | 18 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.52+20631G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17951631 | ||||||
| chr17:17951761
|
G | T | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+20501C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17951761 | ||||||
| chr17:17952033
|
T | C | 1 | a0001c0001t0034g0004 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.52+20229A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952033 | ||||||
| chr17:17952202
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.52+20060T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952202 | ||||||
| chr17:17952282
|
C | T | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+19980G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952282 | ||||||
| chr17:17952283
|
G | A | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.52+19979C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952283 | ||||||
| chr17:17952317
|
C | G | 1 | a0001c0002t0012g0154 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.52+19945G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952317 | ||||||
| chr17:17952376
|
C | CT | 10 | a0001c0001t0001g0166a0001c0001t0002g0182a0001c0001t0002g0183others(7): Show | 10 | HG00733.hp2 HG01358.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.52+19885dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952376
|
CT | C | 31 | a0001c0001t0002g0141a0001c0001t0002g0165a0001c0001t0002g0178others(28): Show | 31 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.52+19885delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952376
|
CTTT | C | 11 | a0001c0001t0005g0012a0001c0001t0005g0013a0001c0001t0005g0014others(8): Show | 11 | HG00609.hp1 HG02135.hp2 NA18949.hp2 others(8): Show |
intron_variant | MODIFIER | c.52+19883_52+19885d others(5): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952376
|
CTTTT | C | 6 | a0001c0001t0001g0152a0001c0001t0009g0159a0001c0001t0010g0148others(3): Show | 6 | HG01433.hp2 HG01891.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+19882_52+19885d others(6): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952376
|
CTTTTT | C | 8 | a0001c0001t0001g0229a0001c0001t0007g0158a0001c0001t0007g0160others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.52+19881_52+19885d others(7): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952376
|
CTTTTTT | C | 13 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0125others(10): Show | 15 | HG02055.hp1 HG02129.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.52+19880_52+19885d others(8): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952376
|
CTTTTTTT | C | 121 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(118): Show | 123 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.52+19879_52+19885d others(9): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952376
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0013g0007a0001c0001t0013g0008 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.52+19876_52+19885d others(12): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952376
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0169 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.52+19874_52+19885d others(14): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952376
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0002g0214 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.52+19873_52+19885d others(15): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952376 | ||||||
| chr17:17952387
|
T | C | 5 | a0001c0001t0001g0049a0001c0001t0001g0050a0001c0001t0001g0125others(2): Show | 5 | HG02559.hp2 NA18988.hp2 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+19875A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952387 | ||||||
| chr17:17952388
|
T | C | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(117): Show | 122 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.52+19874A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952388 | ||||||
| chr17:17952389
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0011g0116a0001c0001t0014g0010 | 3 | HG02896.hp2 HG03209.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.52+19873A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952389 | ||||||
| chr17:17952538
|
C | T | 33 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0001g0233others(30): Show | 35 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.52+19724G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952538 | ||||||
| chr17:17952711
|
T | A | 1 | a0001c0001t0002g0070 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.52+19551A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17952711 | ||||||
| chr17:17953016
|
A | T | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+19246T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17953016 | ||||||
| chr17:17953022
|
C | T | 1 | a0001c0001t0015g0188 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.52+19240G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17953022 | ||||||
| chr17:17953689
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+18573T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17953689 | ||||||
| chr17:17953752
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.52+18510C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17953752 | ||||||
| chr17:17953870
|
G | A | 1 | a0001c0001t0038g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52+18392C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17953870 | ||||||
| chr17:17954312
|
C | CT | 135 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(132): Show | 137 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.52+17949dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17954312 | ||||||
| chr17:17954408
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.52+17854T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17954408 | ||||||
| chr17:17954515
|
G | T | 3 | a0001c0001t0008g0174a0001c0001t0008g0175a0001c0001t0008g0176 | 3 | NA18964.hp2 NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.52+17747C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17954515 | ||||||
| chr17:17954966
|
G | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(128): Show | 133 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.52+17296C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17954966 | ||||||
| chr17:17955008
|
T | A | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+17254A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955008 | ||||||
| chr17:17955325
|
C | CT | 27 | a0001c0001t0001g0009a0001c0001t0001g0030a0001c0001t0001g0045others(24): Show | 27 | HG00558.hp1 HG01109.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.52+16936dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955325 | ||||||
| chr17:17955325
|
CT | C | 40 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0233others(37): Show | 42 | HG01070.hp1 HG01433.hp2 HG01891.hp1 others(39): Show |
intron_variant | MODIFIER | c.52+16936delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955325 | ||||||
| chr17:17955325
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0021g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.52+16926_52+16936d others(13): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955325 | ||||||
| chr17:17955325
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0035 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.52+16925_52+16936d others(14): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955325 | ||||||
| chr17:17955345
|
T | G | 4 | a0001c0001t0001g0026a0001c0001t0004g0131a0001c0001t0009g0159others(1): Show | 4 | HG01346.hp1 HG02135.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+16917A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955345 | ||||||
| chr17:17955346
|
T | G | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.52+16916A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955346 | ||||||
| chr17:17955457
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+16805T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955457 | ||||||
| chr17:17955738
|
G | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(125): Show | 130 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.52+16524C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955738 | ||||||
| chr17:17955840
|
G | C | 1 | a0001c0001t0002g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.52+16422C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955840 | ||||||
| chr17:17955874
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.52+16388C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955874 | ||||||
| chr17:17955888
|
C | T | 1 | a0001c0001t0002g0182 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.52+16374G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955888 | ||||||
| chr17:17955935
|
C | T | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+16327G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17955935 | ||||||
| chr17:17956061
|
GCAA | G | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+16198_52+16200d others(5): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956061 | ||||||
| chr17:17956078
|
G | C | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.52+16184C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956078 | ||||||
| chr17:17956079
|
A | G | 13 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0126others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.52+16183T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956079 | ||||||
| chr17:17956107
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+16155T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956107 | ||||||
| chr17:17956481
|
C | G | 1 | a0001c0001t0002g0179 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.52+15781G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956481 | ||||||
| chr17:17956608
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.52+15654C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956608 | ||||||
| chr17:17956636
|
C | T | 1 | a0001c0001t0038g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52+15626G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956636 | ||||||
| chr17:17956644
|
G | A | 1 | a0001c0001t0040g0235 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.52+15618C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956644 | ||||||
| chr17:17956660
|
C | A | 1 | a0001c0001t0004g0003 | 2 | HG02818.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.52+15602G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956660 | ||||||
| chr17:17956684
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.52+15578C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956684 | ||||||
| chr17:17956689
|
G | A | 2 | a0001c0001t0002g0217a0001c0001t0002g0218 | 2 | HG00280.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.52+15573C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956689 | ||||||
| chr17:17956703
|
A | G | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+15559T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956703 | ||||||
| chr17:17956764
|
G | A | 1 | a0001c0001t0005g0076 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.52+15498C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956764 | ||||||
| chr17:17956786
|
C | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0029a0001c0001t0001g0031others(11): Show | 14 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.52+15476G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956786 | ||||||
| chr17:17956802
|
G | A | 4 | a0001c0001t0002g0129a0001c0001t0004g0126a0001c0001t0004g0127others(1): Show | 4 | HG01934.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+15460C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956802 | ||||||
| chr17:17956817
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0037 | 2 | NA18942.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.52+15445G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956817 | ||||||
| chr17:17956822
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.52+15440G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956822 | ||||||
| chr17:17956836
|
C | T | 1 | a0001c0001t0003g0080 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.52+15426G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956836 | ||||||
| chr17:17956843
|
G | A | 16 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(13): Show | 17 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+15419C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17956843 | ||||||
| chr17:17957012
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0181 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.52+15250G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957012 | ||||||
| chr17:17957057
|
C | A | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.52+15205G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957057 | ||||||
| chr17:17957066
|
C | T | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.52+15196G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957066 | ||||||
| chr17:17957232
|
T | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(180): Show | 187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.52+15030A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957232 | ||||||
| chr17:17957485
|
T | C | 1 | a0001c0001t0007g0158 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.52+14777A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957485 | ||||||
| chr17:17957498
|
T | C | 1 | a0001c0001t0001g0229 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.52+14764A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957498 | ||||||
| chr17:17957534
|
T | C | 1 | a0001c0001t0038g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52+14728A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957534 | ||||||
| chr17:17957879
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+14383G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957879 | ||||||
| chr17:17957888
|
A | G | 1 | a0001c0001t0001g0035 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.52+14374T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957888 | ||||||
| chr17:17957965
|
C | G | 1 | a0001c0001t0037g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.52+14297G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17957965 | ||||||
| chr17:17958046
|
T | C | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(128): Show | 133 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(130): Show |
intron_variant | MODIFIER | c.52+14216A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17958046 | ||||||
| chr17:17958089
|
C | CA | 14 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(11): Show | 14 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.52+14172dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17958089 | ||||||
| chr17:17958089
|
CA | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0031a0001c0001t0001g0032others(3): Show | 6 | HG01070.hp2 HG01261.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.52+14172delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17958089 | ||||||
| chr17:17958180
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.52+14082G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17958180 | ||||||
| chr17:17958544
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.52+13718G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17958544 | ||||||
| chr17:17958555
|
C | T | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+13707G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17958555 | ||||||
| chr17:17958570
|
T | C | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.52+13692A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17958570 | ||||||
| chr17:17958835
|
C | T | 1 | a0001c0001t0004g0126 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.52+13427G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17958835 | ||||||
| chr17:17959083
|
C | T | 9 | a0001c0001t0002g0134a0001c0001t0004g0130a0001c0001t0004g0131others(6): Show | 9 | HG01884.hp2 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.52+13179G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17959083 | ||||||
| chr17:17959410
|
A | T | 1 | a0001c0001t0001g0024 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.52+12852T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17959410 | ||||||
| chr17:17959423
|
C | T | 1 | a0001c0001t0003g0079 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.52+12839G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17959423 | ||||||
| chr17:17959492
|
C | A | 2 | a0001c0001t0001g0075a0001c0001t0005g0076 | 2 | NA19068.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.52+12770G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17959492 | ||||||
| chr17:17959514
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.52+12748C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17959514 | ||||||
| chr17:17959636
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.52+12626C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17959636 | ||||||
| chr17:17959688
|
C | T | 1 | a0001c0001t0002g0179 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.52+12574G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17959688 | ||||||
| chr17:17960222
|
C | G | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+12040G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17960222 | ||||||
| chr17:17960309
|
A | G | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.52+11953T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17960309 | ||||||
| chr17:17960526
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.52+11736G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17960526 | ||||||
| chr17:17960565
|
T | C | 1 | a0001c0001t0005g0022 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.52+11697A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17960565 | ||||||
| chr17:17960619
|
T | C | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+11643A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17960619 | ||||||
| chr17:17960734
|
T | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 172 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.52+11528A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17960734 | ||||||
| chr17:17961070
|
C | T | 1 | a0001c0001t0016g0224 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.52+11192G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961070 | ||||||
| chr17:17961113
|
A | T | 3 | a0001c0001t0008g0172a0001c0001t0008g0173a0001c0001t0031g0171 | 3 | HG02145.hp2 HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.52+11149T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961113 | ||||||
| chr17:17961312
|
C | G | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+10950G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961312 | ||||||
| chr17:17961488
|
T | C | 3 | a0001c0001t0010g0149a0001c0001t0010g0150a0001c0001t0010g0151 | 3 | HG01433.hp2 HG01891.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.52+10774A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961488 | ||||||
| chr17:17961518
|
G | T | 1 | a0001c0001t0002g0141 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.52+10744C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961518 | ||||||
| chr17:17961560
|
A | G | 2 | a0001c0001t0002g0177a0001c0001t0002g0178 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.52+10702T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961560 | ||||||
| chr17:17961728
|
C | T | 5 | a0001c0001t0001g0152a0001c0001t0010g0148a0001c0001t0010g0149others(2): Show | 5 | HG01433.hp2 HG01891.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+10534G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961728 | ||||||
| chr17:17961729
|
G | A | 2 | a0001c0001t0013g0007a0001c0001t0013g0008 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.52+10533C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961729 | ||||||
| chr17:17961871
|
C | CA | 117 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(114): Show | 118 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.52+10390dupT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961871 | ||||||
| chr17:17961871
|
C | CAA | 16 | a0001c0001t0002g0134a0001c0001t0003g0077a0001c0001t0004g0003others(13): Show | 17 | HG00597.hp1 HG01243.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.52+10389_52+10390d others(4): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961871 | ||||||
| chr17:17961943
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(109): Show | 113 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.52+10319G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17961943 | ||||||
| chr17:17962232
|
CA | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+10029delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962232 | ||||||
| chr17:17962324
|
A | AT | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+9937dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962324 | ||||||
| chr17:17962324
|
A | T | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.52+9938T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962324 | ||||||
| chr17:17962324
|
AT | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(109): Show | 113 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.52+9937delA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962324 | ||||||
| chr17:17962352
|
GCT | G | 5 | a0001c0001t0009g0220a0001c0001t0009g0221a0001c0001t0009g0223others(2): Show | 5 | HG01070.hp1 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.52+9908_52+9909del others(2): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962352 | ||||||
| chr17:17962438
|
G | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+9824C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962438 | ||||||
| chr17:17962528
|
G | A | 13 | a0001c0001t0005g0011a0001c0001t0005g0012a0001c0001t0005g0013others(10): Show | 13 | HG00609.hp1 HG02056.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.52+9734C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962528 | ||||||
| chr17:17962534
|
G | A | 1 | a0001c0001t0002g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.52+9728C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962534 | ||||||
| chr17:17962596
|
G | A | 1 | a0001c0001t0002g0093 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.52+9666C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962596 | ||||||
| chr17:17962757
|
G | A | 15 | a0001c0001t0001g0229a0001c0001t0001g0233a0001c0001t0006g0001others(12): Show | 17 | HG02109.hp1 HG02129.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.52+9505C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962757 | ||||||
| chr17:17962876
|
G | A | 24 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0118others(21): Show | 24 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.52+9386C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962876 | ||||||
| chr17:17962956
|
G | A | 1 | a0001c0001t0009g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.52+9306C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17962956 | ||||||
| chr17:17963139
|
G | A | 1 | a0001c0001t0016g0224 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.52+9123C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17963139 | ||||||
| chr17:17963456
|
G | C | 1 | a0001c0001t0002g0093 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.52+8806C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17963456 | ||||||
| chr17:17963528
|
T | C | 1 | a0001c0001t0027g0120 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.52+8734A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17963528 | ||||||
| chr17:17963535
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.52+8727C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17963535 | ||||||
| chr17:17963583
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+8679T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17963583 | ||||||
| chr17:17963724
|
G | T | 1 | a0001c0001t0001g0229 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.52+8538C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17963724 | ||||||
| chr17:17964162
|
C | T | 2 | a0001c0001t0013g0007a0001c0001t0013g0008 | 2 | HG02970.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.52+8100G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17964162 | ||||||
| chr17:17964166
|
T | C | 1 | a0001c0001t0008g0173 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.52+8096A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17964166 | ||||||
| chr17:17964167
|
C | G | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.52+8095G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17964167 | ||||||
| chr17:17964300
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+7962T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17964300 | ||||||
| chr17:17964516
|
C | T | 3 | a0001c0001t0008g0174a0001c0001t0008g0175a0001c0001t0008g0176 | 3 | NA18964.hp2 NA18984.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.52+7746G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17964516 | ||||||
| chr17:17964551
|
T | C | 1 | a0001c0001t0002g0225 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.52+7711A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17964551 | ||||||
| chr17:17964690
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.52+7572A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17964690 | ||||||
| chr17:17964818
|
C | T | 1 | a0001c0001t0038g0132 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.52+7444G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17964818 | ||||||
| chr17:17964916
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.52+7346G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17964916 | ||||||
| chr17:17965042
|
T | C | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.52+7220A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17965042 | ||||||
| chr17:17965400
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.52+6862G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17965400 | ||||||
| chr17:17965457
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01884.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.52+6805G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17965457 | ||||||
| chr17:17965579
|
A | G | 1 | a0001c0001t0036g0006 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.52+6683T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17965579 | ||||||
| chr17:17965668
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.52+6594G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17965668 | ||||||
| chr17:17965797
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+6465A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17965797 | ||||||
| chr17:17966053
|
G | A | 33 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0001g0233others(30): Show | 35 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.52+6209C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17966053 | ||||||
| chr17:17966077
|
C | T | 7 | a0001c0001t0001g0166a0001c0001t0002g0164a0001c0001t0002g0165others(4): Show | 7 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.52+6185G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17966077 | ||||||
| chr17:17966203
|
C | T | 20 | a0001c0001t0001g0144a0001c0001t0002g0081a0001c0001t0002g0093others(17): Show | 20 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.52+6059G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17966203 | ||||||
| chr17:17966328
|
A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.52+5934T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17966328 | ||||||
| chr17:17966355
|
ACT | A | 5 | a0001c0001t0007g0160a0001c0001t0007g0161a0001c0001t0007g0162others(2): Show | 5 | HG02109.hp1 HG02486.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.52+5905_52+5906del others(2): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17966355 | ||||||
| chr17:17967080
|
T | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+5182A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17967080 | ||||||
| chr17:17967361
|
A | G | 2 | a0001c0001t0004g0130a0001c0001t0004g0131 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.52+4901T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17967361 | ||||||
| chr17:17967464
|
A | G | 6 | a0001c0001t0001g0166a0001c0001t0002g0164a0001c0001t0002g0165others(3): Show | 6 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.52+4798T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17967464 | ||||||
| chr17:17967660
|
G | T | 62 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(59): Show | 63 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.52+4602C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17967660 | ||||||
| chr17:17967754
|
C | T | 112 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(109): Show | 113 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.52+4508G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17967754 | ||||||
| chr17:17967761
|
C | T | 4 | a0001c0001t0002g0129a0001c0001t0004g0126a0001c0001t0004g0127others(1): Show | 4 | HG01934.hp1 HG02257.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.52+4501G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17967761 | ||||||
| chr17:17968298
|
A | G | 2 | a0001c0002t0012g0153a0001c0002t0012g0154 | 2 | HG01243.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.52+3964T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17968298 | ||||||
| chr17:17968528
|
G | A | 1 | a0001c0001t0017g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.52+3734C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17968528 | ||||||
| chr17:17968556
|
T | C | 3 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0124 | 3 | HG01256.hp1 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.52+3706A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17968556 | ||||||
| chr17:17968570
|
C | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+3692G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17968570 | ||||||
| chr17:17968601
|
G | A | 33 | a0001c0001t0001g0152a0001c0001t0001g0229a0001c0001t0001g0233others(30): Show | 35 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.52+3661C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17968601 | ||||||
| chr17:17968647
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.52+3615C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17968647 | ||||||
| chr17:17968664
|
CA | C | 153 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(150): Show | 157 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(154): Show |
intron_variant | MODIFIER | c.52+3597delT | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17968664 | ||||||
| chr17:17968929
|
C | G | 1 | a0001c0001t0001g0028 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.52+3333G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17968929 | ||||||
| chr17:17969014
|
C | T | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.52+3248G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969014 | ||||||
| chr17:17969057
|
C | CT | 10 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0152others(7): Show | 10 | HG01433.hp2 HG01891.hp1 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.52+3204dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969057 | ||||||
| chr17:17969218
|
G | A | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+3044C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969218 | ||||||
| chr17:17969223
|
A | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01346.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.52+3039T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969223 | ||||||
| chr17:17969234
|
A | G | 1 | a0001c0001t0005g0011 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.52+3028T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969234 | ||||||
| chr17:17969275
|
T | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(126): Show | 131 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.52+2987A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969275 | ||||||
| chr17:17969434
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.52+2828T>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969434 | ||||||
| chr17:17969514
|
G | A | 17 | a0001c0001t0002g0129a0001c0001t0002g0134a0001c0001t0004g0003others(14): Show | 18 | HG01884.hp2 HG01891.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.52+2748C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969514 | ||||||
| chr17:17969651
|
C | T | 1 | a0001c0001t0037g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.52+2611G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969651 | ||||||
| chr17:17969859
|
T | TTC | 12 | a0001c0001t0001g0144a0001c0001t0001g0229a0001c0001t0001g0233others(9): Show | 14 | HG00438.hp1 HG00597.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.52+2401_52+2402dup others(2): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969859 | ||||||
| chr17:17969859
|
TTC | T | 127 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0009others(124): Show | 129 | HG00099.hp1 HG00280.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.52+2401_52+2402del others(2): Show |
TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969859 | ||||||
| chr17:17969951
|
C | A | 1 | a0001c0001t0040g0235 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.52+2311G>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17969951 | ||||||
| chr17:17970193
|
T | A | 1 | a0001c0001t0009g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52+2069A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970193 | ||||||
| chr17:17970219
|
T | G | 1 | a0001c0001t0009g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52+2043A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970219 | ||||||
| chr17:17970226
|
C | CT | 22 | a0001c0001t0001g0152a0001c0001t0005g0011a0001c0001t0005g0012others(19): Show | 22 | HG00609.hp1 HG01433.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.52+2035dupA | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970226 | ||||||
| chr17:17970365
|
C | T | 4 | a0001c0001t0010g0148a0001c0001t0010g0149a0001c0001t0010g0150others(1): Show | 4 | HG01433.hp2 HG01891.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+1897G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970365 | ||||||
| chr17:17970637
|
G | A | 1 | a0001c0001t0002g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.52+1625C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970637 | ||||||
| chr17:17970685
|
C | T | 1 | a0001c0001t0014g0010 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.52+1577G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970685 | ||||||
| chr17:17970718
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.52+1544T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970718 | ||||||
| chr17:17970828
|
T | A | 1 | a0001c0001t0009g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52+1434A>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970828 | ||||||
| chr17:17970831
|
G | A | 1 | a0001c0001t0009g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52+1431C>T | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970831 | ||||||
| chr17:17970846
|
C | G | 4 | a0001c0001t0013g0007a0001c0001t0013g0008a0001c0001t0036g0006others(1): Show | 4 | HG02258.hp1 HG02970.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.52+1416G>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970846 | ||||||
| chr17:17970849
|
A | T | 1 | a0001c0001t0009g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52+1413T>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970849 | ||||||
| chr17:17970854
|
C | T | 1 | a0001c0001t0009g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52+1408G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970854 | ||||||
| chr17:17970855
|
T | C | 1 | a0001c0001t0009g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52+1407A>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970855 | ||||||
| chr17:17970856
|
G | T | 1 | a0001c0001t0009g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52+1406C>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17970856 | ||||||
| chr17:17971084
|
G | C | 1 | a0001c0001t0037g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.52+1178C>G | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17971084 | ||||||
| chr17:17971172
|
C | T | 144 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0024others(141): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.52+1090G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17971172 | ||||||
| chr17:17971583
|
T | G | 1 | a0001c0001t0009g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.52+679A>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17971583 | ||||||
| chr17:17972028
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0024others(141): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.52+234T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17972028 | ||||||
| chr17:17972093
|
A | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0024others(141): Show | 146 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.52+169T>C | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17972093 | ||||||
| chr17:17972114
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.52+148G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17972114 | ||||||
| chr17:17972175
|
C | T | 1 | a0001c0001t0034g0004 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.52+87G>A | TOM1L2 | ENSG00000175662.18 | transcript | ENST00000379504.8 | protein_coding | 1/14 | chr17 | 17972175 |